Appendix — Azima v. Florida Department of Professional Regulation

Supreme Court brief1986

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| BILED

| APR 2S 1986

CASE NO. SpANIOL, JR.

HOSP ERK

IN THE

SUPREME COURT OF THE UNITED STATES

OCTOBER TERM, 1985

ALI A. AZIMA, M.D., PETITIONER,

v.

FLORIDA DEPARTMENT OF

PROFESSIONAL REGULATION,

BOARD OF MEDICAL EXAMINERS,

RESPONDENT.

APPENDIX TO THE

PETITION FOR WRIT OF CERTIORARI

TO THE DISTRICT COURT OF APPEAL

FOR THE FIRST DISTRICT OF FLORIDA

BERNARD H. DEMPSEY, JR., ESQ.

(Counsel of Record)

FERDINAND M. ROMANO, ESQ.

RICHARD LEE BARRETT, ESQ.

DEMPSEY & GOLDSMITH, P.A.

Suite 500, Day Building

605 East Robinson Street

Post Office Box 1980

Orlando, Florida 32802

(305) 422-5166

Attorneys for Petitioner,

AL] A. AZIMA, M.D.

CASE NO.

IN THE

SUPREME COURT OF THE UNITED STATES

OCTOBER TERM, 1985

ALI A. AZIMA, M.D., PETITIONER,

V.

FLORIDA DEPARTMENT OF

PILCOFESSIONAL REGULATION,

BOARD OF MEDICAL EXAMINERS,

RESPONDENT.

APPENDIX TO THE

PETITION FOR WRIT OF CERTIORARI

TO THE DISTRICT COURT OF APPEAL

FOR THE FIRST DISTRICT OF FLORIDA

BERNARD H. DEMPSEY, JR., ESQ.

(Counsel of Record)

FERDINAND M. ROMANO, ESQ.

RICHARD LEE BARRETT, ESQ.

DEMPSEY & GOLDSMITH, P.A.

Suite 500, Day Building

605 East Robinson Street

Post Office Box 1980

Orlando, Florida 32802

(305) 422-5166

Attorneys for Petitioner,

ALI A. AZIMA, M.D.

TABLE OF CONTENTS

APPENDIX

SECTION I.

Opinion of the District

Court of Appeal, First Dis-

trict, State of Florida.

SECTION II.

Final Ore2r of the Board of

Medical Examiners, State of

Florida.

SECTION III.

Text of Statutes, Regulations

and Constitutional Provisions

Which the Case Involves.

§390.001(7), Fla. Stat.,

Termination of Pregnancies.

§458.331, Fla. Stat., Grounds

for Disciplinary Action;

Action by the Board.

§768.45, Fla. Stat., Medical

Negligence; Standards of

Recovery.

Florida Administrative Pro-

cedure Act, Chapter 120,

Fla. Stat.

Sheeset, Fla. Stat.,

Decisisions Which Affect

Substantial Interests.

§120.68, Fla. Stat.,

Judicial Review.

Fla. Admin. Code,

Rule 10D-72.16.

TABLE OF CONTENTS (Cont'd. )

U.S. Const., Amend. XIV, §l

Citizenship; Privileges and

Immunities; Due Process; Equal

Protection; Apportionment of

Representation; Disqualification

of Officers; Public Debt; En-

forcement.

SECTION IV.

Portion of Record Demonstrating

That Both Federal Questions

Were Timely and Properly Raised.

SECTION V.

Summary of the Case.

1.

Y

3.

The Petitioner.

The Petitioner's Medical

Procedures.

Case History and Testimony

Relating to Holli Schmidt.

Case History and Testimony

on Christine Sellers Kuchar.

Case History and Testimony

Relating to Darlene Baker.

Conclusion.

A-ii-

A-116

A-124

APPENDIX -- SECTION I

I. Opinion of the District Court

of Appeal, First District,

State of Florida.

IN THE DISTRICT COURT

OF APPEAL

FIRST DISTRICT, STATE

OF FLORIDA

ALI A. AZIMA, M.D., NOT FINAL UNTIL TIME

EXPIRES TO FILE MO-

Appellant, TION FOR REHEARING

AND DISPOSITION

vs. THEREOF IF FILED.

DEPARTMENT OF PROFES- CASE NO. BE-368

SIONAL REGULATION,

Appellee.

- f

Opinion filed July 15, 1985.

Appeal from an order of the Department of

Professional Regulation, Board of Medical

Examiners.

Bernard H. Dempsey, Jr. and Richard Lee

Barrett, Orlando, for appellant.

J. Riley Davis, Tallahassee, for appellee.

BARFIELD, J.

Dr. Azima appeals the order of the

Department of Professional Regulation (Depart-

ment) which suspended his license for failure

"to practice medicine with that level of

care, Skill, and treatment which is recog-

nized by a reasonably prudent similar physi-

cian as being acceptable under similar condi-

tions and circumstances." See Fla. Stat.

section 458.331(1)(t)(1981). Appellant con-

tends that the Department's order is not sup-

ported by competent and substantial evidence.

We disagree and affirm,

Dr. Azima operated a clinic in the

Fort Myers area which provided birth control

services and performed pregnancy termination

procedures. The hearing officer found that

Dr. Azima provided substandard care to two of

his patients and the Department accepted her

findings of fact and conclusions of law.

Appellant asserts that the Department erred

because the evidence against him was all in

the form of expert testimony of physicians

who were in direct competition with him.1l

It is his position that under the rationale

of Robinson v. Florida Board of Dentistry,

447 So.2d 930 (Fla. 3d DCA 1984), the compet-

ing physicians' testimony did not provide a

sufficient evidentiary basis to support the

Department's order.

In Robinson, the district court

reversed an order which imposed sanctions

against a dentist for alleged substandard

treatment of a patient. The expert testimony

against Dr. Robinson consisted solely of the

lfhere were six physicians performing

pregnancy terminations outside of the

hospital setting in Fort Myers at the time of

the hearing. Four of appellant's five

competitors testified against him.

opinions of Dr. Beard, the dentist who suc-

ceeded Dr. Robinson in treating the patient.

The court found that where the successor had

an interest in seeing his recommended treat-

ment recognized as "correct" and had a conti-

nuing financial interest in the patient, his

testimony, without more, could not support a

license suspension.

We find that the facts before us dif-

fer from those in Robinson in several signifi-

cant respects. First, four different local

physicians testified against the appellant.

Thus, their testimony presented a much

broader cross-section of the local medical

community than was made available in

Robinson. 2 Moreover, the “interests" of

the testifying physicians here were different

-

2we reject appellant's simplistic argument

that because three of the four witnesses were

partners, their similar views should only be

regarded as a single opinion.

from those present in Robinson. Unlike Dr.

Beard, these physicians did not recommend

totally different courses of treatment but

instead testified that Dr. Azima's care was

substandard by his failure to perform or have

performed certain tests to safeguard his

patients' health. 3 Additionally, there

was no suggestion that any of the physicians

were continuing to treat these patients and,

accordingly, there is no showing of continued

Financial interests in the patients on the

part of the witnesses.

Based on the above, we hold Robinson

inapplicable to the instant case. As the

order of the Department of Professional Regu-

3specifically, appellant failed to use a blood

test to determine pregnancy before inserting

an IUD in a woman who exhibited symptoms of

pregnancy; and failed to determine a woman's

Rh factor and hemoglobin level at the time of

a termination procedure and failed to take

appropriate steps to recognize that he had

not, in fact, terminated the pregnancy.

lation is supported by competent and substan-

tial evidence, it is AFFIRMED.

BOOTH, Chief Judge, and WIGGINTON, J.,

CONCUR.

APPENDIX -- SECTION II

II. Final Order o. the Board of

Medical Examiners, State of

Florida.

BEFORE THE BOARD OF MEDICAL EXAMINERS

DEPARTMENT OF PRO- DPR CASE NOS.

FESSIONAL REGULATION, 0034574, 0014227,

0014657, 0014312,

Petitioner, 0018786

vs.

DOAH CASE NO.

ALI A. AZIMA, M.D., 83-1205, 83-2589,

Respondent. LICENSE NO.

/ ME 20485

FINAL ORDER OF THE

BOARD OF MEDICAL EXAMINERS

This cause came before the Board of

Medical Examiners (Board) pursuant to Section

120.57(1)(b)(9), Florida Statutes, on Decem-

ber 1, 1984, in Miami, Florida for the pur-

pose of considering the hearing officer's

Recommended Order (a copy of which is attach-

ed hereto) in the above-styled cause. Peti-

tioner, Department of Professional Regula-

tion, was represented by William M. Furlow,

Esquire; Respondent was present and repre-

sented by Bernard H. Dempsey, Jr., Esquire

and Richard Lee Barrett.

Upon review of the recommended order,

the argument of the parties, and after a re-

view of the complete record in this case, the

Board makes the following findings and conclu-

sions.

FINDINGS OF FACT

is The exceptions to the recommend-

ed Order filed by Respondent are rejected in

that they would require the Board to reweigh

the evidence presented. This the Board may

not do. Wagner v. Department of Professional

Regulation, 405 So.2d 471. In addition, the

Board finds no reason to believe the hearing

‘otficer failed to consider any of the evi-

dence presented.

a's The hearing officer's findings

of fact are approved and adopted in toto anda

are incorporated by reference herein.

Je There is competent substantial

evidence in the record to support the Board's

findings of fact.

CONCLUSIONS OF LAW

a‘ The Board has jurisdiction of

this matter pursuant to the provision of Sec-

tion 120.57(2), Florida Statutes, and Chapter

458, Fiorida Statutes.

Ss The hearing officer's conclu-

sions of law are approved and adopted in toto

and are incorporated by reference herein.

3% There is competent substantial

evidence in the record to support the Board's

conclusions of law.

DISPOSITION

Upon a review of the complete record

in this case, the Board determines that the

penalty recommended by the hearing officer be

altered. WHEREFORE,

IT IS HEREBY ORDERED AND ADJUDGED

that:

Le Respondent's license to practice

medicine in Florida shall be suspended for a

period of one year, with the specific provi-

sion that in six months Respondent may re-

quest that the Board stay the second six

months of the suspension.

a Upon the termination or stay of

the suspension, Respondent's license to prac-

tice medicine in Florida shall be placed on

probation for a period of three years, sub-

ject to the term and condition that Respon-

dent make semi-annual appearances before the

Board.

36 During the periods of suspension

and probation, Respondent shall earn fifty

(50) hours of Category 1 continuing medical

education annually. This Order takes effect

upon filing.

Pursuant to Section 120.59, Florida

Statutes, the parties are hereby notified

that they may appeal this final order by fil-

ing one copy of a notice of appeal with the

clerk of the agency and by filing the filing

fee and one copy of a notice of appeal with

the District Court of Appeal within thirty

days of the date this order is filed, as pro-

vided in Chapter 120, Florida Statutes, and

the Florida Rules of Appellate Procedure.

DONE AND ORDERED this me day of

January, 1985.

BOARD OF MEDICAL EXAMINERS

Richard J. Feinstein, M.D.

CHAIRMAN :

APPENDIX -- SECTION III.

III. Text of Statutes, 1 Regula-

tions and Constitutional Pro-

visions Which the Case Involve:

§390.001, Fla. Stat., Termination of preg

nancies

* * *

(7) Fetal remains.--Fetal remain:

shall be disposed of in a sanitary and appro

priate manner and in accordance with standar:

health practices, as provided by rule of th

Department of Health and Rehabilitative Servi

ces. Failure to dispose of fetal remains is

accordance with department rules is a misde

meanor of the second degree, punishable a:

provided in s. 775.082, s. 775.083, or s

775.084.

lpfext added to statutes subsequent to January

FOOTNOTE CONTINUED ON NEXT PAGE,

betel

Vl

§458.331, Fla. Stat., Grounds for discipli-

nary action; action by the board

(1) The following acts shail consti-

tute grounds for which the disciplinary

actions specified in subsection (2) may be

taken:

(a) Attempting to obtain, obtaining,

or renewing a license to practice medicine by

bribery, by fraudulent misrepresentations, or

through an error of the department or the

board.

(b) Having a license to practice

medicine revoked, suspended, or otherwise

acted against, including the denial of licen-

16, 1985, when the Board of Medical Examiners

rendered its Final Order is underscored.

Unless otherwise noted (see note 2), there

were no deletions or other revisions to the

Statutes between January 16, 1985, and the

filing date of this Petition for Writ of

Certiorari.

sure, by the licensing authority of anothe

state, territory, Or country.

(c) Being convicted or found guilty

regardless of adjudication, of a crime in an

jurisdiction which directly relates to th

practice of medicine or to the ability t

practice medicine. Any plea of nolo conten

dere shall be considered a conviction fo

purposes of this chapter.

(d) False, deceptive, or misleadin

advertising.

(e) Advertising, practicing, o

attempting to practice under a name othe

than one's own.

(f£) Failing to report to the depart

ment any person whom the licensee knows is i

violation of this chapter or of the rules o

the department or the board. However, if th

licensee verifies that the person is activel

participating in a board-approved program for

the treatment of a physical or mental condi-

tion, he is required only to report such per-

son to an impaired professional consultant.

(g) Aiding, assisting, procuring, or

advising any unlicensed person to practice

medicine contrary to this chapter or to a

rule of the department or the board.

(h) Failing to perform any statutory

or legal obligation placed upon a licensed

physician.

(i) Making or filing a report which

the licensee knows to be false, intentionally

or negligently failing to file a report or

record required by state or federal law, will-

fully impeding or obstructing such filing or

inducing another person to do so. Such

reports or records shall include only those

which are signed in the capacity as a

licensed physician.

(3) Paying or receiving any commis-

sion, bonus, kickback, or rebate, or engaging

in any split~-fee arrangement in any form what-

soever with a physician, organization,

agency, Or person, either directly or in-

directly, for patients referred to providers

of health care goods and services, including,

but not limited to, hospitals, nursing homes,

clinical laboratories, ambulatory surgical

centers, Or pharmacies. The provisions of

this paragraph shall not be construed to pre-

vent a physician from receiving a fee for

professional consultation services.

(k) Exercising influence within a

patient-physician relationship for purposes

of engaging a patient in sexual activity. A

patient shall be presumed to be incapable of

giving free, full, and informed consent to

sexual activity with his or her physician.

(1) Making deceptive, untrue, or

fraudulent representations in the practice of

medicine or employing a trick or scheme in

the practice of medicine when such scheme or

trick fails to conform to the generally pre-

vailing standards of treatment in the medical

community.

(m) Soliciting patients, either per-

sonally or through an agent, through the use

of fraud, intimidation, undue influence, or a

form of overreaching or vexatious conduct. A

solicitation is any communication which

directly or implicitly requests an immediate

Oral response from the recipient.

(n) Failing to keep written medical

records justifying the course of treatment of

the patient, including, but not limited to,

patient histories, examination results, an

test results.

(oOo) Exercising influence on th

patient or client ii such a Manner as t

exploit the patient or client for financiée

gain of the licensee or of a third part

which shall include, but not be limited tc

the promoting or selling of services, goods

appliances, or drugs and the promoting c

advertising on any prescription form of

community pharmacy unless the form shall a's

state "This prescription may be filied at an

pharmacy of your choice."

(p) Performing professional service

which have not been duly authorized by th

patient or client, or his legal representa

tive, except as provided ins. 743.064

s. 768.13, or s. 768.46.

-

(q) Prescribing, dispensing, admini-

stering, mixing, or otherwise preparing a

legend drug, including any controlled sub-

stance, Other than in the course of the physi-

cian's professional practice. For the pur-

poses of this paragraph, it shall be legally

presumed that prescribing, dispensing, admin-

istering, mixing, or otherwise preparing

legend drugs, including all controlled sub-

Stances, inappropriately or in excessive or

inappropriate guantities is not in the best

interest of the patient and is not in the

course of the physician's professional prac-

tice, without regard to his intent.

(r) Prescribing, dispensing, or

administering any medicinal drug appearing on

any schedule set forth in chapter 893 by the

physician to himself, except one prescribed,

dispensed, or administered to the physician

by another practitioner authorized to pre-

scribe,\ dispense, or administer medicinal

drugs.

(s) Being unable to practice medi-

cine with reasonable skill and safety to

patients by reason of illness or use of

alcohol, drugs, narcotics, chemicals, or any

other type of material or as a result of any

mental or physical condition. In enforcing

this paragraph, the department shall have,

upon probable cause, authority to compel a

physician to submit to a mental or physical

examination by physicians designated by the

department. Failure of a physician to submit

to such examination when so directed shall

constitute an admission of the allegations

against him, unless the failure was due to

circumstances beyond his control, consequent

upon which a default and final order may be

A-20

entered without the taking of testimony or

presentation of evidence. A physician

affected under this paragraph shall at reason-

able intervals be afforded an opportunity to

demonstrate that he can resume the competent

practice of medicine with reasonable skill

and safety to patients. In any proceeding

under this paragraph, neither the record of

proceedings nor the order entered by the

board shall be used against a physician in

any other proceeding.

(t) Gross or repeated malpractice

or the failure to practice medicine with that

level of care, skill, and treatment which is

recognized by a reasonably prudent similar

physician as being acceptable under similar

conditions and circumstances. The board

Shall give great weight to the provisions of

Ss. 768.45 when enforcing this paragraph. As

used in this paragraph, “repeated malprac-

tice" includes, but js not limited to, three

Or more claims for medical malpractice within

the previous 5-year period resulting in indem-

nities being paid.in excess of $10,000 each

to the claimant in a judgment or settlement

and which incidents involved negligent con-

duct by the physician. As _ used in this para-

graph, “gross malpractice" or "the failure to

practice medicine with that level of care,

skill, and treatment which is recognized by a

reasonably prudent similar physician as being

acceptable under similar conditions and cir-

cumstances," shall not be construed so as to

require more than one instance, event, or

act.

(u) Performing any procedure or pre-

scribing any therapy which, by the prevailing

Standards of medical practice in the com-

munity, would constitute experimentation on a

human subject, without first obtaining full,

informed, and written consent.

(v) Practicing or offering to prac-

tice beyond the scope permitted by law or

accepting and performing professional respon-

sibilities which the licensee knows or has

reason to know that he is not competent to

perform.

(w) Delegating professional respon-

sibilities to a person when the licensee dele-

gating such responsibilities knows or has

reason to know that such person is net quali-

fied by training, experience, or licensure to

perform them.

(x) Violating any provision of this

chapter, a rule of the board or department,

Or a lawful order of the board or department

previously entered in a disciplinary hearing

or failing to comply with a lawfully issued

subpoena of the department.

(y) Conspiring with another licensee

Or with any other person to commit an act, or

committing an act, which would tend to

coerce, intimidate, or preclude another

licensee from lawfully advertising his ser-

vices.

(z) Procuring, or aiding or abetting

in the procuring of, an unlawful termination

of pregnancy.

(aa) Presigning blank prescription

forms.

(bb) Prescribing any medicinal drug

appearing on schedule II in chapter 893 by

the physician for office use.

(cc) Prescribing, ordering, dispens-

ing, administering, supplying, selling, or

giving any drug which is an amphetamine or

sympathomimetic amine drug or a compound

designated as a Schedule II controlled sub-

stance, pursuant to chapter 893, to or for

any person except for:,

Ba The treatment of narcolepsy;

hyperkinesis; behavioral syndrome in children

characterized by the developmentally inappro-

priate symptoms of moderate to severe dis-

tractability, short attention span, hyper-

activity, emotional lability, and impul-

Sivity; or drug-induced brain dysfunction; or

Zs The differential diagnostic

psychiatric evaluation of depression or the

treatment of depression shown to be refrac-

tory to other therapeutic modalities; or

3. . The clinical investigation of

the effects of such drugs or compounds when

an investigative protocol therefor is submit-

ted to, reviewed, and approved by the board

before such investigation is begun.

(dd) Failing to supervise adequately.

the activities of those physician's assis-

tants, emergency medical technicians, or

advanced registered nurse practitioners act-

ing under the supervision of the physician.

(ee) Prescribing, ordering, dispens-

ing, administering, supplying, selling, or

giving growth hormones, testosterone or its

analogs, human chorionic gonadotropin (HCG),

or other hormones for the purpose of muscle

building or to enhance athletic performance.

For the purposes of this subsection, the term

"muscle building" does not include the treat-

ment of injured muscle. A prescription writ-

ten for the drug products listed above may be

dispensed by the pharmacist with the presump-

tion that the prescription is for legitimate

medical use.

(2) When the board finds any person

guilty of any of the grounds set forth in

subsection (1), it may enter an order impos-

ing one or more of the following penalties:

(a) Refusal to certify to the depart-

ment an application for licensure.

(b) Revocation or suspension of a

license.

(c) Restriction of practice.

(d) Imposition of an administrative

fine not to exceed $1,000 for each count or

separate offense.

(e) Issuance of a reprimand.

(f£) Placement of the physician on

probation for a period of time and subject to

such conditions as the board may specify,

including, but not limited to, requiring the

physician to submit to treatment, to attend

continuing education courses, to submit to

reexamination, or to work under the super-

vision of another physician.

(3) the board shall not reinstate

the license of a physician, or cause a

license to be issued to a person it has

deemed unqualified, until such time as it is

satisfied that he has complied with all the

terms and conditions set forth in the final

order and that such person is capable of safe-

ly engaging in the practice of medicine.

(4) The board shall by rule estab-

lish guidelines for the disposition of dis-

ciplinary cases involving specific types of

violations. Such guidelines may include mini-

mum and maximum fines, periods of supervision

Or probation, or conditions of probation or

reissuance of a license.

(5) Upon the department's receipt

from the Department of Insurance of the name

of a physician having three or more claims

with indemnities exceeding $10,000 each with-

in the previous, 5-year period, including

reports for the 3-year period preceding the

effective date of this act, the department

shall investigate the occurrences upon which

the claims were based and determine if action

by the department against the physician is

warranted.

(6) Upon the department's receipt

from the Department of Health and Rehabilita-

tive Services pursuant to s. 395.041 of the

name Of a physician whose conduct may consti-

tute grounds for disciplinary action by the

department, the department shall investigate

the occurrences upon which the report was

based and determine if action by the

department against the physician is

warranted.

§768.45, Fla. Stat., Medical negligence;

standards of recovery. “

(1) In any action for recovery of

2Effective October 1, 1985, §768.45, Fla.

Stat., was revised as follows: subsection

(1) was rewritten; the last sentence of sub-

section (2)(b) was added; subsection

(2)(c)(2) was rewritten to substitute refer-

ence to “prevailing professional standard"

for “accepted standard" of care in subsec-

tions (3)(a) and (4) and subsection (5) was

added. Prior to the 1985 amendment, subsec-

tions (1) and (2)(c) provided:

(1) In any action for recov-

ery Of damages based on the

death or personal injury of

any person in which it is

alleged that such death or

injury resulted from the neg-

ligence of a health care pro-

vider as defined in s. 768.50

(2)(b), the claimant shall

have the burden of proving by

the greater weight of evi-

dence that the alleged ac-

tions of the health care pro-

vider represented a breach of

the accepted standard of care

for that health care provider.

The accepted standard of care

for a given health care pro-

vider shall be that level of

FOOTNOTE CONTINUED ON NEXT PAGE,

damages based on the death or personal injury

of any person in which it is alleged that

such death or injury resulted from the negli-

gence of a health care provider as defined in

s. 768.50(2)(b), the claimant shall have the

burden of proving by the greater weight of

care, skill, and treatment

which is recognized by a rea-

sonably prudent similar

health care provider as being

acceptable under similar con-

ditions and circumstances.

(2)(c) The purpose of this subsec-

tion is to establish a relative stan-

dard of care for various categories

and classifications of health care

providers. Any health care provider

may testify as an expert in any ac-

tion if he:

Ae Is a "Similar health care

provider" pursuant to paragraph (a)

or (b); or,

as Is not a Similar health

care provider pursuant to paragraph

(a) or (b) but, to the satisfaction

of the court, possesses sufficient

training, experience, and knowledge

to provide such expert testimony as

to the acceptable standard of care in

a given cause.

evidence that the alleged actions of the

health care pruvider represented a breach of

the prevailing professional standard of care

for that health care provider. The prevail-

ing professional standard of care for a given

health care provider shall be that level of

care, Skill, and treatment which, in light of

all relevant surrounding circumstances, is

recognized as acceptable and appropriate by

reasonably prudent similar health care pro-

viders.

(2) (a) If the health care provider

whose negligence is claimed to have created

the cause of action is not certified by the

appropriate American board as being a special-

ist, is not trained and experienced in a medi-

cal specialty, or does not hold himself out

as a specialist, a "Similar health care

provider" is one who:

he Is licensed by the appropriate

regulatory agency of this state;

r Is trained and experienced in

the same discipline or school of practice;

and

: Practices in the same or similar

medical community.

(b) If the health care provider

whose negligence is claimed to have created

the cause of action is certified by the appro-

priate American board as a specialist, is

trained and experienced in a medical special-

ty, or holds himself out as a specialist, a

"similar health care provider" is one who:

+ Is trained and experienced in

the same specialty; and

ae Is certified by the appropriate

American board in the same specialty. How-

ever, if any health care provider described

in this paragraph is providing treatment or

diagnosis for a condition which is not within

his specialty, a specialist trained in the

treatment or diagnosis for that condition

shall be considered a “Similar health care

provider."

(c) The purpose of this subsection

is to establish a relative standard of care

for various categories and classifications of

health care providers. Any health care pro-

vider may testify as an expert in any action

if he:

as Is a Similar health care pro-

vider pursuant to paragraph (a) or paragraph

(b); or

Se Is not a similar health care

provider pursuant to paragraph (a) or para-

graph (b) but, to the satisfaction of the

court, possesses sufficient training, experi-

ence, and knowledge as a resuit of practice

or teaching in the specialty of the defendant

Or practice or teaching in a related field of

medicine, so as to be able to provide such

expert testimony as to the prevailing profes-

sional standard of care in a given field of

medicine. Such training, experience, or

knowledge must be as a result of the active

involvement in the practice or teaching of

medicine within the 5-year period before the

incident giving rise to the claim.

(3) (a) If the injury is claimed to

have resulted from the negligent affirmative

medical intervention of the health care pro-

vider, the claimant must, in order to prove a

breach of the prevailing professional stan-

dard of care, show that the injury was not

within the necessary or reasonably foresee-

able results of the surgical, medicinal, or

diagnostic procedure constituting the medical

intervention, if the intervention from which

the injury is alleged to have resulted was

carried out in accordance with the prevailing

professional standard of care by a reasonably

prudent similar health care provider.

(b) The provisions of this subsec-

tion shall apply only when the medical inter-

vention was undertaken with the informed con-

sent of the patient in compliance with the

provisions of s. 768.46.

(4) The existence of a medical

injury shall not create any inference or pre-

sumption of negligence against a health care

provider, and the claimant must maintain the

burden of proving that an injury was proxi-

mately caused by a breach of the prevailing

professional standard of care by the health

care provider. However, the discovery of the

presence of a foreign body, such as a sponge,

clamp, forceps, surgical needle, or other

paraphernalia commonly used in surgical, exam-

ination, or diagnostic procedures, shall be

prima facie evidence on the part of the

health care provider.

(5) The Legislature is cognizant of

the changing trends and techniques for the

delivery of health care in this state and the

discretion that is inherent in the diagnosis,

care, and treatment of patients by different

health care providers. The failure of a

health care provider to order, perform, or

administer supplemental diagnostic tests

shall not be actionable if the health care

provider acted in good faith and with due

regard for the prevailing professional stan-

dard of care.

FLORIDA ADMINISTRATIVE PROCEDURE ACT, CHAP-

TER 120, FLA. STAT.

§120.57, Fla. Stat., Decisions which affect

substantial interests

The provisions of this section apply

in all proceedings in which the substantial

interests of a party are determined by an

agency, unless such proceedings are exempt

pursuant to subsection (5). Unless waived by

all parties, subsection (1) applies whenever

the proceeding involves a disputed issue of

material fact. Unless otherwise agreed, sub-

section (2) applies in all other cases.

(1) Formal proceedings.--

(a) A hearing officer assigned by

the division shall conduct all hearings under

this subsection, except for:

Sa Hearings before agency heads or

a member thereof other than an agency head or

a member of an agency head within the Depart-

ment of Professional Regulation;

as Hearings before the Unemployment

Appeals Commission in unemployment compensa-

tion appeals, unemployment compensation

appeals referees, and special deputies pur-

Ssuant to s. 443.141;

: Hearings regarding drivers'

licensing pursuant to chapter 322;

4, Hearings conducted within the

Department of Health and Rehabilitative Ser-

vices in the execution of those social and

economic programs administered by the former

Division of Family Services of said depart-

ment prior to the reorganization effected by

cnapter 75-48, Laws of Florida;

. Hearings in which the division

is a party, in which case an attorney

assigned by the Administration Commission

shall be the hearing officer;

6. Hearings which involve student

disciplinary suspensions or expulsions and

which are conducted by educational units;

Vs Hearings of the Public Employees

Relations Commission in which a determination

is made of the appropriateness of the bargain-

ing unit, as provided in s. 447.307; and

8. Hearings held by the Department

of Agriculture and Consumer Services pursuant

to chapter 601.

(b) In any case to which this subsec-

tion is applicable, the following procedures

apply:

a A request for a hearing shall be

granted or denied within 15 days of receipt.

a All parties shall be afforded an

opportunity for a hearing after reasonable

notice of not less than 14 days; however, the

14-day notice requirement may be waived with

the consent of all parties. In a preliminary

hearing for the revocation of parole, no less

than 7 days' notice shall be given. In a

hearing involving a student disciplinary sus-

pension or expulsion conducted by an educa-~

tional unit, the 14-day notice requirement

may be waived by the agency head or the hear-

ing officer without the consent of the par-

ties. The notice shall include:

a. A statement of the time, place,

and nature of the hearing.

b. A statement of the legal author-

ity and jurisdiction under which the hearing

is to be held.

Ce A reference to the particular

sections of the statutes and rules involved.

a. Except for any hearing before an

unemployment compensation appeals referee, a

short and plain statement of the matters

asserted by the agency and by all parties of

record at the time notice is given. If the

agency or any party is unable to state the

matters in sufficient detail at the time ini-

tial notice is given, the notice may be limit-

ed to a statement of the issues involved, and

thereafter, upon timely written application,

a more definite and detailed statement shall

be furnished not less than 3 days prior to

the date set for the hearing.

. Except for any proceeding con-

ducted as prescribed in s. 120.54(4) or

s. 120.56, a petition or request for a hear-

ing under this section shall be filed with

the agency. If the agency elects to request

a hearing officer from the division, it shall

so notify the division within 10 days of re-

ceipt of the petition or request. When the

Florida Land and Water Adjudicatory Commis-

sion receives a notice of appeal pursuant to

s. 380.07, the commission shall notify the

division within 60 days of receipt of the

notice of appeal if the commission elects to

request the assignment of a hearing officer.

On the request of any agency, the division

shall assign a hearing officer with due re-

gard to the expertise required for the partic-

ular matter. The referring agency shall take

no further action with respect to the formal

proceeding, except as a party litigant, as

long as the division has jurisdiction over

the formal proceeding. Any party may request

the disqualification of the hearing officer

by filing an affidavit with the division

prior to the taking of evidence at a hearing,

stating the grounds with particularity.

4. All parties shall have an oppor-

tunity to respond, to present evidence and

argument on all issues involved, to conduct

cross-examination and submit rebuttal evi-

dence, to submit proposed findings of facts

and orders, to file exceptions to any order

or hearing officer's recommended order, and

to be represented by counsel. When appro-

priate, the general public may be given an

opportunity to present oral or written commun-

ications. If the agency proposes to consider

such material, then all parties shall be

given an opportunity to cross-examine or chal-

lenge or rebut it.

- The record in a case governed by

this subsection shall consist only of:

a. All notices, pleadings, motions,

and intermediate rulings;

b. Evidence received or considered;

Ce A statement of matters official-

ly recognized;

d. Questions and proffers of proof

and objections and rulings thereon;

e. Proposed findings and excep-

tions;

f. Any decision, opinion, proposed

Or recommended order, or report by the

officer presiding at the hearing;

g. All staff memoranda or data sub-

mitted to the hearing officer during the hear-

ing or prior to its disposition, after notice

of the submission to all parties, except com-

munications by advisory staff as permitted

under s. 120.66(1), if such communications

are public records;

h. All matters placed on the record

after an ex parte communication pursuant to

s. 120.66(2); and

Ae The official transcript.

6. The agency shall accurately and

completely preserve all testimony in the pro-

ceeding, and, on the request of any party, it

Shall make a full or partial transcript avail-

able at no more than actual cost. In any

proceeding before a hearing officer initiated

by a consumptive use permit applicant pur-

Suant to subparagraph 13, the applicant shall

bear the cost of accurately and completely

preserving all testimony and providing full

Or partial transcripts to the water manage-

ment district. At the request of any party,

full or partial transcripts shall be provided

at no more than cost.

ene

Ve Findings of fact shall be based

exclusively on the evidence or record and on

matters officially recognized.

B Except as provided in subpara-

graph 12, the hearing officer shall complete

and submit to the agency and all parties a

recommended order consisting of his findings

of fact, conclusions of law, interpretation

of administrative rules, and recommended

penalty, if applicable, and any other informa-

tion required by law or agency rule to be

containea in the final order. The agency

Shall allow each party at least 10 days in

which to submit written exceptions to the

recommended order.

Pi The agency may adopt the recom-

mended order as the final order of the agency.

The agency in its final order may reject or

modify the conclusions of law and interpreta-

tion of administrative rules in the recommend-

ed order, buy may not reject or modify the

findings of fact unless the agency first

determines from a review of the complete

record, and states with particularity in the

order, that the findings of fact were not

based upon competent substantial evidence or

that the proceedings on which the findings

were based did not comply with essential

requirements of law. The agency may acccept

the recommended penalty in a recommended

order, but may not reduce or increase it with-

out a review of the complete record and with-

out stating with particularity its reasons

therefor in the order, by citing to the

record in justifying the action. When there

is an appeal, the court in its discretion may

award reasonable attorney's fees and costs to

the prevailing party if the court finds that

the appeal was frivolous, meritless, or an

abuse of the appellate process or that the

agency action which precipitated the appeal

was a gross abuse of the agency's discretion.

10. If the hearing officer assigned

to a hearing becomes unavailable, the divi-

sion shall assign another hearing officer who

shall use any existing record and ieceive any

aGditional evidence or argument, if any,

which the new hearing officer finds neces-

sary.

ll. A hearing officer who is a mem-

ber of an agency head may participate in the

formulation of the final order of the agency,

provided he has completed all his duties as

hearing officer.

12. In any application for a license

or merger pursuant to title XXXVIII which is

referred by the agency to the division for

hearing pursuant to this section, the hearing

officer shall complete and submit to the agen-

cy and to ail parties a written report con-

sisting of findings of fact and rulings on

evidentiary matters. The agency shall allow

each party at least 10 days in which to sub-

mit written exceptions to the report.

13. In any application for a consump-

tive use permit pursuant to oart II of chap-

ter 373, the water managemert district on its

Own motion may, or, at the request of the

applicant for the permit, shall, refer the

matter to the division for the appointment of

a hearing officer to conduct a hearing under

this section.

§120.68 Judicial review.

(1) A party who is adversely affect-

ed by final agency action is entitled to judi-

cial review. For purposes of this section, a

district school board, whose decision is re-

viewed under the provisions of s. 231.36 and

whose final action is modified by a superior

administrative decision, shall be a party

entitled to judicial review of the final ac-

tion. A preliminary, procedural, or interme-

diate agency action or ruling is immediately

reviewable if review of the final agency deci-

sion would not provide an adequate remedy.

(2) Except in matters for which judi-

cial review by the Supreme Court is provided

by law, all proceedings for review shall be

instituted by filing a petition in the dis-

trict court of appeal in the appellate dis-

trict where the agency maintains its headquar-

ters or where a party resides. Review pro-

ceedings shall be conducted in accordance

with the Florida Appellate Rules.

(3) The filing of the petition does

not itself stay enforcement of the agency

decision, but if the agency decision has the

effect of suspending or revoking a license,

supersedeas shall be granted as a matter of

right upon such conditions as are reasonable,

unless the court, upon petition of the agen-

cy, determines that a supersedeas would con-

stitute a probable danger to the health, safe-

ty, or welfare of the state. The agency may

also grant a stay upon appropriate terms,

but, whether or not the action has the effect

of suspending or revoking a license, a peti-

tion to the agency for a stay shall not be a

prerequisite to a petition to the court for

Supersedeas. In any event, the orader shall

specify the conditions, if any, upon which

the stay or supersedeas is granted.

(4) Judicial review of any agency

shall be confined to the record transmitted

and any additions made thereto in accordance

with subsection (6).

(5) The record for judicial review

shall consist of the following:

(a) The agency's written document

expressing the order, the statement of rea-

sons therefore if issued, and the record

under s. 120.57, if review of proceedings

under that section is sought.

(b) The agency's written document

expressing the action, the statement of rea-

sons therefor, if issued, and the materials

considered by the agency under s. 120.54, if

review is sought of proceedings under that

section.

(c) The agency's written document

expressing the j:ction, and other written docu-

ments identified by the agency as having been

considered by it before its action and used

as a basis for its action, if review is

sought of proceedings under s. 120.56 or

s. 120.565 or if there has been no proceeding

unger s. 120.54 or s. 120.57.

(6) When there has been no hearing

prior to agency action and the reviewing

court Finds that the validity of the action

depends upon disputed facts, the court shall

order the agency to conduct a prompt, fact-

finding proceeding under this act after hav-

ing a reasonable opportunity to reconsider

its determination on the record of the pro-

ceedings.

(7) The reviewing court shall deal

separately with disputed issues of agency

procedure, interpretations of law, determina-

tions of fact, or policy within the agency's

exercise of delegated discretion.

(8) The court shall remand the case

for further agency action if it finds that

either the fairness of the proceedings or the

correctness of the action may have been im-

paired by a material error in procedure or a

failure to follow prescribed procedure. Fail-

ure Of any agency to comply with s. 126.53

Shall be presumed to be a material error in

procedure.

(9) If the court finds that the agen-

cy has erroneously interpreted a provision of

law and that a correct interpretation compels

a particular action, it shall:

(a) Set aside or modify the agency

action, or

(b) Remand the case to the agency

for further action under a correct interpreta-

tion of the provision of law.

(10) If the agency's action depends

on any fact found by the agency in a proceed-

ing meeting the requirements of s. 120.57 of

the act, the court shall not substitute its

judgment for that of the agency as to the

weight of the evidence on any disputed find-

ing of fact. The court shall, however, set

aside agency action or remand the case to the

agency if it finds that the agency's action

depends on any finding of fact that is not

Supported by competent substantial evidence

in the record.

(ll) If the agency's action depends

on facts determined pursuant to subsection

(6), the court shall set aside, modify, or

order agency action if the facts compel a

ne

particular action as a matter of law, or it

may remand the case to the agency for further

examination and action within the agency's

responsibility.

(12) The court shall remand the case

to the agency if it finds the agency's exer-

cise of discretion to be:

(a) Outside the range of discretion

delegated to the agency by law;

(b) Inconsistent with an agency

rule, an officially stated agency policy, or

a prior agency practice, if deviation there-

from is not explained by the agency; or

(c) Otherwise in violation of a con-

Stitutional or statutory provision;

but the court shall not substitute its judg-

ment for that of the agency on an issue of

discretion.

(13) (a) The reviewing court's deci-

sion may be mandatory, prohibitory, or declar-

atory in form, and it shall provide whatever

relief is appropriate irrespective of the

original form of the petition. The court

Le Order agency action required by

law, order agency exercise of discretion when

required by law, set aside agency action,

remand the case for further agency proceed-

ings, Or decide the rights, privileges, obli-

gations, requirements, or procedures at issue

between the parties, and

r - Order such ancillary relief as

the court finds necessary to redress the ef-

fects of official action wrongfully taken or

withheld.

(b) If the court sets aside agency

action or remands the case to the agency for

further proceedings, it may make such inter-

locutory order as the court finds necessary

to preserve the interests of any party and

the public further proceedings or agency ac-

tion,

(14) Unless the court finds a ground

for setting aside, modifying, remanding, or

ordering agency action or ancillary celief

under a specified provision of this section,

it shall affirm the agency's action.

Fla. Admin. Code, Rule 10D-72.16

§10D-72.16 Disposal of Fetal Remains.

All fetal remains shall be disposed of in

a sanitary, nuisance free manner. Incinera-

tion or burial of such remains, as well as

other nuisance free methods, are acceptable

so long as the licensing agency is assured

that the disposal method utilized is nuisance

free.

U.S. CONST., AMEND. XIV, §1

CITIZENSHIP; PRIVILEGES AND IMMUNITIES; DUE

PROCESS; EQUAL PROTECTION; APPORTIONMENT OF

REPRESENTATION; DISQUALIFICATION OF OFFICERS;

PUBLIC DEBT; ENFORCEMENT

Section l. All persons born or

naturalized in the United States, and subject

to the jurisdiction thereof, are citizens of

the United States and of the State wherein

they reside. No State shall make or enforce

any law which shall abridge the privileges or

immunities of citizens of the United States;

nor shall any State deprive any person of

life, liberty, or property, without due pro-

cess of law; nor deny to any person within

its jurisdiction the equal protection of the

laws.

ee eT en ae etwas

APPENDIX -~- SECTION IV

IV. Portion of Record Demonstrating

That Both Federal Questions Were

Timely and Properly Raised.

The following excerpts are from Peti-

tioner's briefs to the District Court of Ap-

peal for the First District of Florida. Re-

garding the first question presented:

What is perhaps the most disturbing

feature about prosecutions under §458.331(1)

(t), Fla. Stat., is that doctors [sic] may be

denied the right to practice medicine based

on unwritter and uncodified standards deter-

mined by a loosely assembled group of his

peers. As such, medical licensees are put on

no notice whatsoever regarding what conduct

is prohibited. This leaves the DPR free to

create and enforce standards which are devel-

oped at will, promulgated ad hoc, and en-

forced ex post facto. If a physician cannot

feel safe by following to the letter the writ-

ten promulgated standards of his profession

A-63

without fear of being ambushed by zealous DPR

prosecutors wielding a stable of "interested

physicians," then no doctor anywhere can prac-

tice his profession without performing proce-

dures which are unnecessary yet are performed

"primarily to protect us and the clinic."

[Petitioner's Initial Brief, pp. 39-40].

* * *

The standard by which Appellant is to

be judged, “that level of care, skill and

treatment which is recognized by a reasonably

prudent similar physician as being acceptable

under similar conditions and circumstances,"

is vague, ambiguous and subject to a wide

range of interpretation. The average jurist

has little idea what medical procedures are

appropriate in a given circumstance and even

less understanding about how the procedures

should be performed. [Petitioner's Reply

Brief, p. 1lj.

es eee

nt eet ees, ete ie”

Regarding the second question present-—

What is particularly interesting

about the Robinson case is that the only evi-

dence that Dr. Robinson's treatment was im-

proper came from a doctor who had, as the

court put it, “a professional interest in

having his course of treatment recognized as

being the ‘correct’ or ‘justifiable' one."

What makes the case so revealing in the in-

Stant proceeding is that all of the evidence

that Dr. AZIMA failed to meet medical stand-

ards was offered by Drs. Yankopolus, Water-

man, Cowdin and Sibley who also had an inter-

est in having their course of treatment recog-

nized as being the "correct" or "justifiable"

one. The court in Robinson said:

It should be absolutely self-

evident that suspending a

professional license solely

on the basis of the testimony

of one interested witness

does not even begin to ap-

proach the level of "“compe-

tent substantial evidence" as

A-65

required by section 120.57.

Dr. Beard's opinion as to why

extraction was the only avail-

able option in this case was

certainly relevant testimony.

But the hearing officer and

the petitioner's attorney

should have understood that

Dr. Beard would have a profes-

sional interest in having his

course of treatment recogniz-

ed as being the "correct" or

"justifiable" one. In addi-

tion, Dr. Beard had a continu-

ing financial interest in the

case in that the complainant

was, presumably, still his

patient. Without impugning

Dr. Beard's motives, we find

his testimony suspect. One

professional's opposing opin-

ion, without more, on a par-

ticular treatment is neither

substantial evidence of incom-

petence nor a measure of "gen-

erally prevailing peer perfor-

nance, * Cis. @8cCction

466.028(1)(y), Florida Stat-

utes.

The Department of Profession-

al Regulation, as well as the

specific professional boards

coming under its purview,

must remember that the suspen-

sion of a license which is

essential in the pursuit of

livelihood involves state

action. Such licenses may

not be revoked or suspended

without procedural due pro-

cess. Barry v. Barchi, 433

A-66

aati ha ki i

ented ss

0.8. 35, 99 8.Ct. 2642, 6:

L.86.20 365 (1979).

Id. at 932.

(Footnotes

omitted. Empha-

asis added.)

See also, Davis v. Department of Professional

Regulation, 457 So.2d 1074, 1077 (Fla. lst

DCA 1984); and Johnston v. Department of Pro-

fessional Regulation, 456 So.2d 939, 944

(Fla. lst DCA 1984), which cite Robinson with

approval and hold accordingly.

No more was presented in Petitioner's

hearing in the way of competent substantial

evidence than was presented in the Robinson

case. [Petitioner's Initial Brief, pp.

24-25].

* * *

Because such proceedings are penal in

nature, the courts have universally held that

the proof must be substantially greater than

that which is required to support convention-

al agency action. Bowling v. Department of

Insurance, 394 So.2d 165, 171 (Fla. lst DCA

A-67

1981). In other words, the proof must be

commensurate with the potential penalty.

Henderson Signs, Inc. v. Department of Trans-

———

portation, 397 So.2d 769 (Fla. lst DCA 1981);

Department of Professional Regulation v.

Whitney, 6 FALR 5033, 5045, DOAH Case No.

82-2557 (Final Order of Board of Medical Ex-

aminers, June 29, 1984).

In Bowling, this Court explained:

In a proceeding under a penal

Statute for suspension or

revocation of a valuable busi-

ness or professional license,

the term "competent substan-

tial evidence" takes on vigor-

ous implications that are not

so clearly present on other

occasions for agency action

under Chapter 120.

, ae * *

Evidence which is "substan-

tial" for one purpose may be

less so on another, graver

occezsion. One takes a stran-

ger's name at his word upon a

chance meeting, but wants

better proof to cash his

check.

Id. at 171.

(Footnote

omitted. )

This Court again emphasized its com-

mitment to the principles expressed in Bowl-

ing in its opinion in Davis v. Department of

Professional Regulation, 457 So.2d 1074, 1076

(Fla. lst DCA 1984):

In Bowling the court echoes

the concern expressed by the

Florida Supreme Court in

State v. Pattishail, Supra,

with regard to the higher

seriousness accorded to the

reguirement of substantiality

when the matter at stake is a

license that allows one to

earn a livelihood, saying

"when the proceeding may re-

sult in the loss of a valu-

able business or professional

license, the critical matters

in issue must be shown by

evidence which is indubitably

as ‘substantial’ as the conse-

guences." Bowling, supra, at

ie a In Bowling, the court

rejected the Department's

evidentiary findings on the

ground that they lacked a

substantial basis for estab-

lishing Bowling's guilt on

the eight counts with which

A-69

he was charged. The court

vacated the order revoking

Bowling's license.

[Petitioner's

Initial Brief,

pp. 20-21].

APPENDIX -- SECTION V.

V. Summary of the Case.

Preface

The following summary of testimony

and facts is material to this Court's consi-

deration of the questions presented. This

summary of the record demonstrates that Peti-

tioner had no prior notice of the medical

standards by which he was found guilty of

committing medical malpractice. Nor did the

Department of Professional Reguiation (herein-

after "DPR") prove by a preponderance of com-

petent substantial evidence:

a. that Dr. Azima was legal-

ly obligated to determine the

Rh factor of Ms. Kuchar's

blood;

b. that Dr. Azima did not

determine the Rh factor of

Ms. Kuchar's blood; and

Ce that Dr. Azima was re-

quired by law to send the

abortion tissue for a patho-

logical examination when Peti-

tioner, in full accordance

with the American College o!

OB/GYN standards, aware,

clearly determined through a

detailed visual examination

that fetal remains were

present and the abortion was

successful.

It is also noted that each of the expert wit-

nesses who testified against Dr. AZIMA treat-

ed one or more of the patients named in the

DPR complaint.1 Three of the four doctors

who testified against Petitioner, Drs.

lpr. Cowdin treated both Christine Sellers and

Holli Schmidt. Drs. Yankopolus and Waterman

treated Holli Schmidt, and Dr. Sibley treated

Coleen Lundy, who was also a complaining wit-

ness.

Yankopolus, Cowdin and Waterman, practice

together and that practice is hereinafter

referred to as the Yankopolus group.

1. The Petitioner

Dr. ALI AZIMA, the Petitioner, gradu-

ated from the Medical College at Tehran Uni-

versity, where he received his M.D. degree in

L9Gi . (R. 357-358). During three years of

residency in forensic medicine, he developed

a knowledge and expertise in clinical path-

ology. (R. 358-359). After coming to the

United States, Dr. AZIMA completed four more

years of internship and residency in gynecol-

ogy and obstetrics, including a fellowship in

internal medicine. He is a specialist in

Obstetrics and Gynecology (hereinafter refer-

red to as "OB/GYN") (R. 359) and has estab-

lished three subspecialties in oncology, endo-

crinology, and fetal internal medicine. (R.

360).

In 1974 Dr. AZIMA entered private

practice in Baltimore, Maryland. (R. 360-

361). In 1977, along with his wife, he estab-

lished a women's health clinic in Fort Myers,

Florida. (RR. 369). It was at this women's

health clinic that all of the complaining

patients in the instant proceedings were

treated. The clinic was licensed and met all

Standards and regulations for licensure dur-

ing 1981 and 1982, the relevant time periods

of this case. (R-368, 369).

Dr. AZIMA is a board-certified obste-

trician-gynecologist (R. 363). During all

periods relevant to this case, he was a mem-

ber of the Charlotte County Medical Society,

the Florida Medical Association, the American

Board of OB/GYN, and was also a Fellow of the

American College of Obstetricians and Gyne-

cologists. (R. 364).

A-74

Prior to this case, Dr. AZIMA had

deiivered approximately 5,000 or 6,000

babies, and had in the course of his practice

performed approximately 3,500 terminations of

pregnancy. At the hearing he estimated that

he has implanted as many as 1,000 intrauter-

ine devices. (R. 364-365). Until the in-

Stant proceedings, he had never before been

the subject of any malpractice complaints.

(R. 365).

2. The Petitioner's Medical Procedures

In 1977 Dr. AZIMA established proce-

dures to treat patients for both prenatal and

abortion services at his Ft. Myers clinic.

These procedures were based on his residency

training and textbooks and met with all of

the standards of the American College of Ob-

stetricians and Gynecologists. (R. 369-370).

As a member of the American College of Obste-

tricians and Gynecologists, he received all

of their literature. These publications were

the only published standards of his profes-

sion and from 1977 to the present, there were

no other published standards of his profes-

sion which he could follow. These facts were

not contested or otherwise refuted in the

record.

The procedures in place during 1981

and 1982 in the Fort Myers clinic were as

follows:

Upon entering the clinic, it was stan-

dard procedure for a patient to receive three

documents -- a consent form, an information

sheet, and a post-abortion instruction form.

(R. 371). Every patient had to sign the con-

sent form (R. 372) and the patient registra-

ticn record information sheets or else Dr.

AZIMA would not proceed with treatment. (R.

373). After a patient paid, the nurse brought

the chart to Dr. AZIMA and thereafter brought

the patient to his consultation room. (R.

374). Dr. AZIMA would then review the record

and question the patient. (R. 375).

Dr. AZIMA questioned the patients to

confirm their written information and deter-

mine whether they had overlooked anything,

such as medications or past medical history.

(R. 374-377). He would not proceed with any

pregnancy termination procedure until a preg-

nancy test had been completed and the patient

came to a final conclusion that she wanted

the abortion. (R. 377). To assure pregnan-

cy, Dr. AZIMA always administered a pregnancy

test, generally the UCG Slide test, which is

considered in the medical community to have a

high degree of reliability. (R. 379-380).

Dr. AZIMA testified that these proce-

dures were scrupulously followed for patients

Sellers/Kuchar, Schmidt and Baker, and that

he obtained from each of them information

concerning each patient's age, marital

status, number of prior pregnancies, men-

strual history and date of last menstrual

period. (R. 380-382). For every prenatal

and abortion patient, Dr. AZIMA testified

that he "always" determines the age of the

pregnancy, the blood type and Rh factor.

(R. 381-382). He does not necessarily write

down all information, but he always documents

abnormal findings. (R. 383).

After using an anatomy chart to in-

struct the patient and asking the patient

whether she has any questions (R-384), the

patient leaves the consultation room, voids

her bladder in the clinic lavatory and is led

by a nurse to the examination room where the

patient is prepared for an examination. (R.

385, 389). The detailed physical examination

is described at R. 389 and R. 390.

ee ee

In order to determine the actual age

of the pregnancy (R. 392-393), the OB/GYN

exam includes a pelvic examination. These

procedures clearly comport with required

OB/GYN standards. (R. 381, 391).

After the manual examination, he in-

forms the patient that he is going to insert

the speculum. He inspects the cervix for

abnormalities, cleanses the vagina with an

antiseptic solution, and then gives a para-

cervical block, which is an injection of one

per cent Xylocaine, used to dilate and sound

the uterine cavity. (R. 392-397).

Dilation of the cervix is accomplish-

ed with a cannula which is inserted into the

vagina. The cannula corresponds in size to

the age of the pregnancy. For example, a ten

millimeter cannula is used for a ten-week

pregnancy. (Rs. 397}. the cervix is dilated

one millimeter more than the size of the can-

nula to avoid discomfort to the patient.

(R. 399).

Once the abortion is performed (R.

409), the uterus is massaged to help it con-

tract and to reduce bleeding. (R. 410). At

that point Dr. AZIMA, finished with the opera-

tion, watches the patient, talks with her and

observes her condition. He also checks the

patient's blood pressure at that time. (R.

410-411).

Dr. AZIMA then performs a detailed

examination of the uterine product in order

to identify the products of conception, as

specifically detailed in the American College

of OB/GYN standards. [R. @21);.

If Dr. AZIMA is certain that fetal

parts have been removed, he disposes of tne

uterine product. This fully comports with

all Florida state regulations and statutes

regarding the disposal of such tissue. If

there are any doubts, he sends the specimen

to the pathologist for examination. (R. 412).

There is no requirement by any standard to

send every specimen to pathology. (R. 413).

Finally, the patient's blood pressure

is taken for ccmparison and if it has not

already been determined, the patient's blood

is typed to determine her Rh factor. (R.

438, €233} 4 If the patient is Rh neyative,

she is counseled that she may need RhoGam.

Dr. AZIMA counself Rh negative patients and

only offers the RhoGam, which they may refuse.

(R. 417).

The nurse then asks the patient to

Sit up and see how she feels. The patient is

told to lie down if there is any feeling of

weakness or dizziness. She is told to lie

Gown again if any dizziness occurs, otherwise

she dresses and proceeds to the recovery room.

(R. 417-418).

Dr. AZIMA then talks to the patient

about how she feels, provides medication, and

discusses contraceptive measures. (R. 418).

He instructs the patient to read the pink

instructional sheet again and to return in

one week. (R. 419). Because abortion is a

Surgical procedure, a one-week return visit

was a critical part of Dr. AZIMA's standard

procedures. It is necessary in order to

check for complications. (R. 419-420).

During the hearing, Dr. AZIMA's testi-

mony as to these medical procedures and to

their accordance with accepted professional

standards was detailed and was in no way con-

travened by any evidence or testimony.

3. Case History and Testimony

Relating to Holli Schmidt

(Count II of the March 15, 1983, Complaint)

A. Case History of Holli Schmidt

Dr. AZIMA was specifically found guil-

ANE NAS md MPa os

8 al eRe Rei ons

Odes) cat iets

ty of violating §458.331(1)(t), Fla. Stat.,

for having implanted an IUD into Holli

Schmidt without taking adequate precautions

to ensure that she was not pregnant at the

time of insertion.

Dr. AZIMA first saw Holli Schmidt on

December 1, 1977, three years prior to the

visit which led to these charges. She sought

and received an abortion. (R. 436, 438, 479).

On her follow-up appointment, he inserted an

IUD (R. 438).

Ms. Schmidt again saw Dr. AZIMA on

June 11, 1979, because she was nine days late

with her period and exhibited all the signs

of pregnancy. (R. 481). A pregnancy test,

however, revealed that she was not pregnant

and, therefore, no treatment was administer-

ed.

Her third visit came on February 23,

1981, when she again came to Dr. AZIMA for an

abortion. She claimed her last menstrual

period was six weeks prior and she exhibited

breast tenderness and nausea. These symptoms

were were consistent with her history of show-

ing false signs of pregnancy. Her pregnancy

test was again negative. (R. 436). To con-

firm that she was not pregnant Dr. AZIMA con-

ducted a pelvic examination. He found her

uterus normal and determined that it was not

enlarged. (R. 439). The patient then re-

quested another IUD which was inserted at

that time. She returned for a March 5 follow-

up visit at which time she again exhibited

symptoms of pregnancy. [R. 429% RR. 883).

Both a pelvic exam and another pregnancy test

administered on March 5 again confirmed that

she was not pregnant. (R. 440, 483). Be-

cause the string of the IUD was not visible,

Ta i he

Dr. AZIMA sounded the uterus and thereby

confirmed that the IUD was still in place.

(R. 439).

To ease her concerns and keep abreast

of the situation, Dr. AZIMA scheduled another

appointment nine days later on Saturday,

March 14, 1981. She did not return for that

follow-up appointment. (R. 439, 483).

During the course of the 1981 treat-

ment in question, Dr. AZIMA conducted two

pregnancy tests, two physical examinations

and two pelvic examinations, all of which

showed no indication of pregnancy. (R. 439-

440). He twice determined that her uterus

was not enlarged, (R. 440), which is conclu-

sive evidence that she was not pregnant at

that time.

Dr. Yankopolus examined Ms. Schmidt

nearly two months after she last Saw Dr.

AZIMA. (R. 198, 199). His records disclose

that Holli Schmidt did not tell him the truth.

She told him that AZ1IMA had examined her as

recently as the week before and that AZIMA

put his hands in his pockets, shrugged his

shoulders and could not explain her symptoms.

(R. 199). Dr. Yankopolus did nothing to veri-

fy this erroneous story. (R. 200). Without

conducting a test to assure that the IUD was

Still in place, Dr. Yankopolus advised her of

the dangers of pregnancy with an IUD in place

and counselled regarding an abortion. (R.

224, 225).

Dr. Yankopolus referred Ms. Schmidt

to his partner, Dr. Waterman, in order to

terminate the pregnancy. Two days later,

without first confirming that the IUD was in

fact present, Dr. Waterman performed an abor-

tion on Ms. Schmidt on May 1, 1981. (R. 341).

Waterman testified that he did not

specifically remember removing Holli

Schmidt's IUD and holding it up and showing

it to her. "I do that routinely. Today I

can't sit here and tell you that I did it on

that particular day." Waterman altered Ms.

Schmidt's medical records one year after the

abortion to state that the IUD was removed on

May 1, 1981. On cross-examination he admit-

ted that his only basis for making the correc-

tion was an allegation by Schmidt that it had

been removed. (R. 341).

B. DPR Testimony Against Dr. AZIMA.

(1) Dr. Yankopolus' Testimony.

The DPR presented the testimony of

Dr. Yankopolus who stated that the procedure

that he follows is to "make the determination

that the patient is not pregnant for sure."

"([M]ost often the device is inserted on a

period...." (T-186).

Dr. Yankopolus testified that he ad-

ministers either a urine or a blood pregnancy

test only if there is a doubt that the pa-

tient is not pregnant. (T-178-179). There-

fore his standard respecting insertion of an

IUD device is less protective than the stan-

dards adhered to by Dr. AZIMA who twice per-

formed a pregnancy test on Holli Schmidt.

Dr. Yankopolus also testified that it

was inappropriate for the IUD to have been

inserted because of Ms. Schmidt's overt preg-

nancy signs and symptoms and because he did

not know which type of pregnancy test Dr.

AZIMA performed. It must be remembered, how-

ever, that Holli Schmidt had cnce before ex-

hibited false pregnancy signs and Dr. AZIMA

in this instance not only administered two

pregnancy tests but also performed two pelvic

examinations. (R. 439-440). Approximately

eight weeks after Dr. AZIMA'S examinations

revealed no pregnancy, on April 27, 1981, Dr.

Yankopolus determined that Ms. Schmidt was

pregnant.

(2) Dr. Waterman's Testimony

Dr. Waterman testified that Holli

Schmidt conceived ten to twelve weeks prior

to his May 1 examination of her. (R. 325).

On this basis he testified that it

was inappropriate for Dr. AZIMA to insert the

IUD because the patient could have been preg-

nant. (R. 326). But, On cross-examination

he admitted that the medical standard by

which he was judging Dr. AZIMA was not to be

found any place in particular. Rather, it

was based upon his own medical judgment and

experience and could not be found in any pub-

lished rules or standards (R. 329-330). Fur-

thermore, Dr. AZIMA'sS unopposed testimony

established that a woman may miss a period,

have tenderness or enlargement of the

breasts, gain weight, or even feel something

in her abdomen and yet not be pregnant. (R.

378-379).

C. Response to DPR Testimony.

(1) Dr. Yankopolus' Testimony

Dr. Yankopolus acknowledged that his

diagnosis of Ms. Schmidt and critique of Dr.

AZIMA were based in part upon the erroneous

belief that Holli Schmidt had seen Dr. AZIMA

the week before. (RR. #01,, #02). Dr.

Yankopolus testified that Dr. AZIMA should

have discovered the pregnancy the week prior

to April 27, 1981, if she was twelve weeks

pregnant when Yankopolus saw her on April 27,

1981. (R. 202). However, Dr. AZIMA did not

see her after March 5, 1981.

Dr. Yankopolus further admitted that

IUD's are only 96 percent effective as contra-

ceptives, and he did not know whether Holli

Schmidt fell in the remaining four percent

who become pregnant while using an IUD. (R.

ee ee een ey ey et

Ne RD Mickie nie A

215). He testified that he heard a fetal

heartbeat in Holli Schmidt which can be heard

nine and one-half to ten weeks after concep-

tion. (R. 215). He also admitted on cross-

examination that Holli Schmidt could have

expelled the IUD (R. 222) and that there are

tests that he could have performed but did

not, in order to verify that the IUD was in

place.

Regarding the urine pregnancy tests

which Dr. AZIMA gave Holli Schmidt, Dr.

Yankopolus first stated that some tests are

"potentially" useless, because they are only

85 percent accurate but then acknowledged

that other urine pregnancy tests are 96% ac-

curate. (R. 220-221). He had no idea what

kind of pregnancy test Dr. AZIMA twice gave

to Holli Schmidt in 1981. (R. 221).

Dr. Yankopolus testified that he does

not always do a pregnancy test before insert-

ing an IUD. (R. 223). Yet, even though Dr.

AZIMA performed two pregnancy tests (in addi-

tion to two physical examinations and two

pelvic examinations), Dr. Yankopolus testi-

fied that Dr. AZIMA was negligent. (R. 223-

224). This unsupported testimony of Dr.

Yankopolus discloses no substandard practice

by Dr. AZIMA. Yet the hearing officer found

that Petitioner violated §458.331(1)(t),

Fla. Stat.

(2) Dr. Cowdin's Testimony

Dr. Cowdin testified that he has ex-

perience in prescribing and inserting IUDs

and that he would "generally insert the IUD

while the patient is on her menstruai per-

iod," because "it's technically easier to do

so." (R. 247). Dr. Cowdin admitted that an

IUD does not always prevent conception and he

has actually delivered a baby whereupon an

IUD was expelled during birth, indicating

that the IUD was not effective. cme 29h).

He also acknowledged that an IUD can be invol-

untarily expelled. (R. 294).

When Dr. Cowdin was questioned about

the two sets of tests that Dr. AZIMA had per-

formed upon Schmidt -- pregnancy tests and

pelvic examinations -- he responded that

"there is nothing wrong with that." CR.

292).

When asked when Holli Schmidt became

pregnant, he answered that "conception likely

occurred in the neighborhood of February 15."

(R. 293). While this might not have shown up

on the pregnancy test which was given to

Holli Schmidt on February 23 and again ten

days later (R. 293), if Holli Schmidt had

kept her March 14 appointment with Dr. AZIMA,

a third pregnancy test would have revealed

the pregnancy. (R. 293).

When asked what Dr. AZIMA did wrong,

Dr. Cowdin responded, "I can't answer that.

I don't know what he did to her." (R. 294).

At one point Dr. Cowdin, was asked:

"Do you think that it is within the standard

of care for a doctor to always do a pregnancy

test before inserting an IUD?" He responded

that it was a "question ... difficult to

answer," and that it would depend on circum-

stances, and that those circumstances boiled

down to a medical judgment by the doctor.

(R. 295).

Notwithstanding a diagnosis by the

Yankopolus group that Holli Schmidt was

twelve to fourteen weeks pregnant, Dr. Cowdin

acknowledged that on May 1, 1981, Dr. Water-

man used a number nine cannula on Holli

Schmidt -- a nine millimeter suction catheter

(R. 296). Cowdin also acknowledged the auth-

Oritative character of the publication "Con-

A te ONES: ht on Sin a ih at er

temporary OB/GYN" (R. 297) and a chart corre-

lating the size of the cannula with the size

of the uterus and age of pregnancy.

Cowdin acknowledged that if the cor-

relation procedure contained in the "Contem-

porary OB/GYN" chart was appropriate, then

Holli Schmidt's pregnancy would have been

nine weeks, ¢ (R. 299-301), and therefore

Ms. Schmidt was not pregnant when Dr. AZIMA

inserted the IUD.

Dr. Cowdin, based upon the litera-

ture, "Contemporary OB/GYN" of October 1979,

and the size of the cannula utilized by

Waterman in her abortion, opined that Holli

Schmidt conceived in the neighborhood of

March 13, (R. 299- 300), nearly 3 weeks after

the IUD was inserted by Dr. AZIMA on February

2after performing the abortion, Dr. Waterman

did not request a pathological examination to

determine the age of the fetus. (T-281).

A-95

23. Dr. AZIMA last saw Ms. Schmidt on March

>» (RR. 300).

The admission by Dr. Cowdin of the

likelihood that Ms. Schmidt's pregnancy occur-

red after Dr. AZIMA last saw her, examined

her and confirmed that her IUD was still in

place on March 5, 1981, is cogent and convinc-

ing evidence that Dr. AZIMA did not fall be-

low established standards by implanting the

IUD on February 23, 1981. Moreover, no doc-

tor testified that the IUD must be in place

Only during menstruation.

(3) Dr. Waterman's Testimony

Dr. Waterman was then asked what he

would do if a woman came into his office,

told him that she had an IUD but the string

had disappeared, and that she might wish to

terminate the pregnancy if the IUD was there.

Waterman answered that he would order an ul-

trasound. However, he did not order an ultra-

asian

a aL eS

sound prior to performing an abortion on

Holli Schmidt. (R. 331).

Dr. Waterman admitted that he does

not always do a pregnancy test before insert-

ing an IUD, and in light of the fact that Dr.

AZIMA did two ;,regnancy tests and scheduled a

third one which Holli Schmidt never came back

for, Dr. Waterman testified "I don't know"

what Dr. AZIMA did wrong. (R. 337).

(4) Dr. AZIMA's Testimony

After DPR expert witnesses testified

that the probable age of Holli Schmidt's preg-

nancy on April 27, 1981 was twelve to four-

teen weeks, Dr. AZIMA testified at length,

employing authoritative literature and draw-

ing to scale on the blackboard for the bene-

fit of the Hearing Officer, the impropriety

of such a diagnosis. Uterine size at twelve

weeks of pregnancy is comparable to a large

apple, whereas uterine size at fourteen weeks

of pregnancy is comparable to a large grape-

fruit; so that OB/GYN's do not speak of

"twelve to fourteen weeks," but rather speak

in one-week increments. The difference be-

tween a twelve-week pregnancy and a fourteen-

week pregnancy iS gross and observable, and

cannot be a proper span of measurement. (R.

398-406). It is medically unacceptable to

diagnose a pregnancy as twelve to fourteen

weeks, this being insufficiently precise to

satisfy standards of medical practice. (R.

403).

Dr. AZIMA's unrebutted testimony as

to these matters was based in part on his

teaching as a clinical instructor at Univers-

ity Hospital, Maryland. (R. 406-407).

(5) Dr. Sibley's Testimony

Dr. Craig Sibley acknowledged on

cross-examination that he diagnoses pregnan-

cies in terms of being ten weeks, or nine

ary

A ot ae ae a ml

weeks, or eight weeks. (R. 154-155). Dr.

Sibley also testified that he measures the

age of a pregnancy from the first day of the

last menstrual period. This differs by ap-

proximately two weeks from actual time of

conception. (R. 155). This was contrary to

the testimony of the Yankopolus group.

In support of Dr. AZIMA's procedures,

Dr. Sibley, like the other expert witnesses,

acknowledged that the urine pregnancy test is

a reasonable way to determine whether the

patient is pregnant (R. 170-171). He also

acknowledged that missing a menstrual period

is not proof of pregnancy; that breast tender-

ness is not proof of pregnancy, and that a

physician who performs pregnancy tests, pel-

vic examinations and takes a history, has

performed reasonably. (R. 170-171). Doing

it twice is even more reasonable. CR. 2Fiks

(6) Conclusions

Dr. AZIMA'S procedure for inserting

the IUD in Holli Schmidt deviated in no way

from the standards of the American College of

Obstetricians and Gynecologists, nor from any

other standards published or otherwise. (R.

440). There is no standard that requires

insertion of an IUD only during the menstrual

period. (R. 442).

Within reasonable medical certainty,

Holli Schmidt was not pregnant when she visit-

ed Dr. AZIMA on February 23, 1981. (R. 440).

Within reasonable medical certainty, Holli

Schmidt was not pregnant when she visited Dr.

AZIMA on March 5, 1981. (R. 440). Even if,

arguendo, she was pregnant at that time, cer-

tainly Dr. AZIMA's two pregnancy tests and

two pelvic examinations are sufficient to

absolve him from any claim of medical negli-

gence.

A-100

4. Case History and Testimony

on Christine Sellers Kuchar

(Count I of the March 15, 1983, Complaint)

A. Case History of Ms. Kuchar

Dr. AZIMA was disciplined specifical-

ly for not having sent the aborted tissue

specimen to a pathology laboratory for a de-

tailed examination, and for not having deter-

mined her Rh factor.

Christine Kuchar, formerly Christine

Sellers, came to Dr. AZIMA on February 19,

1981, for an abortion. (R. 52, 430, 467-469).

She had been told two weeks earlier by Dr.

Carver, her attending physician at the Ft.

Myers Community Hospital Emergency Room, that

she was pregnant. (R. St, 33, 830, S34, SOG).

She did not, however, inform Dr. AZIMA that

she had previously seen Dr. Carver and had

been diagnosed pregnant. (R. 441). Not only

did she fail to tell Dr. AZIMA that she had

A-101

previously seen Dr. Carver, but she also fail-

ed to inform him that she had a suspected

ectopic pregnancy? five years earlier,

which she also discussed with Dr. Carver on

February 18. (R. 23, 66, 68, 74, 76, 84, 94,

606). Both of these pieces of information

were very important and would have greatly

facilitated Dr. AZIMA's ability to treat her

under the circumstances. If. Dr. AZIMA had

been told by Ms. Sellers that she had a prior

Suspected ectopic pregnancy, then having iden-

tified recognizable fetal parts in the tissue

he removed from her uterus, he would have

3An ectopic pregnancy occurs when a fertilized

egg implants and grows outside of the uterus;

in most cases it implants and matures in the

fallopian tube and almost always leads to

rupture and removal of the fallopian tube.

(R. 146, 206, 343).

A-102

been put on notice of the possibility of a

combined pregnancy. 4

She did tell Petitioner that her last

menstrual period was January 4, 1981 which

made her seven weeks pregnant. (R. 431). Her

pelvic examination disclosed that her uterus

waS Six or seven weeks in size. Dr. AZIMA

provided a suction curettage and paracervical

block with one per cent Xylocaine. After

performing the abortion, Dr. AZIMA made a

detailed visual inspection of the products of

conception and determined that he had, in

fact, successfully terminated a pregnancy.

There were clearly recognizable fetal parts

in the tissue. (R. 35, 468, 469). She was

given an antibiotic and an appointment was

_—

4n combined or dual pregnancy occurs when two

eggs are fertilized and one implants in the

uterus while the other, at the same time,

implants in the fallopian tube. Thus, a

woman has two viable fetuses inside of her at

the same time. (R. 146, 147, 209, 249, 320,

SSo) «

A-103

made for her to return in one week. (R. 431-

432). Ms. Kuchar did not return.

Ms. Kuchar never conferred or talked

with Dr. AZIMA after the procedure on Febru-

ary 19. (R. 59). One week after the Febru-

ary 19 meeting with Dr. AZIMA, she went to

Dr. Cowdin's office. (R. 60). She testified

that Dr. Cowdin was very upset that she ad

not received a shot of RhoGam after the abor-

tion was performed. She testified also that

she knew that if one had an Rh factor one is

supposed to have a shot of RhoGam -- having

learned that with the birth of her first

child. (R. 61). Although she purported to

have known this, she refused RhoGam during

her February 19 visit with Dr. AZIMA,

One week or less after seeing Dr.

Cowdin, she awakened with pain in her lower

abdomen, went to Dr. Cowdin's office, and was

informed that she had an ectopic or tubal

A-104

pregnancy. (R. 62), She was taken to Lee

Memorial Hospital and had her right fallopian

tube, which had ruptured, removed. (R. 63).

She has recovered and has had no problems

Since. (id.)

The record reveals without contradic~—

tion that Ms. Kuchar had an ectopic pregnancy

which required an operation approximately two

weeks after Petitioner performed the termina-

“tion procedure. (R. 62).

B. Testimony in Response ta DPR Charges.

Dr. AZIMA testified that he definite-

ly asked Ms. Sellers what her Rh factor was,

and she told him that it was Rh negative.

(R. 432). He then testified that he asked

her if she wanted a shot of RhoGam, which is

administered to Rh negative patients who con-

template future pregnancies, and she replied

no since she intended to have her tubes tied.

(R. 433).

A-105

While Ms. Sellers testified that no

one at Dr. AZIMA's office asked her what her

blood type was (R. 61), she never, in any

way, contradicted Dr. AZIMA's testimony that

she refused the shot of RhoGam. What is so

telling about this is that the only reason

for administering RhoGam is to prevent the

sensitization of an Rh negative patient. It

is only called for if a patient is Rh nega-

tive. (R. 133, 244, 245). So, why did Dr.

AZIMA ask Ms. Sellers if she desired a shot

of RhoGam? The answer is self-evident -- he

knew she was Rh negative. (R. 210, 333, 432).

This logical conclusion is uncontradicted by

the testimony and the record.

Because Ms. Kuchar is Rh negative,

she was counselled that she might want RhoGam.

RhoGam is only necessary if "the patient is

considering further pregnancies." (R. 415).

RhoGam is not necessary if the patient does

A-106

not desire future pregnancies or wishes ster-

ilization. (R. 416). Since RhoGam is not

100 percent effective and has some harmful

side effects (R. 416-417), Dr. AZIMA counsels

Rh negative patients, and allows them to make

their own informed decision as to whether to

take the RhoGam, which they may refuse. im.

417).

The DPR's medical witnesses testified

that blood type must be determined, but ack-

nowledged that it need not always be determin-

ed by the drawing of blood. Regarding Ms.

Kuchar, it was acknowledged that Dr. Cowdin

accepted history (R. 267) and it was acknowl-

edged by the other DPR medical witnesses that

this may be reliable. Dr. AZIMA testified =

that he determined blood type in every case,

that he determined from her history that she

was Rh negative and she refused RhoGam be-

cause she wanted to be sterilized. oa. MSS)

A-107

This procedure has not been demonstrated to

be in violation of any medical standard,

rule, statute, or other medical protocol.

It is established by the medical evi-

dence herein that an ectopic pregnancy may be

difficult to detect, and that the only sure

method of detection is exploratory surgery

which is not ethically recommended as a mat-

ter of course.

In order for Ms. Kuchar to have been

found suffering an ectopic pregnancy two

weeks after Dr. AZIMA performed a termination

procedure, one of two possible events must

have occurred. Either Petitioner did not

successfully terminate the pregnancy on Febru-

ary 19, 1981 because it was ectopic, or Ms.

Kuchar had a combined pregnancy, i.e. two

eggs were fertilized, where one egg implanted

in a fallopian tube and the other developed

in her uterus. (Rm. 346).

A-108

If there was only one fertilized egg

then it must have resided in the fallopian

tube and Petitioner's termination procedures

would not have been successful. The exis-

tence of only one egg would have necessarily

been evident by an inability to identify

fetal remains in the uterine product. How-

ever, Dr. AZIMA did clearly identify fetal

parts in the products of conception (R. 435),

thus indicating a combined ectopic pregnancy,

such having a rare occurrence of approximate-

iy one in 30,000. (R.. 209, 265, 320). Fur-

thermore, had Petitioner been told by Ms.

Kuchar that she had a prior suspected ectopic

pregnancy, he would have been on notice of

the possibility of a combined pregnancy when

he performed her abortion. (R. 261, 262).

Had Kuchar told Drs. Cowdin and AZIMA that

she had a possible tubal pregnancy five years

before (R. 261-62), it would have made a dif-

A-109

ference because of the significantly higher

recurrence rate for women who have had ectop-

ic pregnancies. (R 261-62). Having observed

fetal remains there was nothing to be gained

by sending the products of conception for

further pathological examination. (R. 168,

265).

Dr. AZIMA followed his standard proce-

dures with Ms. Kuchar. (T-432). He obtained

her patient history. She told him she was Rh

negative. He offered her RhoGam, but was

told by her that she wanted her tubes to be

tied (permanent sterilization), (R. 98,99),

and she therefore refused the RhoGam. (R.

432-433). Had the patient returned in one

week as scheduled, a pregnancy test would

have been administered and would without

doubt have revealed her ectopic pregnancy.

(R. 433). Dr. AZIMA committed no acts of

either omission or commission which in any

A-110

way deviated from the kiconsare procedures

about which he testified (R. 433-434). Nor

did he do anything that would diverge from

the published standards of the American Col-

lege of Obstetricians and Gynecologists.

(R. 434).

Dr. AZIMA completed the abortion pro-

cedure on Ms. Kuchar on February 19, 1981 and

inspected the products of conception in de-

tail. (R. 435). In that inspection no abnor-

mality or irregularity was found. There was

no published standard by either the American

College of OB/GYN's or the Florida Medical

Association nor was ther2 any rule or reason

which required him to send those particular

products for further pathological examination.

(R. 435-436). He was, however, suspended

specifically for failing to send those prod-

ucts for pathological examination based sole-

A-111

ly upon the testimony of interested physi-

cians.

C. Regarding Ms. Kuchar.

On seme examination, Ms. Kuchar

denied the accuracy of the February 18, 1981,

date on her hospital record (R. 606, 84) and,

therefore, her credibility was significantly

impeached.

On cross-examination the witness ac-

knowledged her name and the date on the hospi-

tal records (R. 66, 67), as well as the name

of a witness, but declared that the records

are wrong. (Rm. 64, 65). Having testified

that the witness, Dr. Carver and the hospital

made a mistake but she did not (R. 68), she

then contradicted Dr. Cowdin's records by

denying that she had told him that she had an

ectopic pregnancy five years before. (R.

68).

A-112

Ms. Kuchar admitted that when Dr.

Cowdin saw her, one week after Dr. AZIMA per-

formed the abortion, Dr. Cowdin did not dis-

cover the ectopic pregnancy. (R. 74). Nor

did Dr. Carver discover it on February 18.

(R. 74).

Ms. Kuchar stated she was not upset

that Dr. Cowdin had missed her ectopic preg-

nancy when she first went to him, although he

did not give her a pregnancy test to confirm

that Dr. AZIMA's abortion had been effective.

(R. 78-79). Ms. Kuchar denied that Dr.

Cowdin said that he was working with DPR to

get Dr. AZIMA and that the DPR agent said

that he was working with Dr. Cowdin to get

Dr. AZIMA (R. 78-79), but was impeached by

her deposition of November 4, 1983 when she

had so testified. (R. 80-81).

Ms. Kuchar's hospital records of Feb-

ruary 18, 1981 indicate that she told Dr.

A-115

Carver about an ectopic pregnancy five years

prior; but in her deposition of November 4,

1983 she denied any pregnancies between 1973

and February 1981 and denied any ectopic preg-

nancies. (R. 82). She also denied any mis-

carriages and any "female trouble" between

1973 and 1981. When confronted with her

November 4, 1983, deposition, she acknowledg-

ed having said that but tried to explain that

she thought she had not had a tubal pregnancy

after all. (R. 83). She was further impeach-

ed by her November 4, 1983 deposition where

she denied having been to any emergency rooms.

(R. 82-84).

Ms. Kuchar admitted that she had not

told Dr. AZIMA that she might have had a

tubal pregnancy five years prior because she

did not think it was an important factor.

(R. 84).

A-114

Ms. Kuchar's testimony materially

contradicted her prior depositional testi-

mony, her medical records in the Yankopolus —

group's office and her hospital records.

(R. 85-86). She was also impeached by her

February 24, 1982, deposition wherein she was

asked whether she scheduled an appointment

with Dr. AZIMA for a week after the abortion

and answered, "No, I didn't." (R. 88). Yet,

at the hearing she testified that before she

left Dr. AZIMA's clinic she Gid schedule an-

other appointment for the next week. (R. 87).

When asked about these contradictory posi-

tions and why she had given the answers she

had, she replied: "I don't know." (R. 88).

Although three doctors, Carver, AZIMA

and Cowdin, all failed to diagnose the ectop-

ic pregnancy, the witness testified that Dr.

Azima was the only one who was negligent in

not discovering it. (R. 94). Ms. Kuchar

A-115

continues to this day to see the Yankopolous

group for treatment. (Id.).

5. Case History and Testimony

Relating to Darlene Baker

(Count I of the August 2, 1983, Complaint)

Dr. AZIMA was disciplined specifical-

ly for not having sent Ms. Baker's aborted

tissue specimen to a pathology laboratory for

a microscopic examination.

Dr. AZIMA first saw Darlene Baker on

January 12, 1981. (R. 422). She was then a

31-year-old married female with two full-term

deliveries, no premature births, one abortion

and one spontaneous or induced termination.

Her last menstrual period was unknown and she

was on the birth control pill. Her physical

examination was noted as normal. Her pelvic

examination disclosed a uterus of eight to

nine weeks size. (R. 423). He performed a

termination of pregnancy, and the details of

A-116

this procedure regarding Darlene Baker are in

the record. (R. 425). Darlene Baker, like

Ms. Kuchar and Ms. Schmidt, did not return

for her one-week follow-up appointment,

(Id. )

On December 23, 1982, approximately

two years later, she returned and was given a

pregnancy test that showed positive. She

asked for another abortion. (Id.) Dr. AZIMA

determined that she was ten weeks pregnant.

(R. 427).

During the 1982 visit Petitioner scru-

pulously followed his standard procedures

with Ms. Baker. The uterine tissue which was

visually inspected was consistent with an

eleven week old fetus. (R. 427). There was

no abnormality in that tissue (R. 427-428).

Having noted clearly recognizable fetal parts

and noting no abnormality, Dr. AZIMA then

disposed of the tisse in a manner which was

A-117

in full compliance with all of the applicable

standards and regulations.

During her 1982 visit, Ms. Baker also

requested an IUD and scheduled an appointment

to have the device inserted the next week.

She, however, did not return for her follow-

up visit. (R. 428).

Ms. Baker complained about her treat-

ment because two months after her abortion

she awakened in a pool of blood and could

think of no other reason for it than the abor-

tion. (R. 43-44). There is no evidence that

the abortion procedures utilized by Dr. AZiMA

were in any way related to the bleeding Ms.

Baxer experienced two months later.

The testimony of Dr. AZIMA is con-

firmed by the medical record, being DPR's

Exhibit "A", (R. 462-466), and is uncontra-

dicted.

6. Testimony Regarding The Standards

For Obstetric & Gynecological

Services.

Regarding the charge that Dr. AZIMA

failed to meet accepted standards or engaged

in gross or repeated malpractice by failing

to send all fetal remains out for a detailed

pathological examination, there are no OB/GYN

protocols or standards for the Lee County

Medical Society, nor were there any in i981

Or 1962. (Rs 3353- 356).

Dr. AZIMA scrupulously followed the

published American College of OB/GYN stan-

dards as a matter of standard procedure and

as to the patients referenced herein, did

make a close and detailed examination of the

tissue and clearly noted fetal parts.

He is sufficiently trained and compe-

tent to make such an examination. (R. 412).

The standards explain that an OB/GYN special-

ist must examine the specimen that he has

A-119

removed in order to be fully familiar with

the pathology of what he has obtained. (R.

412°

If Dr. AZIMA is certain that fetal

parts have been removed, he disposes of the

uterine product. This fully comports with

all Florida state regulations and statutes

regarding the disposal of such tissue. If

there are any doubts, he sends the specimen

to the pathologist for examination. (R. 412).

There is no requirement by any standard to

send every specimen to pathology. (R. 413).

The witnesses were in significant conflict

with one another on this point.

As to the standards of the profes-

sion, i.e., either wnat OB/GYN's in fact do

Or ought to be doing, Dr. Sibley only knew

what four others do. (R. 161). The four

others are the Yankopolus group practice.

(R. 162). That is “the same standard as

A-120

mine." (R. 162). But Dr. Waterman acknowl-

edged that there are places that do not send

Out tissues for pathological examination and

that there is no law that requires this.

(R. 318).

Dr. Sibley testified that a number of

licensed clinics in the State of Florida do

not send out fetal parts to pathology. (R.

157-158). He acknowledged that sending the

products of conception to a laboratory is

done "primarily to protect us and the clinic.

A lot of clinics do not do it; our clinics

happen to do it." (BR. 1297-38). In Dr.

Sibley's opinion, not sending the products to

pathology does not constitute malpractice.

(R. 158). Neither does any rule of law or

rule of the medical examiners of the State of

Florida require that those products be sent

to pathology (R-159).

A-121

A. .Yankopolus Testimony.

Dr. Yankopolus admitted that he was

not competent or capable of examining the

products of conception visually. (KR, 231} %

When asked about the standards for obstetric

and gynecological services published by the

American College of Obstetricians and Gyne-

cologists, he wasn't sure whether he had seen

them, but acknowledged that it is an authori-

tative work and is the standard of his profes-

sion. (R. 231).

The 1982 publication of the Standards

of the American College of Obstetricians and

Gynecologists reports at page 52 that "ina

Situation of selective termination of preg-

nancy, a ohysician should record a descrip-

tion of the gross products definitely being

identified as products of elective interrup-

tions, and if not easily identifiable, they

A-122

must be submitted to a pathologist for gross

and microscopic examination." (R. 231-232).

Nevertheless, evidencing the tenor of

his testimony, Dr. Yankopolus -- who declared

himself to be incompetent to make such an

examination -- declared that he is “above the

standards" of the American College. (R.

232)

B. _Cowdin Testimony

Dr. Cowdin also testified that it

falls below the standards of the profession

if the remains of the abortion are not sent

to pathology. ({(R. 271). Yet he was impeach-

ed by his deposition of March 23, 1982 (R.

268). When he was asked specifically whether

he knew of any "professional obligation, not

legal obligation" to send the products to

pathology, and answered "No." (R. 271). Dr.

Cowdin disagreed with the earlier testimony

A-123

of Dr. Sibley that a lot of clinics do rot

send the remains to pathology. (R. 273).

Dr. Cowdin's credibility was also

called into question when he testified that

it falls below the accepted standard of care

not to record what the products of conception

were (R. 274), but that he does not always

record them. (Id.) He records a description

of the products if he feels there is some-

thing unusual, but does not if he feels there

is nothing unusual. (R. 275).

6. Conclusion

It is not contested in the record

that Dr. AZIMA clearly satisfied the estab-

lished standards of the American College of

Obstetricians and Gynecologists.

The DPR has failed to prove by compe-

tent substantial evidence that Dr. AZIMA en-

gaged in gross or repeated malipractice or

fell below minimally acceptable medical stan-

A-124

\

\

\

dards through his procedures regarding the

products of conception. Nor did the DPR pro-

Vide competent substantial evidence toad

prove that Dr. AZIMA determined Ms. Kuchar'

Rh factor and offered her RhoGam

A-125

This is a copy of a public record, reproduced as it was published. It is not legal advice, and it may not be the version a court would rely on. Check the official source before you cite it.

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