Bennie Scott Whittington v. Woodie L. Mason, M.D. ( 2002 )

IN THE SUPREME COURT OF MISSISSIPPI
NO. 2003-CT-00700-SCT
BENNIE SCOTT WHITTINGTON AND TINA S.
WHITTINGTON
v.
WOODIE L. MASON, M.D. AND HINDS UROLOGY
CLINIC, P.A.
ON WRIT OF CERTIORARI
DATE OF JUDGMENT: 12/03/2002
TRIAL JUDGE: HON. W. SWAN YERGER
COURT FROM WHICH APPEALED: HINDS COUNTY CIRCUIT COURT
ATTORNEYS FOR APPELLANT: DOUGLAS G. MERCIER
WILLIE T. ABSTON
ATTORNEYS FOR APPELLEES: GEORGE QUINN EVANS
LYNDA CLOWER CARTER
NATURE OF THE CASE: CIVIL - MEDICAL MALPRACTICE
DISPOSITION: AFFIRMED - 06/16/2005
MOTION FOR REHEARING FILED:
MANDATE ISSUED:
EN BANC.
DICKINSON, JUSTICE, FOR THE COURT:
¶1. The narrow question presented in this medical negligence case is whether expert
testimony is required to establish the material risks which must be disclosed to a patient in
order to obtain informed consent to a medical procedure.
BACKGROUND
¶2. Because the trial court directed a verdict for the defendants, we begin by setting forth
the facts in the light most favorable to the plaintiffs. After fathering six children, Bennie Scott
Whittington considered having a vasectomy. He and his wife, Tina, visited Dr. Woodie L.
Mason at the Hinds Urology Clinic, P.A. (the “Clinic”), on May 19, 1998, to discuss the
procedure. A nursing assistant directed the Whittingtons to a room where they watched an
informational videotape about the vasectomy procedure. After watching the videotape, the
Whittingtons met with Dr. Mason to discuss the procedure. At some point prior to leaving the
clinic, the Whittingtons were presented with a consent form for the procedure which disclosed
certain risks. The Whittingtons signed the consent form just below the following language
printed on the form: “we have been informed of alternatives and complications.”
¶3. Mr. Whittington returned on May 29, 1998, for the vasectomy, which Dr. Mason
performed as an out-patient procedure. Following the procedure, Mr. Whittington returned
home. Within a few hours, he began to experience severe pain and swelling in his scrotal area.
Mrs. Whittington called Dr. Mason who instructed Mr. Whittington to return to the clinic. Dr.
Mason advised Mr. Whittington to stay off his feet for the remainder of the day, but advised
him that the pain should resolve within a few hours, and he should be able to return to work
within 72 hours.
¶4. Mr. Whittington continued to experience severe pain, bruising and swelling. He
returned to see Dr. Mason on June 2 and again on June 8. During the latter visit, Dr. Mason
released Mr. Whittington to return to work. The next day at work, Mr. Whittington and another
worker were lifting a tire from an “18 wheeler” when Mr. Whittington experienced an episode
of extreme pain on the right side of his scrotum. He was also bleeding in the scrotal area. He
called Dr. Mason who instructed him to return to the clinic the next day.
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¶5. Dr. Mason applied silver nitrate to the scrotal area and then informed Mr. Whittington
that he required a second surgery to remove a granuloma that had developed following the
vasectomy.
¶6. After Dr. Mason removed the granuloma on July 15, Mr. Whittington continued to
experience pain, severe swelling and bruising for six to eight weeks. An open, draining hole
remained at the surgical site, and he was unable to return to work for several weeks.
¶7. When Dr. Mason saw Mr. Whittington again on July 24, he advised that the pain should
subside. On August 3, Dr. Mason released Mr. Whittington to return to work. However,
because he still experienced pain, Mr. Whittington decided to seek a second opinion.
¶8. Sometime around the middle of August, Mr. Whittington scheduled an appointment with
Dr. Bruce Shingleton, who recommended another surgery to remove a granuloma. The
procedure was performed at the end of August. Mr. Whittington continued to experience pain
and severe swelling for several weeks. He remained under Dr. Shingleton’s care for several
months because the pain continued.
¶9. On November 30, Dr. Shingleton released Mr. Whittington. However, because he still
suffered abdominal cramps and pain following sexual activity, Mr. Whittington decided to get
a third opinion.
¶10. On January 29, 1999, Mr. Whittington saw Dr. Lionel Fraser who prescribed a course
of pain therapy and treatment which included a scrotal injection to alleviate the pain. When
these measures did not end the pain, Dr. Fraser removed Mr. Whittington’s right testicle, and
approximately one week later the pain subsided.
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¶11. The Whittingtons filed suit against Dr. Mason and the Clinic, alleging various causes
of action. However, an Agreed Order of Partial Summary Judgment was entered, leaving as the
only relevant issue before the trial court the question of whether Dr. Mason obtained informed
consent to perform the vasectomy.
¶12. At trial, the Whittingtons did not call an expert to establish the material risks which
should have been disclosed in order to obtain informed consent. After the jury failed to reach
a verdict, the trial court directed a verdict for the defendants. The Whittingtons timely filed
an appeal which was assigned to the Court of Appeals.
¶13. In affirming the trial court’s directed verdict for the defendants, the Court of Appeals
stated that “[e]xpert testimony is necessary to determine whether or not the loss of a testicle
is a known risk in a procedure such as a vasectomy.” 2004 WL 2163388 at *3 (Miss. Ct. App.
2004). Because the Whittingtons presented no expert testimony, the Court of Appeals
concluded that the defendants could not be held liable for failure to disclose the loss of a
testicle as a risk of the procedure. The Court of Appeals provided no further analysis of the
Whittingtons’ claim that Dr. Mason failed to adequately inform them of other risks of the
vasectomy including severe, chronic pain and bruising, sperm granuloma, and additional
medical procedures.
¶14. In a motion for rehearing, the Whittingtons directed the Court of Appeals to Dr.
Mason’s own testimony in which he admitted the existence of multiple “known risks” of a
vasectomy. In their brief, the Whittingtons state:
Mr. Whittington suffered an orchiectomy, and the decision of the Court
of Appeals holds that there was no expert testimony at trial to establish that the
“orchiectomy” was a “known risk” of Dr. Mason’s vasectomy. But accepting the
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holding of the Court of Appeals, according to the transcript of the trial
testimony, the same holding cannot be applied to the other “known risks” to
which Dr. Mason testified while being cross-examined in the Plaintiffs’ case-in-
chief at the trial of this civil action. Those other “known risks” of chronic pain,
sperm granuloma and additional surgical procedures represent painful and
compensable complications which were suffered by Scott Whittington as a
result of Dr. Mason’s vasectomy procedure, and those other post-vasectomy
complications are matters on which Scott Whittington presented evidence at
trial.
¶15. We granted the Whittingtons’ petition for writ of certiorari and now proceed to finally
decide the matter.
ANALYSIS
¶16. Every medical procedure involves risks. As discussed infra, no court has ever required
a physician to disclose to a patient every possible risk of a medical procedure. Instead, from
among all possible risks of a procedure, only those which are material must be disclosed in
order to obtain informed consent to the procedure. This begs the question: What must be done
(in the legal sense) to establish what are – and are not – the material risks of a particular
procedure?
¶17. It is apparent from the excellent briefs submitted by both parties that our jurisprudence
regarding “informed consent” is not crystal clear on this point. We shall therefore review in
some detail the prior decisions of this Court which discuss the requirements for informed
consent.
Professional community standard
¶18. Prior to 1985, Mississippi followed the “professional community” standard for a
determination of the material risks which must be disclosed in order to obtain conformed
consent. This professional community standard, in turn, required medical experts to establish
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the acceptable standard within the medical community. For instance, in Ross v. Hodges, 234
So. 2d 905 (Miss. 1970), a patient charged her physician with failure to disclose the risk of
neurological deficit associated with cranial surgery. In affirming the trial court’s directed
verdict on the issue of informed consent, this Court held, “Plaintiff had the burden of proving,
in this respect, the professional standard according to the customs of medical practice of
neurosurgeons in this area.”1 Id. at 909.
Reikes v. Martin
¶19. In 1985, this Court decided Reikes v. Martin, 471 So. 2d 385 (Miss. 1985), wherein
the plaintiff claimed inter alia, that her doctors failed to obtain her informed consent to cobalt
therapy for uterine cancer. In their appeal of a jury verdict of $543,750, the doctors assigned
as error the granting of a jury instruction which provided that “the defendants could be found
liable for failing to fully inform [the plaintiff] of the risk of cobalt therapy, where no evidence
in the record showed she would have elected not to undergo the therapy had she been so
informed.” Id. at 391. In briefly discussing a physician’s duty to inform a patient of risks, the
Reikes Court recognized and cited the authority of Ross v. Hodges. It is important to note at
this juncture that, as to the test for material risks, the Reikes Court neither questioned nor
overruled Ross v. Hodges.
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In Hall v. Hilbun, 466 So. 2d 856, 874-75 (Miss. 1985), the requirement that medical
experts base their opinions on local standards of care was changed to allow testimony based upon the
standard of care of “minimally knowledgeable and competent physicians in the same specialty or
general field of practice. . . .” This change, however, has no bearing on the case before us today.
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¶20. As to the issue of causation (which was the only “informed consent” issue raised on
appeal and discussed in Reikes), this Court began by setting forth the jury instruction at issue,
which stated:
The court instructs the jury that a physician must obtain consent from a
patient to perform the procedure or treatment performed on the patient. To
obtain the required consent, the physician must explain the procedure to the
patient and warn the patient of all material risks or dangers in the procedure or
treatment. The purpose of the explanation is to enable the patient such as [the
plaintiff] to make an intelligent and informed choice about whether to undergo
the treatment or procedure, in this case, cobalt therapy. The physician is
negligent if he fails to disclose to the patient . . . all material information, risks
and warnings.
A risk or danger is material if it would be important to a reasonable
person in the patient’s position in making the decision whether or not to undergo
the procedure or treatment, in this case, cobalt therapy.
The physician is not required to disclose all possible information. The
physician need only disclose information for a reasonable person to make an
intelligent decision.
Reikes, 471 So. 2d at 392. Commenting on the instruction, the Reikes Court then stated:
Although not referred to by name, this instruction applied2 the so-called
prudent patient or materiality of the risk standard in determining what risks must
be revealed to the patient. Under this standard, a physician must disclose those
known risks which would be material to a prudent patient in determining whether
or not to undergo the suggested treatment.
The appellants contend that the above jury instruction was erroneous as
it allowed recovery upon proof that informed consent was not given and without
any showing of causation, i.e., that Mrs. Martin would not have elected to
undergo the treatment if she had been informed of the known risks.
Id. The Reikes Court then addressed the causation issue:
To recover under the doctrine of informed consent, as in all negligence
cases, there must be a causal connection between the breach of duty by the
2
Although the instruction applied the “prudent patient or materiality of the risk standard”
for the determination of which risks must be disclosed, the Reikes Court neither approved nor
adopted the standard.
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defendant and the injuries suffered by the plaintiff. Some states have adopted
a subjective standard, requiring the plaintiff to testify or otherwise prove that
she would not have consented to the proposed treatment if she had been fully
informed. [citations omitted]. A second test, and the one used by the vast
majority of the states, is based upon an objective standard. Under this test, the
question becomes whether or not a reasonably prudent patient, fully advised of
the material known risks, would have consented to the suggested treatment.
Id. The Reikes Court then stated: “[W]e think an objective test is the more desirable and adopt
that test as the one to be applied in this State.” Id. at 393. Critical to an understanding of the
holding in Reikes is that the Court adopted the objective test for causation, but did not make
any finding with respect to the duty to disclose.
¶21. Nevertheless, the Reikes decision would be credited in later cases with adopting the
objective patient-need standard for determining the materiality of a risk. See, e.g., Herrington
v. Spell, 692 So. 2d 93, 98 (Miss. 1997) (“We have adopted [in Reikes] an objective test to
determine what information a physician must disclose. . . .”); Hudson v. Parvin, 582 So. 2d
403, 410 (Miss. 1991) (“We have adopted an objective test [in Reikes] to determine what
information a physician must disclose. . . .”); Phillips ex rel. Phillips v. Hull, 516 So. 2d 488,
493 (Miss. 1987) (“However, recently the Court [in Reikes] recognized the objective patient-
need standard. . . .”).
¶22. Thus, the perceived change from the “professional community” standard to the
“objective patient need” standard for determining material risks, springs from a misapplication
of Reikes. It bears repeating that the adoption by the Reikes Court of the objective standard
for purposes of determining causation is unrelated to the obligation of the plaintiff to
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produce expert testimony to establish the material risks of a medical procedure which should
be disclosed.
¶23. The use of the objective (as opposed to subjective) standard for establishing causation,
as announced in Reikes, is not before us.
¶24. As recognized by the Reikes Court, no doctor could comply with a requirement to
disclose every possible risk to every procedure. 471 So. 2d at 392. Doctors must, however,
disclose material risks associated with a particular procedure. Among the many factors which
could weigh on the question of materiality are frequency of occurrence, potential severity or
danger associated with the risk, and the cost and availability of an alternative procedure. These
factors cannot be established absent expert testimony.
This Court’s holding
¶25. Thus, we hold today that expert testimony is required to assist the finder of fact in
determining whether a particular risk is material, requiring disclosure to the patient prior to
a medical procedure. In the event of conflicting expert testimony, the finder of fact must
evaluate the basis for each expert opinion and decide which is more credible. This
determination is no different from other issues requiring expert testimony.
¶26. The record in the case sub judice indicates that there were several “risks” of the
vasectomy which the Whittingtons claim were not disclosed. However, the Whittingtons
produced no expert testimony to establish that these risks were material and should have been
disclosed. Thus, the Whittingtons’ claim of lack of informed consent must fail.
¶27. Our review of the record in this case leads us to the conclusion that the jury had no
reasonable basis to determine that material risks of a vasectomy included any of the undesired
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results of the procedure which the Whittingtons claim were not disclosed. Any such
determination by the jury would have been pure speculation.
CONCLUSION
¶28. We hold that a plaintiff must produce expert testimony to establish the material risks
and available alternatives of a medical procedure. Absent such expert testimony, a jury may
not consider whether a physician conducted a medical procedure without informed consent.
To the extent this Court’s prior cases – including the cases cited herein – conflict with our
decision today, they are hereby overruled. Because the Whittingtons produced no expert
testimony to assist the jury in determining which complications of the vasectomy were
material risks requiring disclosure or further explanation prior to the procedure, we affirm the
trial court’s grant of judgment in favor of the defendants and the judgment of the Court of
Appeals.
¶29. AFFIRMED.
SMITH, C.J., WALLER AND COBB, P.JJ., CARLSON AND RANDOLPH, JJ.,
CONCUR. GRAVES, J., CONCURS IN RESULT ONLY. EASLEY, J., DISSENTS
WITHOUT SEPARATE WRITTEN OPINION. DIAZ, J., NOT PARTICIPATING.
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