Opinion
Shortly after giving birth to her daughter in 1982, appellant, Sheri R. Traxler, received a blood transfusion. By 1988, when Sheri Traxler first learned that she, tragically, had become one of the approximately 600,000 women worldwide who are now afflicted with Acquired Immune
Facts
After a normal pregnancy under the care of Dr. Chris Cammisa, appellant was admitted to NorthBay Medical Center where Dr. Robert Varady delivered her baby. Since this was Dr. Varady’s first delivery at the NorthBay Medical Center, Dr. James Heinrich was designated as his “proctor.” After appellant gave birth to a normal baby girl by vaginal delivery, Dr. Varady examined the placenta and concluded that it was intact, meaning that no significant amount of placental tissue had been retained in the utems.
Two weeks later, appellant began severe hemorrhaging, was mshed to the hospital and signed a consent form authorizing a dilatation and curettage procedure (D&C). 1 Dr. Cammisa estimated that appellant had already lost approximately two pints of blood and suspected that a blood transfiision might be necessary. He ordered two units of blood to be held for appellant. Dr. Cammisa then performed the D&C and removed some “necrotic-appearing tissue.” Unexpectedly, appellant continued to hemorrhage. After consulting with Dr. Heinrich, Dr. Cammisa placed appellant under general anesthesia and performed a second D&C. Only a few blood clots, which did not explain why appellant continued to hemorrhage, were found.
In the recovery room Dr. Heinrich evaluated appellant’s condition. Her total documented blood loss during this period comprised approximately 30-40 percent of her total blood volume. His primary concern was that she could hemorrhage again at anytime. Renewed hemorrhaging had occurred in
In 1988, after being notified by the Irwin Memorial Blood Bank that she might have received HIV-infected blood, appellant tested positive for the presence of the HIV virus. It was undisputed at trial that in 1982 the HIV virus had not yet been identified and that the risk of receiving HIV-tainted blood through a transfusion was unknown.
Appellant’s theory of liability was that Dr. Varady negligently performed the delivery by failing to ensure that no placental tissue was retained; that his negligence caused her to hemorrhage. She further alleged that Dr. Heinrich ordered an unnecessary transfusion, to which she did not give her informed consent. A unanimous jury found no negligence on the part of any of the defendants.
Analysis
I.
Appellant contends the trial court erred in refusing to give her requested instruction on “negligence per se.”
Appellant’s requested instruction read as follows: “If you find that a party to this action violated Title 22, California [Code of Regulations] Sections 70213(a) and (d); 70231; 70233; 70235; 70703 ; 70706; 70706.2; 70707; 70747; 70749; 70751 (a)(h) and 70753,[ 2 ] the Statutes and code sections just read to you, and that such a violation was a legal cause of injury to another, you will find that such violation was negligence unless such party proves by a preponderance of the evidence that he did what might reasonably be expected of a person of ordinary prudence, acting under similar circumstances, who desired to comply with the law. In order to sustain such burden of proof, such party must prove by a preponderance of the evidence that he was faced with circumstances which prevented compliance or justified noncompliance with the statutes and codes.”
A—Section 70223, Subdivision (g)
We conclude that the trial court correctly refused to give appellant’s requested instruction on section 70223, subdivision (g), because the elements set forth in Evidence Code section 669, defining when an alleged violation of statute or regulation supports a presumption of negligence per se, were not supported by the evidence. 4
Section 669 of the Evidence Code provides that: “(a) The failure of a person to exercise due care is presumed if: (1) He violated a. . . regulation of a public entity; (2) The violation proximately caused death or injury. . . ; (3) The death or injury resulted from an occurrence of the nature which the . . . regulation was designed to prevent; and (4) The person suffering the death or injury to his person . . . was one of the class of persons for whose protection the . . . regulation was adopted.” The burden is on the proponent of a negligence per se instruction to démonstrate that these elements are met.
(Ronald M.
v.
White
(1980)
Section 70223, subdivision (g), of title 22 provides, in part, that “All anatomical parts, tissues and foreign objects removed by operation shall be delivered to a pathologist designated by the hospital and a report of his
Although conceding that “the failure to send the tissue to pathology certainly did not cause appellant to become infected," appellant argues that the evidence supports the inference that Drs. Cammisa and Varady violated section 70223 by failing to send all the tissue they removed in the first D&C procedure to pathology. She alleges this failure to have all the tissue examined by a pathologist prevented “appellant from proving that Dr. Varady’s negligence in the delivery of the placenta [following childbirth] was the first link in the chain of [her] infection.” In other words, appellant argues that she should have been permitted to prove Drs. Varady’s and Cammisa’s alleged violation of section 70223 and have the jury instructed on negligence per se in support of her contention that they concealed proof of Dr. Varady’s primary negligence in the delivery of appellant’s daughter.
Putting aside the very substantial question whether spoliation of evidence is the type of injury section 70223 is designed to prevent, the issue is waived
In her final argument with respect to section 70223, subdivision (g), appellant asserts that the section applied to the original vaginal delivery of the placenta, which should have been sent to a pathologist for examination.
We find no error in refusing the instruction. Section 79223, subdivision (g) has no application to these facts, because the placenta was not removed “by operation.” At trial, exhaustive evidence was presented to the effect that placentas typically are not sent to pathology following a normal, uncomplicated delivery. A placenta in a normal vaginal delivery is expelled by the mother’s uterine contractions and the force of gravity, assisted by the doctor’s application of gentle traction. No reasonable jury would have found that the placenta was removed “by operation.” Therefore the refusal to give the instruction on this theory, if error, would be harmless. (See, e.g.,
Murphy
v.
Atchison, T. & S. F. Railway
(1958)
Appellant speculates that if Dr. Varady had sent the apparently normal and intact placenta to pathology after the childbirth, a pathologist might have discerned that some placental tissue had been retained and, therefore, (assuming that was the cause of the hemorrhaging) the doctor could have taken measures to prevent the hemorrhaging, thereby eliminating the need for the transfusion. Although, appellant was permitted at trial, in the context of a common law negligence claim, to advance her theory that Dr. Varady was negligent in failing to have the placenta examined by a pathologist, she does not cite any evidence that a pathology lab could have discerned that a significant amount of placental tissue had been retained and thereby prevented the hemorrhaging. Appellant has thus failed to show that the alleged violation of section 70223, subdivision (g) proximately caused her injury. (See Evid. Code, § 669, subd. (a)(2).) We therefore are persuaded that refusal to give the instruction, if error, was harmless. (See, e.g., Murphy v. Atchison, T. & S. F. Railway, supra, 162 Cal.App.2d at pp. 822-824.)
B—Section 70707
Appellant also contends that the court should have given a negligence per se instruction based on section 70707.
Appellant again fails to demonstrate that she was prejudiced by the failure to give a “negligence per se" instruction based on this section. Section 70707 requires nothing more than that the patient’s informed consent be obtained. The section does not offer a definition of the term “informed consent" that differs in any significant respect with the common law. In
Cobbs
v.
Grant
(1972)
The jury was fully instructed on the common law duty to obtain a patient’s informed consent, and what constitutes an emergency, excusing the performance of this duty. By its unanimous verdict, the jury concluded that appellant either gave informed consent or her consent was implied under the circumstances. Thus, refusing to give the requested instruction, if error, was harmless. It is not reasonably probable that the result would have been different had the requested instruction been given.
6
(See
Canavin
v.
Pacific Southwest Airlines
(1983)
Appellant next contends that the court erred in refusing her instruction on “informed consent.” Appellant requested the following instruction: “A physician rendering a diagnosis has a duty to inform the patient that other members of the medical profession might render a different diagnosis based on a contrary recognized school of thought.” This instruction is based on dicta in
Jamison
v.
Lindsay
(1980)
Appellant cites no evidence that there were divergent “schools of thought” regarding any of the decisions made by her treating physicians. The requested instruction was, therefore, properly refused.
(Scalere
v.
Stenson
(1989)
Appellant also contends that the court erred in refusing to supplement the instructions given on informed consent with the following language excerpted from
Cobbs
v.
Grant, supra,
The court gave complete instructions on informed consent, including BAJI No. 6.11, which is based on the holding in
Cobbs
v.
Grant, supra,
III.
Finally, appellant contends that the court erred by refusing to instruct the jury on the tort of battery.
Appellant contends she had a cause of action for battery based on her contentions that her written consent to the D&C and “any other therapeutic procedure that (his) (their) judgment may dictate to be advisable for the patient’s well being” did not include consent to the transfusion, and her consent to the transfusion could not be implied because no emergency or other circumstance existed excusing the treating physicians from obtaining a separate consent to the blood transfusion.
In
Cobbs
v.
Grant, supra,
Respondents contend that appellant’s cause of action lay only in negligence. In
Cobbs
the court explained that when the physician obtains a patient’s consent and some undisclosed complication with a low probability of occurrence develops, the patient’s cause of action lies in negligence only.
(Cobbs
v.
Grant, supra,
The jury, by its verdict on appellant’s informed consent cause of action, must have found either that appellant consented or that her consent was implied under the circumstances. Therefore, any error in refusing to instruct on battery was harmless. (See, e.g.,
Lussier
v.
San Lorenzo Valley Water Dist.
(1988)
Conclusion
The judgment is affirmed.
Strankman, P. J., and Dossee, J., concurred.
Notes
The form stated, in pertinent part, as follows: “1.1 authorize and direct Dr. Cammisa my surgeon and/or associates or assistants of his choice, to perform the following operation on me [suction curettage] and/or to do any other therapeutic procedure that (his) (their) judgment may dictate to be advisable for the patient’s well being. The nature of the operation has been explained to me and no warranty or guarantee has been made as to the result or cure. FJ] 2.1 hereby authorize and direct the above-named surgeon and/or his associates or assistants to provide such additional services for me as he or they may deem reasonable or necessary, including but not limited to the administration and maintenance of anesthesia, and the performance of services involving pathology and radiology, and I hereby consent thereto.’’
Unless otherwise noted, all further title and section cites are to the Code of Regulations.
Appellant makes no attempt to demonstrate that the instruction as a whole was proper. Since the court has no duty to refine or revise an incorrect or overbroad instruction, it was properly refused on the basis it was overbroad.
(Travelers Ins. Co.
v.
Lesher
(1986)
We further find that appellant has failed to demonstrate that she was prejudiced by the refusal to give her proposed instruction. It is, therefore, unnecessary for us to address the broader issues raised by the hospital, physician respondents and amicus curiae as to whether, and in what circumstance, any of the title 22 regulations can ever be used to define a standard of care for hospitals or physicians.
The court also found that none of the title 22 regulations could be used to define the standard of care for physicians. It is unnecessary to determine whether this broader aspect of the court’s summary adjudication was correct, because even if section 70223 could, in the appropriate factual circumstances, be used to define the standard of care for physicians, we affirm the court’s determination that the alleged violation of this section did not proximately cause appellant’s injuries.
The hospital argues that this regulation does not impose a duty on the
hospital
to ensure that the treating physicians obtain the patient’s informed consent. The treating physicians in turn contend that this regulation does not define the
physician’s
standard of care in obtaining a patient’s informed consent, which they contend can only be established through expert testimony. We need not address these broader questions because we find the issues of informed consent and whether an emergency existed were fully presented to the jury under
Similarly, where consent is conditional and the doctor proceeds without observing the condition placed on the patient’s consent, the patient may have a cause of action for battery. (See, e.g.,
Ashcraft
v.
King
(1991)
