delivered the opinion of the court:
Plaintiff, Leona Mielke, appeals from an order of the circuit court of Lake County directing a verdict in favor of defendant-appellee Con-dell Memorial Hospital (Condell Hospital) and from a judgment entered on jury verdicts in favor of defendants Burton Miller, M.D., and Robert Munson, M.D. Plaintiff assigns as errors the improper impeachment of its expert witness, the trial court’s reservation of an evidentiary ruling until after cross-examination, the trial court’s order granting Condell Hospital’s motion for a directed verdict, and its exclusion of expert testimony summarizing the medical literature. We affirm.
Plaintiff was admitted to Condell Hospital on December 10, 1978, for emergency treatment of a perforated duodenal ulcer. Her blood pressure was extremely low, her pulse was rapid, she was experiencing severe abdominal pain and had been vomiting blood. Munson, an internist and the attending physician, testified she was in shock. Miller, a board-certified general surgeon, examined plaintiff and recommended she be given penicillin and gentamicin, two antibiotic drugs.
Plaintiff subsequently underwent two surgical procedures, the first to repair a perforated ulcer, and the second to remove an abdominal abscess. Both surgeries were performed by Miller. To combat a potentially serious infection, plaintiff was given gentamicin before and after each of the surgical operations. She also was given Lasix, a diuretic, to counteract fluid which had collected in her lungs following the abdominal abscess surgery. Both drugs have an indicated side effect of autotoxicity.
On December 27, plaintiff complained of a headache and blood was discovered in her urine. At trial, plaintiff’s witness, Dr. M. Reese Guttman, testified that plaintiff suffered loss of her labyrinth, the inner ears’ balance function because of the gentamicin she was given at the hospital. Guttman stated persons suffering from a total loss of labyrinthian function on each side are unable to walk without aid, are housebound, and cannot perform household duties unless they are seated. He further testified the condition was permanent.
At the close of plaintiff’s case, the trial court allowed the motion of Condell Hospital for a directed verdict because of the absence of proof of the hospital’s negligence. Thereafter, the jury returned verdicts of not guilty for the defendant doctors and the trial court entered judgment on the verdicts. Plaintiff’s post-trial motion was denied and she filed a timely notice of appeal.
RESERVATION OF RULING ON ADMISSIBILITY OF EVIDENCE
Plaintiff first assigns as error the trial court’s reservation of its ruling on the admissibility of the drug manufacturer’s insert. During his direct testimony, plaintiff’s expert witness, John W. Frost, M.D., was asked to identify plaintiff’s exhibit No. 3, the gentamicin package insert, and was asked whether the insert embodied the standard of care about which he testified. When Frost responded that it did, plaintiff offered the package insert into evidence. Defense counsel objected on the ground that the standard of care could only be established from physician testimony, the directions were not mandatory, and the foundation for the insert was insufficient. The court elected to reserve its ruling until after the cross-examination of Frost and also reserved its ruling on plaintiff’s exhibit No. 4, the 1977 Physiclan’s Desk Reference (PDR), also identified by Frost as embodying the standard of care. Folio-wing re-cross-examination of Frost, the package insert and the PDR were admitted into evidence by stipulation of all of the parties. The stipulation included the condition that exhibit Nos. 3 and 4 would not go to the jury.
At the close of plaintiffs case, plaintiff’s attorney read the contents of exhibit No. 3 to the jury while the package insert was projected onto a screen in the darkened courtroom. Plaintiffs attorney also used both exhibit Nos. 3 and 4 to cross-examine Drs. Miller and Munson and their expert -witnesses and relied upon both exhibits in her closing argument. The essence of plaintiffs argument, therefore, is solely that the trial court erred by reserving its ruling on the admissibility of the exhibit until after Frost’s direct testimony even though the exhibits were subsequently introduced.
The cases cited by plaintiff do not warrant the conclusion that the trial court erred in the case at bar. The supreme court in Ohligschlager v. Proctor Community Hospital (1973),
Even were these cases directly on point, plaintiff’s argument here must fail because the insert was read to the jury, was used during cross-examination and closing argument, and was admitted into evidence by stipulation. The parties also agreed that the package insert and the PDR were the same. Therefore, the jury was presented with the contents of the package insert and the relevant portion of the PDR. Although plaintiff asserts prejudice because Frost was precluded from using the insert in his direct testimony, we note that plaintiff did not attempt to recall Frost for examination after exhibit Nos. 3 and 4 were admitted. Plaintiff cites no case where the trial court’s reservation of an evidentiary ruling was error when the evidence was subsequently admitted. Contrary to plaintiff’s contention, even if the trial court’s reservation were error, such error would be harmless. The jury heard and read the package insert and was present when defense witnesses were cross-examined with the insert and the PDR. Since the information was presented to the jury, no reversible error was committed by the trial court.
IMPEACHMENT OF EXPERT
Plaintiff contends the trial court erred in allowing repeated impeachment of its expert on immaterial matters. The scope of cross-examination of a witness is within the sound discretion of the trial court. (Eckley v. St. Therese Hospital (1978),
Applying these principles to the instant case, no reversible error is raised by plaintiff. At trial, Frost answered affirmatively that he knew what the standards of care were for administering and monitoring drugs “here” in 1978. In his deposition, however, Frost stated he was not familiar with the standards in the area in 1978 “because I wasn’t in this area in 1978.” Since these answers are inconsistent, they affect his credibility and thus, impeachment on this ground was proper.
Both defendants and their experts agreed that plaintiff was gravely ill with findings consistent with widespread infection and septic shock in the emergency room on December 10, 1978. They further agreed that broad spectrum antibiotic treatment was necessary because of clinical findings of sepsis and shock. Since defendants testified they gave plaintiff gentamicin based on her condition, Frost was properly asked if plaintiff was in shock. While at trial his answer was equivocal as to whether plaintiff was in shock, in his deposition Frost was more certain, stating plaintiff was in shock. The two answers are arguably impeaching, and thus, no error was committed. Both defendant doctors stressed the importance of physician judgment in treating plaintiff’s illness. Therefore, Frost was properly impeached on the issue of whether he could form an opinion as to the care rendered without being present during plaintiff’s treatment. At trial, Frost answered he could reach an opinion concerning treatment solely from the record, but in his deposition stated “it’s rather hard when you are not there to know the circumstances ***.” While in his deposition he nevertheless stated he had formed an opinion based upon his review of the hospital record, his deposition testimony affected his credibility and the weight to be accorded his answer and thus was properly recounted by defense counsel.
Frost also gave two opposite opinions as to whether plaintiff was a “sick lady”, following the discontinuation of the first course of gentamicin. Both defendant doctors and their experts testified plaintiff was gravely ill and exhibited symptoms of recurring sepsis. Plaintiff’s condition, therefore, was material to the decision to again give gentamicin and thus, Frost’s inconsistent answers were properly raised by defense counsel.
Both defendant doctors and their experts testified that the evidence of infection warranted the continuation of gentamicin until the course was finished on the eighth day post-operatively. Therefore, Frost was asked the question whether continuation of gentamicin until the positive identity came back on the culture was good medical practice. Frost stated it was not good medical practice and that he would not have continued gentamicin that long. In his deposition testimony, however, Frost responded he might have continued the gentamicin, depending upon the condition of the patient. The disparity in his answers provided a proper ground for impeachment. Since all of the instances of impeachment concern material issues and were directed toward Frost’s qualifications or credibility, the trial court committed no reversible error.
DIRECTED VERDICT FOR HOSPITAL
Plaintiff contends the trial court erred in granting the hospital’s motion for a directed verdict. A court may direct a verdict when, at the close of all the evidence, the court has determined that even in the light most favorable to the nonmoving party, the evidence could not justify a contrary result. (Pedrick v. Peoria & Eastern R.R. Co. (1967),
Application of the Pedrick standard to medical malpractice cases requires the reviewing court to scrutinize the evidence submitted by the plaintiff in support of its case. (McMillen v. Carlinville Area Hospital (1983),
Plaintiff asserts that the hospital’s standard of care was established by the introduction into evidence of the standards of the Joint Commission on Accreditation of Hospitals (Joint Commission standards), the package insert on gentamicin and the PDR. The parties agreed at trial that the PDR and the package insert were the same. The hospital responds that the trial court properly directed the verdict because plaintiff failed to establish a standard of care by expert testimony. Plaintiff replies that expert testimony is not mandatory in this case.
While plaintiff states that the Joint Commission standards establish a standard of care, she fails to cite any particular standard or to refer us to a place in the record where specific standards were argued to the trial court. Plaintiff cites the testimony of the hospital’s pharmacist that Condell Hospital complied with the Joint Commission standards and argues that the standards are independent evidence of a hospital’s standard of care, but she does not refer to any specific standard upon which she bases her contention. Instead, she simply includes the entire 1977 Accreditation Manual of Hospitals in the appellate record and makes only generalized conclusions that the manual establishes the standard of care. Supreme Court Rule 341(e)(7) requires an appellant’s brief to contain argument with “citation of the authorities and the pages in the record relied on.” (87 Ill. 2d R. 341(e)(7).) Strict adherence to the standard is necessary to expedite and facilitate the administration of justice. (Harvey v. Carponelli (1983),
Apart from the Joint Commission standards, plaintiff relied upon the PDR and the package insert as establishing the hospital’s standard of care. The general rule is that the standard of care must be established by expert testimony. (Biundo v. Christ Community Hospital (1982),
Plaintiff offered no expert testimony on the standard of care of the hospital. Rather, she contends that the record contains sufficient independent evidence of the negligence of the hospital (the PDR and the package insert). If in advancing this argument plaintiff contends that no expert testimony is required because the interaction of the two drugs is within every person’s common knowledge, then we find her position untenable. In a complex situation such as is present here, involving the pharmacological effects of a drug regimen, a layperson cannot be expected to determine without the aid of expert testimony what standard should be used to judge the hospital’s conduct. This case is not a situation where conduct is so grossly negligent “that a layman could readily appraise it, in which event expert testimony may not be necessary.” Casbarra v. St. James Hospital (1980),
Neither do we agree that her reliance on the PDR and the package insert is sufficient to establish the standard in the absence of expert testimony. While we agree that “the standard of care applicable to a hospital may be proved via a number of evidentiary sources” (Greenberg v. Michael Reese Hospital (1980),
Plaintiff also relies on two Federal cases to support her contention that the evidence established the hospital’s standard of care. In Monk v. Doctors Hospital (D.C. Cir. 1968),
The decision in Lucy Webb Hayes National Training School v. Perotti (D.C. Cir. 1969),
Even if the evidence did establish the hospital’s standard of care, plaintiff failed to prove that the hospital breached that standard. Plaintiff’s argument appears to be that the failure of the hospital pharmacy to inform the attending physician concerning the potential adverse interaction between Lasix and gentamicin was a sufficient deviation from the Joint Commission standards to submit the issue of the hospital’s negligence to the jury. Since plaintiff has waived her reliance on the Joint Commission standards, her only bases for establishing a breach of a standard of care are the PDR and the package insert. As noted by plaintiff, the PDR and the insert contain warnings issued by the manufacturers of the drug products to the medical profession concerning the concurrent use of gentamicin and a potent diuretic. While these sources may provide relevant evidence of a standard of care or its breach, such evidence alone is too general to establish even a prima fade case of Condell Hospital’s breach of a standard of care.
Even considering plaintiff’s evidence regarding the Joint Commission standards, no breach of care was established. Plaintiff does not refer to any specific Joint Commission standard or recommendation. The record discloses that the hospital pharmacist testified that Condell Hospital in 1978 complied with the provisions of the Joint Commission on Accreditation of Hospitals, and that the hospital maintained a drug monitoring service in which a registered pharmacist reviewed and judged the drug therapy of each patient. The pharmacist also testified a hospital pharmacist would discuss a particular drug with the physician if it were inappropriate. The pharmacist further stated plaintiff’s drug regimen was reviewed with regard to interactions, interferences, and incompatibilities. Plaintiff did not offer any evidence that lack of communication between the pharmacist and the physician here was a deviation from a standard of care. Plaintiff did not establish that Condell Hospital’s drug monitoring program was deficient. Plaintiff did not cite to any evidence establishing that plaintiff’s drug regimen was inappropriate. The potential adverse interaction of two drugs highlighted in the PDR does not establish a prima fade case that under the facts presented here gentamicin was inappropriately given and that Condell Hospital breached a standard of care. Therefore, the trial court properly directed a verdict in favor of the hospital.
EXPERT TESTIMONY SUMMARIZING HISTORY AND CONTENT OF MEDICAL LITERATURE
Plaintiff’s final argument is that the trial court erred in refusing to allow her expert to testify as to the history and content of medical literature regarding gentamicin and Lasix. At trial, plaintiff’s only expert witness was Frost. During direct examination of Frost, plaintiff asked him to review the literature on the history of gentamicin from 1964 “particularly with emphasis on its ototoxicity and interaction with Lasix.” In answering plaintiff’s question, Frost began reading from notes he had taken on his review of the literature. One defendant objected, arguing Frost’s summary of the articles constituted hearsay. If plaintiff were allowed to present testimony concerning the contents of the articles, defendant contended, the jury would hear evidence which defendants would be unable to challenge on cross-examination. Plaintiff made an offer of proof, wherein Frost stated his notes summarized articles written by well-recognized authorities, his opinion of the standard of care was based upon the notes, and his testimony, if allowed, would parallel his notes. The trial court refused to allow Frost to read from his notes even though plaintiff stated she did not desire to have the notes admitted into evidence. The court agreed “that Frost was not precluded from stating his opinion and the authorities forming the basis of the opinion,” but was prohibited from reading from his notes or from the articles themselves.
While this precise issue has not been decided by an Illinois court, several supreme court decisions have considered similar questions. In Darling v. Charleston Community Memorial Hospital (1965),
In Lawson v. G.D. Searle & Co. (1976),
The more recent case of Walski v. Tiesenga (1978),
“Such is not the law in this jurisdiction at this time, and it is unnecessary for us to decide now whether and under what circumstances a plaintiff may introduce medical treatises as substantive evidence; plaintiff has made no attempt to introduce the treatises used to cross-examine Dr. Tiesenga as substantive evidence.” (72 Ill. 2d 249 , 258-59.)
This statement by the Walski court suggests that the articles cannot be used as substantive evidence here to establish defendant’s standard of care. See Plost v. Lewis A. Weiss Memorial Hospital (1978),
Plaintiff argues the supreme court’s adoption of Federal Rules of Evidence 703 and 705 in Wilson v. Clark (1981),
Several recent decisions have interpreted Ward. In People v. Rhoades (1979),
Similarly, plaintiff here is attempting to introduce the facts in the articles as substantive evidence on direct testimony regarding gentamicin and Lasix. While prior decisions make clear that Frost could base his opinion on the articles and could recite the articles as sources for his opinion, Bailey supports our conclusion that the trial court properly rejected Frost’s summarization of the findings of the articles.
Also supportive of the defendants’ position are Fornoff v. Parke-Davis & Co. (1982),
In Mehochko v. Gold Seal Co. (1966),
“In tests, the essential elements are the results, methods and qualifications of the tester. The method and qualification of the tester (to conduct the test and correctly read its results) give the results their veracity. Dr. Lederer was not testifying from his own knowledge about an exhibit (like the X-ray or myelogram) before the court. He could not be cross-examined about an exhibit before the court. He was not testifying from his own knowledge about an exhibit before the court; he knew no more about the independent tests than he had read (been told). The tests were not before the court and he could not be cross-examined about the method (save what he read about it) nor about the tester’s qualifications to perform the experiments and correctly interpret the results. Dr. Lederer was a stranger to the evidence he introduced. He knew nothing about it save through hearsay; he could not be cross-examined about the essence of the independent tests.” (Mehochko v. Gold Seal Co. (1966),66 Ill. App. 2d 54 , 58,213 N.E.2d 581 , 583.)
Just as did the witness in Mehochko, Frost here was attempting to summarize the results of the tests that he had not conducted and about which he could not testify on cross-examination concerning the test methods and procedures. Plaintiff’s arguments that Mehochko is “inapposite” are unpersuasive. We do not read Wilson as overruling Mehochko as does plaintiff. In Wilson, the court allowed prospectively a nontreating physician to offer his opinion in response to a hypothetical question based upon records not introduced into evidence. Here, and in Mehochko, the experts were not just offering their opinion, but in addition were attempting to summarize tests and studies performed by others. Another distinguishing factor between Mehochko and the instant case on the one hand and Wilson on the other is that the tests in the former cases are significantly less reliable than are hospital records. Finally, in Wilson, the expert witness was answering a hypothetical question based upon facts contained in the plaintiff’s hospital chart. Therefore, those facts were directly pertinent to that litigation. In contrast, the disputed testimony in Mehochko did not concern the plaintiff’s injuries directly, but rather only experiments on the product conducted under potentially different conditions. Likewise, Frost’s testimony which was excluded by the trial court here did not directly concern plaintiff’s treatment, but rather summarized tests some of which occurred many years prior to plaintiff’s injuries and none of which replicated her unique circumstances. For these reasons, we find Mehochko persuasive and conclude the trial court properly prevented Frost from summarizing the medical literature.
The judgment of the circuit court of Lake County is affirmed.
Affirmed.
HOPF and NASH, JJ., concur.
