James v. Nolan

614 A.2d 709, 418 Pa. Super. 425, 1992 Pa. Super. LEXIS 3075
CourtSuperior Court of Pennsylvania
DecidedSeptember 9, 1992
Docket1944
StatusPublished
Cited by18 cases

This text of 614 A.2d 709 (James v. Nolan) is published on Counsel Stack Legal Research, covering Superior Court of Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
James v. Nolan, 614 A.2d 709, 418 Pa. Super. 425, 1992 Pa. Super. LEXIS 3075 (Pa. Ct. App. 1992).

Opinion

ROWLEY, President Judge:

In this appeal from the judgment entered on the jury verdict in favor of appellee Maeve Nolan, M.D., and Firm Labs Service, P.C. (hereinafter “appellees”), appellant Rodney James (hereinafter “appellant”) seeks a new trial based on his contention that the trial court erred in several respects and that the jury’s verdict was inconsistent with the law and the facts of this case. The following four issues have been raised for our consideration: (1) whether the jury’s finding that appellee was negligent but that her negligence was not a substantial factor in causing appellant’s harm was inconsistent 1 ; (2) whether the trial court should have admitted the *428 Pennsylvania Blood Bank statute into evidence 2 ; (3) whether the trial court’s jury instructions adequately addressed the concept of “substantial factor;” and (4) whether the trial court erred in permitting testimony and argument regarding various factors, rather than just the one advanced by appellant, which could have caused appellant’s harm. Having thoroughly reviewed the record and considered the arguments of the parties, we affirm.

Recently, this Court reiterated the standard of review which we utilize in evaluating the appellant’s claims in the instant appeal:

When assessing the denial of a motion for new trial, the Superior Court will reverse only where the [trial] court has clearly and palpably abused its discretion or committed an error of law which controlled the outcome of the case.

Lilley v. Johns-Manville Corporation, 408 Pa.Super. 83, 95, 596 A.2d 203, 209 (1991).

The factual and procedural history of this case is as follows: Appellant filed a negligence suit against various defendants in his own name and as executor of the estate of his wife, a deceased blood technician (Patricia James) who was employed by the McKeesport Hospital’s blood bank prior to her demise. In his action, he claimed damages which resulted from his wife’s contraction of Acquired Immune Deficiency Syndrome (hereinafter’ “AIDS”) in the course of her performance of an apheresis procedure on a patient whose blood had not been tested for the human immunodeficiency virus (hereinafter “HIV”) prior to the procedure, but which would ultimately reveal the presence of HIV. By the time of trial, appellees were the only defendants remaining in the case. Following a *429 jury trial, a verdict was returned in favor of appellees. Post-verdict motions were denied in a comprehensive twenty-eight page memorandum opinion by the trial judge, whereupon the instant appeal was taken.

Patricia James, appellant’s decedent, was employed by the McKeesport Hospital in the capacity of assistant supervisor of the blood bank when the events involved in this case took place. As a result of her position, she was required to act as supervisor in the absence of the blood bank’s regular supervisor, Marilyn McDonough. At all times relevant to this action, Ms. McDonough was on vacation and Patricia James was acting as supervisor of the blood bank.

At the time that this cause of action arose, appellee, Dr. Maeve Nolan, was medical director of the McKeesport Hospital blood bank, but she was not an employee of the hospital. Appellee Nolan owned a professional corporation, appellee Firm Labs Service, which billed the hospital for the professional services of Dr. Nolan.

On December 3,1986, a patient at McKeesport Hospital was in desperate need of a platelet transfusion from a family member. The patient’s attending physician advised appellee Nolan of the immediate need for platelet apheresis because Dr. Nolan, as director of the blood bank, was the only person who could schedule an apheresis procedure. A relative was located and told to report to the blood bank for preliminary blood work in preparation for the potential donation of his blood.

That afternoon, the potential donor arrived at the lab and blood was drawn for tests routinely performed on a prospective donor’s blood. The hemoglobin, hematocrit and white blood cell levels in his blood were tested immediately to ascertain whether the donor could withstand the apheresis process without harming his own health. Within an hour, the results were returned as normal and appellee Nolan scheduled the apheresis procedure for the next day, December 4, 1986.

As a matter of routine, prior to the ultimate transfusion of the platelets into the patient, additional tests (including tests *430 for hepatitis and HXV) were to be performed on the donor’s blood in order to determine whether his platelets would be suitable for transfusion. These tests were to be performed by a lab technician assigned to the task by the blood bank supervisor, or in her absence, the acting supervisor. As the physician in charge of the blood bank, appellee Nolan never did the actual testing of potential donors’ blood. McKeesport Hospital protocol mandated that the blood be tested for HIV during the morning shift because the test requires about four hour’s time and the morning shift is the most heavily staffed.

In the instant case, the donor’s blood was drawn on the afternoon of December 3rd and the apheresis procedure was scheduled for the next morning, December 4th, due to the patient’s urgent need for the platelets. Therefore, due to the medical urgency of the situation, the donor’s blood had not been tested for HIV prior to commencement of the procedure, but was to be so tested prior to ultimate transfusion of the platelets.

During an apheresis procedure, the donor is attached to a centrifuge with a needle in each arm. The donor’s blood continuously flows from one arm into the machine and back into the other arm while the machine separates out the platelets from the other components of the donor’s blood. The procedure requires the participation of two healthcare workers — one to operate the machine and the other to assist the patient.

In the instant case, the decedent, Patricia James, operated the machine with the assistance of Georgia Gentile. In the course of the procedure, technical difficulties ensued with the machine’s tubing, automatically causing the machine to stop. Mrs. James attempted to remedy the problem by removing and replacing the tubing, rather than terminating the process or contacting the blood bank director, appellee Nolan. No reference was made by the two technicians to the machine’s manual.

According to the trial testimony, Mrs. James removed the clogged segments of tubing containing the donor’s blood without clamping them or restricting the flow of blood in any *431 manner. The donor’s blood spurted on the machine and all over Mrs. James’ hands and arms. In violation of the hospital’s infection control policy, and despite the availability of a sink and gloves within several steps of the machine, Mrs. James’ did not wash the blood off herself, but rather, cleaned the machine and mopped up the blood around the area of the machine without wearing gloves.

While Mrs.

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Cite This Page — Counsel Stack

Bluebook (online)
614 A.2d 709, 418 Pa. Super. 425, 1992 Pa. Super. LEXIS 3075, Counsel Stack Legal Research, https://law.counselstack.com/opinion/james-v-nolan-pasuperct-1992.