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Grecco v. University of Medicine and Dentistry of New Jersey

November 07, 2001

CHRISTOPHER GRECCO, A MINOR BY HIS GUARDIAN AD LITEM, RICHARD GRECCO, AND RICHARD GRECCO AND SABRINA GRECCO, INDIVIDUALLY, PLAINTIFFS
v.
UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY, UNIVERSITY HOSPITAL, SUSAN MAKOWSKY, R.N., ANGELA BROWN, R.N., CATHLEEN FALICIANI, R.N., VISWANATHAN NIRANJAN, M.D., AND LING YU SHIH, M.D., DEFENDANTS
GEORGE SAMUELS, JOSEPH LICATA AND UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY, THIRD-PARTY PLAINTIFFS/ RESPONDENTS
v.
SABRINA GRECCO AND RICHARD GRECCO, THIRD-PARTY DEFENDANTS/ APPELLANTS



On appeal from Superior Court of New Jersey, Law Division, Essex County, Docket No. L- 6541-98.

Before Judges Havey, Coburn and Weissbard.

The opinion of the court was delivered by: Havey, P.J.A.D.

NOT FOR PUBLICATION WITHOUT THE APPROVAL OF THE APPELLATE DIVISION

Argued October 9, 2001

In Foldi v. Jeffries, 93 N.J. 533, 546-47 (1983), the Supreme Court preserved the doctrine of parental immunity in cases involving the negligent exercise of parental authority or provision of customary child care. However, if the parents' behavior is willful and wanton, the parental immunity doctrine does not apply. Id. at 547. In this case, plaintiffs Richard and Sabrina Grecco (plaintiffs), individually, and Richard Grecco, as guardian ad litem of their son, plaintiff Christopher Grecco, filed a malpractice action against defendant University of Medicine and Dentistry of New Jersey (UMDNJ) and various hospital employees. Christopher suffers from carbamyl phosphate synthetase deficiency (CPSD). Plaintiffs claim that while Christopher was hospitalized and suffering an episode of hyperammonemia at the University Hospital, the UMDNJ staff negligently administered to Christopher an insufficient dose of medication. Plaintiffs allege that as a result, Christopher suffered severe permanent neurological damage.

UMDNJ filed a third-party action against plaintiffs, asserting that they negligently or intentionally failed to obtain a liver transplant for Christopher, which, it alleges, would have cured Christopher of CPSD. The hospital's claim is predicated on the fact that plaintiffs' older son, Richard, who also suffered from CPSD, successfully underwent a liver transplant for treatment of that disease while an infant. The trial court denied plaintiff's motion for summary judgment to dismiss the third-party complaint. We granted leave to appeal and now reverse.

The salient facts are undisputed. Christopher was born on August 15, 1994, with CPSD, a hereditary genetic disorder involving the absence of a natural enzyme which detoxifies excess nitrogen in the body. Patients with CPSD are subject to toxic buildup of nitrogen, known as hyperammonemia. CPSD is a urea cycle disorder which, if not treated, can cause irreversible and progressive brain damage or death.

Plaintiffs' oldest son, Richard, who was born six years before Christopher, also suffered from CPSD. At sixteen days of age, Richard underwent a successful liver transplant, which involved a seven-month hospital stay. Richard had a good recovery and, since the transplant, has had no complications associated with CPSD.

Christopher was diagnosed with CPSD prenatally. After delivery, he was placed in intensive care and underwent treatment for hyperammonemia. He received several medications including sodium benzoate, sodium phenylacetate and arginine hydrochloride, and was placed on a protein-restricted regimen. On October 18, 1994, two months after Christopher's birth, defendant Dr. Ling Yu Shih, a UMDNJ physician treating Christopher, wrote to plaintiffs' medical insurance carrier seeking approval to treat Christopher by strict dietary control of total protein intake, with special attention given to reducing nonessential amino acids. Dr. Shih recommended use of Cyclinax, a medical food specially designed to manage urea cycle disorders and other protein-free products to supply necessary calories. Dr. Shih also recommended consultations with a qualified nutritionist and clinical biochemical geneticist. He advised that, "[w]ith the appropriate nutritional support and strict medical supervision, I am confident that Christopher Grecco can best achieve his growth and development potential and avoid the devastating consequences of urea cycle disorder." In his deposition, Dr. Shih repeated his view that the dietary protocol recommended by him was "effective." He added that he had utilized the same protocol on at least six of his other patients.

Based on consultations with Dr. Shih, plaintiffs chose to treat Christopher's disorder conservatively by following a strict dietary protocol. During the ensuing months, Christopher experienced brief episodes of hyperammonemia for which he was treated with medication. At one point, in March 1995, he was admitted to Johns Hopkins Hospital after experiencing vomiting and dehydration. His ammonia level was elevated. Christopher had suffered a diffuse cerebral edema. He was thereafter hospitalized on three occasions in June and July 1995. On November 11, 1995, he was admitted to University Hospital where meningitis was diagnosed. Nevertheless, Christopher continued to make progress. He began to walk, he was happy and affectionate, had dressing skills and demonstrated independence.

On November 24, 1996, Christopher was admitted to University Hospital after experiencing vomiting and irritability. Once again, his ammonia levels were elevated. Physician orders directed that Christopher "should receive 3.25 grams each of sodium benzoate, sodium phenylacetate and 26 ml of 10% arginine in 400cc of D10W to run at 17 cc/hr." According to plaintiffs' medical expert, the prescribed dosage concentration was negligently diluted by hospital personnel and, due to the error, "Christopher received only 25% of the medication which he should have been receiving." The expert states that, as a consequence, Christopher suffered an episode of hyperammonemia leaving him with severe permanent neurological damage.

In denying plaintiffs' summary judgment motion to dismiss UMDNJ's third-party complaint, the trial court stated that there were genuine fact issues as to whether plaintiffs' failure to have Christopher undergo a liver transplant was wanton and willful conduct. That conclusion was apparently based on the fact that plaintiffs knew that they were "carriers" of the gene which causes CPSD and that they had opted for a liver transplant for their oldest son, Richard, who suffered from the same disorder.

Foldi, supra, 93 N.J. at 545, holds that "[t]here are certain areas of activities within the family sphere involving parental discipline, care, and control that should and must remain free from judicial intrusion. Parents should be free to determine how the physical, moral, emotional, and intellectual growth of their children can best be promoted." Consequently, the Court retained the doctrine of parental immunity in areas involving the exercise of parental authority or the provision of customary child care. Id. at 546. In Foldi, the Court invoked the doctrine, barring an action against parents who negligently supervised their child, resulting in the child's wandering away from her residence over to a neighbor's residence where she was bitten on the face by a dog. Id. at 535. The Court carved out an exception to the doctrine where the parent's failure to supervise his or her children is "willful or wanton," id. at 549, that is:

It must appear that the defendant with knowledge of existing conditions, and conscious from such knowledge that injury will likely or probably result from his conduct, and with reckless indifference to the consequences, consciously and intentionally does some wrongful act or omits to discharge some duty which produces the injurious ...


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