Didato v. Strehler

554 S.E.2d 42, 262 Va. 617, 2001 Va. LEXIS 119
CourtSupreme Court of Virginia
DecidedNovember 2, 2001
DocketRecord 003030; Record 003031
StatusPublished
Cited by44 cases

This text of 554 S.E.2d 42 (Didato v. Strehler) is published on Counsel Stack Legal Research, covering Supreme Court of Virginia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Didato v. Strehler, 554 S.E.2d 42, 262 Va. 617, 2001 Va. LEXIS 119 (Va. 2001).

Opinion

JUSTICE HASSELL

delivered the opinion of the Court.

In these consolidated appeals from judgments sustaining the defendants’ demurrers in medical negligence actions, we consider whether the plaintiffs’ motions for judgment alleged viable causes of action based upon negligence, the assumption of a duty, and the creation of a special relationship.

I.

Mimi Didato and her husband, Gary Didato, filed separate amended motions for judgment against Paul M. Strehler, M.D., and *620 Chippenham Pediatric & Adolescent Medicine, PC. (Chippenham Pediatric). Mimi Didato and Gary Didato, to whom we will refer jointly as the plaintiffs, alleged in their separate motions for judgment that the defendants breached certain duties owed to them. The defendants filed demurrers to the amended motions for judgment and asserted that the plaintiffs failed to allege viable causes of action against them.

The circuit court sustained the demurrers. The circuit court concluded that: the plaintiffs failed to allege that they were patients of the defendants and, therefore, the defendants owed no duty to the plaintiffs; a special relationship did not exist between the plaintiffs and the defendants and, therefore, the defendants owed no duty to the plaintiffs under that theory of recovery; and the defendants did not assume a duty owed to the plaintiffs.

The circuit court entered judgments in favor of the defendants. We awarded the plaintiffs appeals from the judgments, and we consolidated their cases.

II.

A.

A demurrer “admits the truth of all material facts that are properly pleaded, facts which are impliedly alleged, and facts which may be fairly and justly inferred from alleged facts.” Cox Cable Hampton Roads, Inc. v. City of Norfolk, 242 Va. 394, 397, 410 S.E.2d 652, 653 (1991). Thus, we will state the relevant facts, contained in the plaintiffs’ amended motions for judgment, which are necessary for our resolution of these appeals.

Strehler is a physician licensed to practice medicine in this Commonwealth, and he is engaged in the practice of pediatrics. Chippenham Pediatric is a professional corporation registered to do business in this Commonwealth and provides pediatric services. Strehler is an officer and employee of Chippenham Pediatric. The Didatos are the parents of three children: Matthew, bom on January 21, 1993; Gabrielle, bom on September 28, 1994; and Nicholas, bom on May 12, 1998.

In 1993, the plaintiffs “presented to Dr. Strehler and Chippenham Pediatric and requested that they provide their family including themselves and their infant son Matthew all health care [that] a family should receive from a pediatrician and a professional corporation engaged in providing health care services relating to the practice of pediatrics.” Pursuant to this request, “Dr. Strehler and Chippenham *621 Pediatric agreed to provide the Didato family all health care [that] members of a family should receive from a pediatrician and a professional corporation engaged in providing health care services relating to the practice of pediatrics.” The relationship between the Didato family and the defendants “continued without interruption until 1997,” when the plaintiffs moved from Virginia to Connecticut.

According to the plaintiffs, thalassemia and sickle cell disease are inherited diseases of the blood known as hemoglobinopathies. “Thalassemia is a form of anemia (red blood cell deficiency). Hemoglobin is the oxygen-carrying component of the red blood cells. It is made of two different kinds of proteins, called alpha and beta globins. If the body doesn’t produce both of these two proteins, the red blood cells do not form properly and do not carry sufficient oxygen. The result is anemia that begins in early childhood and persists throughout life. There are a number of varieties of thalassemia. If the body does not produce beta globins, the resultant disease is called beta thalassemia.”

The plaintiffs stated in the amended motions for judgment that “[s]ickle cell disease (also referred to as ‘sickle cell anemia’) is caused by the presence of an abnormal type of hemoglobin called ‘sickle hemoglobin’ in red blood cells. The presence of sickle hemoglobin causes red blood cells to change from their usual biconcave disc shape to a crescent or sickle shape. The abnormal hemoglobin makes the red blood cells unable to carry oxygen and the abnormal shape can also cause the red blood cells to clog small blood vessels forming clots and preventing some organs and tissue from receiving sufficient oxygen. When this occurs, red blood cells are damaged and destroyed producing anemia and the victim of sickle cell disease will experience episodes of severe pain and sustain damage to organs and tissue.”

Continuing, the plaintiffs stated that “[s]ome of the various clinical manifestations of sickle cell disease include painful swelling of the hands and feet caused by ischemic necrosis of the small bones, illnesses accompanied by fever, hypoxia and acidosis, infarction of bone marrow, splenic infarcts, splenic enlargement leading to circulatory collapse, pulmonary infarction, strokes, ischemic damage to heart, liver, kidneys and eyes and priapism (painful penile erections).”

According to the plaintiffs, “[v]ictims of sickle cell disease are susceptible to meningitis, sepsis and other serious infections and a high risk for a lethal, rapid decrease in hemoglobin level (aplastic *622 episode). ... By mid-childhood most victims of sickle cell disease are underweight and have an enlarged heart. Puberty is frequently delayed. Throughout life, the victim of sickle cell disease will suffer a barrage of medical crises and can expect to experience pain in varying levels of intensity on a daily basis. . . . The life expectancy of sickle cell disease victims is dramatically reduced as a consequence of the disease and its sequelae.”

The plaintiffs also pled that “[b]oth thalassemia and sickle cell disease are autosomal recessive disorders. This means these disorders only occur when both parents carry the gene for the disorder. If both parents are carriers of the abnormal gene responsible for producing the disorder, there is a 25 per cent possibility that a child of the parents will have the disorder. A person who carries the gene for thalassemia has the ‘thalassemia trait.’ A person who carries the gene for sickle cell disease has the ‘sickle cell trait.’ ... If one parent is a carrier of the beta thalassemia trait and the other parent is a carrier of sickle cell trait, there is a 25 per cent possibility that a child of the parents will be bom with a type of sickle cell disease known as sickle beta thalassemia.” Continuing, the plaintiffs stated that “[o]ne form of sickle beta thalassemia disease is called sickle beta O thalassemia. This is the most severe form of sickle beta thalassemia.”

“The beta thalassemia trait is found primarily in persons of Mediterranean, African or Southeast Asian origin. . . . [Mr.] Didato is of Sicilian descent and is therefore a person of Mediterranean origin. . . .

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Bluebook (online)
554 S.E.2d 42, 262 Va. 617, 2001 Va. LEXIS 119, Counsel Stack Legal Research, https://law.counselstack.com/opinion/didato-v-strehler-va-2001.