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Title
Severe reactions associated with diphtheria-tetanus-pertussis vaccine: detailed study of children
with seizures, hypotonic-hyporesponsive episodes, high fevers, and persistent crying [see comments]
AuthorBlumberg DA; Lewis K; Mink CM; Christenson PD; Chatfield P; Cherry JD
AddressDept of Pediatrics, UCLA School of Medicine 90024-1752.
Source
Pediatrics,
91:
6, 1993 Jun,
1158-65
AbstractOBJECTIVE. The pathophysiology of severe reactions to diphtheria-tetanus-pertussis (DTP)vaccine
is not well understood. Active pertussis toxin in DTP vaccine has been proposed to cause severe DTP vaccine
reactions. Large doses of pertussis toxin cause hyperinsulinemia and hypoglycemia as well as leukocytosis
with a predominant lymphocytosis in animal models. To learn more about the causes of and risk factors
for severe DTP vaccine reactions, children experiencing severe DTP vaccine reactions were studied. DESIGN.
Prospective, referral-based surveillance. SETTING. Los Angeles, CA. SUBJECTS. Children experiencing
severe reactions within 48 hours of DTP immunization and evaluated within 24 hours of the reaction. Severe
reactions included encephalopathy, persistent crying > or = 3 hours, hypotonic-hyporesponsive
episodes (collapse episodes), fever > or = 40.5 degrees C, or seizures. Some comparisons were made between
children with DTP vaccine-associated seizures and a comparison group of children experiencing
febrile seizures unrelated to immunization. OUTCOME MEASURES. A history and physical examination were
performed. Follow-up examinations were performed 1 month later. Blood was collected for complete blood
cell count with leukocyte differential count, serum chemistry measurements, and insulin and glucose values.
Serum was assayed for active pertussis toxin, both in free and immune-complex masked states.
RESULTS. Sixty children experienced severe reactions within 48 hours of DTP immunization: 32 children
had seizures only, 14 subjects had hypotonic-hyporesponsive episodes, 2 subjects had fever > or = 40.5
degrees C only, 4 subjects had persistent crying > or = 3 hours, 6 children had seizures and fever >
or = 40.5 degrees C, and 2 children had persistent crying and seizures. The children with seizures had
a high rate of personal and family histories of seizures, and 90% had documented fevers (> or = 38 degrees
C). Persistent crying was associated with painful local reactions. Effects that may have been
due to vaccine pertussis toxin were not found. Lymphocytosis did not occur, nor did hypoglycemia. Some
relatively elevated insulin values were noted; however, this finding was also noted in the comparison
group of children experiencing febrile seizures unrelated to immunization. No biologically active pertussis
toxin was found in the acute sera of children experiencing severe DTP vaccine reactions. CONCLUSIONS.
Seizures associated with DTP vaccine have similar clinical characteristics as febrile seizures, and persistent
crying is initiated by painful local reactions. Vaccine endotoxin is a cause of febrile DTP
vaccine reactions. We found no evidence that DTP vaccine pertussis toxin plays a role in severe DTP vaccine
reactions.