Acute Metabolic Crisis Induced By Vaccination in Seven Chinese Patients

Pediatric Neurology

Volumn 35, Issue 2, 2006, Pages 114-118

  Yang, Yanling ^a   Sujan, Sayami ^a   Sun, Fang ^a   Zhang, Yuehua ^a   Jiang, Yuwu ^a   Song, Jinqing ^a   Qin, Jiong ^a   Wu, Xiru ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; ACELLULAR VACCINE; ANTIBIOTIC AGENT; CARNITINE; CYANOCOBALAMIN; DIPHTHERIA PERTUSSIS TETANUS VACCINE; ENCEPHALITIS VACCINE; FLUDROCORTISONE; GLUCOSE; HEPATITIS B VACCINE; HYDROCORTISONE; JAPANESE ENCEPHALITIS VACCINE; MANNITOL; MEASLES VACCINE; SODIUM CHLORIDE; THIAMINE; UBIDECARENONE; VACCINE; VITAMIN;

ABNORMALLY HIGH SUBSTRATE CONCENTRATION IN BLOOD; ADRENAL INSUFFICIENCY; ARTICLE; BRAIN DISEASE; CAUSE OF DEATH; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; COMA; CONTROLLED STUDY; CONVULSION; DEHYDRATION; DIAGNOSTIC VALUE; DIARRHEA; DISEASE SEVERITY; DRUG FEVER; EDEMA; FEMALE; GLUTARIC ACIDURIA TYPE 1; HUMAN; HYPOGLYCEMIA; INFANT; KETOACIDOSIS; LACTIC ACIDEMIA; LEIGH DISEASE; LETHARGY; MALE; METABOLIC ACIDOSIS; METABOLIC DISORDER; METHYLMALONIC ACIDURIA; MOTOR RETARDATION; PIGMENT DISORDER; PRESCHOOL CHILD; PRIORITY JOURNAL; RESPIRATORY FAILURE; RESPIRATORY TRACT DISEASE; SEIZURE; SOMNOLENCE; STEROID 21 MONOOXYGENASE DEFICIENCY; VACCINATION REACTION; VOMITING;

ACID-BASE IMBALANCE; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD, PRESCHOOL; COMA; FATAL OUTCOME; FEMALE; HUMANS; INFANT; MALE; METABOLISM, INBORN ERRORS; VACCINES; WATER-ELECTROLYTE IMBALANCE;

EID: 33746198258     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2005.12.004     Document Type: Article

References (27)

1. Peter G. Immunization practices. In: Behrman R.E., Kliegman R.M., and Jenson H.B. (Eds). Nelson's textbook of pediatrics. 16th ed. (2001), W.B. Saunders, Philadelphia 1081-1089
2. Bjornson G., Scheifele D., Metzger D., Ferguson A., Wensley D., and Whitfield M. Promoting the use of influenza vaccine for children at risk of complications. BC Med J 42 (2000) 89-90
3. Chen R.T., Pless R., and Destefano F. Epidemiology of autoimmune reactions induced by vaccination. J Autoimmun 16 (2001) 309-318
4. Stratton K., Almario D.A., Wizemann T.M., and McCormick M.C. Immunization Safety Review Committee. Immunization safety review. Vaccinations and sudden unexpected death in infancy (2003), National Academy of Sciences, Washington, DC 17-84
5. Weibel R.E., Caserta V., Benor D.E., and Evans G. Acute encephalopathy followed by permanent brain injury or death associated with further attenuated measles vaccines. A review of claims submitted to the National Vaccine Injury Compensation Program. Pediatrics 101 3 Pt 1 (1998) 383-387
6. Levine L.S., and DiGeorge A.M. Congenital adrenal hyperplasia. In: Behrman R.E., Kliegman R.M., and Jenson H.B. (Eds). Nelson's textbook of pediatrics. 16th ed. (2001), W.B. Saunders, Philadelphia 1729-1737
7. Fu X.W., Kimura M., Iga M., and Yamaguchi S. Gas chromatographic-mass spectrometric screening for organic acidemias using dried urine filter paper. Determination of a-ketoacids. J Chromatogr B 758 (2001) 87-94
8. Smeitink J., van den Heuvel L., and DiMauro S. The genetics and pathology of oxidative phosphorylation. Nat Rev Genet 2 (2001) 342-352
9. Speiser P.W., and White P.C. Congenital adrenal hyperplasia. N Engl J Med 349 (2003) 776-788
10. Speiser P.W. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Endocrinol Metab Clin North Am 30 (2001) 31-59
11. Fenton W.A., Gravel R.A., and Rosenblatt D.S. Disorders of propionate and methylmalonate metabolism. In: Scriver C.R., Beaudet A.L., Sly W.S., and Valle D. (Eds). The metabolic and molecular basis of inherited disease. 8th ed. (2001), McGraw-Hill, New York 2165-2193
12. Nyhan W.L., and Ozand P.T. Methylmalonic acidemia. In: Nyhan W.L., and Ozand P.T. (Eds). Atlas of metabolic disease (1998), Chapman & Hall Medical, London 13-23
13. Swaiman K.F. Aminoacidopathies and organic acidemias resulting from deficiency of enzyme activity and transport abnormalities. In: Swaiman K.F., and Ashwal S. (Eds). Pediatric neurology. Principles & practice. 3rd ed. (1999), Mosby Inc, St. Louis 377-410
14. Kimura M., Yamamoto T., and Yamaguchi S. Automatic metabolic profiling and interpretation of GC/MS data for organic acidemia screening. A personal computer-based system. Tohoku J Exp Med 188 (1999) 317-334
15. Nyhan W.L., and Ozand P.T. Glutaric aciduria (type 1). In: Nyhan W.L., and Ozand P.T. (Eds). Atlas of metabolic disease (1998), Chapman & Hall Medical, London 245-251
16. Hoffmann G.F., and Zschocke J. Glutaric aciduria type 1. From clinical, biochemical and molecular diversity to successful therapy. J Inherit Metab Dis 22 (1999) 381-391
17. Brismar J., and Ozand P.T. CT and MR of the brain in glutaric academia type 1. A review of 59 published cases and a report of 5 new patients. Am J Neuroradiol 16 (1995) 675-683
18. Rahman S., Blok R.B., Dahl H.H., et al. Leigh syndrome. Clinical features and biochemical and DNA abnormalities. Ann Neurol 39 (1996) 343-351
19. Leigh D. Subacute necrotizing encephalomyelopathy in an infant. J Neurol Neurosurg Psychiat 14 (1951) 216-221
20. Davis R.L., Kolczak M., Lewis E., et al. Active surveillance of vaccine safety. A system to detect early signs of adverse events. Epidemiology 16 (2005) 336-341
21. Centers for Disease Control and Prevention. Update: Vaccine side effects, adverse reactions, contraindications, and precautions. Recommendations of the Advisory Committee on Immunization Practices. Morbid Mortal Weekly Rept 1996;45(RR-12:1-35.
22. Hori D., Hasegawa Y., Kimura M., Yang Y., Verma I.C., and Yamaguchi S. Clinical onset and prognosis of Asian children with organic acidemias, as detected by analysis of urinary organic acids using GC/MS, instead of mass screening. Brain Dev 27 (2005) 39-45
23. Yang Y.L., Yamaguchi S., Tagami Y., et al. Clinical survey of 71 patients with organic acidurias. J Peking Univ (Health Sci) 34 (2002) 214-218
24. Weiss M., Dorr H.G., Brandmaier R., Schwarz H.P., and Belohradsky B.H. Vaccine tolerance in steroid substituted patients with congenital adrenal hyperplasia. Eur J Med Res 2 (1997) 290-292
25. Munnich A., Rotig A., Cormier-Daire V., and Rustin P. Clinical presentation of respiratory chain deficiency. In: Scriver C.R., Beaudet A.L., Sly W.S., and Valle D. (Eds). The metabolic and molecular bases of inherited disease. Vol. 2. 8th ed. (2001), McGraw-Hill, New York 2261-2274
26. Luo X.P., Wang M.T., Wei H., et al. Application of gas chromatography-mass spectrometry analysis on urine filter paper in the high-risk screening and diagnosis of inherited metabolic diseases. Zhonghua Er Ke Za Zhi 41 (2003) 245-248
27. Han L.S., Gao X.L., Ye J., Qiu W.J., and Gu X.F. Application of tandem mass spectrometry in diagnosis of organic acidemias. Zhonghua Er Ke Za Zhi 43 (2005) 325-330