본문 바로가기
KERD
논문KCI 등재

국내 가와사키병 환아의 약물사용

Drug Utilization in Korean Children with Kawasaki Disease

1

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류약학

초록

Background: Kawasaki disease (KD) is an acute febrile, systemic vasculitis as a leading cause of acquired heart disease inchildren. Intravenous immunoglobulin G (IVIG) and aspirin are the standard initial therapy in the treatment of acute KD. The purposeof this study was to investigate drug utilization in children with KD, and to compare “IVIG + high-dose aspirin” and “IVIG +moderate-dose aspirin” in preventing cardiac complications. Methods: We analyzed pediatric patient sample data compiled by theHealth Insurance Review & Assessment Service from 2010 to 2015. We identified patients with KD using the KCD-6 code of M30.3. We excluded patients in chronic phase or ≥10 years. We also excluded patients who were diagnosed KD in November orDecember. Drug utilization pattern were assessed in acute KD patients and 30-day and 60-day cardiac complications wereinvestigated between “IVIG + high-dose aspirin” group and “IVIG + moderate-dose aspirin” group. Results: In acute phase, IVIGwas administered to 95.8% patients, and 57.1% patients were prescribed moderate-dose aspirin and 25% patients were with highdoseaspirin. Steroid use was rapidly increased from 4.0% in 2010 to 11.3% in 2015. Both 30-day and 60-day cardiac complicationsoccurred less in “IVIG + high-dose aspirin” group compared to “IVIG + moderate-dose aspirin” group, but not statisticallysignificant (0.9% vs 1.8%, p=0.252 for 30-day complication rate; 1.5% vs 2.7%. p=0.073 for 60-day complication rate). Conclusion:We were not able to demonstrate which aspirin therapy is superior for preventing cardiac complications in acute KD patients andfurther research is warranted.

Abstract

Background: Kawasaki disease (KD) is an acute febrile, systemic vasculitis as a leading cause of acquired heart disease inchildren. Intravenous immunoglobulin G (IVIG) and aspirin are the standard initial therapy in the treatment of acute KD. The purposeof this study was to investigate drug utilization in children with KD, and to compare “IVIG + high-dose aspirin” and “IVIG +moderate-dose aspirin” in preventing cardiac complications. Methods: We analyzed pediatric patient sample data compiled by theHealth Insurance Review & Assessment Service from 2010 to 2015. We identified patients with KD using the KCD-6 code of M30.3. We excluded patients in chronic phase or ≥10 years. We also excluded patients who were diagnosed KD in November orDecember. Drug utilization pattern were assessed in acute KD patients and 30-day and 60-day cardiac complications wereinvestigated between “IVIG + high-dose aspirin” group and “IVIG + moderate-dose aspirin” group. Results: In acute phase, IVIGwas administered to 95.8% patients, and 57.1% patients were prescribed moderate-dose aspirin and 25% patients were with highdoseaspirin. Steroid use was rapidly increased from 4.0% in 2010 to 11.3% in 2015. Both 30-day and 60-day cardiac complicationsoccurred less in “IVIG + high-dose aspirin” group compared to “IVIG + moderate-dose aspirin” group, but not statisticallysignificant (0.9% vs 1.8%, p=0.252 for 30-day complication rate; 1.5% vs 2.7%. p=0.073 for 60-day complication rate). Conclusion:We were not able to demonstrate which aspirin therapy is superior for preventing cardiac complications in acute KD patients andfurther research is warranted.

참고문헌 (27)

  1. Uehara R, "Epidemiology of Kawasaki disease in Asia, Europe, and the United States", J Epidemiol, 22, pp.79~85 (2012)
  2. Newburger JW, "Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association", Circulation, 110, pp.2747~2771 (2004)
  3. Abe J, "Elevated granulocyte colony-stimulating factor levels predict treatment failure in patients with Kawasaki disease", J Allergy Clin Immunol, 122, pp.1008~1013.e8 (2008)
  4. Park YW, "Epidemiological features of Kawasaki disease in Korea, 2006-2008", Pediatr Int, 53, pp.36~39 (2011)
  5. Kim GB, "Epidemiology and Clinical Features of Kawasaki Disease in South Korea, 2012-2014", Pediatr Infect Dis J, 36, pp.482~485 (2017)
  6. Research Committee of the Japanese Society of Pediatric C, "Guidelines for medical treatment of acute Kawasaki disease: report of the Research Committee of the Japanese Society of Pediatric Cardiology and Cardiac Surgery (2012 revised version)", Pediatr Int, 56, pp.135~158 (2014)
  7. Zhou C, "IVIG inhibits TNFalpha-induced MMP9 expression and activity in monocytes by suppressing NF-kappaB and P38 MAPK activation", Int J Clin Exp Pathol, 8, pp.15879~15886 (2015)
  8. Matsuda A, "Anti-inflammatory effects of high-dose IgG on TNF-alpha-activated human coronary artery endothelial cells", Eur J Immunol, 42, pp.2121~2131 (2012)
  9. Durongpisitkul K, "The prevention of coronary artery aneurysm in Kawasaki disease : A meta-analysis on the efficacy", Pediatrics, 96, pp.1057~ (1995)
  10. Terai M, "Prevalence of coronary artery abnormalities in Kawasaki disease is highly dependent on gamma globulin dose but independent of salicylate dose", J Pediatr, 131, pp.888~893 (1997)
  11. McCrindle BW, "Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association", Circulation, 135, pp.e927~e99 (2017)
  12. Kato H, "Kawasaki disease : effect of treatment on coronary artery involvement", Pediatrics, 63, pp.175~179 (1979)
  13. Kobayashi T, "Efficacy of immunoglobulin plus prednisolone for prevention of coronary artery abnormalities in severe Kawasaki disease (RAISE study): a randomised, open-label, blindedendpoints trial", Lancet, 379, pp.1613~1620 (2012)
  14. Kobayashi T, "Prediction of intravenous immunoglobulin unresponsiveness in patients with Kawasaki disease", Circulation, 113, pp.2606~2612 (2006)
  15. Egami K, "Prediction of resistance to intravenous immunoglobulin treatment in patients with Kawasaki disease", J Pediatr, 149, pp.237~240 (2006)
  16. Sano T, "Prediction of non-responsiveness to standard high-dose gamma-globulin therapy in patients with acute Kawasaki disease before starting initial treatment", Eur J Pediatr, 166, pp.131~137 (2007)
  17. Sundel RP, "Gamma globulin re-treatment in Kawasaki disease", J Pediatr, 123, pp.657~659 (1993)
  18. Weiss JE, "Infliximab as a novel therapy for refractory Kawasaki disease", J Rheumatol, 31, pp.808~810 (2004)
  19. Tremoulet AH, "Calcineurin inhibitor treatment of intravenous immunoglobulin-resistant Kawasaki disease", J Pediatr, 161, pp.506~512.e1 (2012)
  20. Akagi T, "Salicylate treatment in Kawasaki disease:high dose or low dose?", Eur J Pediatr, 150, pp.642~646 (1991)
  21. Saguil A, "Diagnosis and management of kawasaki disease", Am Fam Physician, 91, pp.365~371 (2015)
  22. Yong-WonPark, "Epidemiologic Study of Kawasaki Disease in Korea, 1997-1999: Comparison with Previous Studies During 1991-1996", Journal of Korean Medical Science, 17(4), pp.453~456 (2002), 대한의학회
  23. Park YW, "Epidemiologic picture of Kawasaki disease in Korea, 2000-2002", Pediatr Int, 47, pp.382~387 (2005)
  24. 하상미, "Epidemiologic Study on Kawasaki Disease in Korea, 2007-2014: Based on Health Insurance Review & Assessment Service Claims", Journal of Korean Medical Science, 31(9), pp.1445~1449 (2016), 대한의학회
  25. Kuo HC, "High-Dose Aspirin is Associated with Anemia and Does Not Confer Benefit to Disease Outcomes in Kawasaki Disease", PLoS One, 10, pp.e0144603~ (2015)
  26. Baumer JH, "Salicylate for the treatment of Kawasaki disease in children", Cochrane Database Syst Rev, pp.Cd004175~ (2006)
  27. Hamada H, "Aspirin treatment for patients with Kawasaki disease", Nihon Rinsho, 72, pp.1612~1616 (2014)

관련 논문AI추천

이 간행물의 다른 논문 (9건)