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      Pyrazinamide에 의한 전격성 간부전 = A Case of Pyrazinamide Induced Fulminant Hepatic Failure

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      https://www.riss.kr/link?id=A75040506

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      다국어 초록 (Multilingual Abstract)

      Standard antituberculous therapy, including isoniazid (INH), rifampin, ethambutol, and pyrazinamide (PZA), is widely used to treat active tuberculosis. The most important side effect is hepatotoxicity. In a standard four-drug regimen, PZA was the most...

      Standard antituberculous therapy, including isoniazid (INH), rifampin, ethambutol, and pyrazinamide (PZA), is widely used to treat active tuberculosis. The most important side effect is hepatotoxicity. In a standard four-drug regimen, PZA was the most common cause of drug-induced hepatitis and was dose-related. The incidence of drug-induced hepatitis is high at doses of 40∼70 mg/kg per day but has fallen significantly since the recommended dose was reduced. Liver toxicity induced by PZA is rare at doses of 25 mg/kg per day or less. PZA-induced fulminant hepatic failure is also rare but fatal. We report a case of fulminant hepatic failure caused by a re-challenge of PZA. (Tuberc Respir Dis 2007;63:435-439)

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      참고문헌 (Reference)

      1 "Risk factors of acute hepatic failure during antituberculosis treatment: two cases and literature review" 64 : 377-384, 2006

      2 "Risk factors for side-effect of isoniazide, rifampin and pyrazinamide in patients hospitalized for pulmonary tuberculosis" 9 : 2026-2030, 1996

      3 "Risk factors for hepatotoxicity associate with rifampin and pyrazinamide for the treatment of latent tuberculosis infection: experience from three pubic health tuberculosis clinics" 6 : 995-1000, 2002

      4 "National survey to measure rates of liver injury, hospitalization, and death associated with rifampin and pyrazinamide for latent tuberculosis infection" 41 : 1125-1133, 2005

      5 "Incidence of serious side effects from first-line antituberculosis drugs among patients treated for active tuberculosis" 167 : 1472-1477, 2003

      6 "Hepatotoxicity of antituberculosis drugs" 51 : 111-113, 1996

      7 "Deleterious influence of pyrazinamide on the outcome of patients with fulminant or subfulminant liver failure during antituberculous treatment including isoniazid" 21 : 929-932, 1995

      8 "Controlled clinical trial of four short-course regimens of chemotherapy for two durations in the treatment of pulmonary tuberculosis" 39-48, amrevrespirdis1978;118

      9 "Clinical trial of three 6-month regimens of chemotherapy given intermittently in the continuation phase in the treatment of pulmonary tuberculosis" 374-8, amrevrespirdis1985;132

      10 "Clinical trial of six-month and four-month regimens of chemotherapy in the treatment of pulmonary tuberculosis" 579-85, amrevrespirdis1979;119

      1 "Risk factors of acute hepatic failure during antituberculosis treatment: two cases and literature review" 64 : 377-384, 2006

      2 "Risk factors for side-effect of isoniazide, rifampin and pyrazinamide in patients hospitalized for pulmonary tuberculosis" 9 : 2026-2030, 1996

      3 "Risk factors for hepatotoxicity associate with rifampin and pyrazinamide for the treatment of latent tuberculosis infection: experience from three pubic health tuberculosis clinics" 6 : 995-1000, 2002

      4 "National survey to measure rates of liver injury, hospitalization, and death associated with rifampin and pyrazinamide for latent tuberculosis infection" 41 : 1125-1133, 2005

      5 "Incidence of serious side effects from first-line antituberculosis drugs among patients treated for active tuberculosis" 167 : 1472-1477, 2003

      6 "Hepatotoxicity of antituberculosis drugs" 51 : 111-113, 1996

      7 "Deleterious influence of pyrazinamide on the outcome of patients with fulminant or subfulminant liver failure during antituberculous treatment including isoniazid" 21 : 929-932, 1995

      8 "Controlled clinical trial of four short-course regimens of chemotherapy for two durations in the treatment of pulmonary tuberculosis" 39-48, amrevrespirdis1978;118

      9 "Clinical trial of three 6-month regimens of chemotherapy given intermittently in the continuation phase in the treatment of pulmonary tuberculosis" 374-8, amrevrespirdis1985;132

      10 "Clinical trial of six-month and four-month regimens of chemotherapy in the treatment of pulmonary tuberculosis" 579-85, amrevrespirdis1979;119

      11 "Chemotherapy and management of tuberculosis in the United Kingdom: recommendations 1998" 53 : 536-548, 1998

      12 "Antituberculous therapy-induced fulminant hepatic failure: successful treatment with liver transplantation and nonstandard antituberculous therapy" 12 : 1427-1430, 2006

      13 "Anti-tuberculosis medication and the liver: dangers and recommendations in management" 8 : 1384-1388, 1995

      14 "American Thoracic Society/Centers for Disease Control/Infectious Diseases Society of America Treatment of tuberculosis" 167 : 603-662, 2003

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      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-07-30 학술지명변경 한글명 : 결핵 및 호흡기질환 -> Tuberculosis and Respiratory Diseases KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      2000-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.21 0.21 0.2
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.19 0.15 0.475 0.2
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