PMID- 15618844 OWN - NLM STAT- MEDLINE DCOM- 20050317 LR - 20190906 IS - 0954-691X (Print) IS - 0954-691X (Linking) VI - 16 IP - 12 DP - 2004 Nov TI - Liver disease is a major cause of mortality following allogeneic bone-marrow transplantation. PG - 1347-54 AB - BACKGROUND: Liver disease is an important cause of morbidity and mortality among recipients of bone-marrow transplantation (BMT). The aim of this retrospective study was to determine the incidence, risk factors and clinical evolution of liver disease following allogeneic BMT. METHODS: A total of 103 patients (mean age 22.8 years (SD 10.9); 31.1% aged < 18 years; 66% males) transplanted in a single institution were enrolled. Data on donors and recipients were collected, including hematological disease, alanine transaminase, alkaline phosphatase, bilirubin, hepatitis B virus (HBV) and hepatitis C virus (HCV) markers (including HBV-DNA and HCV-RNA). RESULTS: Fifty six of 103 patients died, with liver disease the main cause of death (27 of 56, 48%). Overall the incidence of liver failure attributed to hepatic graft-versus-host-disease (GVHD) was 22.3% (23 of 103; 74% HBV/HCV infected) and veno-occlusive disease (VOD) was 9.7% (10 of 103; 80% HBV/HCV infected). Fourteen patients had hepatitis reactivations (four hepatic GVHD and three VOD). Donors' HCV-RNA status and serum bilirubin above 2 mg/dl were predictive of hepatic GVHD [adjusted odds ratio (AOR) 11.1, 95% confidence interval (CI) 0.99-33.12; AOR 3.93, 95% CI 1.09-14.62; P < 0.05, respectively] and an abnormal alkaline phosphatase could predict severe liver disease (AOR 2.78, 95% CI 1.01-7.54; P < 0.05). Development of severe liver disease (hepatic GVHD or VOD) was a significant predictor of mortality (AOR 4.57, 95% CI 1.09-20.32; P < 0.05) with a low probability of survival (19.3%, SD 7.9%) compared with those without liver disease (52.1%, SD 7.6%; log-rank P = 0.0003). CONCLUSIONS: Hepatic GVHD is a common complication following BMT and an important cause of liver-related mortality. The high prevalence of HCV and HBV may have contributed to the outcome of hepatic GVHD and VOD. Therefore, antiviral therapy should be considered early to prevent relentless progression of liver disease. FAU - El-Sayed, Manal H AU - El-Sayed MH AD - Pediatric Department, Hematology/Oncology Division, Children's Hospital, Ain Shams University, Cairo, Egypt. manalhelsayed@yahoo.com FAU - El-Haddad, Alaa AU - El-Haddad A FAU - Fahmy, Omar A AU - Fahmy OA FAU - Salama, Iman I AU - Salama II FAU - Mahmoud, Hossam K AU - Mahmoud HK LA - eng PT - Journal Article PL - England TA - Eur J Gastroenterol Hepatol JT - European journal of gastroenterology & hepatology JID - 9000874 RN - 0 (RNA, Viral) RN - RFM9X3LJ49 (Bilirubin) SB - IM MH - Adolescent MH - Adult MH - Bilirubin/blood MH - Bone Marrow Transplantation/*adverse effects MH - Child MH - Child, Preschool MH - Female MH - Graft vs Host Disease/etiology/mortality MH - Hepacivirus/isolation & purification MH - Hepatic Veno-Occlusive Disease/etiology/mortality MH - Hepatitis/etiology/mortality MH - Hepatitis B virus/isolation & purification MH - Humans MH - Liver Diseases/etiology/*mortality MH - Male MH - Middle Aged MH - Prognosis MH - RNA, Viral/blood MH - Retrospective Studies MH - Risk Factors MH - Survival Analysis MH - Transplantation, Homologous EDAT- 2004/12/25 09:00 MHDA- 2005/03/18 09:00 CRDT- 2004/12/25 09:00 PHST- 2004/12/25 09:00 [pubmed] PHST- 2005/03/18 09:00 [medline] PHST- 2004/12/25 09:00 [entrez] AID - 00042737-200412000-00019 [pii] AID - 10.1097/00042737-200412000-00019 [doi] PST - ppublish SO - Eur J Gastroenterol Hepatol. 2004 Nov;16(12):1347-54. doi: 10.1097/00042737-200412000-00019.