Clinical investigation on the treatment of HCMV hepatitis in children.
- Author:
Fen-hua CHEN
1
;
Qing-wen WANG
;
Si-nian PAN
;
Hui-qin CHEN
;
Jing-zhi JI
;
Zheng-xian HE
Author Information
- Publication Type:Clinical Trial
- MeSH: Antiviral Agents; therapeutic use; Cytomegalovirus; genetics; Cytomegalovirus Infections; drug therapy; DNA, Viral; analysis; Drug Therapy, Combination; Female; Follow-Up Studies; Ganciclovir; therapeutic use; Hepatitis, Viral, Human; drug therapy; virology; Humans; Immunoglobulins, Intravenous; therapeutic use; Infant; Male; Treatment Outcome
- From: Chinese Journal of Experimental and Clinical Virology 2004;18(1):76-79
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effective therapeutic method of human cytomegalovirus (HCMV) hepatitis in children.
METHODSTwenty-five children with HCMV hepatitis were randomly assigned to a treated group (n=13) or a control group (n=12). Both groups were treated with prednisone, glucurone, luminal and Xiaoyanlidanpian. But the treated group was given ganciclovir (GCV) + intravenous immunoglobulin (IVIG) in addition. Each infant of the two groups was checked for blood routine, liver function and HCMV copy numbers on admission and before discharge. They were seen at the third, sixth and ninth month after discharge. On each visit blood specimens were collected for HCMV copy numbers (fluorescence quantitative PCR, FQ-PCR).
RESULTSThe viral load of the treated group decreased significantly. A significant difference in viral copy numbers was found between the two groups on admission, discharge, and third, sixth and ninth month after discharge (P less than 0.001). The number of HCMV DNA copy fell to 10(3) copies/ml on discharge while that of the control group fell to the same level after the third month. The differences between the two groups in the length of hospitalization, time of initial jaundice disappearance and complete disappearance were statistically significant (P less than 0.05). The need for transfusion in the treated group was significantly less than that in the control group (chi-square=4.012, P less than 0.05).
CONCLUSIONCombination of GCV with a high dosage of IVIG to treat HCMV active infection could decrease viral load remarkably; The duration of disease, severity of symptoms, degree of anemia and the need for blood transfusion were reduced. No adverse effects related to the combination of GCV with IVIG therapy were observed.