File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1111/j.1440-1797.2006.00662.x
- Scopus: eid_2-s2.0-33846999883
- PMID: 17295655
- WOS: WOS:000244752700004
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Pilot study of pegylated interferon-alpha 2a in dialysis patients with chronic hepatitis C virus infection
Title | Pilot study of pegylated interferon-alpha 2a in dialysis patients with chronic hepatitis C virus infection |
---|---|
Authors | |
Keywords | Dialysis Hepatitis C Pegylated interferon |
Issue Date | 2007 |
Publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/NEP |
Citation | Nephrology, 2007, v. 12 n. 1, p. 11-17 How to Cite? |
Abstract | Aim: Pegylated interferon (PEG-IFN) combined with ribavirin is recommended for the treatment of chronic hepatitis C virus (HCV) infection in patients without renal failure. The optimal treatment of hepatitis C in dialysis patients remains to be established. A high incidence of adverse effects has been observed with conventional interferon and PEG-IFN alpha-2b in dialysis patients. Methods: We conducted a prospective study to investigate the tolerability and efficacy of PEG-IFN alpha-2a (135 μg weekly for 48 weeks) in six dialysis patients with chronic HCV infection. Results: Two patients completed 48 weeks of treatment. Treatment was stopped in three patients (beyond 24 weeks) when they developed unrelated complications, and stopped in one patient due to failure of viral clearance. None required treatment discontinuation due to adverse effects, and PEG-IFN alpha-2a was subjectively well tolerated. Marrow suppression with mild anaemia, leucopenia, or thrombocytopenia remained common. Two patients (infected with genotypes 3a and 1b, respectively) had sustained virological response. Conclusions: Results from this pilot study showed that PEG-IFN alpha-2a appeared relatively well tolerated in dialysis patients with chronic HCV infection, and about one-third of patients could achieve sustained virological response. © 2006 The Authors. |
Persistent Identifier | http://hdl.handle.net/10722/76682 |
ISSN | 2023 Impact Factor: 2.4 2023 SCImago Journal Rankings: 0.641 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chan, TM | en_HK |
dc.contributor.author | Ho, SKN | en_HK |
dc.contributor.author | Tang, CSO | en_HK |
dc.contributor.author | Tse, KC | en_HK |
dc.contributor.author | Lam, MF | en_HK |
dc.contributor.author | Lai, KN | en_HK |
dc.contributor.author | Yung, S | en_HK |
dc.date.accessioned | 2010-09-06T07:23:49Z | - |
dc.date.available | 2010-09-06T07:23:49Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Nephrology, 2007, v. 12 n. 1, p. 11-17 | en_HK |
dc.identifier.issn | 1320-5358 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/76682 | - |
dc.description.abstract | Aim: Pegylated interferon (PEG-IFN) combined with ribavirin is recommended for the treatment of chronic hepatitis C virus (HCV) infection in patients without renal failure. The optimal treatment of hepatitis C in dialysis patients remains to be established. A high incidence of adverse effects has been observed with conventional interferon and PEG-IFN alpha-2b in dialysis patients. Methods: We conducted a prospective study to investigate the tolerability and efficacy of PEG-IFN alpha-2a (135 μg weekly for 48 weeks) in six dialysis patients with chronic HCV infection. Results: Two patients completed 48 weeks of treatment. Treatment was stopped in three patients (beyond 24 weeks) when they developed unrelated complications, and stopped in one patient due to failure of viral clearance. None required treatment discontinuation due to adverse effects, and PEG-IFN alpha-2a was subjectively well tolerated. Marrow suppression with mild anaemia, leucopenia, or thrombocytopenia remained common. Two patients (infected with genotypes 3a and 1b, respectively) had sustained virological response. Conclusions: Results from this pilot study showed that PEG-IFN alpha-2a appeared relatively well tolerated in dialysis patients with chronic HCV infection, and about one-third of patients could achieve sustained virological response. © 2006 The Authors. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/NEP | en_HK |
dc.relation.ispartof | Nephrology | en_HK |
dc.subject | Dialysis | en_HK |
dc.subject | Hepatitis C | en_HK |
dc.subject | Pegylated interferon | en_HK |
dc.subject.mesh | Adolescent | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Antiviral Agents - adverse effects - therapeutic use | en_HK |
dc.subject.mesh | Cohort Studies | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Hepatitis C, Chronic - complications - drug therapy | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Interferon-alpha - adverse effects - therapeutic use | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Pilot Projects | en_HK |
dc.subject.mesh | Polyethylene Glycols - adverse effects - therapeutic use | en_HK |
dc.subject.mesh | RNA, Viral - analysis | en_HK |
dc.subject.mesh | Recombinant Proteins | en_HK |
dc.subject.mesh | Renal Dialysis | en_HK |
dc.subject.mesh | Time Factors | en_HK |
dc.subject.mesh | Treatment Outcome | en_HK |
dc.title | Pilot study of pegylated interferon-alpha 2a in dialysis patients with chronic hepatitis C virus infection | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1320-5358&volume=12&spage=11&epage=17&date=2007&atitle=Pilot+study+of+pegylated+interferon-alpha+2a+in+dialysis+patients+with+chronic+hepatitis+C+virus+infection | en_HK |
dc.identifier.email | Chan, TM: dtmchan@hku.hk | en_HK |
dc.identifier.email | Lai, KN: knlai@hku.hk | en_HK |
dc.identifier.email | Yung, S: ssyyung@hku.hk | en_HK |
dc.identifier.authority | Chan, TM=rp00394 | en_HK |
dc.identifier.authority | Lai, KN=rp00324 | en_HK |
dc.identifier.authority | Yung, S=rp00455 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1440-1797.2006.00662.x | en_HK |
dc.identifier.pmid | 17295655 | - |
dc.identifier.scopus | eid_2-s2.0-33846999883 | en_HK |
dc.identifier.hkuros | 130461 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33846999883&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 12 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 11 | en_HK |
dc.identifier.epage | 17 | en_HK |
dc.identifier.isi | WOS:000244752700004 | - |
dc.publisher.place | Australia | en_HK |
dc.identifier.scopusauthorid | Chan, TM=7402687700 | en_HK |
dc.identifier.scopusauthorid | Ho, SKN=36839065300 | en_HK |
dc.identifier.scopusauthorid | Tang, CSO=55225422400 | en_HK |
dc.identifier.scopusauthorid | Tse, KC=7102609864 | en_HK |
dc.identifier.scopusauthorid | Lam, MF=35300050600 | en_HK |
dc.identifier.scopusauthorid | Lai, KN=7402135706 | en_HK |
dc.identifier.scopusauthorid | Yung, S=22636568800 | en_HK |
dc.identifier.citeulike | 1089689 | - |
dc.identifier.issnl | 1320-5358 | - |