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- PMID: 21532006
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Article: Clinical course and outcomes of single-organism enterococcus peritonitis in peritoneal dialysis patients
Title | Clinical course and outcomes of single-organism enterococcus peritonitis in peritoneal dialysis patients |
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Authors | |
Keywords | Enterococcus peritonitis Renal failure |
Issue Date | 2011 |
Publisher | Multimed, Inc. The Journal's web site is located at http://pdiconnect.com |
Citation | Peritoneal Dialysis International, 2011, v. 31 n. 5, p. 522-528 How to Cite? |
Abstract | Background and Objectives: Enterococci are part of the normal flora of the gastrointestinal tract. They can cause enteric peritonitis, which is a serious complication of peritoneal dialysis (PD). However, the clinical course and outcome of PD-related Enterococcus peritonitis remainsunclear. Methods: We reviewed all Enterococcus peritonitis episodes occurring in our dialysis unit from 1995 to 2009. Results: During the study period, 1421 episodes of peritonitis were recorded. Of 29 episodes (2.0%) that were attributable to single-organism Enterococcus, 12 episodes were caused by E. faecalis; 9, by E. faecium; and the remaining 8, by other Enterococcus species. The overall rate of ampicillin resistance was 41.4%. Recent use of antibiotics was associated with the development of ampicillin-resistant Enterococcus (ARE) peritonitis (hazard ratio: 12.53; p = 0.04). The primary response rate of Enterococcus peritonitis was significantly higher than that of Escherichia coli peritonitis (89.7% vs. 69.9%, p = 0.038), but the primary response rate was not significantly lower for ARE peritonitis than for ampicillin- susceptible Enterococcus (ASE) peritonitis (83.3% vs. 94.1%, p = 0.553). However, significantly more patients with ARE had received vancomycin (83.3% vs. 23.5%, p = 0.003), with a longer mean duration of vancomycin treatment (11.8 ± 6.9 days vs. 3.7 ± 6.8 days, p = 0.005). Conclusions: Recent use of antibiotics was a risk factor for the development of ARE peritonitis. Outcomes in ASE and ARE peritonitis were similar, but vancomycin was required during treatment for ARE peritonitis, in turn possibly predisposing the patients to infections caused by vancomycin-resistant organisms. © 2011 International Society for Peritoneal Dialysis. |
Persistent Identifier | http://hdl.handle.net/10722/137412 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.933 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yip, T | en_HK |
dc.contributor.author | Tse, KC | en_HK |
dc.contributor.author | Ng, F | en_HK |
dc.contributor.author | Hung, I | en_HK |
dc.contributor.author | Lam, MF | en_HK |
dc.contributor.author | Tang, S | en_HK |
dc.contributor.author | Lui, SL | en_HK |
dc.contributor.author | Lai, KN | en_HK |
dc.contributor.author | Chan, TM | en_HK |
dc.contributor.author | Lo, WK | en_HK |
dc.date.accessioned | 2011-08-26T14:24:32Z | - |
dc.date.available | 2011-08-26T14:24:32Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Peritoneal Dialysis International, 2011, v. 31 n. 5, p. 522-528 | en_HK |
dc.identifier.issn | 0896-8608 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/137412 | - |
dc.description.abstract | Background and Objectives: Enterococci are part of the normal flora of the gastrointestinal tract. They can cause enteric peritonitis, which is a serious complication of peritoneal dialysis (PD). However, the clinical course and outcome of PD-related Enterococcus peritonitis remainsunclear. Methods: We reviewed all Enterococcus peritonitis episodes occurring in our dialysis unit from 1995 to 2009. Results: During the study period, 1421 episodes of peritonitis were recorded. Of 29 episodes (2.0%) that were attributable to single-organism Enterococcus, 12 episodes were caused by E. faecalis; 9, by E. faecium; and the remaining 8, by other Enterococcus species. The overall rate of ampicillin resistance was 41.4%. Recent use of antibiotics was associated with the development of ampicillin-resistant Enterococcus (ARE) peritonitis (hazard ratio: 12.53; p = 0.04). The primary response rate of Enterococcus peritonitis was significantly higher than that of Escherichia coli peritonitis (89.7% vs. 69.9%, p = 0.038), but the primary response rate was not significantly lower for ARE peritonitis than for ampicillin- susceptible Enterococcus (ASE) peritonitis (83.3% vs. 94.1%, p = 0.553). However, significantly more patients with ARE had received vancomycin (83.3% vs. 23.5%, p = 0.003), with a longer mean duration of vancomycin treatment (11.8 ± 6.9 days vs. 3.7 ± 6.8 days, p = 0.005). Conclusions: Recent use of antibiotics was a risk factor for the development of ARE peritonitis. Outcomes in ASE and ARE peritonitis were similar, but vancomycin was required during treatment for ARE peritonitis, in turn possibly predisposing the patients to infections caused by vancomycin-resistant organisms. © 2011 International Society for Peritoneal Dialysis. | en_HK |
dc.language | eng | en_US |
dc.publisher | Multimed, Inc. The Journal's web site is located at http://pdiconnect.com | en_HK |
dc.relation.ispartof | Peritoneal Dialysis International | en_HK |
dc.subject | Enterococcus peritonitis | en_HK |
dc.subject | Renal failure | en_HK |
dc.subject.mesh | Abdominal Pain - microbiology | - |
dc.subject.mesh | Anti-Bacterial Agents - therapeutic use | - |
dc.subject.mesh | Gram-Positive Bacterial Infections - drug therapy - etiology | - |
dc.subject.mesh | Peritoneal Dialysis - adverse effects | - |
dc.subject.mesh | Peritonitis - drug therapy - microbiology | - |
dc.title | Clinical course and outcomes of single-organism enterococcus peritonitis in peritoneal dialysis patients | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Hung, I: ivanhung@hkucc.hku.hk | en_HK |
dc.identifier.email | Tang, S: scwtang@hku.hk | en_HK |
dc.identifier.email | Lai, KN: knlai@hku.hk | en_HK |
dc.identifier.authority | Hung, I=rp00508 | en_HK |
dc.identifier.authority | Tang, S=rp00480 | en_HK |
dc.identifier.authority | Lai, KN=rp00324 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.3747/pdi.2009.00260 | en_HK |
dc.identifier.pmid | 21532006 | - |
dc.identifier.scopus | eid_2-s2.0-84856138178 | en_HK |
dc.identifier.hkuros | 190905 | en_US |
dc.identifier.hkuros | 211520 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84856138178&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 31 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 522 | en_HK |
dc.identifier.epage | 528 | en_HK |
dc.identifier.isi | WOS:000295842800005 | - |
dc.publisher.place | Canada | en_HK |
dc.identifier.scopusauthorid | Yip, T=7004283977 | en_HK |
dc.identifier.scopusauthorid | Tse, KC=7102609864 | en_HK |
dc.identifier.scopusauthorid | Ng, F=7103125634 | en_HK |
dc.identifier.scopusauthorid | Hung, I=7006103457 | en_HK |
dc.identifier.scopusauthorid | Lam, MF=35300050600 | en_HK |
dc.identifier.scopusauthorid | Tang, S=7403437082 | en_HK |
dc.identifier.scopusauthorid | Lui, SL=7102379130 | en_HK |
dc.identifier.scopusauthorid | Lai, KN=7402135706 | en_HK |
dc.identifier.scopusauthorid | Chan, TM=36110804400 | en_HK |
dc.identifier.scopusauthorid | Lo, WK=7201502414 | en_HK |
dc.identifier.issnl | 0896-8608 | - |