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- Publisher Website: 10.3747/pdi.2016.00123
- Scopus: eid_2-s2.0-85029595297
- PMID: 27680764
- WOS: WOS:000397949800009
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Article: Epidemiology and Clinical Characteristics of Acinetobacter Peritoneal Dialysis-Related Peritonitis in Hong Kong—With a Perspective on Multi-Drug and Carbapenem Resistance
Title | Epidemiology and Clinical Characteristics of Acinetobacter Peritoneal Dialysis-Related Peritonitis in Hong Kong—With a Perspective on Multi-Drug and Carbapenem Resistance |
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Authors | |
Keywords | Acinetobacter Peritoneal dialysis Peritonitis Multidrug resistance Carbapenem resistance Hong Kong |
Issue Date | 2017 |
Publisher | Multimed, Inc. The Journal's web site is located at http://pdiconnect.com |
Citation | Peritoneal Dialysis International, 2017, v. 37 n. 2, p. 177-182 How to Cite? |
Abstract | Background:
Acinetobacter spp. is an important cause of peritoneal dialysis (PD)-related peritonitis, but studies on Acinetobacter peritonitis have been scarce. In view of the rising concern of carbapenem-resistant Acinetobacter (CRA) and multidrug-resistant Acinetobacter (MDRA) infections, we conducted this study on the incidence of Acinetobacter peritonitis and the impact of CRA and MDRA on its outcome.
Methods:
We retrospectively evaluated the clinical characteristics, prevalence, antibiotic sensitivity patterns, outcomes, and factors associated with treatment failure over the past 16 years in our patients with Acinetobacter PD-related peritonitis.
Results:
Out of 2,389 episodes of peritonitis, there were 66 episodes (3%) of Acinetobacter peritonitis occurring in 59 patients. Twelve episodes were caused by MDRA (18%), of which 5 were CRA (8%). There was a progressive increase in the incidence of MDRA and CRA infections over the study period. Most isolates were sensitive to sulbactam combinations (ampicillin-sulbactam [95.4%] and cefoperazone-sulbactam [93.9%]), aminoglycosides (amikacin [92.4%], tobramycin [90.9%], and gentamicin [89.4%]), and carbapenems (imipenem [92.2%]). There was 1 case of relapse. Fifteen episodes resulted in catheter removal (23%), and 7 patients died (11%). Hypoalbuminemia (odds ratio [OR] = 0.85, p = 0.006) and carbapenem resistance (OR = 18.2, p = 0.049) were significantly associated with higher rates of treatment failure.
Conclusion:
Both carbapenem resistance and hypoalbuminemia were significantly associated with treatment failure. Up to 80% of peritonitis episodes by CRA resulted in catheter loss or mortality. Sulbactam combinations and/or aminoglycosides remained effective for the majority of Acinetobacter isolates. There seemed to be an increasing relative incidence of MDRA and CRA infections over the past 16 years. |
Persistent Identifier | http://hdl.handle.net/10722/241798 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.933 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Li, PH | - |
dc.contributor.author | Cheng, VCC | - |
dc.contributor.author | Yip, T | - |
dc.contributor.author | Yap, DYH | - |
dc.contributor.author | Lui, SL | - |
dc.contributor.author | Lo, WK | - |
dc.date.accessioned | 2017-06-20T01:48:43Z | - |
dc.date.available | 2017-06-20T01:48:43Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Peritoneal Dialysis International, 2017, v. 37 n. 2, p. 177-182 | - |
dc.identifier.issn | 0896-8608 | - |
dc.identifier.uri | http://hdl.handle.net/10722/241798 | - |
dc.description.abstract | Background: Acinetobacter spp. is an important cause of peritoneal dialysis (PD)-related peritonitis, but studies on Acinetobacter peritonitis have been scarce. In view of the rising concern of carbapenem-resistant Acinetobacter (CRA) and multidrug-resistant Acinetobacter (MDRA) infections, we conducted this study on the incidence of Acinetobacter peritonitis and the impact of CRA and MDRA on its outcome. Methods: We retrospectively evaluated the clinical characteristics, prevalence, antibiotic sensitivity patterns, outcomes, and factors associated with treatment failure over the past 16 years in our patients with Acinetobacter PD-related peritonitis. Results: Out of 2,389 episodes of peritonitis, there were 66 episodes (3%) of Acinetobacter peritonitis occurring in 59 patients. Twelve episodes were caused by MDRA (18%), of which 5 were CRA (8%). There was a progressive increase in the incidence of MDRA and CRA infections over the study period. Most isolates were sensitive to sulbactam combinations (ampicillin-sulbactam [95.4%] and cefoperazone-sulbactam [93.9%]), aminoglycosides (amikacin [92.4%], tobramycin [90.9%], and gentamicin [89.4%]), and carbapenems (imipenem [92.2%]). There was 1 case of relapse. Fifteen episodes resulted in catheter removal (23%), and 7 patients died (11%). Hypoalbuminemia (odds ratio [OR] = 0.85, p = 0.006) and carbapenem resistance (OR = 18.2, p = 0.049) were significantly associated with higher rates of treatment failure. Conclusion: Both carbapenem resistance and hypoalbuminemia were significantly associated with treatment failure. Up to 80% of peritonitis episodes by CRA resulted in catheter loss or mortality. Sulbactam combinations and/or aminoglycosides remained effective for the majority of Acinetobacter isolates. There seemed to be an increasing relative incidence of MDRA and CRA infections over the past 16 years. | - |
dc.language | eng | - |
dc.publisher | Multimed, Inc. The Journal's web site is located at http://pdiconnect.com | - |
dc.relation.ispartof | Peritoneal Dialysis International | - |
dc.subject | Acinetobacter | - |
dc.subject | Peritoneal dialysis | - |
dc.subject | Peritonitis | - |
dc.subject | Multidrug resistance | - |
dc.subject | Carbapenem resistance | - |
dc.subject | Hong Kong | - |
dc.title | Epidemiology and Clinical Characteristics of Acinetobacter Peritoneal Dialysis-Related Peritonitis in Hong Kong—With a Perspective on Multi-Drug and Carbapenem Resistance | - |
dc.type | Article | - |
dc.identifier.email | Li, PH: liphilip@hku.hk | - |
dc.identifier.email | Yap, DYH: desmondy@hku.hk | - |
dc.identifier.authority | Li, PH=rp02669 | - |
dc.identifier.authority | Yap, DYH=rp01607 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.3747/pdi.2016.00123 | - |
dc.identifier.pmid | 27680764 | - |
dc.identifier.scopus | eid_2-s2.0-85029595297 | - |
dc.identifier.hkuros | 272794 | - |
dc.identifier.volume | 37 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 177 | - |
dc.identifier.epage | 182 | - |
dc.identifier.isi | WOS:000397949800009 | - |
dc.publisher.place | Canada | - |
dc.identifier.issnl | 0896-8608 | - |