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Can EPS development be avoided with early interventions? The potential role of tamoxifen--a single-center study.
- Source :
-
Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis [Perit Dial Int] 2014 Sep-Oct; Vol. 34 (6), pp. 582-93. Date of Electronic Publication: 2014 Mar 01. - Publication Year :
- 2014
-
Abstract
- Background: Encapsulating peritoneal sclerosis (EPS) is a severe complication of peritoneal dialysis (PD). Identification of patients at high risk for EPS ("EPS-prone") and delivery of appropriate interventions might prevent its development. Our aim was to evaluate the clinical characteristics and outcomes of all EPS and EPS-prone patients diagnosed at our PD unit.<br />Methods: For a 30-year period representing our entire PD experience, we retrospectively identified all patients with EPS (diagnosed according to International Society for Peritoneal Dialysis criteria) and all patients defined as EPS-prone because they met at least 2 established criteria (severe peritonitis, PD vintage greater than 3 years, severe hemoperitoneum, overexposure to glucose, and acquired ultrafiltration failure).<br />Results: Of 679 PD patients, we identified 20 with EPS, for an overall prevalence of 2.9%. Mean age at diagnosis was 50.2 ± 16.4 years, with a median PD time of 77.96 months (range: 44.36 - 102.7 months) and a median follow-up of 30.91 months (range: 4.6 - 68.75 months). Of patients with EPS, 10 (50%) received tamoxifen, 10 (50%) received parenteral nutrition, and 2 (10%) underwent adhesiolysis, with 25% mortality related to EPS. Another 14 patients were identified as EPS-prone. Median follow-up was 54.05 months (range: 11.9 - 87.04 months). All received tamoxifen, and 5 (36%) received corticosteroids; none progressed to full EPS. We observed no differences in baseline data between the groups, but the group with EPS had been on PD longer (84 ± 53 months vs 39 ± 20 months, p = 0.002) and had a higher cumulative number of days of peritoneal inflammation from peritonitis (17.2 ± 11.1 days vs 9.8 ± 7.9 days, p = 0.015). Overall mortality was similar in the groups. The incidence of EPS declined during our three decades of experience (5.6%, 3.9%, and 0.3%).<br />Conclusions: Being a serious, life-threatening complication of PD, EPS requires high suspicion to allow for prompt diagnosis and treatment. Early detection of EPS-prone states and delivery of appropriate intervention might prevent EPS development. Tamoxifen seems to be a key strategy in prevention, but caution should be used in interpreting our results. Additional randomized controlled studies are needed.<br /> (Copyright © 2014 International Society for Peritoneal Dialysis.)
- Subjects :
- Adult
Aged
Aged, 80 and over
Cohort Studies
Databases, Factual
Early Diagnosis
Female
Follow-Up Studies
Humans
Kidney Failure, Chronic diagnosis
Kidney Failure, Chronic mortality
Male
Middle Aged
Monitoring, Physiologic methods
Peritoneal Dialysis methods
Peritoneal Fibrosis etiology
Peritoneal Fibrosis mortality
Primary Prevention methods
Retrospective Studies
Risk Assessment
Statistics, Nonparametric
Survival Analysis
Treatment Outcome
Kidney Failure, Chronic therapy
Peritoneal Dialysis adverse effects
Peritoneal Fibrosis prevention & control
Tamoxifen administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 1718-4304
- Volume :
- 34
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis
- Publication Type :
- Academic Journal
- Accession number :
- 24584614
- Full Text :
- https://doi.org/10.3747/pdi.2012.00286