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Variation in Peritoneal Dialysis-Related Peritonitis Outcomes in the Peritoneal Dialysis Outcomes and Practice Patterns Study (PDOPPS).
Al Sahlawi, Muthana; Zhao, Junhui; McCullough, Keith; Fuller, Douglas S; Boudville, Neil; Ito, Yasuhiko; Kanjanabuch, Talerngsak; Nessim, Sharon J; Piraino, Beth M; Pisoni, Ronald L; Teitelbaum, Isaac; Woodrow, Graham; Kawanishi, Hideki; Johnson, David W; Perl, Jeffrey.
Afiliação
  • Al Sahlawi M; Division of Nephrology, St. Michael's Hospital and the Keenan Research Center in the Li Ka Shing Knowledge Institute, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada; Department of Internal Medicine, College of Medicine, King Faisal University, Al-Hasa, Saudi Arabia.
  • Zhao J; Arbor Research Collaborative for Health, Ann Arbor, MI.
  • McCullough K; Arbor Research Collaborative for Health, Ann Arbor, MI.
  • Fuller DS; Arbor Research Collaborative for Health, Ann Arbor, MI.
  • Boudville N; Medical School, University of Western Australia, Perth, Australia.
  • Ito Y; Aichi Medical University, Nagakute, Japan.
  • Kanjanabuch T; Center of Excellence in Kidney Metabolic Disorders and Division of Nephrology, Department of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Nessim SJ; Division of Nephrology, Jewish General Hospital, McGill University, Montreal, QC, Canada.
  • Piraino BM; University of Pittsburgh, Pittsburgh, PA.
  • Pisoni RL; Arbor Research Collaborative for Health, Ann Arbor, MI.
  • Teitelbaum I; University of Colorado, Aurora, CO.
  • Woodrow G; Renal Unit, St. James's University Hospital, Leeds, United Kingdom.
  • Kawanishi H; Akane Foundation, Tsuchiya General Hospital, Nakaku, Hiroshima, Japan.
  • Johnson DW; Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia; Translational Research Institute, Brisbane, Australia.
  • Perl J; Division of Nephrology, St. Michael's Hospital and the Keenan Research Center in the Li Ka Shing Knowledge Institute, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada. Electronic address: jeff.perl@utoronto.ca.
Am J Kidney Dis ; 79(1): 45-55.e1, 2022 01.
Article em En | MEDLINE | ID: mdl-34052357
ABSTRACT
RATIONALE &

OBJECTIVE:

Peritoneal dialysis (PD)-associated peritonitis is a significant PD-related complication. We describe the likelihood of cure after a peritonitis episode, exploring its association with various patient, peritonitis, and treatment characteristics. STUDY

DESIGN:

Observational prospective cohort study. SETTING &

PARTICIPANTS:

1,631 peritonitis episodes (1,190 patients, 126 facilities) in Australia, New Zealand, Canada, Japan, Thailand, the United Kingdom, and the United States. EXPOSURE Patient characteristics (demographics, patient history, laboratory values), peritonitis characteristics (organism category, concomitant exit-site infection), dialysis center characteristics (use of icodextrin and low glucose degradation product solutions, policies regarding antibiotic self-administration), and peritonitis treatment characteristics (antibiotic used).

OUTCOME:

Cure, defined as absence of death, transfer to hemodialysis (HD), PD catheter removal, relapse, or recurrent peritonitis within 50 days of a peritonitis episode. ANALYTICAL

APPROACH:

Mixed-effects logistic models.

RESULTS:

Overall, 65% of episodes resulted in a cure. Adjusted odds ratios (AOR) for cure were similar across countries (range, 54%-68%), by age, sex, dialysis vintage, and diabetes status. Compared with Gram-positive peritonitis, the odds of cure were lower for Gram-negative (AOR, 0.41 [95% CI, 0.30-0.57]), polymicrobial (AOR, 0.30 [95% CI, 0.20-0.47]), and fungal (AOR, 0.01 [95% CI, 0.00-0.07]) peritonitis. Odds of cure were higher with automated PD versus continuous ambulatory PD (AOR, 1.36 [95% CI, 1.02-1.82]), facility icodextrin use (AOR per 10% greater icodextrin use, 1.06 [95% CI, 1.01-1.12]), empirical aminoglycoside use (AOR, 3.95 [95% CI, 1.23-12.68]), and ciprofloxacin use versus ceftazidime use for Gram-negative peritonitis (AOR, 5.73 [95% CI, 1.07-30.61]). Prior peritonitis episodes (AOR, 0.85 [95% CI, 0.74-0.99]) and concomitant exit-site infection (AOR, 0.41 [95% CI, 0.26-0.64]) were associated with a lower odds of cure.

LIMITATIONS:

Sample selection may be biased and generalizability may be limited. Residual confounding and confounding by indication limit inferences. Use of facility-level treatment variables may not capture patient-level treatments.

CONCLUSIONS:

Outcomes after peritonitis vary by patient characteristics, peritonitis characteristics, and modifiable peritonitis treatment practices. Differences in the odds of cure across infecting organisms and antibiotic regimens suggest that organism-specific treatment considerations warrant further investigation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peritonite / Diálise Peritoneal / Diálise Peritoneal Ambulatorial Contínua Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Am J Kidney Dis Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Arábia Saudita

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peritonite / Diálise Peritoneal / Diálise Peritoneal Ambulatorial Contínua Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Am J Kidney Dis Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Arábia Saudita
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