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Propensity score matching and persistence correction to reduce bias in comparative effectiveness: the effect of cinacalcet use on all-cause mortality.
Gillespie, Iain A; Floege, Jürgen; Gioni, Ioanna; Drüeke, Tilman B; de Francisco, Angel L; Anker, Stefan D; Kubo, Yumi; Wheeler, David C; Froissart, Marc.
Afiliação
  • Gillespie IA; Amgen Ltd, Uxbridge, UK.
  • Floege J; Division of Nephrology, Medizinische Klinik II, RWTH University Hospital Aachen, Aachen, Germany.
  • Gioni I; on behalf of Amgen Ltd, UK.
  • Drüeke TB; Inserm Unit 1088, UFR de Médecine et de Pharmacie, Université de Picardie, Amiens, France.
  • de Francisco AL; Servicio de Nefrología, Hospital Universitario Valdecilla, Universidad de Cantabria, Santander, Spain.
  • Anker SD; Department of Innovative Clinical Trials, University Medical Centre Göttingen, Göttingen, Germany.
  • Kubo Y; Amgen Inc, Thousand Oaks, CA, USA.
  • Wheeler DC; Center for Nephrology, University College London, UK.
  • Froissart M; Amgen Europe GmbH, Zug, Switzerland.
Pharmacoepidemiol Drug Saf ; 24(7): 738-47, 2015 Jul.
Article em En | MEDLINE | ID: mdl-26011775
ABSTRACT

PURPOSE:

The generalisability of randomised controlled trials (RCTs) may be limited by restrictive entry criteria or by their experimental nature. Observational research can provide complementary findings but is prone to bias. Employing propensity score matching, to reduce such bias, we compared the real-life effect of cinacalcet use on all-cause mortality (ACM) with findings from the Evaluation of Cinacalcet Therapy to Lower Cardiovascular Events (EVOLVE) RCT in chronic haemodialysis patients.

METHODS:

Incident adult haemodialysis patients receiving cinacalcet, recruited in a prospective observational cohort from 2007-2009 (AROii; n = 10,488), were matched to non-exposed patients regardless of future exposure status. The effect of treatment crossover was investigated with inverse probability of censoring weighted and lag-censored analyses. EVOLVE ACM data were analysed largely as described for the primary composite endpoint.

RESULTS:

AROii patients receiving cinacalcet (n = 532) were matched to 1790 non-exposed patients. The treatment effect of cinacalcet on ACM in the main AROii analysis (hazard ratio 1.03 [95% confidence interval (CI) 0.78-1.35]) was closer to the null than for the Intention to Treat (ITT) analysis of EVOLVE (0.94 [95%CI 0.85-1.04]). Adjusting for non-persistence by 0- and 6-month lag-censoring and by inverse probability of censoring weight, the hazard ratios in AROii (0.76 [95%CI 0.51-1.15], 0.84 [95%CI 0.60-1.18] and 0.79 [95%CI 0.56-1.11], respectively) were comparable with those of EVOLVE (0.82 [95%CI 0.67-1.01], 0.83 [95%CI 0.73-0.96] and 0.87 [95%CI 0.71-1.06], respectively).

CONCLUSIONS:

Correcting for treatment crossover, we observed results in the 'real-life' setting of the AROii observational cohort that closely mirrored the results of the EVOLVE RCT. Persistence-corrected analyses revealed a trend towards reduced ACM in haemodialysis patients receiving cinacalcet therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diálise Renal / Estudos Observacionais como Assunto / Calcimiméticos / Cinacalcete / Hiperparatireoidismo / Falência Renal Crônica Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diálise Renal / Estudos Observacionais como Assunto / Calcimiméticos / Cinacalcete / Hiperparatireoidismo / Falência Renal Crônica Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article