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Comparison of the Effects of Intermittent Boluses to Simple Continuous Infusion on Patients' Global Perceived Effect in Intrathecal Therapy for Pain: A Randomized Double-Blind Crossover Study.
Eldabe, Sam; Duarte, Rui V; Madzinga, Grace; Batterham, Alan M; Brookes, Morag E; Gulve, Ashish P; Perruchoud, Christophe; Raphael, Jon H; Lorenzana, David; Buchser, Eric.
Afiliación
  • Eldabe S; Department of Pain and Anaesthesia, The James Cook University Hospital, Middlesbrough, UK.
  • Duarte RV; College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
  • Madzinga G; Department of Pain and Anaesthesia, The James Cook University Hospital, Middlesbrough, UK.
  • Batterham AM; Health and Social Care Institute, Teesside University, Middlesbrough, UK.
  • Brookes ME; Department of Pain and Anaesthesia, The James Cook University Hospital, Middlesbrough, UK.
  • Gulve AP; Department of Pain and Anaesthesia, The James Cook University Hospital, Middlesbrough, UK.
  • Perruchoud C; Anaesthesia and Pain Management Department, EHC-Hôpital de Morges, Morges, Switzerland.
  • Raphael JH; Department of Pain Management, Russells Hall Hospital, Dudley, UK.
  • Lorenzana D; Anaesthesia and Pain Management Department, Kantonsspital, Luzern, Switzerland.
  • Buchser E; Anaesthesia and Pain Management Department, EHC-Hôpital de Morges, Morges, Switzerland.
Pain Med ; 18(5): 924-931, 2017 05 01.
Article en En | MEDLINE | ID: mdl-27651513
ABSTRACT

Objective:

Intrathecal drug delivery (ITDD) is commonly used for intractable pain management. A paucity of good-quality studies in chronic noncancer patients and concerns over increased dosages have focused interest on different modes of administration. The aim of this international multicenter randomized double-blind crossover trial was to compare the efficacy of the same daily dose of drugs administered by intermittent boluses vs simple continuous infusion.

Methods:

Eligible patients implanted with a programmable ITDD device were randomized to receive two weeks of either intermittent boluses or a simple continuous flow in period 1, followed by a crossover to the alternative mode of administration. The primary outcome measure was the Patients' Global Impression of Change (PGIC) scale.

Results:

The mean proportion of positive responders (at least "minimally improved") was 38.4% in the continuous condition vs 37.3% in the bolus (difference in proportions = 1.1%, 95% confidence interval [CI] = -21.8-24.0%, P = 0.93). The mean PGIC in the continuous condition was 3.8 vs 3.9 in the bolus (mean difference = -0.1, -0.6-0.4, P = 0.72). Exploratory analyses revealed a tendency for the mean proportion of positive responders to be higher at low vs high flow rates for both bolus and continuous administrations. Two patients were withdrawn from the study due to adverse events during the bolus phase, both with symptoms of increased pain, and one patient with additional symptoms of numbness and urinary retention.

Conclusion:

The mean PGIC and proportion of positive responders was not substantially different after intermittent bolus vs continuous administration.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dolor Intratable / Dimensión del Dolor / Bombas de Infusión Implantables / Autoevaluación Diagnóstica / Analgésicos Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dolor Intratable / Dimensión del Dolor / Bombas de Infusión Implantables / Autoevaluación Diagnóstica / Analgésicos Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article