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Extended-Release Morphine for Chronic Breathlessness in Pulmonary Arterial Hypertension-A Randomized, Double-Blind, Placebo-Controlled, Crossover Study.
Ferreira, Diana H; Ekström, Magnus; Sajkov, Dimitar; Vandersman, Zac; Eckert, Danny J; Currow, David C.
Afiliación
  • Ferreira DH; Discipline, Palliative and Supportive Services, Flinders University, Adelaide, South Australia, Australia. Electronic address: ferr0158@uni.flinders.edu.au.
  • Ekström M; Division of Respiratory Medicine & Allergology, Department of Clinical Sciences, Lund University, Lund, Sweden.
  • Sajkov D; Australian Respiratory and Sleep Medicine Institute and Department of Respiratory and Sleep Medicine, Flinders Medical Centre, Adelaide, Australia.
  • Vandersman Z; IMPACCT, Faculty of Health, University of Technology Sydney, Sydney, New South Wales, Australia.
  • Eckert DJ; Neuroscience Research Australia (NeuRA) and School of Medical Sciences, University of New South Wales, Sydney, Australia.
  • Currow DC; Discipline, Palliative and Supportive Services, Flinders University, Adelaide, South Australia, Australia; IMPACCT, Faculty of Health, University of Technology Sydney, Sydney, New South Wales, Australia; Wolfson Centre for Palliative Care Research, University of Hull, Hull, England.
J Pain Symptom Manage ; 56(4): 483-492, 2018 10.
Article en En | MEDLINE | ID: mdl-30031217
CONTEXT: Pulmonary arterial hypertension (PAH) affects people of all ages and is associated with poor prognosis. Chronic breathlessness affects almost all people with PAH. OBJECTIVES: This randomized, placebo-controlled, double-blind, crossover study aimed to evaluate the effects of regular, low-dose, extended-release (ER) morphine for PAH-associated chronic breathlessness. METHODS: Participants with PAH-associated chronic breathlessness were randomized to 1) seven days of ER morphine 20 mg, 2) seven-day washout, and 3) seven days of identically looking placebo, or vice versa. Primary end points were breathlessness "right now"-morning and evening-measured with a Visual Analogue Scale. Secondary end points included additional breathlessness measures, quality of life, function, harms, and blinded treatment preference (ACTRN12609000209291). RESULTS: Within a period of seven years, 50 patients were assessed in detail and 23 (46%) were randomized (despite broad eligibility criteria). Four participants withdrew while taking morphine. Nineteen participants completed the study. Breathlessness "right now" was higher on morphine compared with placebo both for morning [mean (M) ± SD 31.7 ± 25 mm vs. 26.9 ± 22 mm; effect size (80% CI) = -0.22 (-0.6 to 0.2)] and evening [(M ± SD 33.5 ± 28 mm vs. 25.6 ± 21 mm; effect size (80% CI) = -0.33 (-0.8 to 0.1)]. All secondary measures of breathlessness were higher with morphine as were nausea and constipation. CONCLUSION: This study does not support a Phase III study of ER morphine for people with PAH-associated chronic breathlessness. Recruiting to the target sample size was difficult, the direction of effect in every measure of breathlessness favored placebo and morphine generated more harms.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Cardiovasculares / Disnea / Hipertensión Pulmonar / Morfina Tipo de estudio: Clinical_trials / Prognostic_studies Aspecto: Patient_preference Límite: Female / Humans / Male / Middle aged Idioma: En Revista: J Pain Symptom Manage Asunto de la revista: NEUROLOGIA / PSICOFISIOLOGIA / TERAPEUTICA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Cardiovasculares / Disnea / Hipertensión Pulmonar / Morfina Tipo de estudio: Clinical_trials / Prognostic_studies Aspecto: Patient_preference Límite: Female / Humans / Male / Middle aged Idioma: En Revista: J Pain Symptom Manage Asunto de la revista: NEUROLOGIA / PSICOFISIOLOGIA / TERAPEUTICA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos