Literature DB >> 15373309

Long-term non-invasive positive pressure ventilation among cystic fibrosis patients awaiting lung transplantation.

Ori Efrati1, Dalit Modan-Moses, Asher Barak, Yoram Boujanover, Arie Augarten, Amir M Szeinberg, Isaak Levy, Yaacov Yahav.   

Abstract

BACKGROUND: Pulmonary disease is the most frequent cause of morbidity and mortality in cystc fibrosis patients. New techniques such as non-invasive positive pressure ventilation have resulted in prolongation of life expectancy in CF patients with end-stage lung disease.
OBJECTIVES: To determine the role of NIPPV in CF patients awaiting lung transplantation.
METHODS: Between 1996 and 2001 nine CF patients (5 females) with end-stage lung disease were treated with bi-level positive airway pressure ventilation in the "spontaneous" mode.
RESULTS: The patients' mean age at initiation of BiPAP was 15 years (range 13-40 years) and the mean duration of BiPAP usage was 8 months (range 3-16 months). Four patients underwent successful lung transplantation, three patients died while awaiting transplantation, and the remaining two are still on NIPPV while waiting for transplantation. Patients' body mass index increased significantly (P < 0.05) during BiPAP therapy (from 16.1 to 17.2 kg/m2). Blood pH, PaCO2, and bicarbonate improved significantly (from 7.31 to 7.38, 90.8 to 67.2 mmHg, and 48.9 to 40.3 mEq/L, respectively). Pulmonary function tests were not affected by BiPAP usage. The patients experienced a significant alleviation in morning headaches and improvement in quality of sleep (P < 0.003). There were no major complications during BiPAP usage.
CONCLUSIONS: We demonstrated that long-term NIPPV can stabilize and improve physiologic parameters such as ventilation, arterial blood gases and body mass index, as well as subjective symptoms such as sleep pattern, daily activity level, and morning headaches in CF patients with end-stage lung disease. Further prospectively controlled studies are needed to evaluate the potential of BiPAP therapy and its influence on morbidity and mortality in the post-lung transplantation period.

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Year:  2004        PMID: 15373309

Source DB:  PubMed          Journal:  Isr Med Assoc J            Impact factor:   0.892


  3 in total

1.  Improved survival following lung transplantation with long-term use of bilevel positive pressure ventilation in cystic fibrosis.

Authors:  Ori Efrati; Mordechai R Kremer; Asher Barak; Arie Augarten; Nira Reichart; Amir Vardi; Dalit Modan-Moses
Journal:  Lung       Date:  2007-03-28       Impact factor: 2.584

Review 2.  Sleep disorders in cystic fibrosis: A systematic review and meta-analysis.

Authors:  Joel Reiter; Alex Gileles-Hillel; Malena Cohen-Cymberknoh; Dennis Rosen; Eitan Kerem; David Gozal; Erick Forno
Journal:  Sleep Med Rev       Date:  2020-02-19       Impact factor: 11.609

Review 3.  Sleep in children with cystic fibrosis: More under the covers.

Authors:  Joel Reiter; Oded Breuer; Malena Cohen-Cymberknoh; Erick Forno; Alex Gileles-Hillel
Journal:  Pediatr Pulmonol       Date:  2021-05-20
  3 in total

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