Literature DB >> 30284025

Objective and Subjective Sleep Efficiency in Adult Patients with Cystic Fibrosis and Impact on Quality of Life.

Marta Íscar-Urrutia1, Claudia Janeth Madrid-Carbajal2, Gemma Rubinos-Cuadrado2, Ramón Fernández-Álvarez2, María José Vázquez-López2, Cristina Hernández-González2, Ana Isabel Enríquez-Rodríguez2, Marta García-Clemente2.   

Abstract

INTRODUCTION: Poor sleep quality and excessive daytime sleepiness are common in patients with cystic fibrosis (CF), and both are negatively correlated with health-related quality of life (HRQoL). The objective of our study was to evaluate subjective and objective sleep quality in adult CF patients and its effect on HRQoL.
MATERIALS AND METHODS: This was a descriptive, prospective, cross-sectional study of CF patients > 18 years of age. Patients underwent nocturnal polysomnography (PSG) and were administered the Pittsburgh Sleep Quality Index questionnaire (PSQI) and the Cystic Fibrosis Quality of Life Questionnaire (CFQR 14 + Spain).
RESULTS: The study included 23 patients, 14 women (61%). The mean age of the participants was 32 + 18 years. The mean PSQI score was 5.57 + 3.55; 13 (56.5%) of the patients were poor sleepers, and 13% reported poor sleep quality; seven (30%) had sleep latency > 30 min, 10 (43.5%) had sleep efficiency < 85%. Nineteen underwent polysomnography. According to PSG measurements, sleep efficiency was less than 90% in 61% of the patients. Pathological values were found for the following parameters: intra-sleep wakefulness in 12 patients (63%); microarousal index in 12 patients (63%); and apnea-hypopnea index (AHI) in 2 patients. The desaturation time with SpO2 < 90% (T90) was > 30% in 3 patients. We observed a significant correlation between PSQI and all dimensions of CFQR 14.
CONCLUSIONS: Subjective and objective sleep efficiency decreases in adult CF patients. Sleep quality has an impact on HRQoL. The PSQI questionnaire was able to discriminate sleep quality.

Entities:  

Keywords:  Airflow obstruction; Cystic fibrosis; Nocturnal hypoxaemia; Quality of life; Sleep quality

Mesh:

Substances:

Year:  2018        PMID: 30284025     DOI: 10.1007/s00408-018-0167-x

Source DB:  PubMed          Journal:  Lung        ISSN: 0341-2040            Impact factor:   2.584


  29 in total

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2.  Diagnosis and treatment of sleep apnea-hypopnea syndrome. Spanish Society of Pulmonology and Thoracic Surgery.

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3.  Predicting sleep-disordered breathing in patients with cystic fibrosis.

Authors:  M A Milross; A J Piper; M Norman; G N Willson; R R Grunstein; C E Sullivan; P T Bye
Journal:  Chest       Date:  2001-10       Impact factor: 9.410

4.  Mechanism of hemoglobin desaturation during rapid-eye-movement sleep in normal subjects and in patients with cystic fibrosis.

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5.  Hypoxemia and hypercapnia during exercise and sleep in patients with cystic fibrosis.

Authors:  S Bradley; P Solin; J Wilson; D Johns; E H Walters; M T Naughton
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6.  Cystic fibrosis patients have poor sleep quality despite normal sleep latency and efficiency.

Authors:  Larry Jankelowitz; Kathryn J Reid; Lisa Wolfe; Joanne Cullina; Phyllis C Zee; Manu Jain
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7.  Patient-reported pain and impaired sleep quality in adult patients with cystic fibrosis.

Authors:  Patrick A Flume; Jody Ciolino; Susan Gray; Mary K Lester
Journal:  J Cyst Fibros       Date:  2009-08-08       Impact factor: 5.482

8.  Long-term survival and nutritional data in patients with cystic fibrosis treated in a Danish centre.

Authors:  M Nir; S Lanng; H K Johansen; C Koch
Journal:  Thorax       Date:  1996-10       Impact factor: 9.139

9.  Comparison of oxygen desaturation during sleep and exercise in patients with cystic fibrosis.

Authors:  M J Coffey; M X FitzGerald; W T McNicholas
Journal:  Chest       Date:  1991-09       Impact factor: 9.410

10.  Nocturnal home oxygen in the treatment of hypoxemic cystic fibrosis patients.

Authors:  R Zinman; M Corey; A L Coates; G J Canny; J Connolly; H Levison; P H Beaudry
Journal:  J Pediatr       Date:  1989-03       Impact factor: 4.406

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  2 in total

Review 1.  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

2.  Association between habitual physical activity (HPA) and sleep quality in patients with cystic fibrosis.

Authors:  Sarah Dietz-Terjung; Wolfgang Gruber; Sivagurunathan Sutharsan; Christian Taube; Margarete Olivier; Uwe Mellies; Cordula Koerner-Rettberg; Stefanie Dillenhöfer; Florian Stehling; Matthias Welsner
Journal:  Sleep Breath       Date:  2020-07-14       Impact factor: 2.816

  2 in total

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