Advanced Lung Disease in Patients with Cystic Fibrosis Is Associated with Low Diffusion capacity.


Journal

The Israel Medical Association journal : IMAJ
ISSN: 1565-1088
Titre abrégé: Isr Med Assoc J
Pays: Israel
ID NLM: 100930740

Informations de publication

Date de publication:
Dec 2020
Historique:
entrez: 31 12 2020
pubmed: 1 1 2021
medline: 13 1 2021
Statut: ppublish

Résumé

The single-breath diffusing capacity of the lungs (DLCOSB) test measures the extent to which carbon monoxide (CO) passes from the lung air sacs into the blood. The accessible alveolar volume (VASB) is measured by inert gas during a 10-second period. The single-breath transfer coefficient of the lung for carbon monoxide (KCOSB) is the DLCOSB divided by VASB. Cystic fibrosis (CF) disease comprises progressive airway obstruction with bronchiectasis and parenchyma fibrosis. Yet, the KCOSB appears insignificant in the assessment of pulmonary function in CF. To challenge the precision of normal KCOSB in CF. The authors collected pulmonary function tests (PFT) data from 74 confirmed CF patients (mean age 26 ± 10 years) with various levels of pulmonary disease severity. Tests included spirometry, DLCOBP, and body plethysmography (BP). Anatomical dead space was calculated by deducting anatomical dead space from total lung capacity TLC(BP) to establish alveolar volume (VABP) and to determine KCOBP. We also included individual data of arterial pCO2 blood-gas level. KCOSB values were normal or higher in most patients, regardless of patient FEV1 value (R2 = 0.2204; P < 0.02). In contrast, the measurements of KCOBP were low corresponding with low FEV1 values, and negatively correlated with the elevation of trapped air and pCO2 levels (R2 = 0.1383; P = 0.0133, P > 0.05, respectively). The 10- second perfusion time of the inert gas during DLCOSB represent the communicative alveolar volume in CF patients with advanced pulmonary disease. The findings justify the use of DLCOSB with the deterioration of FEV1 and elevation of pCO2 levels.

Sections du résumé

BACKGROUND BACKGROUND
The single-breath diffusing capacity of the lungs (DLCOSB) test measures the extent to which carbon monoxide (CO) passes from the lung air sacs into the blood. The accessible alveolar volume (VASB) is measured by inert gas during a 10-second period. The single-breath transfer coefficient of the lung for carbon monoxide (KCOSB) is the DLCOSB divided by VASB. Cystic fibrosis (CF) disease comprises progressive airway obstruction with bronchiectasis and parenchyma fibrosis. Yet, the KCOSB appears insignificant in the assessment of pulmonary function in CF.
OBJECTIVES OBJECTIVE
To challenge the precision of normal KCOSB in CF.
METHODS METHODS
The authors collected pulmonary function tests (PFT) data from 74 confirmed CF patients (mean age 26 ± 10 years) with various levels of pulmonary disease severity. Tests included spirometry, DLCOBP, and body plethysmography (BP). Anatomical dead space was calculated by deducting anatomical dead space from total lung capacity TLC(BP) to establish alveolar volume (VABP) and to determine KCOBP. We also included individual data of arterial pCO2 blood-gas level.
RESULTS RESULTS
KCOSB values were normal or higher in most patients, regardless of patient FEV1 value (R2 = 0.2204; P < 0.02). In contrast, the measurements of KCOBP were low corresponding with low FEV1 values, and negatively correlated with the elevation of trapped air and pCO2 levels (R2 = 0.1383; P = 0.0133, P > 0.05, respectively).
CONCLUSIONS CONCLUSIONS
The 10- second perfusion time of the inert gas during DLCOSB represent the communicative alveolar volume in CF patients with advanced pulmonary disease. The findings justify the use of DLCOSB with the deterioration of FEV1 and elevation of pCO2 levels.

Identifiants

pubmed: 33381950

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

770-774

Auteurs

Daphna Vilozni (D)

Department of Pediatric Pulmonology, the National Center for Cystic Fibrosis, Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel, associated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Adi Dagan (A)

Department of Pediatric Pulmonology, the National Center for Cystic Fibrosis, Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel, associated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Ifat Sarouk (I)

Department of Pediatric Pulmonology, the National Center for Cystic Fibrosis, Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel, associated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Bat-El Bar-Aluma (BE)

Department of Pediatric Pulmonology, the National Center for Cystic Fibrosis, Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel, associated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Moshe Ashkenazi (M)

Department of Pediatric Pulmonology, the National Center for Cystic Fibrosis, Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel, associated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Yael Bezalel (Y)

Department of Pediatric Pulmonology, the National Center for Cystic Fibrosis, Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel, associated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Ori Efrati (O)

Department of Pediatric Pulmonology, the National Center for Cystic Fibrosis, Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel, associated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH