PULMONARY FUNCTION TESTING IN CHILDREN WITH CHRONIC LIVER DISEASE

El-Shabrawi MHF1, El-Karaksy HM1, Okasha S1, Kotb MA1, Mohsen NA1, El-Koofy N1, El-Sayed HM1, Isa MA1, Hassan AM1 and Ibrahim A2

1 Department of Pediatrics, Faculty of Medicine, Cairo University, Cairo, Egypt

2 Department of Physiology, Faculty of Medicine, Cairo University, Cairo, Egypt

 

Objective: Arterial hypoxemia due to intrapulmonary shunting is a rare but severe complication in children with chronic liver disease (CLD) that may necessitate ��urgent�� liver transplantation. We aimed at studying the feasibility and usefulness of pulmonary function testing (PFT) in diagnosis of lung affection(s) in children with CLD.

Methods: Twenty-five children (14 males) aged 10-16 (median 12.4) years were investigated; 12 had frank cirrhosis and 13 non-cirrhotic and none was ascitic. All had arterial blood gas determination at rest in 21% oxygen (O2) and after breathing 100% O2 for 15 minutes. PFT was performed using a dry-seal spirometer in the sitting position with nose clips taking the largest of 3 consecutive readings for each child. Carbon monoxide (CO) diffusion capacity (DLco) was estimated by the single breath method using a spirometer containing a gas mixture of nitrogen, 21% O2,10% helium and 0.3% CO .Pulmonary artery pressure was also measured at rest and after maximal exercise by a bicycle ergometer.

Results: Arterial hyoxemia (PaO2 <80 mmHg) was present in 10 patients.Forced expiratory volume in 1 minute(FEV 1)was < 80% predicted in 15 patients, forced vital capacity(FVC) was< 80% predicted in15 and a ratio FEV 1/ FVC was< 65% predicted in 20 patients. DLco was < 80% predicted in 15 patients. These results indicate obstrucive airway as well as a diffusion defect.

Conclusion: Arterial hypoxemia is not uncommon in childern with CLD.PFT is a tedious but non-invasive investigation in children with CLD; it does demonstrate both obstructive airway as well as diffusion defects in these children. Therefore; we may recommend PFT in the work-up of children with CLD in order to detect pulmonary affections early; particularly if liver transplantation is contemplated.

 

 

 
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