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Scintiscanning in diagnostics of hepatopulmonary syndrome in children
M Teisseyre1, M Szymczak, E Swiatek-Rawa
1Clinic of Gastroenterology, Hepatology and Nutrition, Memorial Child Health Centre Institute, Aleja Dzieci Polskich 20, 04-730 Warsaw, Poland.
Insights
Arteriovenous shunts, a hallmark of hepatopulmonary syndrome (HPS), were detected in 28.6% of pediatric liver cirrhosis patients. The severity of these shunts did not correlate with the cause or stage of liver disease.
Area of Science:
- Pediatric Gastroenterology
- Pulmonary Medicine
- Radiology
Background:
- Hepatopulmonary syndrome (HPS) involves arterial oxygenation disturbances in liver cirrhosis patients.
- It is caused by intrapulmonary arteriovenous shunts and vascular dilatation.
- This study focuses on pediatric patients with suspected HPS and liver cirrhosis.
Purpose of the Study:
- To determine the incidence of arteriovenous shunts in children with liver cirrhosis.
- To assess the correlation between shunt severity and the etiology or clinical stage of cirrhosis.
Main Methods:
- Scintiscanning with technetium-labeled microspheres was used to detect arteriovenous shunts.
- The shunt index (SI) was calculated by comparing radioactivity in the brain to the lungs.
- 21 children (1.2-17.7 years) with various types of liver cirrhosis were investigated.
Main Results:
- Arteriovenous shunts were identified in 6 out of 21 (28.6%) pediatric patients.
- Shunt Index (SI) values ranged from 0.06% to 51%.
- No correlation was found between SI values and the etiology of cirrhosis or the Child-Pugh clinical score.
Conclusions:
- Scintiscanning is effective in detecting pulmonary arteriovenous shunts in pediatric liver cirrhosis.
- A significant proportion of children with liver cirrhosis exhibit arteriovenous shunts.
- The severity of HPS, indicated by shunts, is not linked to the underlying liver disease factors studied.
Background:
Arterial blood oxygenation disturbances accompanying liver cirrhosis are referred to as hepatopulmonary syndrome (HPS). HPS develops due to the formation of intrapulmonary arteriovenous shunts and dilatation of the vascular bed. The aim of the study was to assess the incidence of arteriovenous shunts in children with hepatic cirrhosis and HPS suspected on the basis of clinical signs, qualified for liver transplantation.
Material And Methods:
The study was carried out in a group of 21 children aged from 1.2 to 17.7 years (mean age 8.4); 8 girls and 13 boys. The patients were diagnosed as follows: biliary cirrhosis due to extrahepatic bile duct impatency--12, post-inflammatory liver cirrhosis due to infection with HVB--2, autoimmune hepatitis--2, fibrosis of the liver--2, alpha 1-antitrypsin deficiency--1, progressive familial intrahepatic cholestasis--1, cystic fibrosis--1. The presence of arteriovenous anastomoses in the lungs was detected by scintiscanning utilizing microspheres (albumin macroaggregates). Under physiologic conditions, technetium-labeled microspheres injected i.v. are accumulated in pulmonary capillaries. Radioactivity detected in other organs (kidneys, brain) indicates the presence of pathologic shunts omitting the alveoli. A percentage ratio of radioactivity detected in the brain to that present in the lungs serves as the index of blood flow through the anastomosis (SI--shunt index). According to Grimon, the mean SI value for healthy children amounts to 0.43%, the values ranging from 1% to 2% are regarded as borderline ones, and those above 2% allow unequivocal diagnosis of HPS.
Results:
The SI values obtained in the study ranged from 0.06 to 51%. In 7 patients SI exceeded 1%, reaching 1.23% in one, and over 3% in the remaining 6 patients. No correlations were found either between SI value and the etiology of cirrhosis, or between the index and clinical condition of the patient assessed according to Child-Pugh scale.
Conclusions:
1. Scintiscanning revealed the presence of arteriovenous shunts in the lungs of 6/21 (28.6%) investigated patients. 2. No correlation was found between the severity of HPS and the etiology and stage of the underlying disease.
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