Document Detail

Effects of cyanosis and hypothermic circulatory arrest on lung function in neonatal lambs.
MedLine Citation:
PMID:  10475419     Owner:  NLM     Status:  MEDLINE    
BACKGROUND: Lung function is often impaired after cardiac surgery and cardiopulmonary bypass (CPB), particularly in chronically cyanotic patients. This study aimed to evaluate lung function in a surgically created chronic cyanotic neonatal lamb model after CPB and deep hypothermic circulatory arrest (DHCA) and to assess the role of nitric oxide (NO) in the pathogenesis of increased pulmonary vascular resistance. METHODS: A chronic cyanosis model was surgically created in 7 lambs (4.7+/-0.8 days old) by anastomosing the pulmonary artery (PA) to the left atrium (LA). Another 7 lambs underwent a sham operation (control). One week later, the animals underwent shunt takedown and CPB with 90 minutes of DHCA at 18 degrees C. Cardiac index (CI), pulmonary vascular resistance index (PVRI), lung dynamic compliance (Cdyn), alveolar-arterial oxygen difference (AaDO2), left atrial plasma nitrate/nitrite (NO metabolites) levels, and pulmonary cGMP production (concentration difference between LA and PA) were measured before CPB and at 1 and 2 hours after reperfusion. RESULTS: The cyanosis model consistently produced significantly lower arterial oxygen tension (34.8+/-2.3 vs 93.1+/-8.8 torr in control, p < 0.001) and Qp/Qs (0.6+/-0.1 vs 1.0+/-0.0 in control, p < 0.001) than controls. Postoperative PVRI was significantly lower in the cyanosis group than in controls, although CPB with DHCA significantly elevated PVR in both cyanotic and control animals. There were no significant differences in AaDO2 and Cdyn after CPB between groups. The level of NO metabolites did not change before or after CPB in either cyanotic or acyanotic animals. NO metabolite levels tended to be higher in the cyanotic animals (p = 0.08). There was no significant difference in pulmonary cGMP production between both groups. CONCLUSIONS: These findings suggest that CPB with DHCA, per se, does not affect NO production in cyanotic or acyanotic neonatal lambs but causes increased PVR in both groups. Chronic cyanosis does not result in reduced pulmonary function after CPB with DHCA, and is associated with lower PVR. The mechanism may involve an increased NO production in cyanotic animals.
M Nagashima; U Stock; G Nollert; J Sperling; D Shum-Tim; S Hatsuoka; J E Mayer
Related Documents :
24244459 - Regulation of vascular smooth muscle tone by adipose-derived contracting factor.
12438669 - Vascular endothelial growth factor causes pulmonary vasodilation through activation of ...
119419 - Anaphylaxis in the monkey: pulmonary oedema after pre-treatment of beta-receptor stimul...
7112459 - Reduced baroreceptor sensitivity in patients with chronic obstructive pulmonary disease.
11332949 - Uncertainties about the use of inhaled nitric oxide in preterm infants.
20496069 - Pulmonary survival study in 91 patients with systemic sclerosis.
19524559 - Anomaly in aortic arch alters pathological outcome of transient global ischemia in rhes...
15216109 - Eversion endarterectomy: a new application of an old technique.
21530669 - Use of ultra pure nitric oxide generated by the reduction of nitrogen dioxide to revers...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  The Annals of thoracic surgery     Volume:  68     ISSN:  0003-4975     ISO Abbreviation:  Ann. Thorac. Surg.     Publication Date:  1999 Aug 
Date Detail:
Created Date:  1999-09-15     Completed Date:  1999-09-15     Revised Date:  2003-11-14    
Medline Journal Info:
Nlm Unique ID:  15030100R     Medline TA:  Ann Thorac Surg     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  499-504; discussion 504-5     Citation Subset:  AIM; IM    
Department of Cardiovascular Surgery, Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Animals, Newborn
Cardiac Output / physiology
Cardiopulmonary Bypass*
Chronic Disease
Cyanosis / physiopathology*
Cyclic GMP / blood
Disease Models, Animal
Endothelium, Vascular / physiopathology
Heart Arrest, Induced*
Lung / blood supply*
Lung Compliance / physiology
Nitrates / blood
Nitric Oxide / physiology*
Nitrites / blood
Pulmonary Diffusing Capacity / physiology
Vascular Resistance / physiology*
Reg. No./Substance:
0/Nitrates; 0/Nitrites; 10102-43-9/Nitric Oxide; 7665-99-8/Cyclic GMP

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  On-pump versus off-pump coronary revascularization: evaluation of renal function.
Next Document:  Pediatric coronary artery bypass for Kawasaki congenital, post arterial switch, and iatrogenic lesio...