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Pulmonary vein stenosis: the UK, Ireland and Sweden collaborative study.

Seale, A N (author)
Webber, S A (author)
Uemura, H (author)
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Partridge, J (author)
Roughton, M (author)
Ho, S Y (author)
McCarthy, K P (author)
Jones, S (author)
Shaughnessy, L (author)
Sunnegårdh, Jan, 1948 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Hanséus, Katarina (author)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine
Rigby, M L (author)
Keeton, B R (author)
Daubeney, P E F (author)
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 (creator_code:org_t)
2009-09-07
2009
English.
In: Heart (British Cardiac Society). - : BMJ. - 1468-201X .- 1355-6037. ; 95:23, s. 1944-9
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • OBJECTIVE: To describe clinical features, morphology, management and outcome of pulmonary vein stenosis (PVS) in childhood. DESIGN AND SETTING: Retrospective international collaborative study involving 19 paediatric cardiology centres in the UK, Ireland and Sweden. PATIENTS: Cases of PVS presenting between 1 January 1995 and 31 December 2004 were identified. Cases where pulmonary veins connected to a morphological left atrium were included. Functionally univentricular hearts and total anomalous pulmonary venous connection were excluded. All available data and imaging were reviewed. RESULTS: 58 cases were identified. In 22 cases (38%) there was premature delivery. 46 (79%) had associated cardiac lesions; 16 (28%) had undergone previous cardiac surgery before PVS diagnosis. 16 children (28%) had a syndrome or significant extracardiac abnormality. 36 presented with unilateral disease of which 86% was on the left. Where there was adequate sequential imaging, disease progression was shown with discrete stenosis leading to diffusely small pulmonary veins. Collateral vessels often developed. 13 patients had no intervention. Initial intervention was by catheter in 17 and surgery in 28. Overall 3-year survival was 49% (95% CI 35% to 63%) with patients undergoing initial surgical intervention having greater freedom from death or re-intervention (hazard ratio 0.44, 95% CI 0.2 to 0.99, p = 0.023). CONCLUSIONS: PVS is a complex disease of uncertain cause and frequently associated with prematurity. Early intervention may be indicated to deter irreversible secondary changes.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Keyword

Adolescent
Child
Child
Preschool
Constriction
Pathologic
mortality
pathology
therapy
Disease Progression
Female
Great Britain
Heart Defects
Congenital
complications
mortality
Humans
Infant
Infant
Newborn
Infant
Premature
Infant
Premature
Diseases
mortality
pathology
therapy
Ireland
Kaplan-Meiers Estimate
Male
Pulmonary Veins
abnormalities
pathology
Pulmonary Veno-Occlusive Disease
etiology
pathology
therapy
Retrospective Studies
Sweden
Treatment Outcome

Publication and Content Type

ref (subject category)
art (subject category)

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