Histopathological features of open lung biopsies in children treated with extracorporeal membrane oxygenation (ECMO)

被引:8
作者
Sebire, NJ [1 ]
Ramsay, AD [1 ]
Malone, M [1 ]
机构
[1] Great Ormond St Hosp Sick Children, Dept Paediat Pathol, Camelia Botnar Labs, London WC1N 3JH, England
关键词
extracorporeal membrane oxygenation (ECMO); alveolar capillary dysplasia; pulmonary hypertension;
D O I
10.1016/j.earlhumdev.2004.11.004
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Extracorporeal membrane oxygenation (ECMO) has become an established treatment for severe respiratory distress in a range of pediatric conditions. This study describes the histopathotogical features in a series of 22 children receiving ECMO therapy in whom open lung biopsy was carried out. Aims: To describe the histopathological features of open lung biopsies in children receiving ECMO therapy. Study design: Retrospective review of clinical material. Subjects: Children receiving ECMO therapy in whom open lung biopsy was carried out. Results: In those investigated in infancy, open lung biopsy allowed a definite diagnosis to be made of the underlying condition in more than 90% of cases. In older children, the histopathological changes were more non-specific and, although providing useful clinical information, a definitive diagnosis could often not be made. In about a quarter of cases, there are additional pathological features, which may be related to ECMO treatment, such as significant intra-alveolar haemorrhage, but ECMO does not in itself impair the diagnostic usefulness of open lung biopsy in these selected patients. Conclusion: Open lung biopsy provides clinically useful information in infants receiving ECMO therapy. The histopathological changes may be complex and represent both the effects of ECMO and progression of the underlying disease. (c) 2004 Elsevier Ireland Ltd. AR rights reserved.
引用
收藏
页码:455 / 460
页数:6
相关论文
共 21 条
[1]   Open lung biopsy in pediatric patients on extracorporeal membrane oxygenation [J].
Bond, SJ ;
Lee, DJ ;
Stewart, DL ;
Buchino, JJ .
JOURNAL OF PEDIATRIC SURGERY, 1996, 31 (10) :1376-1378
[2]   The incidence and characteristics of neonatal irreversible lung dysplasia [J].
Cassidy, J ;
Smith, J ;
Goldman, A ;
Haynes, S ;
Smith, E ;
Wright, C ;
Haworth, S ;
Davis, P ;
Firmin, R ;
Kasem, K ;
Davis, C .
JOURNAL OF PEDIATRICS, 2002, 141 (03) :426-428
[3]   MISALIGNMENT OF LUNG VESSELS AND ALVEOLAR CAPILLARY DYSPLASIA - A CAUSE OF PERSISTENT PULMONARY-HYPERTENSION [J].
CATER, G ;
THIBEAULT, DW ;
BEATTY, EC ;
KILBRIDE, HW ;
HUNTRAKOON, M .
JOURNAL OF PEDIATRICS, 1989, 114 (02) :293-300
[4]  
CHELLIAH BP, 1995, PEDIATRICS, V96, P1159
[5]   PULMONARY CHANGES FOLLOWING EXTRACORPOREAL MEMBRANE-OXYGENATION - AUTOPSY STUDY OF 23 CASES [J].
CHOU, P ;
BLEI, ED ;
SHENSCHWARZ, S ;
GONZALEZCRUSSI, F ;
REYNOLDS, M .
HUMAN PATHOLOGY, 1993, 24 (04) :405-412
[6]   Pulmonary alveolar proteinosis: A review [J].
deMello, DE ;
Lin, ZW .
PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE, 2001, 20 (05) :413-432
[7]   Histological changes in the hearts of non-survivors of the UK Collaborative Trial of Neonatal ECMO (extra corporeal membrane oxygen) [J].
Evans, MJ ;
Keeling, JW .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1999, 81 (01) :F30-F34
[8]   PATHOLOGICAL COMPLICATIONS OF NONSURVIVORS OF NEWBORN EXTRACORPOREAL MEMBRANE-OXYGENATION [J].
EVANS, MJ ;
MCKEEVER, PA ;
PEARSON, GA ;
FIELD, D ;
FIRMIN, RK .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1994, 71 (02) :F88-F92
[9]   Alveolar capillary dysplasia, with and without misalignment of pulmonary veins: An association of congenital anomalies [J].
Garola, RE ;
Thibeault, DW .
AMERICAN JOURNAL OF PERINATOLOGY, 1998, 15 (02) :103-107
[10]   CONGENITAL PULMONARY LYMPHANGIECTASIA [J].
HUBER, A ;
SCHRANZ, D ;
BLAHA, I ;
SCHMITTMECHELKE, T ;
SCHUMACHER, R .
PEDIATRIC PULMONOLOGY, 1991, 10 (04) :310-313