Page last updated: 2024-10-28

halothane and Esophageal Atresia

halothane has been researched along with Esophageal Atresia in 2 studies

Esophageal Atresia: Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA.

Research Excerpts

ExcerptRelevanceReference
"In 100 patients congenital stridor was found, in 55 children the stridor was considered to be acquired."1.30Stridor in the neonate and infant. Implications for the paediatric anaesthetist. Prospective description of 155 patients with congenital and acquired stridor in early infancy. ( Holzki, J; Laschat, M; Stratmann, C, 1998)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Holzki, J1
Laschat, M1
Stratmann, C1
Conroy, PT1
Bennett, NR1

Other Studies

2 other studies available for halothane and Esophageal Atresia

ArticleYear
Stridor in the neonate and infant. Implications for the paediatric anaesthetist. Prospective description of 155 patients with congenital and acquired stridor in early infancy.
    Paediatric anaesthesia, 1998, Volume: 8, Issue:3

    Topics: Airway Obstruction; Anesthesia, Inhalation; Anesthetics, Inhalation; Arytenoid Cartilage; Bronchial

1998
Management of tracheomalacia in association with congenital tracheo-oesophageal fistula.
    British journal of anaesthesia, 1987, Volume: 59, Issue:10

    Topics: Anesthesia, Inhalation; Atracurium; Esophageal Atresia; Female; Halothane; Humans; Infant, Newborn;

1987