2016
DOI: 10.1590/s1806-37562016000000269
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An initial experience with a digital drainage system during the postoperative period of pediatric thoracic surgery

Abstract: Objective:To report an initial experience with a digital drainage system during the postoperative period of pediatric thoracic surgery. Methods:This was a prospective observational study involving consecutive patients, ≤ 14 years of age, treated at a pediatric thoracic surgery outpatient clinic, for whom pulmonary resection (lobectomy or segmentectomy via muscle-sparing thoracotomy) was indicated. The parameters evaluated were air leak (as quantified with the digital system), biosafety, duration of drainage, l… Show more

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Cited by 3 publications
(3 citation statements)
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“…Of the 13 included studies, there were six RCTs [ 7 , 12 , 14 16 , 18 ], three observational comparative studies that used propensity matching for their analysis [ 20 22 ], three observational studies with no comparative element [ 9 , 13 , 17 ] and one prospective comparative study [ 19 ]. The comparators in almost all of the RCTs and comparative observational studies were traditional analogue chest drainage systems that used wall-mounted suction.…”
Section: Review Of Clinical Effectiveness Evidencementioning
confidence: 99%
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“…Of the 13 included studies, there were six RCTs [ 7 , 12 , 14 16 , 18 ], three observational comparative studies that used propensity matching for their analysis [ 20 22 ], three observational studies with no comparative element [ 9 , 13 , 17 ] and one prospective comparative study [ 19 ]. The comparators in almost all of the RCTs and comparative observational studies were traditional analogue chest drainage systems that used wall-mounted suction.…”
Section: Review Of Clinical Effectiveness Evidencementioning
confidence: 99%
“…Cedar did not find comparative evidence on the use of Thopaz for fluid loss measurement, an outcome in the scope. One identified paper looked at the use of Thopaz in a paediatric cohort [ 13 ]. Although non-comparative, this study was included to provide evidence for use in children in line with the sub-groups defined in the scope.…”
Section: Review Of Clinical Effectiveness Evidencementioning
confidence: 99%
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