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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/20911
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dc.contributor.authorRazumovsky, A.Yu.
dc.contributor.authorAlkhasov, A.B.
dc.contributor.authorBataev, S.M.
dc.contributor.authorMitupov, Z.B.
dc.contributor.authorRachkov, V.Ye.
dc.contributor.authorStepanenko, N.S.
dc.contributor.authorKulikova, N.V.
dc.contributor.authorIgnatyev, R.O.
dc.date.accessioned2022-06-07T09:03:23Z
dc.date.available2022-06-07T09:03:23Z
dc.date.issued2017
dc.identifier.citationRAZUMOVSKY, A.Yu., ALKHASOV, A.B., BATAEV, S.M., et al. Slide tracheoplasty in children with congenetal tracheal stenosis. In: Moldavian Journal of Pediatric Surgery. 2017, no. 1, p. 117. ISSN 2587-3229.en_US
dc.identifier.issn2587-3210
dc.identifier.issn2587-3229
dc.identifier.urihttps://sncprm.info.md/journal
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/20911
dc.description.abstractIntroduction. Congenital tracheal stenosis (CTS) is a rare life-threatening condition that often requires early surgical intervention. Treatment of CTS remains challenging. Patients and methods. Between 2011 and 2016, 16 patients underwent slide tracheoplasty. The median age at surgery was 14.9 months (range, 18 days - 10.5 years). The median body weight was 9.4 kg (range, 1.8- 32.8kg) at operation. Thirteen (81%) patients had long-segment CTS (>50% of total tracheal length), including 6 (38%) patients withtracheal stenosis extended to the bronchus. Abnormal bronchial arborization presented by an anomalous right upper lobe bronchus was detected in 6 patients. Fourteen (88%) patients had associated cardiovascularmalformations, which were previously operated on 5(31%) patients and simultaneously operated on 8(50%) patients. These defects and CTS were repaired with intraoperative usage of ECMO in 9(56%) patients versus conventional ventilatory support under cardiopulmonary bypass (CPB) in 7(44%) patients. Results. There was no airway-associated mortality. One child died for some technical reason. Another died of multiple organ failure one year after the STP. The median follow-up period for the survivors was2.2 years (range, 0.2 – 5.1 years). In these15 patients, the median duration of ventilatory support was 8 (range, 1-25) days. The median duration of postoperative hospitalization period was 36 (range, 8-64) days, including the median duration of ICU stay 26 (range, 6-42) days. Post-STP airway intervention (bougienage or laser photocoagulation) was necessary in 6 of our patients, no one required additional surgical procedures, stenting was not required either.All survivors (100%, 15 out of 15) were asymptomaticat last follow-up. Conclusions. Our data suggest that children with CTS benefit from the usage of ECMO and the policy of simultaneous surgical treatment of associated cardiovascular malformations. Moreover, using intraoperative ECMO provides comfort conditions for surgeons facilitating a technically complicated operation and decreasing intra- and postoperative risks of common complications.en_US
dc.language.isoenen_US
dc.publisherNational Society of Pediatric Surgery of the Republic of Moldovaen_US
dc.relation.ispartofMoldavian Journal of Pediatric Surgery: Pediatric Surgery International Conference “Performances and perspectives in the pediatric surgery development”, September 14-16, 2017, Chisinau, Republic of Moldovaen_US
dc.titleSlide tracheoplasty in children with congenetal tracheal stenosisen_US
dc.typeOtheren_US
Appears in Collections:Moldavian Journal of Pediatric Surgery

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