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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2022
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/21032
Title: | Chest malformations in children. Literature review |
Authors: | Plămădeală, Liviu |
Keywords: | Chest wall deformities;Pectus Excavatum;Pectus Carinatum;Procedure Nuss;Abramson technique |
Issue Date: | 2022 |
Publisher: | Nicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldova, Association of Medical Students and Residents |
Citation: | PLĂMĂDEALĂ, Liviu. Chest malformations in children. Literature review. In: MedEspera: the 9th International Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2022, p. 267. |
Abstract: | Introduction. Chest malformations in children (CMC) can be divided into two types - primary, also called
congenital, have a multifactorial etiology, and secondary or acquired: (post-traumatic), iatrogenic and
syndromal (due to Marfan syndrome, Ehlers-Danlos syndrome, etc.), all together appear, according to
various authors, in 2-7% of the population. Congenital malformations of the chest wall can be classified
into common entities such as pectus excavatum (PE) representing 90% and pectus carinatum (PC) - 7%,
and rare entities such as sternum cleft, asphyxiating thoracic dystrophy (Jeune syndrome), Poland syndrome
and spondylothoracic dysplasia (Jarcho-Levin syndrome), accounting for 3-4% of all cases. Cosmetic
defects are the most common causes of referral to a doctor, and in more severe forms there are pathological
changes in the cardiovascular and respiratory system, which serve as indications for thoracoplasty.
Aim of study. To provide an overview of current diagnostic and surgical treatment of minimally invasive
thoracoplasty.
Methods and materials. We selected the articles published in the period 2016-2021, from the PubMed
database, HINARI, according to the following keywords: "Chest wall deformities", "Pectus Excavatum",
"Pectus Carinatum", "Procedure Nuss", "Abramson technique".
Results. For preoperative evaluation of the manners of CMC surgery, Rx thoracic, thoracic CT scan,
electrocardiograph and color Doppler echocardiography are deemed mandatory by nearly all of the
responders, with a proportion of 89-98%, A pulmonary function test is considered to be necessary by
54.12% of the surveyed cohort. Referring to the indications of surgery for PE, a Haller index of >3.25 of
thoracic CT scan. Restricted pulmonary ventilation disorder, abnormal in ECG and accompanied with
mitral valve prolapse are agreed as indications of surgery . Severe deformity and ongoing deterioration of
deformity and severe social-psychological problems from deformity and cosmetic requests. Minimally
invasive repair of pectus excavatum using the Procedure Nuss, is the most common and preferred operative
correction of pectus excavatum. Variations in intraoperative techniques included sternal elevator (SE) use,
the number of bars placed behind the sternum and the use of bilateral stabilization sutures. Minimally
invasive repair of pectus carinatum using the Abramson technique using a pectus bar that is placed
anteriorly to the sternum. The procedure is less invasive and less risky than a pectus bar inserted for pectus
excavatum, but the lateral fixation of the pectus bar in the Abramson procedure remains a challenge.
Conclusion. Placement of multiple bars and SE use are associated with significantly higher odds of certain
complications. Minimally invasive repair of PE and PC the patient is discharged usually between the fifth
and seventh postoperative day and is seen in the outpatient clinic after 2 weeks, 6 weeks, 3 months, 6
months, and 12 months, with very good results. |
metadata.dc.relation.ispartof: | MedEspera: The 9th International Medical Congress for Students and Young Doctors, May 12-14, 2022, Chisinau, Republic of Moldova |
URI: | https://medespera.asr.md/en/books http://repository.usmf.md/handle/20.500.12710/21032 |
Appears in Collections: | MedEspera 2022
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