| Literature DB >> 35223699 |
Francesco Macchini1, Genny Raffaeli2,3, Ilaria Amodeo2, Martina Ichino1, José Luis Encinas4, Leopoldo Martinez4, Lucas Wessel5, Giacomo Cavallaro2.
Abstract
Recurrence is one of the most common surgical complications in Congenital Diaphragmatic Hernia (CDH). It could remain clinically silent for a long time or present as an acute complication week, months, or even years after the primary surgery. Several risk factors have been identified so far. An extended diaphragmatic defect represents one of the leading independent risk factors, together with indirect signs of large defect such as the liver position related to the diaphragm and the use of the prosthetic patch and with the use of a minimally invasive surgical (MIS) approach. However, the exact contribution of each factor and the overall risk of recurrence during the life span still need to be fully understood. This mini-review aims to give an overview of the current knowledge regarding CDH recurrence, focusing on predisposing factors, clinical presentation, management and follow-up of high-risk patients, and future perspectives.Entities:
Keywords: FETO; congenital diaphragmatic hernia; hernia recurrence; minimally invasive surgery; mortality; prosthetic patch; pulmonary hypertension
Year: 2022 PMID: 35223699 PMCID: PMC8864119 DOI: 10.3389/fped.2022.823180
Source DB: PubMed Journal: Front Pediatr ISSN: 2296-2360 Impact factor: 3.418
Figure 1Intraoperative imaging of patch repair. (A,B) Dome-shape patch repair. (C,D) Cone-shape patch repair.
Figure 2Radiological image of the major recurrence of left side CDH after a first patched diaphragmatic closure. (A,B) Chest X-ray image, (C–F) computed tomography image.