Outcomes following prosthetic patch repair in newborns with congenital diaphragmatic hernia

2013 ◽  
Vol 100 (13) ◽  
pp. 1833-1837 ◽  
Author(s):  
W. B. Jawaid ◽  
E. Qasem ◽  
M. O. Jones ◽  
N. J. Shaw ◽  
P. D. Losty
Author(s):  
Mariatu A. Verla ◽  
Candace C. Style ◽  
Timothy C. Lee ◽  
Alicia D. Menchaca ◽  
Patricio E. Lau ◽  
...  

2020 ◽  
Vol 55 (8) ◽  
pp. 1522-1527 ◽  
Author(s):  
Etienne Suply ◽  
Clare Rees ◽  
Kate Cross ◽  
Hesham Elagami ◽  
Simon Blackburn ◽  
...  

2010 ◽  
Vol 45 (8) ◽  
pp. 1748-1750 ◽  
Author(s):  
Hiroaki Komuro ◽  
Sumi Kudou ◽  
Masaki Matsubara ◽  
Noriko Hoshino

2018 ◽  
Vol 29 (01) ◽  
pp. 120-124 ◽  
Author(s):  
Robin Wigen ◽  
Wenming Duan ◽  
Theo Moraes ◽  
Priscilla Chiu

Purpose The aim is to identify prognostic markers of long-term pulmonary morbidity among congenital diaphragmatic hernia (CDH) survivors. Methods A single-institution, retrospective review was performed on all CDH patients from 2000 and 2012 (REB#1000053383). Liver position, patch use, and pulmonary function tests (PFTs) (forced expiratory volume at 1 second [FEV1] and forced vital capacity [FVC] expressed as mean % predicted + SD) were recorded. Data were analyzed using analysis of variance. Results Patients with acceptable and reproducible PFT (n = 72 for 202 total PFT) with patch repair and liver up (n = 28) had significantly lower FEV1 (72.4 + 17.6) than those with no patch and liver down (n = 98, FEV1= 86.3 + 15.9, p = 0.002). Patients with patch repair and liver down (n = 40) also had significantly lower FEV1 (76.6 + 14.4) than those with liver down and no patch (p = 0.0463). Patients with liver up and patch repair had PFT results consistent with moderate reduction of lung function, while the remainder had mild to no decrease in lung function. All CDH patients older than 14 years had a reduction in FEV1/FVC consistent with obstructive phenotype, with a mean FEV1/FVC = 62.3 for patch repair group and FEV1/FVC = 76.1 in the no patch group. Conclusion Decreased pulmonary function of CDH survivors correlated with the use of patch repair and liver position. CDH lung disease should be monitored in adulthood.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Kim Heiwegen ◽  
Ivo de Blaauw ◽  
Sanne M. B. I. Botden

AbstractLarge studies comparing the surgical outcome of primary versus patch repair in congenital diaphragmatic hernia (CDH) patients are rare. This study aims to evaluate the incidence of surgical complications in both types of CDH repair. PubMed, EMBASE, Cochrane and Web of Science were searched for peer-reviewed articles. Studies on CDH between 1991 and August 2020 were systematically screened and meta-analyses were performed. Primary outcomes of this review were: haemorrhage, chylothorax, recurrences and small bowel obstruction (SBO). A total of 6436 abstracts were screened, after which 25 publications were included (2910 patients). Patch repaired patients have a 2.8 times higher risk on developing a recurrence (20 studies) and a 2.5 times higher risk on developing a chylothorax (five studies). Moreover, they have a two times higher risk on developing a SBO. No studies could be included that evaluated the incidence of surgical haemorrhage between these patients. Although the quality of the studies was relatively low, patch repaired patients have a higher risk on developing a recurrence, chylothorax and small bowel obstruction. Large prospective studies are required to adjust for severity of disease, to reveal the true causative factors in order to minimize the risk on these surgical complications in both types of patients.


2008 ◽  
Vol 23 (1) ◽  
pp. 215-215 ◽  
Author(s):  
Sohail R. Shah ◽  
George K. Gittes ◽  
Katherine A. Barsness ◽  
Timothy D. Kane

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