scholarly journals The surgical repair of a congenital peritoneopericardial diaphragmatic hernia in Maine Coon cat

2021 ◽  
Vol 19 (3) ◽  
pp. 439-447
Author(s):  
Chattida Panprom ◽  
◽  
Palin Jiwaganont ◽  
Ratikorn Bootcha ◽  
Soontaree Petchdee ◽  
...  
2010 ◽  
Vol 46 (6) ◽  
pp. 398-404 ◽  
Author(s):  
Angela C. Banz ◽  
Sharon D. Gottfried

The records of 31 cats and eight dogs undergoing surgical correction of peritoneopericardial diaphragmatic hernia (PPDH) from 2000 through 2007 were reviewed. Weimaraners and long-haired cats of varying breeds, particularly Maine Coon cats, appear to be at higher risk of PPDH. Presenting complaints were most commonly related to the respiratory and gastrointestinal tracts in both dogs and cats, although respiratory signs were more prevalent in cats, and gastrointestinal signs were more common in dogs. The most common herniated organs were liver, gallbladder, and small intestine. Mortality associated with surgical repair of PPDH in cats and dogs was low in the first 2 weeks postoperatively, and prognosis for return to normal function was excellent. Peri-and postoperative complications were typically minor and self-limiting.


2018 ◽  
Vol 67 (3) ◽  
pp. 189
Author(s):  
X. NIKIPHOROU ◽  
R. CHIOTI ◽  
M. N. PATSIKAS ◽  
L. G. PAPAZOGLOU

Peritoneopericardial diaphragmatic hernia (PPDH) is a congenital communication between the pericardial sac and the abdominal cavity allowing displacement of abdominal organs to the pericardial sac. Peritoneopericardial diaphragmatic hernia is thought to occur due to a failure of the development of septum transversum. Vomiting, exercise intolerance and respiratory distress are the most common clinical signs. Diagnosis of PPDH is based on plain radiography. Physical examination and diagnostic imaging may detect the presence of other congenital anomalies. Surgical repair of the PPDH is the treatment of choice for animals with clinical signs. Prognosis following surgical repair of PPDH is favorable. Animals with no clinical signs related to PPDH may not undergo surgical repair.


PEDIATRICS ◽  
1996 ◽  
Vol 97 (6) ◽  
pp. 810-810

This report suggests that stabilization of the intrauterine to extrauterine transitional circulation, combined with a respiratory care strategy that avoids pulmonary overdistension, takes advantage of inherent biological cardiorespiratory mechanics, and very delayed surgery for congenital diaphragmatic hernia results in improved survival and decreases the need for extracorporeal membrane oxygenation (ECMO). This retrospective review of a 10-year experience in which the respiratory care strategy, ECMO availability, and technique of surgical repair remained essentially contant describes the evolution of this method of management of congenital diaphragmatic hernia.


2017 ◽  
Vol 05 (01) ◽  
pp. e51-e54
Author(s):  
Zbyněk Straňák ◽  
Karel Pýcha ◽  
Simona Feyereislova ◽  
Jaroslav Feyereisl ◽  
Michal Rygl

Background Delayed surgery after stabilization of infants with congenital diaphragmatic hernia (CDH) is an accepted strategy. However, the evidence favoring delayed versus immediate surgical repair is limited. We present an extremely rare case of a very low-birth-weight infant with prenatally diagnosed left-sided CDH and unexpected transmural bowel perforations developing within the postnatal stabilization period. Case Report A neonate born at 31st week of gestation with a birth weight of 1,470 g with antenatally diagnosed left-sided CDH presented with bowel dilation leading to transmural bowel perforations on the 2nd day of life. Meconium pleuroperitonitis resulted in severe systemic inflammatory response syndrome, pulmonary hypertension, multiple organ failure, and death. Conclusion In neonates with CDH deteriorating under standard postnatal management, intestinal perforation, and early surgical intervention should be considered.


1987 ◽  
Vol 111 (3) ◽  
pp. 432-438 ◽  
Author(s):  
Hirokazu Sakai ◽  
Masanori Tamura ◽  
Yuhei Hosokawa ◽  
A. Charles Bryan ◽  
Geoffrey A. Barker ◽  
...  

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