臨床小児皮膚科 オープンアクセス

抽象的な

Pediatric Cardiology 2015: Hypoplastic left heart repair - Daniela Poli - Centro Cardiologico Pediatrico del Mediterraneo

Daniela Poli

Purpose: Hypoplastic left heart syndrome (HLHS) is a gathering of imperfections of the heart and enormous veins. A child is brought into the world with this condition (inherent heart imperfection). It happens when some portion of the heart doesn't create as it ought to during the initial two months of pregnancy. In HLHS, a large portion of the left half of the heart is little, immature, or both. The mixture approach for the treatment of patients with hypoplastic left heart disorder most regularly incorporates twofold methodology for transcatheter arrangement of a stent in the blood vessel conduit by means of femoral crotch and careful situation of groups on the branch pneumonic courses through middle sternotomy. We present our results of an early single stage technique for new-borns influenced by hypoplastic left heart disorder. There is huge fluctuation in the basic imperfections of the left heart–aorta complex that all fall under the term hypoplastic left heart condition. The writing for the most part saves this term for aortic atresia or stenosis, mitral atresia or stenosis, or both with serious underdevelopment of the left ventricle, which is unequipped for supporting the foundational course. We have recognized a subset of patients with hypoplastic left heart condition without inborn valvular stenosis and utilize the term hypoplastic left heart complex (HLHC) to depict this subset. Hypoplastic left heart complex comprises of different hypoplastic structures of the left heart–aorta complex including the mitral valve (MV), the left ventricle, the left ventricular surge tract (LVOT), and the aortic valve (AV).

Methods: From October 2011 to September 2014 at Centro Cardiologico Pediatrico del Mediterraneo-OPBG-Taormina, 41 continuous patients experienced an early single stage crossover approach technique for determination of HLHS (23 HLHS, 12 HLHS like, 6 HLHS complex). In 31 cases pre-birth finding was accessible and conveyance was endeavored in our emergency clinic with ICU back up. Every one of them got consistent prostaglandins imbuement, 17 of them required intubation or inotropic support before methodology. All patients were moved to Hybrid Cat Lab, checked by outspread course, focal vein catheter, right hand and right foot beat oxymetry and NIRS. After middle sternotomy, the left and right aspiratory were united by goretex 3 or 3.5 (as indicated by the heaviness of the patients and size of the pneumonic branches) and afterward the stent was conveyed in the blood vessel pipe by means of a 7 French catheter situated in the principle pneumonic conduit.

Results: All of them were treated during the initial 24 hours after birth; middle weight was 3.07 Kg (extend 1.5 kg to 4.5 Kg). For stenting blood vessel ductus we utilized pre-mounted stents in measurement from 7 to 10 and length from 12 to 19 mm Genesis in 5 cases pneumonic courses banding was performed by 3 mm custom goretex tube, while 3 patients 3.5 mm was utilized. All patients made due to the strategy. Mean medical clinic stay length was 19 days (go from 6 to 70 days), mean ICU remain was 11 days (run from 2 to 70 days). Procedural entanglements happened in four patients and in one patient was deffered sternal conclusion. At the middle follow up of 90 days, all patients are as yet alive on clinical treatment. Interstage period was portrayed by careful atrial septal imperfection development in four cases and atrial septal stent was situated in seven cases and inflatable dilatation was acted in three casas. Ductal stenting was not acted in two cases because of extreme breadth of the ductus. In eight cases was performed swell dilatation of ductal stent and in three cases restenting. Fourteen patients experienced fruitful exhaustive stage 2 method and eleven patients experienced biventricular fix.

Conclusion: as far as we can tell, single stage half breed approach for different kinds of HLHS, showed to be wellbeing and viability, with low grimness rate. Patients with HLHS are in danger for interstage dismalness and mortality, particularly between the first and second stages after the half and half technique. A thorough interstage follow up is compulsory so as to distinguish potential significant anatomical issues with respect to measurements of atrial septal deformity, right ventricular systolic capacity, tricuspid spewing forth, deterrent in the proximal or distal blood vessel pipe, gained or local retrograde hindrance of the aortic curve. Strategies ought to be acted in a devote cath lab by an accomplished group as indicated by an institutional program.