Prophylactic peritoneal dialysis catheter does not decrease time to achieve a negative fluid balance after the Norwood procedure: a randomized controlled trial
Lindsay M Ryerson, Andrew S Mackie, Joseph Atallah, Ari R Joffe, Ivan M Rebeyka, David B Ross, Ian Adatia, Lindsay M Ryerson, Andrew S Mackie, Joseph Atallah, Ari R Joffe, Ivan M Rebeyka, David B Ross, Ian Adatia
Abstract
Objective: Infants and children who undergo cardiopulmonary bypass and cardiac surgery are at risk of postoperative fluid overload. Peritoneal dialysis catheter (PDC) and peritoneal dialysis are reported to be effective means of postoperative fluid management. We sought to test the hypothesis that PDC insertion in the operating room at the time of Norwood palliation would decrease the time to achieve a negative fluid balance in a group of neonates with hypoplastic left heart syndrome.
Methods: A single center randomized controlled trial was performed. We randomized neonates with hypoplastic left heart syndrome to prophylactic PDC, with or without dialysis, or standard care (ie, no PDC).
Results: Twenty-two neonates were included; 10 were randomized to PDC and 12 were randomized to standard care. The mean time to first postoperative negative fluid balance was 2.70 ± 1.06 days for the prophylactic PDC group and 2.67 ± 0.65 days for the standard care group (P = .93). There was no difference between the 2 groups in time to lactate ≤ 2 mmol/L, maximum vasoactive-inotrope score on postoperative days 2 to 5, time to sternal closure, time to first extubation, modified clinical outcome score, or hospital length of stay. Twenty-one patients (95%) survived to hospital discharge. Four patients randomized to prophylactic PDC had 1 or more serious adverse events compared with no patients in the standard care group (P = .03).
Conclusions: Prophylactic PDC, with or without dialysis, did not decrease the time to achieve a negative fluid balance after the Norwood procedure, did not alter physiological variables postoperatively, and was associated with more severe adverse events.
Trial registration: ClinicalTrials.gov NCT01215240.
Copyright © 2015 The American Association for Thoracic Surgery. Published by Elsevier Inc. All rights reserved.
Source: PubMed
今後の臨床試験
-
Magnus MedicalCongressionally Directed Medical Research Programs募集
-
Nicholas ButowskiSiren Biotechnologyまだ募集していません神経膠腫 | 脳腫瘍 | 再発性の高悪性度神経膠腫アメリカ
-
State University of New York at Buffaloまだ募集していません
-
Poitiers University Hospitalまだ募集していません
-
Assistance Publique - Hôpitaux de Parisまだ募集していません
-
University of California, Irvine募集脳腫瘍 | 中枢神経系がん | 神経系がん | 脳癌転移性アメリカ
-
Guangdong Raynovent Biotech Co., Ltdまだ募集していません
-
The Hong Kong Polytechnic UniversityWu Jieh Yee Charitable Foundation募集
-
Shanghai General Hospital, Shanghai Jiao Tong University...まだ募集していません
-
Sun Yat-sen Universityまだ募集していません禁煙 | AIエージェント | Early-Stage Cancer
-
Affiliated Hospital of Nantong Universityまだ募集していません