Venovenous versus venoarterial extracorporeal membrane oxygenation in congenital diaphragmatic hernia

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Abstract

Background: Extracorporeal membrane oxygenation (ECMO) has a significant role as a final rescue modality in severe respiratory failure of the newborn with congenital diaphragmatic hernia (CDH). The objective of this study was to compare the efficiency of venovenous (VV) versus venoarterial (VA) ECMO in newborns with CDH.

Methods: A retrospective report of 11 years experience (1990 through 2001) of a single center, comparing VV and VA ECMO is given. VV ECMO was the preferred rescue modality for respiratory failure unresponsive to maximal medical therapy. Only when the placement of a VV ECMO 14F catheter was not possible, VA ECMO was used. Forty-six patients met ECMO criteria; 26 were treated with VV ECMO and 19 with VA ECMO. One patient underwent conversion from VV to VA ECMO.

Results: Before ECMO, there was no difference between VV and VA ECMO patients in mean oxygenation index (83 v 83), mean airway pressure (18.4 v 18.9 cm H2O), ECMO cannulation age (28 v 20 hours), or in the percentage of patients who needed dopamine and dobutamine (100% v 100%). From November 1994, nitric oxide (NO) was available; before ECMO, 11 of 14 (79%) VV ECMO patients received NO versus 9 of 10 (90%) patients in the VA group. VV ECMO patients were larger (3.34 v 2.77 kg; P < .05) and of advanced gestational age (39.0 v 36.9 wk; P < .05) compared with VA ECMO patients. There was no significant difference between VV and VA ECMO patients in survival rate (18 of 26, 69% v 13 of 19, 68%), ECMO duration (152 v 150 hours), time of extubation (32.0 v 33.5 days), age at discharge (73 v 81 days), or incidence of short-term intracranial complications (3.8% v 10.5%) or myocardial stun (3.8% v 15.8%).

Conclusions: The authors conclude that VV ECMO is as reliable as VA ECMO in newborns with CDH in severe respiratory failure who need ECMO support and who can accommodate the VV double-lumen catheter. Because of its potential advantages, VV ECMO may be the preferred ECMO method in these infants.

Section snippets

Materials and methods

VV ECMO was introduced at Huntington Memorial Hospital (Pasadena, CA) in October 1990. Only infants with intractable respiratory failure unresponsive to maximal medical therapy who met ECMO criteria and whose parents gave informed consent were placed on ECMO. VV ECMO was the preferred mode of ECMO. An attempt was made to place a 14 F double-lumen VV catheter (Kendall Infant ECMO Catheter, catalog No. 5914; Kendall Healthcare Products Co, Mansfield, MA) in all infants who met ECMO criteria. The

Results

There were 99 patients with CDH treated at our institution during the time of the study; 46 (46%) of these infants were treated with ECMO. A total of 27 newborns with CDH received VV ECMO. One of them required conversion to VA ECMO (this infant survived). Nineteen newborns with CDH were treated with VA ECMO (Fig 1).

Patient characteristics are given in Table 1. VV ECMO patients were larger and of advanced gestational age compared with VA ECMO patients. This probably was dictated by the ability

Discussion

Our study found that VV ECMO was as efficient as VA ECMO in supporting newborn infants with CDH with intractable respiratory failure who could accommodate the 14 F VV ECMO double-lumen catheter. Our report is based on a retrospective review of 26 VV ECMO and 19 VA ECMO patients in a single center that had made preference of the VV ECMO with a surgical team experienced in this technique. Patients placed on VV ECMO had a comparable severity of their respiratory as well as of their cardiovascular

Acknowledgements

The authors thank the neonatologists and the staff of the Neonatal ECMO Program at Huntington Memorial Hospital for their contributions and support with the study. Dr. Ernesto Gangitano works for Pediatrix Medical Group Inc.

References (26)

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