Dear Editor,
Low cardiac output syndrome (LCOS) affects approximately 25% of children undergoing open heart surgery (OHS) and is associated with increased morbidity and mortality [1]. Evidence for preventive drug therapy for LCOS is derived primarily from the PRIMACORP study [1], which reported a reduction in LCOS risk after administration of high-dose milrinone, using a bolus of 75 μg/kg, followed by a maintenance infusion of 0.75 μg kg−1 min−1 over 35 h. Low-dose milrinone (25 μg/kg bolus and 0.25 μg kg−1 min−1 infusion) was not more effective than placebo. Other drugs may be also used but are not supported by safety and efficacy data [2, 3]. Data on drug use for LCOS prevention in children with OHS is not available for Europe. Therefore, the aim of this study was to characterise hospital practices related to preventive drug therapy for LCOS in children undergoing OHS as a basis for improving the standard of care in this setting.
A Web-based questionnaire was developed to survey 125 specialised hospitals from 36 European countries between January and August 2009. It included 15 questions allocated to 4 sections: prescribing resources and LCOS treatment (data not shown), LCOS prevention, and participant characteristics and comments. The questions on LCOS prevention enquired about the target patient group (all, at risk, none) and mode of drug administration, which was not further stratified. The hospitals were notified by email; of those, 90 hospitals from 31 countries responded (72.0% response rate). Respondents included clinicians (98.9%) and pharmacists (1.1%), specialising primarily in paediatric intensive care, anaesthesiology, cardiology, and cardiothoracic surgery. Nearly all respondents (94.4%) had at least 5 years of experience in caring for children undergoing OHS.
Most European hospitals (70 out of 90) reported preventive drug therapy for LCOS, from which the majority (57 hospitals) selectively targeted patients at risk. However, the drug use was highly variable. In total, 24 different drug regimens were reported, including 17 drugs from 7 therapeutic drug classes. Overall, 70.7% of the drug regimen reports included milrinone, making this the most commonly used drug. Dopamine, dobutamine, epinephrine, and levosimendan were reported significantly less often (Table 1). The dosage and duration of drug administration differed substantially among hospitals.
Table 1.
Summary characteristics of the drugs commonly reported for LCOS prevention
| Druga | Frequency of drug use | Drug administration | ||||
|---|---|---|---|---|---|---|
| N | % | 95% CI | Bolusb (μg/kg) | Maintenance infusionb (μg kg–1 min–1) | Durationb (h) | |
| Milrinone | 53 | 70.7 | 59.6–79.8 | 50 (20–300) | 0.5 (0.2–1.5) | 39 (6–168) |
| Dopamine | 14 | 18.7 | 11.5–28.9 | –c | 5 (0–15) | 36 (8–72) |
| Dobutamine | 12 | 16 | 9.4–25.9 | 7d (6–8) | 5 (2–14) | 36 (6–48) |
| Epinephrine | 12 | 16 | 9.4–25.9 | 1 (1–1) | 0.065 (0.003–0.3) | 9 (6–12) |
| Levosimendan | 12 | 16 | 9.4–25.9 | 12 (12–12) | 0.15 (0.1–0.2) | 24 (24–48) |
| Methylprednisolone | 4 | 5.3 | 2.1–12.9 | 25e (10–35) | – | – |
The analysis was based on 75 drug regimens reported from 69 hospitals. Two hospitals provided three different drug regimens and another two hospitals provided two drug regimens based on the clinical condition of the patient and the type of open heart surgery. One hospital did not fill in the information on drug dosing
aOnly 6 out of 17 drugs were reported more than twice and are listed in the table. The following drugs were reported once or twice: alprostadil, bosentan, calcium, enoximone, glyceryl trinitrate, inhaled nitric oxide, norepinephrine, phenoxybenzamine, phenylephrine, nitroprusside, and thiopental
bData are median with range in parenthesis
cNot reported
dBolus dose in μg kg−1 min−1
eBolus dose in mg/kg
The results of this survey present the current pattern of drug use for LCOS prevention in children with OHS across Europe, which is characterised by a marked variability. In addition, the dose of milrinone appears to be lower than that supported by PRIMACORP. Although our survey shows that milrinone is the most frequently used drug in Europe, neither the dosing nor the duration of drug administration coincide with those demonstrating efficacy in PRIMACORP (Table 1). Reasons for the reduced dose of milrinone may be attributable to concerns about potential side effects, especially hypotension [4], and the role of age-specific pharmacokinetic differences in the elimination of milrinone [5]. Nonetheless, these factors cannot explain the generally lower dose of milrinone used across all paediatric age groups, which needs to be addressed in future clinical research.
In summary, preventive drug therapy for LCOS in children undergoing OHS is highly variable across Europe, and the data available to support current hospital practices are insufficient. Given the importance of balancing benefits and risks with preventive drug therapy, this survey emphasises the need for further studies that will substantiate effective and safe LCOS prevention.
Acknowledgments
The results presented in this Letter to the Editor are part of the PhD work of Ms Vogt, carried out at Heinrich Heine University of Düsseldorf. The authors would like to thank all of the members of the expert panel in the field of paediatric cardiology, anaesthesiology, intensive care, cardiac surgery, general medicine, and psychology for their support during the questionnaire development, the survey participants for taking the time to complete the questionnaire, and the European Congenital Heart Disease Organisation members for establishing contact with various hospitals. We would also like to thank Dr. Lechner for review and comments on the manuscript.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
References
- 1.Hoffman TM, Wernovsky G, Atz AM, Kulik TJ, Nelson DP, Chang AC, Bailey JM, Akbary A, Kocsis JF, Kaczmarek R, Spray TL, Wessel DL. Efficacy and safety of milrinone in preventing low cardiac output syndrome in infants and children after corrective surgery for congenital heart disease. Circulation. 2003;107:996–1002. doi: 10.1161/01.CIR.0000051365.81920.28. [DOI] [PubMed] [Google Scholar]
- 2.Baldasso E, Garcia PCR, Piva JP, Branco RG, Tasker RC. Pilot safety study of low-dose vasopressin in non-septic critically ill children. Intensive Care Med. 2009;35:355–359. doi: 10.1007/s00134-008-1392-1. [DOI] [PubMed] [Google Scholar]
- 3.Pasquali SK, Hall M, Li JS, Peterson ED, Jaggers J, Lodge AJ, Marino BS, Goodman DM, Shah SS. Corticosteroids and outcome in children undergoing congenital heart surgery: analysis of the Pediatric Health Information Systems database. Circulation. 2010;122:2123–2130. doi: 10.1161/CIRCULATIONAHA.110.948737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Brierley J, Peters M. Hemodynamics of milrinone loading in critically ill children. Crit Care Med. 2006;34:A63. doi: 10.1097/00003246-200612002-00220. [DOI] [Google Scholar]
- 5.Bailey JM, Hoffman TM, Wessel DL, Nelson DP, Atz AM, Chang AC, Kulik TJ, Spray TL, Akbary A, Miller RP, Wernovsky G. A population pharmacokinetic analysis of milrinone in pediatric patients after cardiac surgery. J Pharmacokinet Pharmacodyn. 2004;31:43–59. doi: 10.1023/B:JOPA.0000029488.45177.48. [DOI] [PubMed] [Google Scholar]
