|
|
||||||||
J Thorac Cardiovasc Surg 2006;131:506
© 2006 The American Association for Thoracic Surgery
Letter to the Editor |
a Division of Cardiology, The Montreal Children's Hospital, Montreal, Quebec, Canada
b Director, Cardiovascular Intensive Care, Lucile Packard Children's Hospital, Stanford, Calif
c Associate Cardiologist-in-Chief, Children's Hospital Boston, Boston, Mass
We appreciate the interest of Haas and Camphausen in our recently published trial of triiodothyronine (T3) in neonatal heart surgery.
1
The points they raised are addressed below.
Our center, like many other centers performing infant heart surgery in the United States, routinely uses high-dose intravenous loop and thiazide diuretics rather than peritoneal dialysis to manage postoperative fluid overload. We agree that the results of our study cannot be generalized to patients who are treated with peritoneal dialysis.
The inotrope score used in our study, adapted from Wernovsky and associates,
2
was determined by the use of dopamine, dobutamine, milrinone, epinephrine, and norepinephrine. The cumulative dose of dopamine in particular did not differ between treatment groups during the first 5 days after the operation. Vasodilator use was also similar between treatment groups: milrinone was used routinely in our patients, with no difference in cumulative milrinone dose between treatment arms at 5 days. A single patient (randomized to the T3 group) received nitroprusside; no patients received phenoxybenzamine. Amiodarone was not used in any subject.
We planned our trial so that cardiac output was one of two primary outcome measures. The technique used (direct measurement of oxygen consumption by real-time gas exchange) provides an objective determination of cardiac output in children who are sedated, ventilated, and stable.
3
During the study period, infants were weaned from mechanical ventilation at increasingly shorter times after surgery, rendering this measurement infeasible at 48 hours after surgery in several subjects. However, the proportion of patients in each treatment group in whom this end point could not be measured (9/22 in the T3 group and 5/20 in the placebo group) was not statistically significant (P = .34).
| References |
|---|
|
|
|---|
Related Article
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |