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Published on: June 12, 2021
Impact of pharmacotherapy on interstage outcomes in single ventricle infants
Brady S Moffett1, Raphael Mattamal, Elena C Ocampo
1Department of Pharmacy, Texas Children's Hospital, Houston, TX 77030, USA. bsmoffet@texaschildrens.org
Insights
Infants with single ventricle heart disease face a high medication burden between surgeries. Current drug regimens, including digoxin and high-dose furosemide, do not appear to improve interstage weight gain in these vulnerable patients.
Area of Science:
- Pediatric Cardiology
- Pharmacology
- Congenital Heart Disease
Background:
- Single ventricle heart disease (SVHD) requires staged surgical palliation.
- The interstage period between surgical palliation stages is critical for infant growth.
- Optimizing pharmacotherapeutic regimens is essential for improving outcomes in SVHD infants.
Purpose of the Study:
- To characterize medication use in infants with SVHD during the interstage period.
- To determine the impact of outpatient medications on interstage weight gain.
- To identify factors influencing somatic growth in SVHD infants.
Main Methods:
- Retrospective review of 161 SVHD patients undergoing neonatal surgical palliation (2002-2009).
- Analysis of outpatient medication regimens during the interstage period.
- Logistic and linear regression models to assess medication effects on weight-for-age z-score (WAZ) and daily weight gain.
Main Results:
- Patients received a median of four medications, commonly aspirin, furosemide, and ACE inhibitors.
- Most patients (71%) experienced a decrease in WAZ during the interstage period.
- Digoxin and high-dose furosemide were associated with decreased WAZ; ACE-I and other GI medications showed no benefit.
Conclusions:
- Infants with SVHD have a significant medication burden during the interstage period.
- Current pharmacotherapeutic strategies show limited efficacy in improving interstage weight gain.
- Further research is needed to optimize medical management for SVHD infants.
Objective:
To characterize the pharmacotherapeutic regimens used in infants with single ventricle heart disease and determine the influence of outpatient medications on interstage weight gain.
Design:
Retrospective review.
Setting:
Tertiary care pediatric hospital.
Patients:
All patients discharged from our institution with single ventricle heart disease that underwent neonatal first stage surgical palliation between 2002 and 2009 were included. Patients who died prior to second stage palliation or underwent orthotopic heart transplantation were excluded.
Outcome Measures:
Outpatient medication regimens during the interstage period were reviewed. Medication regimens were compared between surgical eras and between patient groups experiencing different outcomes. A logistic regression model was developed to determine independent factors for an interstage increase in weight-for-age z-score (WAZ) and a linear regression model to determine medications significant for an increase in weight gain per day.
Results:
The study cohort consisted of 161 patients (58% male). Most patients in this cohort had either hypoplastic left heart syndrome (51%) or unbalanced complete atrioventricular canal (29%). Patients were placed on a median of four medications (range 1-9) at discharge from first surgical palliation, with aspirin (79%), furosemide (79%), and angiotensin converting enzyme inhibitors (ACE-I) (73%) most commonly prescribed. A median of six medication doses per day (range 2-18) were prescribed at discharge. Most patients (71%) had a decrease in WAZ during the interstage period. Use of digoxin (P < 0.01) and high-dose furosemide (P = .02) were associated with a decrease in WAZ score during the interstage period. Additionally, the use of ACE-I, ranitidine, proton-pump inhibitors, or promotility agents was not associated with improved somatic growth during the interstage period.
Conclusions:
Infants with single ventricle heart disease have a high-medication burden during the interstage period. Despite the focused and intensified use of medications to improve feeding tolerance and somatic growth, current pharmacotherapeutic regimens appear to have little effect on interstage weight gain.
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