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Prolonged furosemide exposure and risk of abnormal newborn hearing screen in premature infants
Laura A Wang1, P Brian Smith2, Matthew Laughon3
1Duke University, Durham, NC, USA.
Insights
Prolonged exposure to furosemide in premature infants did not significantly increase the risk of abnormal hearing screening before hospital discharge. Further audiology follow-up is recommended to assess furosemide
Area of Science:
- Neonatal research
- Pediatric audiology
- Clinical pharmacology
Background:
- Furosemide is known to cause ototoxicity in adults at high doses.
- The risk of hearing loss from furosemide in premature infants is not well understood.
Purpose of the Study:
- To evaluate the association between prolonged furosemide exposure and abnormal hearing screening in premature infants.
Main Methods:
- Propensity score matching was used to compare infants with prolonged (≥28 days) furosemide exposure to those never exposed.
- The study included premature infants (501-1250g birth weight, 23-29 weeks gestational age) from US neonatal intensive care units (2004-2013).
- Abnormal hearing screen was defined as 'fail' or 'refer' for either ear prior to hospital discharge.
Main Results:
- 1020 furosemide-exposed infants were matched with 790 never-exposed infants.
- The proportion of infants with abnormal hearing screens was not significantly higher in the furosemide-exposed group (absolute difference 3.0%, P=0.07).
- Baseline characteristics were similar between matched groups after adjustment for covariates.
Conclusions:
- Prolonged furosemide exposure showed a non-significant trend towards increased abnormal hearing screening in premature infants.
- Further studies including post-discharge audiology follow-up are necessary to fully assess furosemide's safety in this population.
Background:
At very high doses, furosemide is linked to ototoxicity in adults, but little is known about the risk of hearing loss in premature infants exposed to furosemide.
Aims:
Evaluate the association between prolonged furosemide exposure and abnormal hearing screening in premature infants.
Study Design:
Using propensity scoring, infants with prolonged (≥28 days) exposure to furosemide were matched to infants never exposed. The matched sample was used to estimate the impact of prolonged furosemide exposure on the probability of an abnormal hearing screen prior to hospital discharge.
Subjects:
A cohort of infants 501-1250 g birth weight and 23-29 weeks gestational age discharged home from 210 neonatal intensive care units in the United States (2004-2013).
Outcome Measures:
We defined abnormal hearing screen as a result of either "fail" or "refer" for either ear.
Results:
Altogether, 1020 infants exposed to furosemide for ≥28 days were matched to 790 unique infants never exposed, yielding a total of 1042 matches due to sampling with replacement and propensity score ties. Matching resulted in a population similar in baseline characteristics. After adjusting for covariates, the proportion of infants with an abnormal hearing screen in the furosemide-exposed group was not significantly higher than the never-exposed group (absolute difference 3.0% [95% CI -0.2-6.2%], P = 0.07).
Conclusions:
Prolonged furosemide exposure was associated with a positive, but not statistically significant, difference in abnormal hearing screening in premature infants. Additional studies with post-hospital discharge audiology follow-up are needed to further evaluate the safety of furosemide in this population.
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