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Transpyloric Feeding in Severe Bronchopulmonary Dysplasia

Children's Hospital of Philadelphia (CHOP) logo

Children's Hospital of Philadelphia (CHOP)

Status

Completed

Conditions

Bronchopulmonary Dysplasia

Treatments

Other: gastric feeding
Other: transpyloric feeding

Study type

Interventional

Funder types

Other

Identifiers

NCT02142621
14-010924

Details and patient eligibility

About

Bronchopulmonary dysplasia (BPD) is the most common complication of extreme preterm birth. It impacts 10,000-15,000 infants in the US annually, including approximately 50% of infants with birth weight < 1000g. BPD is associated with multiple long-term adverse outcomes including chronic cardiopulmonary and neurodevelopmental impairments. Infants with severe BPD, defined as a need for ≥ 30% inspired oxygen and/or mechanical respiratory support at 36 weeks postmenstrual age (PMA), suffer the greatest burden of these chronic sequelae. Recurrent episodes of hypoxemia and prolonged exposure to supplemental oxygen are linked to the development of these impairments. Gastroesophageal reflux (GER) contributes to these mechanisms by exacerbating pulmonary inflammation and inducing bronchospasm. Unfortunately, clinically available methods to diagnose GER in infants are unreliable. Moreover, acid suppressive agents are both ineffective and carry high risk of serious life-threatening morbidity. Simple transpyloric feeding has promise, but has not been evaluated in BPD.

This study will pilot N-of-1 trials to assess whether transpyloric feeds reduce airway complications of GER and and whether this methodology can aid in identifying individual infants with severe BPD who are likely to benefit from prolonged use of transpyloric feeds.

Aim 1. To determine for each enrolled infant with severe BPD whether transpyloric compared to gastric feeds reduce the number of daily intermittent hypoxemic events (primary outcome) and improve a validated BPD severity score (secondary outcome).

The investigators hypothesize that 80% percent of enrolled infants will have significantly fewer daily intermittent hypoxemic events with transpyloric compared to gastric feeds and will have this feeding method formally recommended.

Aim 2. To pool results from multiple N-of-1 trials to determine whether transpyloric compared to gastric feeds reduce airway complications of GER in infants with severe BPD.

The investigators hypothesize that transpyloric compared to gastric feeds will be associated overall with a 15% reduction in number of daily intermittent hypoxemic events.

Enrollment

15 patients

Sex

All

Ages

4 to 24 weeks old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Gestational age ≤ 32 weeks
  • Severe BPD (FiO2 ≥ 30% and/or mechanical ventilation or non-invasive positive pressure respiratory support at the time of enrollment)
  • Post menstrual age of 36-45 6/7 weeks at enrollment
  • Parent and/or guardian permission (informed consent)

Exclusion criteria

  • Prior intolerance to transpyloric feeds
  • History of surgical anti-reflux procedure
  • Congenital heart disease (not including patent ductus arterioles and hemodynamically insignificant ventricular septal defect or atrial septal defect)
  • Structural abnormalities of the upper airway, lungs, or chest wall
  • Other congenital malformations or syndromes that adversely affect life expectancy or cardio-pulmonary development
  • Parent, guardian, or subject who, in the opinion of the investigators, are unlikely to participate for the duration of the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

15 participants in 2 patient groups

transpyloric tube feeds
Active Comparator group
Description:
Continuous transpyloric tube feeds administered through an oral/nasal feeding tube.
Treatment:
Other: transpyloric feeding
gastric tube feeds
Active Comparator group
Description:
Continuous gastric tube feeds administered through an oral/nasal feeding tube.
Treatment:
Other: gastric feeding

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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