Stress Ulcer Prophylaxis Versus Placebo in Critically Ill Infants With Congenital Heart Disease

NCT ID: NCT03667703

Last Updated: 2022-09-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-03-10
• Study Completion Date: 2022-06-30

Brief Summary

Infants with congenital heart disease often require an intervention during their first year of life. Infants are generally admitted to a cardiac intensive care unit and are routinely prescribed stress ulcer prophylaxis to decrease acid release from the stomach to prevent stress ulcer formation. However, these medicines may not be safe and could put infants at increased risk for hospital-acquired infections, necrotizing enterocolitis and alteration to the infant's microbiome. The investigators plan to assess the feasibility of conducting a prospective, blinded randomized control trial to determine the safety of withholding stress ulcer prophylaxis in critically ill infants with congenital heart disease. In addition, the investigators plan to examine the changes to the infant's microbiome through oral, gastric and stool samples and compare hospital-acquired infections.

Detailed Description

Background & Significance. Approximately 36,000 infants are born with congenital heart disease (CHD) in the United States each year, often requiring surgical intervention in the first year of life. They are vulnerable to postoperative morbidities including infection, growth failure and neurodevelopmental delay. Upon admission to the cardiac intensive care unit (CICU), infants are routinely prescribed stress ulcer prophylaxis (SUP) to decrease acid release from the stomach thus preventing ulcer-induced upper gastrointestinal (UGI) bleeding. Although adopted from the adult literature, this practice is expensive and has not been shown to be effective in infants. More importantly, recent literature suggests that this may not be safe. Studies show an increased risk of hospital-acquired infections, necrotizing enterocolitis and alterations in the evolving healthy gut flora in infants. The study investigators have recently demonstrated an increased risk of infection in children receiving SUP and also reported differences in microbial diversity among children in the CICU. It is necessary to proceed with a prospective trial to determine the safety of withholding SUP in critically ill children with CHD.

Specific Aims & Hypothesis. The overarching hypothesis of the proposal is withholding SUP from critically ill infants with CHD is safe and results in favorable microbial diversity, thus decreasing hospital-acquired infections. Primary Aim 1 of the study is to assess the feasibility of this pilot randomized, controlled clinical trial of SUP versus placebo in infants admitted to the CICU. The study investigators hypothesize that a priori feasibility measures will be achieved during the study period. Primary Aim 2 of the study is to examine the differences of UGI bleeding in critically ill infants with CHD receiving SUP versus those receiving placebo. The study investigators hypothesize that the rate of UGI bleeding will be no different between infants exposed to SUP and to placebo. Secondary Aim 1 of the study is to compare the differences in the abundance of microbial taxa and functional profiles of the aerodigestive tract microbiome between infants receiving SUP and those receiving placebo and before/after the start of SUP. The study investigators hypothesize that there will be significant differences in the abundance of microbial taxa and the functional profiles between the 2 groups - with a more favorable microbial profile present in infants in the placebo group. Secondary Aim 2 is to examine the difference in the incidence of hospital-acquired infections in critically ill infants with CHD receiving SUP versus placebo. The study investigators hypothesize the rate of hospital-acquired infections will be higher in patients exposed to SUP when compared to placebo.

Study Design & Methods. A single-center, prospective, double-blinded, randomized, controlled trial will be conducted as a feasibility study for a larger multicenter trial. Consecutive infants < 12 months of age with CHD admitted to the CICU and anticipated to require respiratory support for > 24 hours will be enrolled and randomized to receive a histamine-2 receptor antagonist (H2RA) medication or study placebo. Patients will remain in the study until discontinuation of respiratory support, discharge from the CICU or study day 14. Oral, gastric and stool samples will be obtained prior to receiving the first dose of study drug and subsequently at the end of the study. The samples will be analyzed for 16S RNA and metagenomic shotgun sequencing for microbiome composition. Gastric pH will be recorded on all gastric samples. Demographics, nutrition variables, medications, and respiratory data will be collected for all patients while enrolled in the study. An independent Drug Safety and Monitoring Board (DSMB) will monitor patient safety every 6 months and after any significant adverse event.

Outcomes. The primary outcomes will be study feasibility and incidence of clinically significant UGI bleeding. Feasibility will be defined as: 1) > 80% screening of eligible patients, 2) > 20% consent rate, 3) > 80% receive timely first dose of study drug, and 4) > 80% protocol adherence. Clinically significant UGI bleeding will be defined as new-onset bleeding with subsequent pre-defined physiologic or hemodynamic changes. The secondary outcomes of the study will be observed differences in the aerodigestive microbial diversity between study groups, mortality, length of stay, duration of respiratory support, bleeding events, incidence of necrotizing enterocolitis and incidence of hospital-acquired infections (ventilator-associated pneumonia, central line-associated bloodstream infections, catheter-associated urinary tract infections, superficial sternal infection or mediastinitis).

Conditions

Congenital Heart Disease; Upper Gastrointestinal Bleeding; Stress Ulcer; Infection

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: QUADRUPLE

Study Groups

Placebo

Subjects randomized to placebo will receive an equivalent volume (mL) of normal saline intravenously or Ora-plus orally based on weight and age.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Patients will be randomized to either receive a placebo or famotidine (study drug).

Study Drug

Subjects randomized to study drug will receive famotidine, a histamine-2 receptor antagonist. Dosing will be weight based and age-dependent. Infants \< 90 days old will receive either 0.5mg/kg intravenously daily or 0.5mg/kg orally twice a day of famotidine. Infants ≥ 90 days or older will receive 0.25mg/kg intravenously every 12 hours or 0.5mg/kg orally twice a day.

Group Type: ACTIVE_COMPARATOR

Famotidine

Intervention Type: DRUG

Patients will be randomized to either receive a placebo or famotidine (study drug).

Interventions

Famotidine

Patients will be randomized to either receive a placebo or famotidine (study drug).

Intervention Type: DRUG

Placebo

Patients will be randomized to either receive a placebo or famotidine (study drug).

Intervention Type: DRUG

Other Intervention Names

Pepcid; Normal saline or stevoside-free syrup

Eligibility Criteria

Inclusion Criteria

1. < 12 months of age (including premature newborns),

2. diagnosed with congenital heart disease (including anatomic, myopathic and arrhythmic conditions),

3. received ≤ 1 dose of SUP (including histamine-2 receptor antagonists, proton pump inhibitors, and sucralfate) during current admission, AND

4. anticipated to require respiratory support for > 24 hours during their CICU stay. Respiratory support includes mechanical ventilation, non-invasive positive-pressure ventilation and high-flow oxygen therapy.

Exclusion Criteria

1. prior use of antacids (including histamine-2 receptor antagonists, proton pump inhibitors, or sucralfate) in the past month for > 7 days,

2. active gastrointestinal bleeding,

3. active Helicobacter pylori infection,

4. administration of high-dose steroids (equivalent dosing to 15 mg/kg/day of methylprednisolone),

5. will receive ketorolac (intravenous nonsteroidal anti-inflammatory drug) during admission,

6. exposed to specific anticoagulants (high-dose aspirin, direct thrombin inhibitors and GPIIbIIIa inhibitors),

7. planned to undergo or recently has undergone gastrointestinal surgery (i.e. repair of duodenal atresia)

8. supported by extracorporeal membrane oxygenator (ECMO) or ventricular assist device (VAD),

9. currently enrolled in another intervention trial,

10. known to be allergic to H2RAs,

11. admitted for palliative care,

12. prior enrollment in the study, OR

13. primary provider declines enrollment.

• Minimum Eligible Age: 1 Minute
• Maximum Eligible Age: 12 Months
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

The Gerber Foundation

OTHER

Sponsor Role: collaborator

Boston Children's Hospital

OTHER

Sponsor Role: lead

Responsible Party

Kimberly I. Mills, MD

Assistant in Cardiology, Instructor in Pediatrics

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Kimberly I Mills, MD

Role: PRINCIPAL_INVESTIGATOR

Boston Children's Hospital

Ben D Albert, MD

Role: PRINCIPAL_INVESTIGATOR

Boston Children's Hospital

Nilesh M Mehta, MD

Role: PRINCIPAL_INVESTIGATOR

Boston Children's Hospital

Locations

Boston Children's Hospital

Boston, Massachusetts, United States

Countries

United States

References

Mills KI, Albert BD, Bechard LJ, Chu S, Duggan CP, Kaza A, Rakoff-Nahoum S, Sleeper LA, Newburger JW, Priebe GP, Mehta NM. Stress Ulcer Prophylaxis Versus Placebo-A Blinded Pilot Randomized Controlled Trial to Evaluate the Safety of Two Strategies in Critically Ill Infants With Congenital Heart Disease. Pediatr Crit Care Med. 2024 Feb 1;25(2):118-127. doi: 10.1097/PCC.0000000000003384. Epub 2024 Jan 19.

Reference Type: DERIVED

PMID: 38240536 (View on PubMed)

Mills KI, Albert BD, Bechard LJ, Duggan CP, Kaza A, Rakoff-Nahoum S, Vlamakis H, Sleeper LA, Newburger JW, Priebe GP, Mehta NM. Stress ulcer prophylaxis versus placebo-a blinded randomized control trial to evaluate the safety of two strategies in critically ill infants with congenital heart disease (SUPPRESS-CHD). Trials. 2020 Jun 29;21(1):590. doi: 10.1186/s13063-020-04513-w.

Reference Type: DERIVED

PMID: 32600393 (View on PubMed)

Other Identifiers

IRB-P00028715

Identifier Type: -

Identifier Source: org_study_id