Proton Pump Inhibitors vs. Histamine-2 REceptor Blockers for Ulcer Prophylaxis Therapy in the Intensive Care Unit
A multi-centre, cluster randomised, crossover, registry trial comparing the safety and efficacy of proton pump inhibitors with histamine-2 receptor blockers for ulcer prophylaxis in intensive care patients requiring invasive mechanical intervention.
Medical Research Institute of New Zealand
26,797 participants
Aug 1, 2016
Interventional
Conditions
Summary
Patients who require treatment in the Intensive Care Unit (ICU) can develop stomach ulcers or duodenal (small intestine) ulcers. This occurs most commonly when life support (a breathing machine) is required or when the patient develops a bleeding tendency as a result of their illness. These kinds of ulcers are known as ‘stress ulcers’ and may cause life-threatening bleeding. Patients who require life support in the ICU are typically given one of two types of medicine to try and prevent the development of stress ulcers. The two types of medicines are called ‘proton pump inhibitors’ (PPIs) and ‘histamine-2 receptor blockers’ (H2RBs). While the prevention of stress ulcers is very important, the medicines used to prevent ulcers may have important side effects including an increased risk of developing certain kinds of infections. The risk of side effects may depend on the medication used. This study will establish which of the two types of medicines that are commonly used for stress ulcer prophylaxis in ICU patients who require life support leads to the lowest risk of upper gastrointestinal bleeding, prolonged mechanical ventilation, and Clostridium difficile infection. The study will use a design known as a ‘cluster crossover registry design’. In this type of study, data are collected primarily from existing data sources rather than the medical records of individual patients. There will be two study treatment periods. During the first treatment period, half of the participating ICUs will be randomly (like the toss of a coin) instructed to use PPIs for stress ulcer prophylaxis in patients who require life-support while the other half will use H2RBs. During the second treatment period each ICU will swap to using the opposite treatment. This means that, in situations where PPIs and H2RBs are regarded as being equivalent by the treating clinician, the treatment administered to the patients will be determined based on the treatment assigned to the patient’s ICU. However, if there is a specific indication for either PPI treatment or H2RB treatment (for example, an allergy), the treatment indicated for the particular patient concerned will be administered irrespective of the treatment assigned to the ICU.
Eligibility
Inclusion Criteria1
- All patients aged 18 years or older who are mechanically ventilated within 24 hours of ICU admission.
Exclusion Criteria1
- Patients who are admitted to ICU with upper GI bleeding (APACHE III admission diagnostic codes 303, 305, and 1403)
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Interventions
Study treatment is open label Proton Pump Inhibitors (PPIs) vs. Histamine-2 Receptor Blockers (H2RBs) as the default routine therapy for ulcer prophylaxis. Each study ICU will use PPIs or H2RBs as routine therapy for a period of six months. At the end of this six month period, the ICU will then swap to the opposite routine ulcer prophylaxis strategy which will then be used for the next six months. The specific PPI or H2RB, dose, mode of administration and duration of study treatment will be the individual ICU clinician’s decision or until the patient is discharged from ICU (whichever is shorter). The PPI and H2RBs will be given as per routine medication (usually by the ICU nurse). Study treatment will only be administered in situations where the treating clinician believes ulcer prophylaxis is in the patient’s best interests and, irrespective of the treatment assigned to the ICU, either a PPI or an H2RB can be used for an individual patient, if the treating clinician believes that a particular treatment is indicated. Intervention adherence will not be checked for individual patients; however once a month, at a set time, stress ulcer prophylaxis use will be recorded for all mechanically ventilated patients.
Locations(4)
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ACTRN12616000481471