Children with severe malnutrition who are admitted sick to hospitals have a high mortality(death rate), usually because of infection. All children with severe malnutrition admitted to hospitals are treated with antibiotics(medication used to kill bacteria). However, the current antibiotics used in hospitals may not be the most effective. It is possible that the antibiotics that are currently used after initial antibiotics should be used first. No studies have been carried out to determine if the current antibiotics used for treating malnourished children who are sick and admitted in hospital are the most appropriate. The aim of this study is to find out if a changed antibiotic system for children with malnutrition is safe, reduces the risk of death and improves nutritional recovery.
Children with complicated severe acute malnutrition (SAM) admitted to hospital in sub-Saharan Africa have a case fatality(death rate) between 12% and more than 20%. Because children with SAM may not exhibit the usual signs of infection, WHO guidelines recommend routine antibiotics(medication used to kill bacteria). However, this is based on "low quality evidence". There is evidence that because of bacterial resistance to the currently recommended first-line antibiotics (gentamicin plus ampicillin or penicillin) could be less effective than potential alternatives. Some hospitals in Africa are already increasing use of ceftriaxone as a first-line treatment. However, this is not based on any data that ceftriaxone actually improves outcomes. Of concern is that ceftriaxone use may also lead to increased antimicrobial resistance, including inducing extended spectrum beta-lactamase (ESBL) and other classes of resistance. A further area where evidence for policy is lacking is the use of metronidazole in severely malnourished children. The WHO guidelines recommend "Metronidazole 7.5 mg/kg every 8 h for 7 days may be given in addition to broad-spectrum antibiotics; however, the efficacy of this treatment has not been established in clinical trials." Metronidazole is effective against anaerobic bacteria, small bowel bacterial overgrowth, Clostridium difficile colitis and also Giardia, which is common amongst children with SAM. Small cohort studies of metronidazole usage suggest there may be benefits for nutritional recovery in malnourished children. However, metronidazole can cause nausea and anorexia, potentially impairing recovery from malnutrition and may also rarely cause liver and neurological toxicity. This multi-centre clinical trial will assess the efficacy of two interventions, ceftriaxone and metronidazole, on mortality and nutritional recovery in sick, severely malnourished children in a 2x2 factorial design. There will also be an analysis of antimicrobial resistance and an economic analysis. To extend our understanding of metronidazole and ceftriaxone pharmacokinetics, additional pharmacokinetic data for the dosing schedule used in the trial will be collected from 120 participants in a sub-study. The trial will be conducted at Kilifi County Hospital, Coast General Hospital, Mbagathi Hospital in Kenya and Mbale Regional Referral Hospital in Uganda. The trial will assess antimicrobial resistance that is carried by children in their intestines and in invasive bacterial isolates. A further sub-study will examine the relative costs of care for SAM for health facilities and for families, including antimicrobial usage will also be assessed. Clear data on the benefits, risks and costs of these antimicrobials will influence policy on case management and antimicrobial stewardship in this vulnerable population.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
2,000
Ceftriaxone a third-generation cephalosporin. Ceftriaxone is active against a broad spectrum of Gram positive and Gram negative bacteria.
The currently recommended first-line antibiotics for the treatment of severe acute malnutrition are gentamicin plus ampicillin or penicillin.
The WHO guidelines recommend that Metronidazole may be given in addition to broad-spectrum antibiotics, "however, the efficacy of this treatment has not been established in clinical trials."
Suspension manufactured to match metronidazole
The currently recommended first-line antibiotics for the treatment of severe acute malnutrition are gentamicin plus ampicillin or penicillin.
Kemri Wellcome Trust Research Programme
Kilifi, Coast Province, Kenya
Kilifi County Hospital
Kilifi, Coast, Kenya
KEMRI WT Clinical Trials Facility
Kilifi, Kenya
Kilifi County Hospital
Kilifi, Kenya
Coast General Hospital - Study site
Mombasa, Kenya
Mbagathi District Hospital
Nairobi, Kenya
Mbagathi Hospital
Nairobi, Kenya
Mbale Regional Referral Hospital
Mbale, Uganda
Mortality
Mortality is measured using source documents from medical records, verbal autopsy, or death or burial certificates in the community.
Time frame: 90 days after enrolment.
Mortality during the first 7 days
Mortality during the first 7 days
Time frame: 7 days
Mortality during the first 30 days
Mortality during the first 30 days
Time frame: 7 days
Index admission inpatient mortality
Mortality during the index hospitalisation, measured using inpatient records.
Time frame: Through index hospital admission, an average of 7 days.
Mortality after discharge from index admission.
Mortality occurring after discharge from the index hospital admission is measured using inpatient medical records, verbal autopsy, or death or burial certificates in the community.
Time frame: 90 days after enrolment
Grade 4 toxicity
Grade 4 toxicity events are measured according to the Division of AIDS Tables for Grading the Severity of Adverse Events using medical records.
Time frame: Up to 7 days following enrolment
Serious adverse events
Serious adverse events are measured using inpatient and outpatient medical records.
Time frame: 90 days after enrolment.
Tolerability - relevant side effects during the first 7 day
Vomiting, diarrhoea, NG tube in place and convulsions during the first 7 days
Time frame: 7 days
Causes of death.
Causes of death, as determined by an endpoint review committee.
Time frame: 90 days after enrolment
Re-admission to hospital.
Re-admission to hospital defined as at least one overnight stay in a hospital or health facility are measured using inpatient records.
Time frame: From discharge from hospital to 90 days after enrolment
Duration of hospitalisation.
Total duration of hospitalisation is measured in days using inpatient records at the start and end of each admission to hospital.
Time frame: 90 days after enrolment.
Duration of administration of antibiotics.
Duration of administration of intravenous antibiotics measured using inpatient records.
Time frame: 90 days after enrolment.
Change in nutritional status
Change in nutritional status is measured using mid-upper arm circumference, weight-for-length, weight-for-age and length-for-age compared to at enrollment.
Time frame: 90 days after enrolment.
Faecal carriage of bacteria expressing Extended Spectrum Lactamase (ESBL)
Faecal carriage of bacteria expressing Extended Spectrum Lactamase (ESBL) is measured using microbial culture and sensitivity testing of rectal swabs.
Time frame: Through study completion an average of 90 days.
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