This study group has developed a new method for diagnosing methanol poisoning using a single drop of blood with a point-of-care (POC) device, eliminating the need for laboratory equipment. The device measures formate, present only in cases of methanol poisoning.
The research comprises two studies. The initial observational study (Study 1a) will assess the sensitivity and specificity of the POC formate assay compared to the laboratory formate assay (the gold standard). If the sensitivity is greater than 0.80, a feasibility three-arm cluster randomized controlled trial (RCT) (Study 1b) will follow to determine the feasibility of recruiting hospitals to a cluster RCT of formate diagnostic approaches.
This design will be used in the second study to test the clinical- and cost-effectiveness of incorporating the formate POC assay into routine clinical use.
Primary Objectives:
Study 1a: Determine the sensitivity and specificity of the POC formate assay compared to the laboratory formate assay.
Study 1b: Assess the feasibility of recruiting hospitals for a cluster RCT of formate diagnostic approaches.
Secondary Objectives:
Study 1a: Evaluate the use of the POC formate assay to identify methanol poisoning across diverse healthcare systems.
Study 1b: Compare clinical and resource use when introducing the POC formate assay into routine clinical practice.
Primary Endpoints:
Study 1a: Sensitivity and specificity of the POC formate test for diagnosing methanol poisoning.
Study 1b: Number of hospitals successfully recruited to the study.
Secondary Endpoints for Study 1a:
Time from patient arrival at the emergency department to sample collection.
Time from sample collection to result display by the POC assay and the laboratory assay.
Delay between result displays by the POC and the laboratory assay.
Time from sample collection until the clinician is informed of the results.
Time to initiation of antidote treatment and stopping unnecessary therapy in patients without methanol poisoning.
Secondary Endpoints for Study 1b:
Time to stopping unnecessary therapy in patients without methanol poisoning.
Proportion of patients with management changes based on the laboratory formate assay.
Clinical outcomes such as deaths, intubations, and dialysis needs.
Cost comparison between the POC formate assay, the laboratory assay, and no assay.
The study will include patients suspected of methanol poisoning or unexplained metabolic acidosis at large referral hospitals in Bangladesh and India. The study aims to determine whether the POC formate test can speed up the initiation of appropriate treatment, reduce unnecessary treatment costs, and improve clinical outcomes.
Study Population:
Patients presenting with suspected methanol poisoning or unexplained metabolic acidosis.
Number of Participants:
Study 1a: 1,620 participants.
Study 1b: 4,500 participants.
Inclusion Criteria:
Patients with suspected methanol poisoning or metabolic acidosis of unknown cause, including children aged 16-17 (with assent), adults (with consent), and those with relatives who can provide consent.
Exclusion Criteria:
Individuals unwilling to provide assent or consent.
Unaccompanied unconscious patients or those without a relative to provide consent.
Previously recruited individuals.
These studies aim to raise awareness of the methanol poisoning crisis, improve early detection and treatment, and establish high-quality protocols for patient care. They also aim to encourage junior doctors to pursue academic careers and practice good clinical habits. Raising awareness will help warn the public about dangerous alcohol and prevent further poisonings.
