Every year, over 150,000 people die from drinking pesticides in suicide attempts, mostly in poor rural Asian communities, and two-thirds of those deaths involve organophosphorus or carbamate insecticides. Current treatment for this poisoning has not changed in 50 years and often fails. These pesticides block an enzyme that normally breaks down acetylcholine, causing it to build up in nerves and stop breathing. No new medicine has been introduced despite millions of deaths. Carefully reducing calcium flow into nerve cells with cheap, widely available drugs—calcium channel blockers or magnesium—might counteract the pesticides' effects, but existing studies are too small and results are mixed. This trial will recruit around 3,100 patients across four Bangladeshi hospitals. One-third will receive routine care, one-third will get additional calcium channel blockers, and one-third will get additional magnesium. The researchers will compare death rates (currently about 11% with standard treatment) and the need for mechanical ventilation. If either treatment works, it would be the first new therapy for these poisonings in half a century, potentially saving tens of thousands of lives annually. The trial will also build research infrastructure in Bangladesh and train local clinical researchers.
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Attempted suicide by drinking pesticides used in farming (called 'pesticide self-poisoning') is the second most important global means of suicide, killing over 150,000 people each year, mostly in poor rural Asian communities. The pesticide used is often stored in the home and easily available at moments of stress or anger. Importantly, survival after self-poisoning allows families, community, and medical/social services to support the person, to help them find reasons not do it again. Pesticides called organophosphorus (OP) and carbamate insecticides are responsible for about two thirds of these deaths across the world. They both inhibit an enzyme called acetylcholinesterase, which usually breaks down the chemical acetylcholine found in the brain and nerves. Because its breakdown is now stopped, acetylcholine accumulates and causes problems with breathing which may be severe enough to kill, even with best available treatment. Unfortunately, no new medicine has been introduced into medical practice for 50 years, despite thousands of studies and millions of deaths. Current treatment does not always work; new treatments are urgently required. Flow of calcium salt into the nerve cells is essential for allowing nerves to work and communicate with other cells in the body. Carefully reducing this flow of calcium with medicines that partially block channels in the nerve cell - calcium channel blocking medicines [CCB] or the magnesium salt - may reduce the pesticides' effects and prevent deaths. Eight studies of magnesium have already been done in poisoned patients; some have suggested benefit from this treatment but overall the studies have been too small and the results mixed. There is no clear information on whether these medicines work. We propose to set up a big study (or randomised controlled trial, RCT) of patients with OP or carbamate poisoning admitted to 4 large Bangladeshi hospitals where this poisoning is a major problem, killing thousands of people each year. We will recruit around 3,100 patients to the study over 3 1/2 years. One third of the patients selected at random will receive routine treatment, while 1/3 will get additional CCB medicines and 1/3 will get the additional magnesium. The extra treatments will be given for 2 days. We will check how many patients die (currently about 11% die with normal treatment) and how many need to go to the intensive care ward for help with their breathing (called mechanical ventilation where a machine breathes for them) across the three groups. We will look to see whether these additional treatments reduce the number of patients dying or needing mechanical ventilation. Our group has a great deal of experience treating and studying poisoned patients, having done similar studies of pesticide poisoning in Sri Lanka and Bangladesh and led recent global improvements in treatment. The study will provide proof about whether these relatively cheap, widely available treatments help the poisoned patients. It potentially will result in the first new treatment for these forms of poisoning for 50 years being introduced in routine hospital practice across the world. The results will be shared with the World Health Organisation and our colleagues in poison centres and hospitals across Asia. Better treatment offers the opportunity to save tens of thousands of lives amongst some of the poorest communities in rural Asia and reduce the heartbreak of suicide amongst children, families, and communities. There will be other benefits from the study. It will set up high-quality infrastructure in Bangladesh that other doctors and researchers will be able to use to set up studies for patients with other diseases and problems. The study will offer useful experience to clinical researchers that they will be able to use for their own research. We will also work with academic laboratories to do studies that will help us better understand the effects of these poisons on human bodies.
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