Despite encouraging declines in maternal mortality over the last two decades, women in resource-poor areas of the world still bear a disproportionate burden. Worldwide, around 10 million women develop preeclampsia each year and about 10-25% of cases in developing countries lead to death. Women in developing countries bear a disproportionate burden - they are seven times more likely to experience preeclampsia than a woman in developed countries.
Preeclampsia is a disorder defined clinically by hypertension and proteinuria, with or without pathologic edema, and can progress to eclampsia. Eclampsia is a serious condition that can cause seizures, kidney and liver damage, and death. There are currently no ways to accurately predict preeclampsia, but urinalysis and blood pressure readings can be used to diagnose the disorder. In place where resources are scarce, urine dipsticks are used instead of urinalysis, but results are not always reliable.
In response to these problems, Maternova partnered with HOPE Foundation Bangladesh to conduct a study looking at the feasibility of a novel urinalysis technology powered by an Android device and cuboid light box called the uChek device. Funded by Merck for Mothers, the study took place at a rural hospital in Ramu, Cox’s Bazar, Bangladesh, near the country’s border with Myanmar, and aimed to look at whether midwives could effectively use the device to conduct enhanced urinalysis. At the beginning of the study, half of the midwives found the device to be “daunting”, but at the end of the study, all of them agreed that the uChek provided faster and more reliable results. Furthermore, these results showed that these smartphone enabled medical devices could be incorporated with minimal additional training or resources - important considerations in places without a lot of resources.
Devices such as the uChek can prove to be invaluable in early diagnoses of preeclampsia, which in turn can mean many saved lives. Early diagnosis can allow for better planning and preparation; for example, if warning signs are detected at 20 weeks gestation, the device can be programmed to prompt the provider to prescribe the appropriate supplements, frequent antenatal checks, and to plan with an obstetrician for special preparations during and post-delivery. This study adds to the growing body of evidence showing that smartphone technology is becoming an increasingly important tool for medical diagnosis in remote areas.
Jean M. Bouquet, DO, is an Assistant Professor of Family Medicine and Co-Director of the Urban Underserved Track at the Rocky Vista University College of Osteopathic Medicine. He is the founder of the Bouquet Speculum, an innovative and FDA-cleared medical device that helps to screen women for cervical cancer. Dr. Bouquet also started the Cure Cervical Cancer nonprofit. The following blog post was written by Dr. Bouquet about his journey to creating the Bouquet Speculum.
Dr. Daniel Kimani is a trained and licensed medical officer in Kenya, holding a Bachelor of Medicine & Surgery, and a post-graduate certificate on basic oncology training. Dr. Kimani is the founder of the Global Cancer Care and Research Institute, and is an expert in clinical colposcopy — a procedure to examine the cervix, vagina, and vulva.