Objective:To assess the cost-effectiveness of a non-pneumatic anti-shock garment (NASG) for obstetric hemorrhage in tertiary hospitals in Egypt and Nigeria.Methods:We combined published data from pre-intervention/NASG-intervention clinical trials with costs from study sites. For each country, we used observed proportions of initial shock level (mild: mean arterial pressure [MAP] >60 mmHg; severe: MAP ≤60 mmHg) to define a standard population of 1,000 women presenting in shock. We examined three intervention scenarios: no women in shock receive the NASG, only women in severe shock receive the NASG, and all women in shock receive the NASG. Clinical data included frequencies of adverse health outcomes (mortality, severe morbidity, severe anemia), and interventions to manage bleeding (uterotonics, blood transfusions, hysterectomies). Costs (in 2010 international dollars) included the NASG, training, and clinical interventions. We compared costs and disability-adjusted life years (DALYs) across the intervention scenarios.Results:For 1000 women presenting in shock, providing the NASG to those in severe shock results in decreased mortality and morbidity, which averts 357 DALYs in Egypt and 2,063 DALYs in Nigeria. Differences in use of interventions result in net savings of $9,489 in Egypt (primarily due to reduced transfusions) and net costs of $6,460 in Nigeria, with a cost per DALY averted of $3.13. Results of providing the NASG for women in mild shock has smaller and uncertain effects due to few clinical events in this data set.Conclusion:Using the NASG for women in severe shock resulted in markedly improved health outcomes (2-2.9 DALYs averted per woman, primarily due to reduced mortality), with net savings or extremely low cost per DALY averted. This suggests that in resource-limited settings, the NASG is a very cost-effective intervention for women in severe hypovolemic shock. The effects of the NASG for mild shock are less certain. © 2013 Sutherland et al.
We assessed the cost-effectiveness of adding the NASG to standard hypovolemic shock management. We used clinical data from two published intervention trials, in Egypt and Nigeria, on the effects of the NASG added to standard care on maternal morbidity and mortality at tertiary facilities.[8] The analysis focused on a standardized group of 1,000 women presenting in shock, with the proportions of severe (mean arterial pressure [MAP] 60 mmHg) shock specified by country to reflect patient characteristics in the clinical trials. We then examined three intervention scenarios: (a) no use of the NASG (i.e., standard care, as the reference case) for any woman in shock; (b) women in severe shock receive the NASG and women in mild shock receive standard care; and (c) all women in shock receive the NASG, regardless of initial shock status. Each scenario was compared incrementally to the reference group (No NASG for any woman in shock). Clinical outcomes (mortality and morbidities) were translated into disability adjusted life years (DALYs), and compared incrementally across scenarios. Costs for the NASG (materials, training, personnel) were collected from project records, and treatments for maternal hemorrhage (e.g., emergency hysterectomy, blood transfusion, and uterotonics) were obtained from local investigators and published sources. All costs were converted into 2010 international dollars. Net cost (or savings) for the NASG was calculated considering the sum of costs for NASG and for clinical management of maternal hemorrhage. Cost-effectiveness was calculated as the cost per DALY averted, which represents the cost for each unit of “disease burden” that the intervention prevents. We conducted a one-way sensitivity analysis. Methods are further described below and in the Technical appendix S1. We obtained clinical information from two studies that used a two-phase design (pre-intervention (standard care) and NASG intervention plus standard care), conducted in four sites in Nigeria and two sites in Egypt. Funding for these studies came from The John D. and Catherine T. MacArthur Foundation. The pre-intervention phase employed standard care including etiology identification, fluid resuscitation, and uterotonic administration for those with uterine atony.[13] The intervention phase added the NASG. A total of 1,442 patients with obstetric hemorrhage of any etiology (ranging from ectopic pregnancy to ruptured uterus) were studied. The six participating facilities logged over 100,000 deliveries during the study period, with a severe hemorrhage rate of 1.4%. Women with MAP<60 had a significantly greater risk of morbidity and mortality and required additional care.[8] Severe morbidity was defined by the Mantel criteria as end-stage organ dysfunction.[14] Additional information is available in the original study manuscripts.[8], [15], [16]. The NASG (Zoex Corporation, Colma, CA) resembles the bottom half of a neoprene wetsuit with an abdominal foam compression ball and Velcro closures that allow perineal and abdominal access; circumferential pressure reduces blood flow to the pelvis and lower extremities and increases cardiac and cerebral perfusion (Figure 1). During the pre-intervention phase, women with hypovolemic shock secondary to obstetric hemorrhage from any etiology were treated with a standardized shock/hemorrhage protocol.[16] Their outcomes were compared to outcomes for similar women treated with the same protocol and the NASG during the intervention phase. * Both the provider and patient have given informed consent, as outlined in the PLOS consent form, to publication of their photograph. Variables selected for this analysis were in two categories: treatments and outcomes (Table 1). Treatment variables included mean uterotonic doses, mean units transfused blood, emergency hysterectomies for women with a primary diagnosis of uterine atony and hysterectomies for women with any obstetric hemorrhage etiology. Outcome variables included mean measured blood loss after drape placement, mean discharge hemoglobin and total number of women with severe anemia or hemoglobin<7.0 g/dl on discharge (approximated from hematocrit by dividing by a factor of 2.95, rounded to 3, for Nigeria[17]), severe morbidity and mortality. We omitted variables that did not differ significantly in the trials by NASG status including other surgeries and procedures. Deaths were translated to DALYs using a value of 24 DALYs per death in Egypt and 22 per death in Nigeria. This was based on the difference between median age at maternal death, 28 and 30 and life expectancy at age 70 and 64 for Egypt and Nigeria respectively.[18] DALYs per other adverse event ranged from 0.09 for transient severe anemia to 2.5 for infertility secondary to emergency hysterectomy and 9 for long-term motor deficit (which occurred once, in Nigeria). Details on DALYs are provided in the Technical appendix S1. We included treatment costs in both clinical study phases, as well as program costs in the intervention phase. The following equations were used to calculate costs: Cost categories included clinical material (disposable and reusable), facility, provider, and laboratory. Unit cost data were collected from local investigators at El Galaa Maternity Hospital in Cairo, Egypt, Assiut University Women’s Health Center in Assiut, Egypt, University College Hospital in Ibadan, Nigeria and Katsina General Hospital in Katsina, Nigeria (Table 2). Respondents reported using internal cost accounting systems and hospital charges to patients in order to estimate costs. Due to wide (30-fold) differences in uterotonic unit costs across the Nigerian hospitals, we used a conservative market price.[19] We examined uncertainty in unit costs in the sensitivity analyses. We developed a cost-effectiveness model in Microsoft Excel 2004 to calculate net costs and DALYs from adding the NASG to a standard protocol for obstetric hemorrhage and hypovolemic shock. Calculations were performed for 1,000 women experiencing life-threatening obstetric hemorrhage, using standard economic methods, and reflecting the country-specific observed proportions of women in mild and severe shock (Table 3) [20]. Net costs (or savings) were calculated across intervention scenarios (no NASG for women in shock, NASG for severe shock only, and NASG for all women in shock), for each country (Table 4). Cost-effectiveness was calculated as net cost per DALY averted, or reported as “dominant” for intervention scenarios with lower costs and better health outcomes. Training costs to treat 1,000 women were annualized assuming that training effects would last 10 years. Training components (venues, trainee per diems, and trainer salaries) and prices were estimated based on the experience in the Nigerian and Egyptian studies. Intractable uterine atony is the only hemorrhage etiology for which emergency hysterectomy can be directly reduced by the NASG, because pelvic vascular compression can control blood loss until uterine contraction occurs. However, women who present with shock secondary to other obstetric hemorrhage etiologies (e.g., abruption placenta, ruptured uterus) and are stabilized with the NASG may then survive long enough to have the chance to receive the needed hysterectomy. For this reason, costs were examined in two ways: for hysterectomies secondary to primary uterine atony and for hysterectomies of all etiologies. Results were similar for both approaches, so we present results using the narrower scope and can provide the broader analysis on request. All costs were converted from Egyptian Pounds and Nigerian Naira to 2010 international dollars using the most recently available conversation factors.[21] We conducted sensitivity analyses to take into account possible variation in our baseline values. A one-way sensitivity analysis adjusted input parameters by 50% above or below the base case or used published ranges if available from prior NASG trials[8], [22] (Table 5 and Technical appendix S1). We also examined different approaches to assigning unit costs in Nigeria due to the very different costs between Northern and Southern Nigeria.