219 research outputs found
The MamaMiso study of self-administered misoprostol to prevent bleeding after childbirth in rural Uganda: a community-based, placebo-controlled randomised trial
BACKGROUND: 600 mcg of oral misoprostol reduces the incidence of postpartum haemorrhage (PPH), but in previous research this medication has been administered by health workers. It is unclear whether it is also safe and effective when self-administered by women. METHODS: This placebo-controlled, double-blind randomised trial enrolled consenting women of at least 34 weeks gestation, recruited over a 2-month period in Mbale District, Eastern Uganda. Participants had their haemoglobin measured antenatally and were given either 600 mcg misoprostol or placebo to take home and use immediately after birth in the event of delivery at home. The primary clinical outcome was the incidence of fall in haemoglobin of over 20% in home births followed-up within 5 days. RESULTS: 748 women were randomised to either misoprostol (374) or placebo (374). Of those enrolled, 57% delivered at a health facility and 43% delivered at home. 82% of all medicine packs were retrieved at postnatal follow-up and 97% of women delivering at home reported self-administration of the medicine. Two women in the misoprostol group took the study medication antenatally without adverse effects. There was no significant difference between the study groups in the drop of maternal haemoglobin by >20% (misoprostol 9.4% vs placebo 7.5%, risk ratio 1.11, 95% confidence interval 0.717 to 1.719). There was significantly more fever and shivering in the misoprostol group, but women found the medication highly acceptable. CONCLUSIONS: This study has shown that antenatally distributed, self-administered misoprostol can be appropriately taken by study participants. The rarity of the primary outcome means that a very large sample size would be required to demonstrate clinical effectiveness. TRIAL REGISTRATION: This study was registered with the ISRCTN Register (ISRCTN70408620)
Incorporating social practices in BDI agent systems
When agents interact with humans, either through embodied agents or because
they are embedded in a robot, it would be easy if they could use fixed
interaction protocols as they do with other agents. However, people do not keep
fixed protocols in their day-to-day interactions and the environments are often
dynamic, making it impossible to use fixed protocols. Deliberating about
interactions from fundamentals is not very scalable either, because in that
case all possible reactions of a user have to be considered in the plans. In
this paper we argue that social practices can be used as an inspiration for
designing flexible and scalable interaction mechanisms that are also robust.
However, using social practices requires extending the traditional BDI
deliberation cycle to monitor landmark states and perform expected actions by
leveraging existing plans. We define and implement this mechanism in Jason
using a periodically run meta-deliberation plan, supported by a
metainterpreter, and illustrate its use in a realistic scenario.Comment: An extended abstract of this paper has been accepted for the
Eighteenth International Conference on Autonomous Agents and Multiagent
Systems (AAMAS), 201
Postpartum haemorrhage: Case definition and guidelines for data collection, analysis, and presentation of immunization safety data.
Levels and Correlates of Non-Adherence to WHO Recommended Inter-Birth Intervals in Rufiji, Tanzania.
Poorly spaced pregnancies have been documented worldwide to result in adverse maternal and child health outcomes. The World Health Organization (WHO) recommends a minimum inter-birth interval of 33 months between two consecutive live births in order to reduce the risk of adverse maternal and child health outcomes. However, birth spacing practices in many developing countries, including Tanzania, remain scantly addressed. METHODS: Longitudinal data collected in the Rufiji Health and Demographic Surveillance System (HDSS) from January 1999 to December 2010 were analyzed to investigate birth spacing practices among women of childbearing age. The outcome variable, non-adherence to the minimum inter-birth interval, constituted all inter-birth intervals <33 months long. Inter-birth intervals >=33 months long were considered to be adherent to the recommendation. Chi-Square was used as a test of association between non-adherence and each of the explanatory variables. Factors affecting non-adherence were identified using a multilevel logistic model. Data analysis was conducted using STATA (11) statistical software. RESULTS: A total of 15,373 inter-birth intervals were recorded from 8,980 women aged 15--49 years in Rufiji district over the follow-up period of 11 years. The median inter-birth interval was 33.4 months. Of the 15,373 inter-birth intervals, 48.4% were below the WHO recommended minimum length of 33 months between two live births. Non-adherence was associated with younger maternal age, low maternal education, multiple births of the preceding pregnancy, non-health facility delivery of the preceding birth, being an in-migrant resident, multi-parity and being married. CONCLUSION: Generally, one in every two inter-birth intervals among 15--49 year-old women in Rufiji district is poorly spaced, with significant variations by socio-demographic and behavioral characteristics of mothers and newborns. Maternal, newborn and child health services should be improved with a special emphasis on community- and health facility-based optimum birth spacing education in order to enhance health outcomes of mothers and their babies, especially in rural settings
Preface
Reproductive tract bleeding in women is a naturally occurring event during menstruation and childbirth. In women with menorrhagia, however, congenital bleeding disorders historically have been underdiagnosed. This consensus is intended to allow physicians to better recognize bleeding disorders as a cause of menorrhagia and consequently offer effective disease-specific therapies. © 2009 Mosby, Inc. All rights reserved
Incidence of Postpartum Infection after Vaginal Delivery in Viet Nam
This study assessed the incidence of postpartum infection which is
rarely clinically evaluated and is probably underestimated in
developing countries. This prospective study identified infection after
vaginal delivery by clinical and laboratory examinations prior to
discharge from hospital and again at six weeks postpartum in Ho Chi
Minh City, Viet Nam. Textbook definitions, physicians' diagnoses,
symptomatic and verbal autopsy definitions were used for classifying
infection. Logistic regression was used for determining associations of
postpartum infection with socioeconomic and reproductive
characteristics. In total, 978 consecutive, eligible consenting women
were followed up at 42\ub17 (range 2-45) days postpartum (not
associated with incidence). Ninety-eight percent took 'prophylactic'
antibiotics. The most conservative estimate of the incidence of
postpartum infection was 1.7%. The incidence of serious infection was
0.5%, but increased to 4.6% when verbal autopsy and symptomatic
definitions were used. Postpartum infection, particularly serious
infection, is greatly underestimated. Just preventing or treating
infection could have a substantial impact on reducing maternal
mortality in developing countries
Client preferences and acceptability for medical abortion and MVA as early pregnancy termination method in Northwest Ethiopia
<p>Abstract</p> <p>Background</p> <p>Increasing access to safe abortion services is the most effective way of preventing the burden of unsafe abortion, which is achieved by increasing safe choices for pregnancy termination. Medical abortion for termination of early abortion is said to safe, effective, and acceptable to women in several countries. In Ethiopia, however, medical methods have, until recently, never been used. For this reason it is important to assess women's preferences and the acceptability of medical abortion and manual vacuum aspiration (MVA) in the early first trimester pregnancy termination and factors affecting acceptability of medical and MVA abortion services.</p> <p>Methods</p> <p>A prospective study was conducted in two hospitals and two clinics from March 2009 to November 2009. The study population consisted of 414 subjects over the age of 18 with intrauterine pregnancies of up to 63 days' estimated gestation. Of these 251 subjects received mifepristone and misoprostol and 159 subjects received MVA. Questionnaires regarding expectations and experiences were administered before the abortion and at the 2-week follow-up visit.</p> <p>Results</p> <p>The study groups were similar with respect to age, marital status, educational status, religion and ethnicity. Their mean age was about 23, majority in both group completed secondary education and about half were married. Place of residence and duration of pregnancy were associated with method choice. Subjects undergoing medical abortions reported significantly greater satisfaction than those undergoing surgical abortions (91.2% vs 82.4%; <it>P </it>< .001). Of those women who had medical abortion, (83.3%) would choose the method again if needed, and (77.4%) of those who had MVA would also choose the method again. Ninety four percent of women who had medical abortion and 86.8% of those who had MVA would recommend the method to their friends.</p> <p>Conclusions</p> <p>Women receiving medical abortion were more satisfied with their method and more likely to choose the same method again than were subjects undergoing surgical abortion. We conclude that medical abortion can be used widely as an alternative method for early pregnancy termination.</p
The role of ethics and ideology in our contribution to global health The topic of this article has vividly interested the author for many years. It is fascinating to him that the issues at stake have not changed for the last 30 years or so. As proof of this – and on purpose – references quoted are both those published before 1985 and after 1995 (Table 1). Considerable material on this topic was already available from the mid 1970s on. The end result has been the (re)construction of a scenario that has been stubborn to change and that looks into most of the, still highly relevant, burning questions of then and now on the issues pertaining to the title of this contribution for debate. It will be of interest to the reader to see how we often need to be reminded of the things our peers had evidence of and wrote about long before us – as the examples of Dr. Virchov and of the Alma Ata Declaration, for instance, show.
What drives public health professionals in their daily work? Presumably it is the appeal of working, either locally or globally, to alleviate the suffering caused by (preventable) ill-health. This article explores the political awareness of health professionals, the political implications of their daily activities and suggests an enhanced role for them in the battle against preventable ill-health worldwide. The starting point for this article is the motivating principles behind these professionals as individuals. It challenges established paradigms in health, medicine, development and academia with a focus on health professionals' political, ethical and ideological motivations and awareness plus the implications of their actions in the realm of global health in the future. It further has implications for the everyday practice of health care providers, public health practitioners, epidemiologists and social scientists in academia
Foley catheter vs. oral misoprostol to induce labour among hypertensive women in India: a cost-consequence analysis alongside a clinical trial
ObjectiveTo determine the effectiveness and economic impact oftwo methods for induction of labour in hypertensive women, inlow-resource settings.DesignCost-consequence analysis of a previously reportedmulticentre, parallel, open-label randomised trial.Setting & populationA total of 602 women with a live fetus, aged≥18 years requiring delivery for pre-eclampsia or hypertension, intwo public hospitals in Nagpur, India.MethodsWe performed a formal economic evaluation alongsidethe INFORM clinical trial. Women were randomised to receivetranscervical Foley catheterisation or oral misoprostol 25 mcg.Healthcare expenditure was calculated using a provider-sidemicrocosting approach.Main outcome measuresRates of vaginal this delivery within24 hours of induction, healthcare expenditure per completedtreatment episode.ResultsInduction with oral misoprostol resulted in a (meandifference) 123.59 ( ) 0.24 to $7.50 per 25 mcg tablet and remain cost-saving
Two prophylactic medication approaches in addition to a pain control regimen for early medical abortion < 63 days’ gestation with mifepristone and misoprostol: study protocol for a randomized, controlled trial
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