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Background
About 2·1 million Palestinians live in Jordan, and 370?000 Palestinians live in Jordanian refugee camps. Conflict in their country of origin, poverty, unemployment, and squalid camp conditions are some of the environmental factors that render Palestine refugees susceptible to mental health problems. The aim of this study was to identify the barriers that contribute to the treatment gap in mental health-care services for Palestinian refugees in the Baqa'a refugee camp north of Amman, Jordan.Methods
In this cross-sectional study, qualitative, semi-structured interviews of health-care professionals working at health centres for Palestine refugees in Jordan were done by a British researcher in the English language in the presence of an interpreter. All interviews were recorded, transcribed, and thematically analysed. Ethical approval was granted by the United Nations Relief and Works Agency for Palestine Refugees in the Near East (UNRWA) and the University of Leeds. Written consent was obtained from all participants.Findings
16 health-care professionals were interviewed during a 3 week period in May, 2015. 14 participants were based in health-care centres at the Baqa'a refugee camp, and two participants were based at the Field Office of the UNRWA in Amman, Jordan. All (100%) participants reported that underfunding was the most common barrier to accessing treatment. Other major barriers were sex (reported by 15 [94%] participants), stigma and religion (12 [75%]), and culture (ten [63%]).Interpretation
We suggest the following policy recommendations to overcome the barriers to accessing and using mental health-care services in Palestinian refugee camps in Jordan: (1) allocation of more resources for the provision of mental health-care services; (2) establishing a health and social care model that adopts a holistic approach to treating mental health problems in Palestinian refugees, incorporating a framework that facilitates enhanced communication and cooperation between faith leaders and health-care providers; and (3) launching anti-stigma campaigns that are culturally and religiously sensitive and specific.Funding
None. 相似文献Background
Cardiac implantable electrical devices (CIEDs) are subject to advisories and complications that can result in morbidity and mortality for patients; there is currently no system in Canada to track these.Methods
This was a multicenter, prospective cohort study conducted at 5 centers to determine feasibility. Patients with a de novo high-voltage (HV) lead implantation were included and followed for a minimum of 1 year.Results
There were 611 leads enrolled into the registry over 18 months. The mean age was 62.4 ± 12.8 years; 144 (23.6%) women were enrolled. The indication for lead implantation was for primary prevention in 65.5%. There were 497 (82.1%) de novo devices (single chamber: 54.5%, dual chamber: 20.5%, cardiac resynchronization therapy [CRT] 25.0%); the remainder of the procedures was a system revision for either upgrade (8.1%) or lead revision (9.8%). The lead revision rate at 1 year was 3.4%, with the primary reason being lead dislodgements. Mortality rate was 3.8% at 1 year. The rate of any device-related complication was 2.0% at 30 days, with the highest rate in CRT implants (4.9%, P = 0.0105). At 1 year, the complication rate was 4.5%, with no significant difference among device types.Conclusions
This study demonstrates that device surveillance is feasible and highlights (1) the need for CIED surveillance to track device-related complications, (2) the scope of this should be larger, and (3) mandatory participation should be considered. This system could predict CIEDs that may be susceptible to higher than usual rates of failure, mitigating adverse outcomes in patients. 相似文献Electronic supplementary material
The online version of this article (doi:10.1007/s13311-014-0310-1) contains supplementary material, which is available to authorized users. 相似文献Retrospective, cross-sectional estimates of pregnancy intention, as used in the Demographic Health Survey (DHS), are the global norm. The London Measure of Unplanned Pregnancy (LMUP) is a newer, psychometrically validated measure which may be more reliable. This paper assesses the reliability of the LMUP and the DHS question over the first postnatal year and explores the effects of maternal characteristics or pregnancy outcome on reported pregnancy intention.
MethodsWe compared the test–retest reliability of the LMUP (using the AC coefficient) and DHS question (using the weighted Kappa) over the first postnatal year using data from Malawian women. We investigated the effect of maternal characteristics and pregnancy outcome using t-tests, Chi squared or Fisher’s exact tests, and calculated odds ratios to estimate effect size.
ResultsThe DHS question was associated with a statistically significant decrease in the prevalence of unplanned pregnancies from 1-to-12 months postnatally; the LMUP was not. The LMUP had moderate to substantial reliability (0.51–0.66); the DHS had moderate reliability (0.56–0.58). The LMUP’s stability was not related to any of the factors examined; the stability of the DHS varied by marital status (p?=?0.033), number of children (p?=?0.048) and postnatal depression (p?<?0.001). Both underestimated unintended pregnancy postnatally vis-à-vis the LMUP in pregnancy.
Conclusions for PracticeThe LMUP is a more reliable measure of pregnancy intention than the DHS in the first postnatal year and does not vary by maternal characteristics or pregnancy outcome. The LMUP should become the gold-standard for measuring pregnancy intention and should be collected in pregnancy or at the first postnatal opportunity.
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