1,429 research outputs found
Gulf War syndrome: an emerging threat or a piece of history?
‘Gulf War syndrome’ is a phrase coined after the 1991 Gulf War to group together disparate, unexplained health symptoms in Gulf veterans. This paper examines the many hypotheses that have been put forward about the origins of the concept and gives an overview of the studies that have attempted to explain the lasting health effects associated with Gulf service. Our review finds that although in the UK there has not yet been evidence of a new Gulf War syndrome as a result of the current conflicts in Iraq and Afghanistan, there is a rise in post-conflict psychiatric disorders now being reported in the USA. We postulate that after conflicts military personnel will always face some form of post-conflict syndrome and the nature of the threats experienced is likely to dictate the form the syndrome might take. We also postulate that media reporting is likely to have influenced and to continue unhelpfully to influence the health of service personnel
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Covid conspiracies: misleading evidence can be more damaging than no evidence at all.
‘What’s it like to have ME?’ The discursive construction of ME in computer-mediated communication and face-to-face interaction
ME/CFS (chronic fatigue syndrome) is a debilitating illness for which no cause or medical tests have been identified. Debates over its nature have generated interest from qualitative researchers. However, participants are difficult to recruit because of the nature of their condition. Therefore, this study explores the utility of the internet as a means of eliciting accounts. We analyse data from focus groups and the internet in order to ascertain the extent to which previous research findings apply to the internet domain. Interviews were conducted among 49 members of internet (38 chatline, 11 personal) and 7 members of two face-to-face support groups. Discourse analysis of descriptions and accounts of ME/CFS revealed similar devices and interactional concerns in both internet and face-to-face communication. Participants constructed their condition as serious, enigmatic and not psychological. These functioned to deflect problematic assumptions about ME/CFS and to manage their accountability for the illness and its effects
Headache in 25 consecutive patients with atrial septal defects before and after percutaneous closure – a prospective case series
In contrast to patent foramen ovale, that is highly prevalent in the general population, atrial
septal defect (ASD) is a rare congenital heart defect. The effect of ASD closure on headache
and migraine remains a matter of controversy. The objectives of the study were (i) to
determine headache prevalence in consecutive patients with ASD scheduled for percutaneous
closure for cardiologic indications, using the classification of the International Headache
Society and (ii) to compare headache characteristics before and after closure of ASD. In this
observational case series no a priori power analysis was performed. Twenty-five consecutive
patients were prospectively included over 27 months. Median duration of follow-up was 12
months, [Interquartile range 0]. Prevalence of active headache seemed to be increased
compared to the general population: Any headaches 88% (95% confidence interval 70-96),
migraine without aura 28% (14-48), migraine with aura 16% (6-35). After ASD closure, we
observed a slightly lower headache frequency (median frequency 1.0 [2.6] vs. 0.3 [1.5]
headaches per month; p=0.067). In patients with ongoing headaches, a significant decrease in
headache intensity (median VAS 7 [3] vs. 5 [4]; p=0.036) was reported. Three patients with
migraine with aura before the intervention reported no migraine with aura attacks at followup,
two of them reported ongoing tension-type headache, one migraine without aura. In
summary, this prospective observational study confirms the high prevalence of headache,
particularly migraine, in ASD patients and suggests a possible small beneficial effect of ASD
closure
H-index pathology: Implications for medical researchers and practitioners
The h-index has quickly become the standard method by which medical schools judge the impact of medical researchers. Rob Horne, Keith Petrie, and Simon Wessely describe a cluster of potentially pathological behaviours associated with the index
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