scholarly journals Body location of “New World” cutaneous leishmaniasis lesions and its impact on the quality of life of patients in Suriname

2020 ◽  
Vol 14 (10) ◽  
pp. e0008759
Author(s):  
Ricardo V. P. F. Hu ◽  
Sahienshadebie Ramdas ◽  
Pythia Nieuwkerk ◽  
Ria Reis ◽  
Rudy F. M. Lai A Fat ◽  
...  
2015 ◽  
Vol 5 ◽  
pp. 344-348 ◽  
Author(s):  
Enver Turan ◽  
Hasan Kandemir ◽  
Yavuz Yeşilova ◽  
Suat Ekinci ◽  
Osman Tanrıkulu ◽  
...  

2013 ◽  
Vol 107 (5) ◽  
pp. 335-336 ◽  
Author(s):  
A. C. d. C. Toledo ◽  
R. E. da Silva ◽  
R. F. Carmo ◽  
T. A. Amaral ◽  
Z. M. P. Luz ◽  
...  

2019 ◽  
Author(s):  
Malini Pires ◽  
Barry Wright ◽  
Paul M. Kaye ◽  
Virgínia Conceição ◽  
Rachel C. Churchill

ABSTRACTBackgroundLeishmaniasis is a neglected tropical parasitic disease endemic in South Asia, East Africa, South America and the Middle East. It is associated with low socioeconomic status (SES) and responsible for considerable mortality and morbidity. Reports suggest that patients with leishmaniasis may have a higher risk of mental illness (MI), psychosocial morbidity (PM) and reduced quality of life (QoL), but this is not well characterised. The aim of this study was to conduct a systematic review to assess the reported impact of leishmaniasis on mental health and psychosocial wellbeing.MethodsA systematic review of the literature was carried out. Pre-specified criteria were applied to identify publications including observational quantitative studies or systematic reviews. Two reviewers screened all of the titles, abstracts and full-studies and a third reviewer was consulted for disagreements. Data was extracted from papers meeting the criteria and quality appraisal of the methods was performed using the Newcastle-Ottowa Scale or the Risk of Bias in Systematic Review tool.ResultsA total of 14 studies were identified from 12,517 records. Nine cross-sectional, three case-control, one cohort study and one systematic review were included. Eleven assessed MI outcomes and were measured with tools specifically designed for this; nine measured PM and 12 measured QoL using validated measurement tools. Quality appraisal of the studies showed that six were of good quality. Cutaneous leishmaniasis and post kala-azar dermal leishmaniasis showed evidence of associated MI and PM including depression, anxiety and stigma, while all forms of disease showed decreased QoL. The findings were used to inform a proposed model and conceptual framework to show the possible links between leishmaniasis and mental health outcomes.ConclusionThere is evidence that leishmaniasis has an impact on MI, PM or QoL of patients and their families and this occurs in all the main subtypes of the disease. There are however large gaps in the evidence. Further research is required to understand the full extent of this problem and its mechanistic basis.AUTHOR SUMMARYLeishmaniasis is a parasitic disease prevalent in many low-and middle-income countries worldwide. In this study the authors looked for evidence as to whether leishmaniasis affected the mental health and quality of life of patients. To conduct the review, a wide search of the literature was conducted, where a total of 14 full articles were included and analysed. It was found that different forms of leishmaniasis (visceral leishmaniasis, cutaneous leishmaniasis and post kala-azar dermal leishmaniasis) do cause a significant impact on patients’ mental health and quality of life through societal factors such as stigma, lack of knowledge, culture and low self-esteem among others. However, no evidence of biological mechanisms was found linking leishmaniasis to mental illness or decreased quality of life. Despite being a very incapacitating disease physically, leishmaniasis also leads to mental illness and decreased quality of life, and should therefore be a priority on the global health agenda for both researchers and policy makers.


Author(s):  
Megan A. Perry

Perry’s research in Jordan spans the divide between investigations of the imperialism and colonialism in the Old World versus the New World, and between prehistory versus history. She probes the effects of the early Byzantine empire on health and quality of life at the sites of Faynan and Aila in Jordan. With textual, material, and archaeological data, she notes that life under imperial rule in these regions was not as drastically different as life under imperial rule by the Europeans, since the Nabataeans had established social and political structures that were influenced by Greco-Roman ones. However, she is able to establish that as influence of Byzantine imperial rule waxed and waned, lives and health of the imperial subjects at Faynan and Aila similarly wavered. She explores quality of life and health through the exploration of dental enamel hypoplasias, periostitis, porotic hyperostosis/cribra orbitalia, as well as strontium ratios, which may act as proxies for either population movement or for dietary diversity.


2018 ◽  
Vol 57 (12) ◽  
pp. 1442-1446
Author(s):  
Wardha F. Refai ◽  
Nayani P. Madarasingha ◽  
Buthsiri Sumanasena ◽  
Sudath Weerasingha ◽  
Rohini Fernandopulle ◽  
...  

2020 ◽  
Vol 29 (4) ◽  
pp. 2097-2108
Author(s):  
Robyn L. Croft ◽  
Courtney T. Byrd

Purpose The purpose of this study was to identify levels of self-compassion in adults who do and do not stutter and to determine whether self-compassion predicts the impact of stuttering on quality of life in adults who stutter. Method Participants included 140 adults who do and do not stutter matched for age and gender. All participants completed the Self-Compassion Scale. Adults who stutter also completed the Overall Assessment of the Speaker's Experience of Stuttering. Data were analyzed for self-compassion differences between and within adults who do and do not stutter and to predict self-compassion on quality of life in adults who stutter. Results Adults who do and do not stutter exhibited no significant differences in total self-compassion, regardless of participant gender. A simple linear regression of the total self-compassion score and total Overall Assessment of the Speaker's Experience of Stuttering score showed a significant, negative linear relationship of self-compassion predicting the impact of stuttering on quality of life. Conclusions Data suggest that higher levels of self-kindness, mindfulness, and social connectedness (i.e., self-compassion) are related to reduced negative reactions to stuttering, an increased participation in daily communication situations, and an improved overall quality of life. Future research should replicate current findings and identify moderators of the self-compassion–quality of life relationship.


2020 ◽  
Vol 29 (4) ◽  
pp. 685-690
Author(s):  
C. S. Vanaja ◽  
Miriam Soni Abigail

Purpose Misophonia is a sound tolerance disorder condition in certain sounds that trigger intense emotional or physiological responses. While some persons may experience misophonia, a few patients suffer from misophonia. However, there is a dearth of literature on audiological assessment and management of persons with misophonia. The purpose of this report is to discuss the assessment of misophonia and highlight the management option that helped a patient with misophonia. Method A case study of a 26-year-old woman with the complaint of decreased tolerance to specific sounds affecting quality of life is reported. Audiological assessment differentiated misophonia from hyperacusis. Management included retraining counseling as well as desensitization and habituation therapy based on the principles described by P. J. Jastreboff and Jastreboff (2014). A misophonia questionnaire was administered at regular intervals to monitor the effectiveness of therapy. Results A detailed case history and audiological evaluations including pure-tone audiogram and Johnson Hyperacusis Index revealed the presence of misophonia. The patient benefitted from intervention, and the scores of the misophonia questionnaire indicated a decrease in the severity of the problem. Conclusions It is important to differentially diagnose misophonia and hyperacusis in persons with sound tolerance disorders. Retraining counseling as well as desensitization and habituation therapy can help patients who suffer from misophonia.


ASHA Leader ◽  
2010 ◽  
Vol 15 (15) ◽  
pp. 5-6
Author(s):  
Anne Skalicky ◽  
Brenda Schick ◽  
Donald Patrick
Keyword(s):  

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