Vitiligo is a common acquired, idiopathic and often familiar depigmentation disorder that affects both sexes equally worldwide.
Although not painful or life-threatening, this disfiguring disorder can have a devastating effect on a patient’s psychosocial wellbeing and social life
This document discusses a study that explored quality of life issues important to patients with hematological malignancies. Researchers interviewed and surveyed 57 patients and identified 21 key quality of life themes, including limitations in social activities, strain on relationships, fatigue, and inability to do activities. The study also identified 5 categories of common symptoms reported, such as breathlessness, fractures, and anaemia. The researchers concluded there is a need for new patient-reported outcome measures that comprehensively assess the impacts of hematological malignancies on patients' quality of life and symptoms.
1. Social and economic factors may have changed between the time periods studied, such as increases in unemployment, poverty, or family disruption, which could impact rates of psychiatric morbidity.
2. Changes may have occurred in how psychiatric disorders are diagnosed and classified between 1977 and 1985 that could influence prevalence findings.
3. Increased awareness, destigmatization of mental health issues, and expansion of treatment services between the periods may have impacted help-seeking behaviors and the proportion of cases identified.
treatment seeking behaviour of leprosy patientsAshok Kanuri
The document summarizes research on the treatment seeking behavior of leprosy patients in Visakhapatnam, India. It finds that socio-demographic factors like age, sex, occupation, and type of diagnosis influence the delay in seeking treatment. Males and daily laborers experienced longer delays. Stigma around leprosy was also found to negatively impact patients' quality of life, education, employment, and marital prospects. Scales to measure perceived, internalized, and enacted stigma showed high rates of stigma among the patients studied. Overcoming misconceptions around leprosy's curability and eliminating discrimination were identified as key to reducing stigma.
This document summarizes a statistics survey project conducted by a group of students on diabetes. The survey included 200 male respondents aged 21-30 and collected data on their knowledge of diabetes facts, symptoms, transmission, treatment costs and more. Key findings from the statistical analysis include: most respondents believed males are more likely to be diagnosed with diabetes; the ratio of diabetics in Malaysia is estimated at 2-3 out of 10; and financial costs of medication and treatment were viewed as having the biggest lifestyle impact for diabetics. The conclusions indicate some questions were difficult to estimate but provide an overview of public understanding of diabetes.
Vitiligo in Croatia: a case report Vedrana Bulat, Mirna Šitum Department of...VR Foundation
INTRODUCTION
Vitiligo is an acquired chronic disease characterized by depigmented macular patches due to loss of epidermal melanocytes. It affects 1,6% of the general population in Croatia.
Female patients are more affected (53,95%) than male patients, with no difference in the severity of vitiligo. Most of our patients were in generally good health, showing no association of vitiligo with thyroid dysfunction, diabetes mellitus, pernicious anemia nor gonadal failure. Localized form of vitiligo most frequently affects 21 to 28-year-old patients, while generalized form prevails in the age group from 29 to 36 years. Patients older than 77 years of age are very rarely affected. The most common localized type was focal (93,28%), and the most common generalized type was vitiligo vulgaris (53,7%). Most of our patients were admitted in September, probably due to increased contrast between involved and uninvolved skin. Most patients attribute the onset of their disease to specific life events (physical injury, emotional distress, illness or pregnancy).
AIMS
The aim of this case report was to present our patient suffering from vitiligo vulgaris, and to evaluate clinical presentation, diagnostic and therapeutic difficulties in this condition.
CASE REPORT
A 23-year-old Caucasian female patient was admitted to our Hospital in September 2010, due to prominent, generalized depigmented patches.
The disease begun acutely, “over night” (in patients` own words), and progressed in the following order: dorsal aspects of hands, upper extremities, trunk, face and lower extremities. Within a few weeks 60% of her body was affected.
On admission to our Hospital her height was 175 centimeters and weight was 60 kilograms, body mass index was normal (19,6).
The affected area had no associated scaling. There was a lack of cutaneous induration or sclerosis. Skin lesions were asymptomatic and lack clinical sings of inflammation. During dermatological examination leukotrichia of the occipital area was found. There was no mucosal involvement. She was without any subjective difficulties (e.g. pain, fever, weight loss).
There was family history of this disorder (her 12-year-old brother has acrofacial vitiligo). The disease appeared almost simultaneously with his sister`s condition. She attributed the onset of her disease to emotional stress, while her parents died in a car accident six months before she has noticed first signs of vitiligo.
She had also noticed new depigmented lesions in sites of physical injury (Koebner phenomena).
History of chronic sun exposure was negative. She was non-smoker.
Illumination with Wood`s lamp showed no fluorescence of the affected depigmented skin.CL has been diagnosed based on the clinical picture and pathohistological appearance.
- Disclaimer-
This PPT is loaded as student material "as is", from the VRF Vitiligo Master Class Barcelona November 2011; VRF does not endorse or otherwise approve it.
Vitiligo is an acquired pigmentary disorder of the skin and mucous membranes characterized by circumscribed depigmented macules and patches that result from a progressive loss of functional melanocytes that are selectively destroyed.
Vitiligo is a condition characterized by patches of skin that lose pigmentation due to the absence of melanocytes. It is caused by the destruction or malfunction of melanocytes, which may be due to autoimmune, neural, or endogenous factors. Treatment aims to repigment the skin and prevent further depigmentation, and involves topical agents like steroids and calcipotriol, phototherapy with UVB or PUVA, and surgical grafting in resistant cases. Vitiligo has no cure and treatment outcomes vary depending on the individual.
Vitiligo is an autoimmune skin disorder that causes loss of skin color in patches due to lack of melanin production. The exact cause is unknown but may involve genetic and environmental factors. Symptoms include white patches that appear on the skin in three patterns - focal, segmental, or generalized. Treatment options include surgical skin grafts, medical therapies like photochemotherapy, and adjunctive therapies like cosmetics and counseling. Vitiligo affects 1% of the world population regardless of age, gender, or race.
This document discusses a study that explored quality of life issues important to patients with hematological malignancies. Researchers interviewed and surveyed 57 patients and identified 21 key quality of life themes, including limitations in social activities, strain on relationships, fatigue, and inability to do activities. The study also identified 5 categories of common symptoms reported, such as breathlessness, fractures, and anaemia. The researchers concluded there is a need for new patient-reported outcome measures that comprehensively assess the impacts of hematological malignancies on patients' quality of life and symptoms.
1. Social and economic factors may have changed between the time periods studied, such as increases in unemployment, poverty, or family disruption, which could impact rates of psychiatric morbidity.
2. Changes may have occurred in how psychiatric disorders are diagnosed and classified between 1977 and 1985 that could influence prevalence findings.
3. Increased awareness, destigmatization of mental health issues, and expansion of treatment services between the periods may have impacted help-seeking behaviors and the proportion of cases identified.
treatment seeking behaviour of leprosy patientsAshok Kanuri
The document summarizes research on the treatment seeking behavior of leprosy patients in Visakhapatnam, India. It finds that socio-demographic factors like age, sex, occupation, and type of diagnosis influence the delay in seeking treatment. Males and daily laborers experienced longer delays. Stigma around leprosy was also found to negatively impact patients' quality of life, education, employment, and marital prospects. Scales to measure perceived, internalized, and enacted stigma showed high rates of stigma among the patients studied. Overcoming misconceptions around leprosy's curability and eliminating discrimination were identified as key to reducing stigma.
This document summarizes a statistics survey project conducted by a group of students on diabetes. The survey included 200 male respondents aged 21-30 and collected data on their knowledge of diabetes facts, symptoms, transmission, treatment costs and more. Key findings from the statistical analysis include: most respondents believed males are more likely to be diagnosed with diabetes; the ratio of diabetics in Malaysia is estimated at 2-3 out of 10; and financial costs of medication and treatment were viewed as having the biggest lifestyle impact for diabetics. The conclusions indicate some questions were difficult to estimate but provide an overview of public understanding of diabetes.
Vitiligo in Croatia: a case report Vedrana Bulat, Mirna Šitum Department of...VR Foundation
INTRODUCTION
Vitiligo is an acquired chronic disease characterized by depigmented macular patches due to loss of epidermal melanocytes. It affects 1,6% of the general population in Croatia.
Female patients are more affected (53,95%) than male patients, with no difference in the severity of vitiligo. Most of our patients were in generally good health, showing no association of vitiligo with thyroid dysfunction, diabetes mellitus, pernicious anemia nor gonadal failure. Localized form of vitiligo most frequently affects 21 to 28-year-old patients, while generalized form prevails in the age group from 29 to 36 years. Patients older than 77 years of age are very rarely affected. The most common localized type was focal (93,28%), and the most common generalized type was vitiligo vulgaris (53,7%). Most of our patients were admitted in September, probably due to increased contrast between involved and uninvolved skin. Most patients attribute the onset of their disease to specific life events (physical injury, emotional distress, illness or pregnancy).
AIMS
The aim of this case report was to present our patient suffering from vitiligo vulgaris, and to evaluate clinical presentation, diagnostic and therapeutic difficulties in this condition.
CASE REPORT
A 23-year-old Caucasian female patient was admitted to our Hospital in September 2010, due to prominent, generalized depigmented patches.
The disease begun acutely, “over night” (in patients` own words), and progressed in the following order: dorsal aspects of hands, upper extremities, trunk, face and lower extremities. Within a few weeks 60% of her body was affected.
On admission to our Hospital her height was 175 centimeters and weight was 60 kilograms, body mass index was normal (19,6).
The affected area had no associated scaling. There was a lack of cutaneous induration or sclerosis. Skin lesions were asymptomatic and lack clinical sings of inflammation. During dermatological examination leukotrichia of the occipital area was found. There was no mucosal involvement. She was without any subjective difficulties (e.g. pain, fever, weight loss).
There was family history of this disorder (her 12-year-old brother has acrofacial vitiligo). The disease appeared almost simultaneously with his sister`s condition. She attributed the onset of her disease to emotional stress, while her parents died in a car accident six months before she has noticed first signs of vitiligo.
She had also noticed new depigmented lesions in sites of physical injury (Koebner phenomena).
History of chronic sun exposure was negative. She was non-smoker.
Illumination with Wood`s lamp showed no fluorescence of the affected depigmented skin.CL has been diagnosed based on the clinical picture and pathohistological appearance.
- Disclaimer-
This PPT is loaded as student material "as is", from the VRF Vitiligo Master Class Barcelona November 2011; VRF does not endorse or otherwise approve it.
Vitiligo is an acquired pigmentary disorder of the skin and mucous membranes characterized by circumscribed depigmented macules and patches that result from a progressive loss of functional melanocytes that are selectively destroyed.
Vitiligo is a condition characterized by patches of skin that lose pigmentation due to the absence of melanocytes. It is caused by the destruction or malfunction of melanocytes, which may be due to autoimmune, neural, or endogenous factors. Treatment aims to repigment the skin and prevent further depigmentation, and involves topical agents like steroids and calcipotriol, phototherapy with UVB or PUVA, and surgical grafting in resistant cases. Vitiligo has no cure and treatment outcomes vary depending on the individual.
Vitiligo is an autoimmune skin disorder that causes loss of skin color in patches due to lack of melanin production. The exact cause is unknown but may involve genetic and environmental factors. Symptoms include white patches that appear on the skin in three patterns - focal, segmental, or generalized. Treatment options include surgical skin grafts, medical therapies like photochemotherapy, and adjunctive therapies like cosmetics and counseling. Vitiligo affects 1% of the world population regardless of age, gender, or race.
Shaun Staunton (Tascahrd) reports on a Qld study of HIV nurses and recommends that HIV nurses could play a greater role in HIV health promotion and prevention. This presentation was given at the AFAO/NAPWA Gay Men's HIV Health Promotion Conference in May 2012.
The AD8 screening test was evaluated on 334 Turkish geriatric outpatients with memory complaints. [1] The AD8 was found to be a valid and reliable tool for detecting mild cognitive impairment and dementia in this population. [2] It demonstrated high sensitivity (100%) and specificity (96.3%) for diagnosing MCI and dementia according to DSM-5 criteria. [3] The AD8 is a practical screening test that can help diagnose cognitive impairment, especially in primary care settings.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
Challenge of integration care of clp (acpm 2014)Andri Andri
This document summarizes the results of an online survey of 75 healthcare providers in Indonesian general hospitals about psychiatric services. It finds that 20-40% of medical inpatients have psychiatric disorders like depression, anxiety, and dementia. However, 52.8% of hospitals reported having no psychiatrist on staff. The most common psychiatric cases seen were depression (34.7%), anxiety (27.8%), and insomnia (11.1%). While 98.6% of providers felt a psychiatric consultation-liaison team was needed, 75% reported their hospital had no such team. The survey concludes there is evidence integrated medical-psychiatric care can improve outcomes for patients with co-occurring conditions.
This document summarizes a study on the impact of chronic contact dermatitis on quality of life and burden on family. The study evaluated 50 patients in Jaipur, India with contact dermatitis for over 6 months. It found that quality of life was average overall but poorer for female patients. The burden on families was generally mild to moderate. Chronic contact dermatitis was shown to significantly affect patients' daily activities and quality of life.
Journal Club Presentation on Depression, Anxiety in DiabetesDnyaneshwariMate1
This study aimed to determine the prevalence of depression and anxiety in Malaysian diabetic patients and identify associated factors. The study found depression in 20% of patients and anxiety in 9%. Multiple logistic regression identified several predictors of anxiety and depression. Higher neuroticism and depression increased odds of anxiety, while higher conscientiousness and psychological quality of life decreased odds. The findings indicate a need to screen diabetic patients for mental health issues and address psychosocial factors in their care.
This poster, presented at ISPOR 6th Asia-Pacific Conference in September 2014, reports on an investigation into the use of time trade off and discrete choice experiments to value health states. No EQ-5D-5L value sets are available now to guide health care decision making in the UAE, despite increasing interest in using patient-preference data in decisions about drug coverage.
This study, based on 320 interviews, finds that religious and spiritual beliefs made it difficult to explain the 'worse than death' (WTD) concept used in TTO and that fewer respondent than in other countries rated health states as WTD. The importance of dimensions also differed, with the majority of respondents considering mobility to be most important and anxiety/depression least important.
The authors conclude that, for TTO, adaptation of methods may be required. No issues were encountered using DCE.
For additional information, contact Koonal Shah at OHE.
The document summarizes findings from the Saudi Health Interview Survey (SHIS) conducted in 2013. Some key findings include:
- 15.1% of Saudis ages 15 or older are hypertensive, 40.5% are borderline hypertensive
- 8.5% are hypercholesterolemic and 20% are borderline hypercholesterolemic
- 13.4% are diabetic and 16.3% are borderline diabetic
- 28.7% of Saudis are obese
This document outlines a prospective study on the effect of pandemic restrictions on quality of life and medication adherence in diabetes patients. It discusses the introduction, aims and objectives, methodology, results and conclusion of the study. The study aims to assess the impact of COVID-19 pandemic restrictions on quality of life and medication adherence in 110 diabetes patients in Bangalore, India over 6 months. Preliminary results show that quality of life was reduced for most patients due to restrictions, while medication adherence decreased initially but increased after counselling. New diabetes cases and complications were also observed due to reduced activity and increased weight during the pandemic. The study concludes that the prevalence of diabetes has increased overall due to pandemic restrictions.
Katherine Promer Flores, MD (she/her)
Staff Physician
Division of Infectious Diseases and Global Public Health
Department of Medicine
University of California San Diego
1. The document provides information about the roles, referrals, and linkages of Integrated Counselling and Testing Centres (ICTCs) in India.
2. ICTCs aim to reduce HIV transmission by increasing access to voluntary HIV testing and counselling. They provide counselling, testing, and link people to medical, psychological, and social support services.
3. ICTCs are located in various public and private health facilities. They require infrastructure like counselling rooms and laboratories, as well as staff like counsellors, medical officers, and laboratory technicians.
Health Promotion and Education program in prevention and control of H...Arjun Hamal
This document outlines a health promotion program to prevent HIV/AIDS using the PRECEDE-PROCEED framework. It begins with an introduction and objectives. Baseline data is presented on the target population which shows some risky behaviors. A needs assessment is then conducted using the PRECEDE components which examine social, epidemiological, behavioral, educational, and policy factors. Objectives are set and a program is designed which includes awareness activities, condom demonstrations, and monitoring. The program aims to increase knowledge of HIV prevention and promote safe sexual practices to reduce new HIV cases in the target area by 50% by 2022.
This document summarizes research on quality of life for bladder cancer patients. Quantitative studies found that muscle-invasive bladder cancer patients reported worse quality of life and more symptoms than non-muscle-invasive patients. Both groups experienced problems with urinary and sexual symptoms. Qualitative interviews found patients endorsed having a navigator to help with treatment, monitoring, and managing symptoms. Future research plans include developing a bladder cancer navigation intervention and studying quality of life and distress over time. The goal is to improve survivorship care through tailored interventions.
Rasch analysis of the Dermatology Life Quality Questionnaire (DLQI)Stephen McKenna
The document discusses a Rasch analysis of the Dermatology Life Quality Questionnaire (DLQI), a 10-item patient-reported outcome measure used to assess quality of life for patients with various skin conditions. The analysis identified several issues with the DLQI, including misfitting items, disordered response thresholds, and differential item functioning. This suggests problems with the scale's development methodology and raises concerns about its use in clinical trials and treatment decisions. The document advocates for improved scale development using modern psychometric methods like Rasch analysis and qualitative research with patients.
Evaluation of the Quality of Life for Parents and Caregivers of Adults with I...Remedypublications1
The quality of life is an important component in the development of target interventions related
to the inclusion of families in the wider social community. The goal of this research was to test the
degree of the quality of life for parents and custodians of adults with intellectual disabilities as a
whole and by domains and to check the relationship of the quality of life and socio-demographic
features of the participants in this research. Forty parents of adults with intellectual disability took
part in the study. A convenience sample from the area of the city of Zagreb and the Zagreb County
was used in referential centres and associations caring for adult with intellectual disabilities older
than 21 years of age. For the purpose of this study, we have used the Personal Wellbeing Index for
the evaluation of the quality of life and welfare of parents and custodians of persons with intellectual
disabilities. The results of the research indicate that the perceived quality of life of the parents does
not deviate from the values that can be found in the healthy population. Parents have also evaluated
the quality of life of their children and the result has shown that they are moderately satisfied. There
is a major connection between the evaluation of the quality of life of the parents and their evaluation
of the quality of life of their children. The more satisfied parents are with their quality of life, i.e.
the better they estimate their personal welfare, the better are the evaluations for the quality of life
of their children. The research results point that there is no statistically significant difference in the
evaluation of the quality of life between the groups that differ with regard to: gender, inclusion in the
physical activity and presence of other disabilities.
Clinical and epidemiological characteristics of childhoodtloanphan
This study analyzed clinical and epidemiological data from 701 children with vitiligo who were seen at a dermatology clinic in Brazil between 2006-2014. The main findings were:
1) Most patients were female (62%) and the average age of onset was 5.9 years. The most common subtype was generalized vitiligo (53.8%).
2) The most affected initial site was the head/neck region (44.2%). Emotional stressors were reported as triggering factors in 67% of patients.
3) Segmental and nonsegmental vitiligo differed significantly in characteristics like age of onset, presence of the Koebner phenomenon, associations with autoimmune diseases, and family
Clinical and epidemiological characteristics of childhood vitiligo a study of...tloanphan
This study analyzed clinical and epidemiological data from 701 children with vitiligo who were seen at a dermatology clinic in Brazil between 2006-2014. The main findings were:
1) Vitiligo was more common in females (62% of cases) and the average age of onset was 5.9 years.
2) The most common subtype was generalized vitiligo (53.8% of cases) and the most common initial site was the head/neck region (44.2% of cases).
3) Associated autoimmune diseases, family history of vitiligo, and the Koebner phenomenon were present in 6.5%, 16.9%, and 38.2% of
The document discusses using an integrated data-driven approach to tackle chronic diseases. It summarizes that chronic diseases are becoming the norm, with over half of those over 45 having multi-morbidity. A paradigm shift is needed from reactive to proactive care. Clalit Health Services in Israel provides an example of an integrated system with universal coverage and strong data infrastructure. Case studies show how Clalit uses data to develop policies and programs around readmissions reduction, predictive prevention, reducing disparities, and proactive care for complex patients. Key requisites for success include data sharing and analytic capacity.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Shaun Staunton (Tascahrd) reports on a Qld study of HIV nurses and recommends that HIV nurses could play a greater role in HIV health promotion and prevention. This presentation was given at the AFAO/NAPWA Gay Men's HIV Health Promotion Conference in May 2012.
The AD8 screening test was evaluated on 334 Turkish geriatric outpatients with memory complaints. [1] The AD8 was found to be a valid and reliable tool for detecting mild cognitive impairment and dementia in this population. [2] It demonstrated high sensitivity (100%) and specificity (96.3%) for diagnosing MCI and dementia according to DSM-5 criteria. [3] The AD8 is a practical screening test that can help diagnose cognitive impairment, especially in primary care settings.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
Challenge of integration care of clp (acpm 2014)Andri Andri
This document summarizes the results of an online survey of 75 healthcare providers in Indonesian general hospitals about psychiatric services. It finds that 20-40% of medical inpatients have psychiatric disorders like depression, anxiety, and dementia. However, 52.8% of hospitals reported having no psychiatrist on staff. The most common psychiatric cases seen were depression (34.7%), anxiety (27.8%), and insomnia (11.1%). While 98.6% of providers felt a psychiatric consultation-liaison team was needed, 75% reported their hospital had no such team. The survey concludes there is evidence integrated medical-psychiatric care can improve outcomes for patients with co-occurring conditions.
This document summarizes a study on the impact of chronic contact dermatitis on quality of life and burden on family. The study evaluated 50 patients in Jaipur, India with contact dermatitis for over 6 months. It found that quality of life was average overall but poorer for female patients. The burden on families was generally mild to moderate. Chronic contact dermatitis was shown to significantly affect patients' daily activities and quality of life.
Journal Club Presentation on Depression, Anxiety in DiabetesDnyaneshwariMate1
This study aimed to determine the prevalence of depression and anxiety in Malaysian diabetic patients and identify associated factors. The study found depression in 20% of patients and anxiety in 9%. Multiple logistic regression identified several predictors of anxiety and depression. Higher neuroticism and depression increased odds of anxiety, while higher conscientiousness and psychological quality of life decreased odds. The findings indicate a need to screen diabetic patients for mental health issues and address psychosocial factors in their care.
This poster, presented at ISPOR 6th Asia-Pacific Conference in September 2014, reports on an investigation into the use of time trade off and discrete choice experiments to value health states. No EQ-5D-5L value sets are available now to guide health care decision making in the UAE, despite increasing interest in using patient-preference data in decisions about drug coverage.
This study, based on 320 interviews, finds that religious and spiritual beliefs made it difficult to explain the 'worse than death' (WTD) concept used in TTO and that fewer respondent than in other countries rated health states as WTD. The importance of dimensions also differed, with the majority of respondents considering mobility to be most important and anxiety/depression least important.
The authors conclude that, for TTO, adaptation of methods may be required. No issues were encountered using DCE.
For additional information, contact Koonal Shah at OHE.
The document summarizes findings from the Saudi Health Interview Survey (SHIS) conducted in 2013. Some key findings include:
- 15.1% of Saudis ages 15 or older are hypertensive, 40.5% are borderline hypertensive
- 8.5% are hypercholesterolemic and 20% are borderline hypercholesterolemic
- 13.4% are diabetic and 16.3% are borderline diabetic
- 28.7% of Saudis are obese
This document outlines a prospective study on the effect of pandemic restrictions on quality of life and medication adherence in diabetes patients. It discusses the introduction, aims and objectives, methodology, results and conclusion of the study. The study aims to assess the impact of COVID-19 pandemic restrictions on quality of life and medication adherence in 110 diabetes patients in Bangalore, India over 6 months. Preliminary results show that quality of life was reduced for most patients due to restrictions, while medication adherence decreased initially but increased after counselling. New diabetes cases and complications were also observed due to reduced activity and increased weight during the pandemic. The study concludes that the prevalence of diabetes has increased overall due to pandemic restrictions.
Katherine Promer Flores, MD (she/her)
Staff Physician
Division of Infectious Diseases and Global Public Health
Department of Medicine
University of California San Diego
1. The document provides information about the roles, referrals, and linkages of Integrated Counselling and Testing Centres (ICTCs) in India.
2. ICTCs aim to reduce HIV transmission by increasing access to voluntary HIV testing and counselling. They provide counselling, testing, and link people to medical, psychological, and social support services.
3. ICTCs are located in various public and private health facilities. They require infrastructure like counselling rooms and laboratories, as well as staff like counsellors, medical officers, and laboratory technicians.
Health Promotion and Education program in prevention and control of H...Arjun Hamal
This document outlines a health promotion program to prevent HIV/AIDS using the PRECEDE-PROCEED framework. It begins with an introduction and objectives. Baseline data is presented on the target population which shows some risky behaviors. A needs assessment is then conducted using the PRECEDE components which examine social, epidemiological, behavioral, educational, and policy factors. Objectives are set and a program is designed which includes awareness activities, condom demonstrations, and monitoring. The program aims to increase knowledge of HIV prevention and promote safe sexual practices to reduce new HIV cases in the target area by 50% by 2022.
This document summarizes research on quality of life for bladder cancer patients. Quantitative studies found that muscle-invasive bladder cancer patients reported worse quality of life and more symptoms than non-muscle-invasive patients. Both groups experienced problems with urinary and sexual symptoms. Qualitative interviews found patients endorsed having a navigator to help with treatment, monitoring, and managing symptoms. Future research plans include developing a bladder cancer navigation intervention and studying quality of life and distress over time. The goal is to improve survivorship care through tailored interventions.
Rasch analysis of the Dermatology Life Quality Questionnaire (DLQI)Stephen McKenna
The document discusses a Rasch analysis of the Dermatology Life Quality Questionnaire (DLQI), a 10-item patient-reported outcome measure used to assess quality of life for patients with various skin conditions. The analysis identified several issues with the DLQI, including misfitting items, disordered response thresholds, and differential item functioning. This suggests problems with the scale's development methodology and raises concerns about its use in clinical trials and treatment decisions. The document advocates for improved scale development using modern psychometric methods like Rasch analysis and qualitative research with patients.
Evaluation of the Quality of Life for Parents and Caregivers of Adults with I...Remedypublications1
The quality of life is an important component in the development of target interventions related
to the inclusion of families in the wider social community. The goal of this research was to test the
degree of the quality of life for parents and custodians of adults with intellectual disabilities as a
whole and by domains and to check the relationship of the quality of life and socio-demographic
features of the participants in this research. Forty parents of adults with intellectual disability took
part in the study. A convenience sample from the area of the city of Zagreb and the Zagreb County
was used in referential centres and associations caring for adult with intellectual disabilities older
than 21 years of age. For the purpose of this study, we have used the Personal Wellbeing Index for
the evaluation of the quality of life and welfare of parents and custodians of persons with intellectual
disabilities. The results of the research indicate that the perceived quality of life of the parents does
not deviate from the values that can be found in the healthy population. Parents have also evaluated
the quality of life of their children and the result has shown that they are moderately satisfied. There
is a major connection between the evaluation of the quality of life of the parents and their evaluation
of the quality of life of their children. The more satisfied parents are with their quality of life, i.e.
the better they estimate their personal welfare, the better are the evaluations for the quality of life
of their children. The research results point that there is no statistically significant difference in the
evaluation of the quality of life between the groups that differ with regard to: gender, inclusion in the
physical activity and presence of other disabilities.
Clinical and epidemiological characteristics of childhoodtloanphan
This study analyzed clinical and epidemiological data from 701 children with vitiligo who were seen at a dermatology clinic in Brazil between 2006-2014. The main findings were:
1) Most patients were female (62%) and the average age of onset was 5.9 years. The most common subtype was generalized vitiligo (53.8%).
2) The most affected initial site was the head/neck region (44.2%). Emotional stressors were reported as triggering factors in 67% of patients.
3) Segmental and nonsegmental vitiligo differed significantly in characteristics like age of onset, presence of the Koebner phenomenon, associations with autoimmune diseases, and family
Clinical and epidemiological characteristics of childhood vitiligo a study of...tloanphan
This study analyzed clinical and epidemiological data from 701 children with vitiligo who were seen at a dermatology clinic in Brazil between 2006-2014. The main findings were:
1) Vitiligo was more common in females (62% of cases) and the average age of onset was 5.9 years.
2) The most common subtype was generalized vitiligo (53.8% of cases) and the most common initial site was the head/neck region (44.2% of cases).
3) Associated autoimmune diseases, family history of vitiligo, and the Koebner phenomenon were present in 6.5%, 16.9%, and 38.2% of
The document discusses using an integrated data-driven approach to tackle chronic diseases. It summarizes that chronic diseases are becoming the norm, with over half of those over 45 having multi-morbidity. A paradigm shift is needed from reactive to proactive care. Clalit Health Services in Israel provides an example of an integrated system with universal coverage and strong data infrastructure. Case studies show how Clalit uses data to develop policies and programs around readmissions reduction, predictive prevention, reducing disparities, and proactive care for complex patients. Key requisites for success include data sharing and analytic capacity.
Similar to DLQI SCORE IN VITILIGO PATIENTS IN RE-MEDIKA HOSPITAL Cross-sectional study - Dr.Teovska (20)
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
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share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
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• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Histololgy of Female Reproductive System.pptxAyeshaZaid1
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Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
3. Vitiligo
Vitiligo is a common acquired, idiopathic and often
familiar depigmentation disorder that affects both
sexes equally worldwide.
Although not painful or life-threatening, this
disfiguring disorder can have a devastating effect
on a patient‟s psychosocial wellbeing and social
life
4. Patients often experience stigmatization, including
curiosity, by other people, rejection and discrimination
at work, low self-esteem, embarrassment, impaired
quality of life and a higher prevalence of sexual
difficulties, especially in women .
Stigmatization is the most influential factor in the
variance of Dermatology Life Quality Index (DLQI)
measurements.
5. Doctor/patients relationship
Additionally, many healthcare professionals still
regard vitiligo as a harmless cosmetic skin
problem, truly underestimating the importance of
treating these patients.
The emotional aspect of diseases vitiligo is gravely
underestimated because clinicians fail to include
the psychological and sociological components
that are so closely tied to this disease
6. Quality of life-QL
Definition
Quality of Life as individuals perception of their
position in life in the context of the culture and
value systems in which they live and in relation to
their goals, expectations, standards and concerns.
It is a broad ranging concept affected in a complex
way by the person's physical health, psychological
state, level of independence, social relationships,
personal beliefs and their relationship to salient
features of their environment.
7. Quality of life at dermatology
patients
• Dermatology-specific Quality of Life instruments
• Skindex
• DLQI
• Dermatology Quality of Life Scales
• Chronic Skin Disease on Daily Life).
8. DLQI Dermatology Life
Quality Index
DLQI Dermatology Life Quality Index
• First
• The most used questionnaire
• Simple questionnaire self administrated who used
to measure the health-related quality of life of
adult patients suffering from a skin disease.
9. DLQI
(Dermatology Life Quality Index)
• It is a simple 10-question validated questionnaire
which has been used in 33 different skin
conditions in 32 countries and is available in 55
languages.
• Its use has been described in over 500
publications including 30 multinational studies.
10. DLQi scores for vitiligo patients
-review the literature worldwide
-Porter et al. studied the effect of vitiligo on sexual
relationships and found that embarrassment during
sexual relationships was especially frequent for men
with vitiligo
-Salzer and Schallreuter reported that 75% found their
disfigurement moderately or severely intolerable
-Weiss et al compared the difficulties faced by patients
with vitiligo with those with leprosy in India
-Al-Abadie et al. indicated that psychological stress
increases levels of neuroendocrine hormones, affects
the immune system and alters the level of
neuropeptides, which may be the initial steps in
pathogenesis of vitiligo
11. DLQi scores for vitiligo patients
-review the literature worldwide
Sampogna, Patients older than 40 years old, have lower
QoL. Patients with vitiligo reported a higher prevalence
of both alexithymia (a state of deficiency in
understanding, processing, or describing emotions) and
depression or anxiety than the general population.
In white populations, the prevalence's of depression and
alexithymia are both estimated as approximately 10%,
while in this study the prevalence was 39%, and of
patients with alexithymia 24%
12. DLQi scores for vitiligo patients
-review the literature worldwide
Papadopoulos et All.have shown that psychological
counseling not only helps to improve body image,
self-esteem and quality of life of patients with
vitiligo, but also provides better control of disease.
Ongenae K, Quality of life in female patients has
shown to be more impaired than men and was
equal to the impairment caused by psoriasis.
14. Motivation
• Knowledge: What is the knowledge of health
information regarding his/her dermatology
illness.
• Attitude: What is the attitude of the patient
regarding his dermatology condition?
• Behaviors: What exactly the patient is doing
regarding his dermatology condition?
• Group behaviors: What is the group behavior
in accepting of patient with dermatology
illness?
• Behavior of health system: What the health
system is doing to change to change this
15. Aim of the study
• To determine score od DLQI in patients with
vitiligo in ReMedika general hospital, Skopje,
R.Macedonia.
• To determine the dominate factors that affects on
quality of life
• From the conclusion of this study to get the
information's in order to start with interventions for
improving and strength the quality of life in
patients with vitiligo
16. Materials and Methods
• Study design: prospective research-(cross
section) study for every new patient with vitiligo
attending the clinic. Using a standard “forward-
backward” translation procedure, the English
language version of the questionnaire was
translated into Macedonian.
• Place of study: Dermatology department,
ReMedika general hospital. Skopje, Macedonia
17. DLQI questionnaire
(Cardiff University's )
1. Questions about basic demographics characters
2. Symptoms and feelings (questions 1 and 2),
3. Daily activities (questions 3 and 4),
4. Leisure (questions 5 and 6),
5. Personal relationships (questions 8 and 9)
6. Work and school (question 7),
7. and treatment (question10) .
18. DLQI questionnaire
(Cardiff University's )
• The DLQI is calculated by summing the score of
each question resulting in a maximum of 30 and
a minimum of 0.
• The higher the score, the more quality of life is
impaired.
• The DLQI can also be expressed as a
percentage of the maximum possible score of 30.
19. Materials and Methods
There were no restrictions on patient selection with
regard to extension of lesions.
The patients were introduced to the subject of this
study and informed about the personal nature of
the questionnaire, and all those who gave consent
were given the DLQI questionnaire to complete.
20. Selection of patients
Criteria for participation
All the patients who are coming in dermatology
department
Criteria for elimination
Children, babies.
Patients with other dermatology condition.
Defined time
May-2011 to May 2012
21. Statistical analyses
Responses on the DLQI will be scored according to
the guidelines of Finlay and Khan.
All statistical analyses is carried out using the
Statistical Package for the Social Sciences (SPSS
11.0 for Windows).
To test the reliability, the internal consistency of the
questionnaire will be assessed by Cronbach's α
coefficient and α equal to or greater than 0.70 was
considered satisfactory.
22. Bias in Research Study
• Selection bias
-Only patients from Re-Medika hospital
dermatology department is involved in this study
• Bias from nonresponse -refusing from patients
• Reporting bias-lack of information regarding their
condition
24. Results
From May –October 2011
• Age of patients
25 - 85 (middle age 53). Most of them (49, 49%)
were 45-65 years old.
Place of living:
½ of the patients (53, 53%) are from Skopje.
25. Demographics characteristics of patients
Parameters Number %
Gender 50 %
Male 16 32%
Female 34 68%
Age
25-34 11 22%
35-44 2 4%
45-54 15 30%
55-64 12 24%
65-74 10 20%
Над 75 1 2%
Place of living
Skopje 35 70,00%
Out side Skopje 15 30,00%
26. Distribution of patients regarding
the age
16 15
14
12 25-34
12 11
10 35-44
10
45-54
8
55-64
6
65-74
4
2 Над 75
2 1
0
27. Comparison of mean DLQI scores
and demographic variables
Sex Mean DLQI
Male 7,50
Female 9,53
Marital status
Single 8,23
Maried 7,25
Place of living
Skopje 9,25
Out side from Skopje 7,38
28. Comparison of mean DLQI scores
and demographic variables
Educational level DLQI
Illiterate 8,00
Under graduate 8,20
Graduate 8,38
Bachelor degree 9,56
Doctorate 7,00
Visibility of lesion
Exposed 9,45
Unexposed 8,23
29. As a conclusion
The chronic nature of disease, long term
treatment, lack of uniform effective therapy and
unpredictable prognosis of disease/therapy make
the patients suffer more from the disease.
30. DLQI score in vitiligo patients
Questions Parameters Mean DLQI
1. Symptoms 1,16
2 Feelings 2,22
3 Daily activities 1,56
4 Kind of clothes 2,22
5 Social or leisure activities 2,16
6 Physical exercise 2,11
7 Educational activities 2,02
8 Interpersonal relationships 2,88
9 Sexual activities 1,06
10 Treatment 1,86
31. Why is important in Macedonia?
• Pilot project first one in Macedonia
• At the end of this study we will give the answer of
influence of demographics characteristics of
patients in Macedonia regarding the quality of life
Review from literature is showing that DLQI not
only can measure the quality of life but can also
be used as a instrument of measuring the quality
of doctors working.
32. Conclusions
Our study quantifies the burden on the quality of life
caused by vitiligo and indicates specific areas of
patients' lives which are most affected by the disease..
These results should awake the
interest of physicians in this „cosmetic‟ disease, since
appropriate treatment is likely to improve the quality of
life of vitiligo patients.
33. Suggestions activities
Holistic approaching is not only treatment of illness
of the patients but it is treatment of a patient as
human been and not only threatening illness.
So thinking about the DLQI at patient with
dermatology illness is thinking about the factors
who determinate the quality of life which are
individual and changeable.
DLQI can help in identifying the dominant needs and
searching of the patients the solution for those.
.
34. Conclusion
With more effective treatment options and a closer
patient/ physician relationship, patients can
improve their quality of life and overall well-being.
Before beginning on a specific treatment course,
both patient and healthcare provider should be
aware of patient's current QoL and monitor it
closely throughout the course of a treatment
regimen.
35. Conclusion
• Doctor must give the right and adequate
information and education regarding the condition
of the patient
• On this way educated patient will have more
control of his disease and he will accept emotional
more his condition.
• So with this DLQI will became a part of every
clinical examinations of the patients, and with this
we will increase the relationships between doctors
and patient.