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1.
Niger J Clin Pract ; 23(9): 1295-1304, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32913171

ABSTRACT

AIMS: The present study aimed to evaluate the incidence of LBP and related factors in over 18-year-olds. MATERIALS AND METHODS: This research was a cross-sectional study involving individuals over 18 years of age with any complaints in the period from May 2015-June 2016 at different hospitals. The research data were evaluated by the SPSS 15.0 statistical package program. Descriptive statistics were presented as mean (±) standard deviation, median (min, max), frequency distribution, and percentage. Pearson's Chi-square test, Yates corrected Chi-square test, and Fisher's test were used as statistical methods. Statistical significance was accepted as P < 0.05. RESULTS: A total of 5,989 people admitted during that period and 50% unknown frequency were taken to reach 1715 subject persons with 2% deviation and 95% confidence interval which reached 1720. The sociodemographic status, occupational conditions, the frequency of low back pain, and risk factors have been evaluated. Around 92.9% of individuals of 65 years of age and older have lifelong LPB while 57.1% have present LBP. The difference was statistically significant for "the satisfaction of working people" and "individuals working more than 41 h a week." (P < 0.001). CONCLUSION: Low back pain is still a serious problem that can be avoided by ensuring optimal working conditions and a healthier life.


Subject(s)
Low Back Pain/diagnosis , Low Back Pain/psychology , Occupational Diseases/epidemiology , Occupational Exposure/adverse effects , Quality of Life , Adolescent , Adult , Age Distribution , Aged , Cross-Sectional Studies , Female , Humans , Low Back Pain/epidemiology , Low Back Pain/etiology , Magnetic Resonance Imaging/methods , Male , Middle Aged , Occupational Diseases/etiology , Occupational Exposure/prevention & control , Occupational Exposure/statistics & numerical data , Personal Satisfaction , Prevalence , Risk Factors , Sex Distribution , Sickness Impact Profile , Socioeconomic Factors , Turkey/epidemiology
2.
Public Health ; 172: 146-152, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31235210

ABSTRACT

OBJECTIVES: Turkey is a principal destination and transit country for refugees from diverse countries. Turkey currently hosts Syrian refugees and provides free access to shelter, education and health care. The aim of this study is to determine the health needs and document the healthcare services available to Syrian refugees in Turkey. STUDY DESIGN: Literature review. METHODS: An examination of the scientific literature, reports and government policies about refugees in Turkey was performed. In addition, literature focussing on the understanding and development of the healthcare needs and systems in crisis situations in Turkey was analysed. RESULTS: The Turkish government has made several regulations for Syrian refugees, which allow them to benefit from emergency care units and primary, secondary and tertiary healthcare centres in Turkey's 81 provinces free of charge; the financial costs of these benefits are covered by the Disaster and Emergency Management Authority. Effectiveness of healthcare services for refugees is limited by language barriers, mobility of the refugees and some legal restrictions. Mental health and rehabilitation services are relatively weak because of the inadequate number of qualified practitioners. CONCLUSIONS: The current migration rules in Turkey do not enable refugees to access all human rights. Because the number of refugees has increased, there has been a subsequent increase in the financial and human resources needed for healthcare services. Multidynamic refugee-friendly systems, the provision of preventive health care (including primary and secondary prevention opportunities) and increasing the number of national and international organisations may help improve the health of refugees.


Subject(s)
Health Services Accessibility , Health Services Needs and Demand , Refugees , Humans , Syria/ethnology , Turkey
3.
Arch Gynecol Obstet ; 279(4): 505-9, 2009 Apr.
Article in English | MEDLINE | ID: mdl-18690468

ABSTRACT

OBJECTIVE: To evaluate the net effect of raloxifene on overall quality of life and sexual function in postmenopausal women. METHODS: The study was performed in the Gynecology and Obstetrics outpatient clinic of Gazi University Faculty of Medicine between January 2002 and February 2005. Fifty postmenopausal women, in whom raloxifene was indicated for prevention and treatment of osteoporosis, were considered the study group. Fifty postmenopausal women who were not osteoporotic were enrolled as the control group. Participants completed a questionnaire composed of several parts (GRISS, BDI and ISI), at the beginning and end of the 12-month treatment period. RESULTS: Two groups were similar to each other with respect to total GRISS scores at the beginning and at the end of the study (P=0.929 and P=0.508; respectively). Raloxifene was associated with a significant improvement from baseline in the total scores of BDI (P=0.0001), whereas this improvement was not significantly different from the control group (P=0.216). With regard to ISI scores, there were no differences between groups in total scores. Raloxifene use did not seem to affect subscores of ISI either. CONCLUSIONS: This study failed to prove any deleterious effect of raloxifene on quality of life and sexual functions.


Subject(s)
Bone Density Conservation Agents/pharmacology , Quality of Life , Raloxifene Hydrochloride/pharmacology , Selective Estrogen Receptor Modulators/pharmacology , Sexual Behavior/drug effects , Aged , Bone Density Conservation Agents/therapeutic use , Female , Humans , Middle Aged , Osteoporosis, Postmenopausal/drug therapy , Postmenopause , Raloxifene Hydrochloride/therapeutic use , Selective Estrogen Receptor Modulators/therapeutic use , Surveys and Questionnaires
4.
Child Care Health Dev ; 34(4): 475-81, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18485025

ABSTRACT

BACKGROUND: The aim of the present study was to determine the patterns of toilet training and the factors that may be related to its timing and duration and the approaches of different sociocultural groups within a developing country. METHODS: This cross-sectional survey was performed on 745 children who live in three different sociocultural settlements. The factors that might have affected initiation and completion age and duration of toilet training were assessed with t-test, ANOVA and logistic regression analysis. RESULTS: Mean initiation and completion ages were 22.05 +/- 6.73, 28.05 +/- 8.40 months respectively. The families living in rural and semi-urban settlements, mothers educated for less than 5 years, unoccupied mothers, children living in houses which do not have a toilet inside, families who use washable diapers, who use Turkish style toilets and who use punishment methods started training earlier. In the infants whose mothers had an education over 12 years, completion age was later than others and the earliest completion age was seen in families who used punishment method. Mean duration needed to complete toilet training was 6.84 +/- 7.16 months. The duration of training was longer in families living in rural and semi-urban settlements, mothers educated for less than 5 years, unoccupied mothers, children living in houses which do not have a toilet inside, families who use washable diapers and when the initiation was before the child was 18 months old. CONCLUSION: Toilet training shows differences among cultures. The age of initiation may be increased as the parents are educated better and a child-orientated approach becomes more popular than the parent-orientated approach.


Subject(s)
Child Development/physiology , Mothers/psychology , Toilet Training , Age Factors , Child Behavior , Child, Preschool , Cross-Cultural Comparison , Diapers, Infant/statistics & numerical data , Epidemiologic Methods , Female , Humans , Infant , Infant Behavior , Male , Rural Health , Socioeconomic Factors , Time Factors , Turkey , Urban Health
5.
Cell Biol Int ; 31(3): 289-92, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17175181

ABSTRACT

As raloxifene is a mixed estrogen receptor agonist and antagonist, it exerts different effects on apoptosis in different tissues. In this study, we aimed to evaluate apoptosis in the peripheral lymphocytes of postmenopausal women treated with raloxifene and compare it with untreated control subjects. In this way, we expected to deduce some results about the effect of raloxifene on the immune system and to serve as a guide for future studies on this newly proposed effect of a well-known agent. Twenty osteoporotic postmenopausal women treated with raloxifene for 12 months were included in this study. Another 20 osteoporotic postmenopausal women matched for age and postmenopausal years, but without any medication, were chosen as the control group. Apoptosis was evaluated using a morphological and DNA fragmentation assay, in the peripheral lymphocytes of these women. Our results revealed a decrease in the apoptosis percentages of the patients treated with raloxifene (14.6%) with respect to the control subjects (15.8%), but the difference was not statistically significant (p=0.467). This study indicated that raloxifene treatment had no apoptotic effect on peripheral human lymphocytes compared to controls.


Subject(s)
Apoptosis/drug effects , Lymphocytes/drug effects , Osteoporosis, Postmenopausal/drug therapy , Raloxifene Hydrochloride/administration & dosage , Selective Estrogen Receptor Modulators/administration & dosage , Aged , Apoptosis/immunology , Female , Humans , Lymphocytes/immunology , Middle Aged , Treatment Outcome
6.
Folia Microbiol (Praha) ; 50(3): 263-7, 2005.
Article in English | MEDLINE | ID: mdl-16295666

ABSTRACT

The relationship between inflammatory bowel disease and microorganisms was evaluated. The presence of Candida albicans-specific IgM and IgG antibodies in serum samples and the presence of C. albicans in stool and colonal mucosa samples of the patients did not exhibit any significant difference between 21 patients in active stage and 15 patients in remission of ulcerative colitis (UC) (compared with 19 control patients). The invasion of yeast cells to the colonal mucosa was demonstrated by detecting C. albicans DNA using specific PCon1, PCon2, and PspA2 primers in PCR assay. Eighteen of 36 patients (50%) were found to be DNA positive while in 19 controls only 4 (21%) were found to be positive. The presence of DNA in the association of the positive serological reactivity is suggested as an important diagnostic marker of UC.


Subject(s)
Candida albicans/isolation & purification , Colitis, Ulcerative/microbiology , Antibodies, Fungal/blood , Base Sequence , Candida albicans/genetics , Candida albicans/immunology , Candida albicans/pathogenicity , Case-Control Studies , Colitis, Ulcerative/etiology , Colitis, Ulcerative/immunology , Colitis, Ulcerative/pathology , DNA, Fungal/analysis , DNA, Fungal/genetics , Feces/microbiology , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Intestinal Mucosa/microbiology , Models, Biological , Polymerase Chain Reaction
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