Pub Date : 2014-12-14eCollection Date: 2014-01-01DOI: 10.4137/CMWH.S19182
Maria Co Lordello, Carolina C Ambrogini, Ana L Fanganiello, Teresa R Embiruçu, Marina M Zaneti, Laise Veloso, Livia B Piccirillo, Bianca L Crude, Mauro Haidar, Ivaldo Silva
Introduction: Self-esteem and self-image are psychological aspects that affect sexual function.
Aims: To validate a new measurement tool that correlates the concepts of self-esteem, self-image, and sexuality.
Methods: A 20-question test (the self-esteem/self-image female sexuality [SESIFS] questionnaire) was created and tested on 208 women. Participants answered: Rosenberg's self-esteem scale, the female sexual quotient (FSQ), and the SESIFS questionnaire. Pearson's correlation coefficient was used to test concurrent validity of the SESIFS against Rosenberg's self-esteem scale and the FSQ. Reliability was tested using the Cronbach's alpha coefficient.
Result: The new questionnaire had a good overall reliability (Cronbach's alpha r = 0.862, p < 0.001), but the sexual domain scored lower than expected (r = 0.65). The validity was good: overall score r = 0.38, p < 0.001, self-esteem domain r = 0.32, p < 0.001, self-image domain r = 0.31, p < 0.001, sexual domain r = 0.29, p < 0.001.
Conclusions: The SESIFS questionnaire has limitations in measuring the correlation among self-esteem, self-image, and sexuality domains. A new, revised version is being tested and will be presented in an upcoming publication.
自尊和自我形象是影响性功能的心理方面。目的:验证一种新的测量工具,它将自尊、自我形象和性的概念联系起来。方法:采用自尊/自我形象女性性行为问卷(SESIFS)对208名女性进行问卷调查。参与者回答:罗森博格自尊量表、女性性商(FSQ)和SESIFS问卷。采用Pearson相关系数检验SESIFS与Rosenberg自尊量表和FSQ的并发效度。采用Cronbach’s alpha系数检验信度。结果:新问卷总体信度较好(Cronbach’s alpha r = 0.862, p < 0.001),但性别领域得分低于预期(r = 0.65)。效度较好:总分r = 0.38, p < 0.001,自尊领域r = 0.32, p < 0.001,自我形象领域r = 0.31, p < 0.001,性领域r = 0.29, p < 0.001。结论:SESIFS问卷在测量自尊、自我形象和性取向之间的相关性方面存在局限性。一个新的修订版本正在测试中,并将在即将出版的出版物中提出。
{"title":"Creation and Validation of the Self-esteem/Self-image Female Sexuality (SESIFS) Questionnaire.","authors":"Maria Co Lordello, Carolina C Ambrogini, Ana L Fanganiello, Teresa R Embiruçu, Marina M Zaneti, Laise Veloso, Livia B Piccirillo, Bianca L Crude, Mauro Haidar, Ivaldo Silva","doi":"10.4137/CMWH.S19182","DOIUrl":"https://doi.org/10.4137/CMWH.S19182","url":null,"abstract":"<p><strong>Introduction: </strong>Self-esteem and self-image are psychological aspects that affect sexual function.</p><p><strong>Aims: </strong>To validate a new measurement tool that correlates the concepts of self-esteem, self-image, and sexuality.</p><p><strong>Methods: </strong>A 20-question test (the self-esteem/self-image female sexuality [SESIFS] questionnaire) was created and tested on 208 women. Participants answered: Rosenberg's self-esteem scale, the female sexual quotient (FSQ), and the SESIFS questionnaire. Pearson's correlation coefficient was used to test concurrent validity of the SESIFS against Rosenberg's self-esteem scale and the FSQ. Reliability was tested using the Cronbach's alpha coefficient.</p><p><strong>Result: </strong>The new questionnaire had a good overall reliability (Cronbach's alpha r = 0.862, p < 0.001), but the sexual domain scored lower than expected (r = 0.65). The validity was good: overall score r = 0.38, p < 0.001, self-esteem domain r = 0.32, p < 0.001, self-image domain r = 0.31, p < 0.001, sexual domain r = 0.29, p < 0.001.</p><p><strong>Conclusions: </strong>The SESIFS questionnaire has limitations in measuring the correlation among self-esteem, self-image, and sexuality domains. A new, revised version is being tested and will be presented in an upcoming publication.</p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"7 ","pages":"37-43"},"PeriodicalIF":0.0,"publicationDate":"2014-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/CMWH.S19182","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32964838","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-07-24eCollection Date: 2014-01-01DOI: 10.4137/CMWH.S11071
Sarah Bandali
The global fight against HIV is progressing; however, women living in rural areas particularly in sub-Saharan Africa (SSA) continue to face the devastating consequences of HIV and AIDS. Lack of knowledge and geographical barriers to HIV services are compounded by gender norms often limiting the negotiation of safe sexual practices among women living in rural areas. This paper discusses findings from a qualitative study conducted in rural areas of Mozambique examining factors that influenced women to engage in HIV risk-reduction practices. The findings from this study led to the emergence of an HIV and AIDS risk assessment and reduction (HARAR) model, which is described in detail. The model helps in understanding gender-related factors influencing men and women to engage in risk-reduction practices, which can be used as a framework in other settings to design more nuanced and contextual policies and programs.
{"title":"Women Living with HIV in Rural Areas. Implementing a Response using the HIV and AIDS Risk Assessment and Reduction Model.","authors":"Sarah Bandali","doi":"10.4137/CMWH.S11071","DOIUrl":"10.4137/CMWH.S11071","url":null,"abstract":"<p><p>The global fight against HIV is progressing; however, women living in rural areas particularly in sub-Saharan Africa (SSA) continue to face the devastating consequences of HIV and AIDS. Lack of knowledge and geographical barriers to HIV services are compounded by gender norms often limiting the negotiation of safe sexual practices among women living in rural areas. This paper discusses findings from a qualitative study conducted in rural areas of Mozambique examining factors that influenced women to engage in HIV risk-reduction practices. The findings from this study led to the emergence of an HIV and AIDS risk assessment and reduction (HARAR) model, which is described in detail. The model helps in understanding gender-related factors influencing men and women to engage in risk-reduction practices, which can be used as a framework in other settings to design more nuanced and contextual policies and programs. </p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"7 ","pages":"25-35"},"PeriodicalIF":0.0,"publicationDate":"2014-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116384/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32557203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-06-16eCollection Date: 2014-01-01DOI: 10.4137/CMWH.S13955
Mara Z Vitolins, Brandy-Joe Milliron, Judith O Hopkins, Artie Fulmer, Julia Lawrence, Susan Melin, Douglas Case
Numerous studies have found that increased body size (weight or body mass index) is a risk factor for breast cancer development, recurrence, and death. The detrimental relationship between body size and breast cancer recurrence may be more pronounced among women with estrogen receptor (ER)/progesterone receptor (PR)-negative breast cancer. Considering the limited availability of treatments, and the association between body size and recurrence, alternative treatments are needed for ER/PR-negative breast cancer survivors, particularly overweight survivors. The objective of this pilot study was to examine the feasibility of a 12-week, multi-component meal-replacement weight loss intervention among overweight or obese ER/PR-negative breast cancer survivors; and to obtain preliminary data on changes in anthropometrics, biomarkers, and health-related quality of life (QOL). The 12-week intervention included a portion-controlled diet (including meal replacements) and a multi-component intervention (including behavioral techniques, diet modification, physical activity, and social support). The goal of the intervention was to help participants lose 5% or more of their initial weight by reducing their caloric intake and increasing their physical activity (to at least 15 minutes each day). Paired t-tests assessed changes in continuous measures. Body weight was measured weekly and mixed-model regression analysis assessed change in weight over time. Nineteen ER/PR-negative breast cancer survivors with a mean age of 59 years participated in the study. All but two of the participants completed the 12-week intervention. Women lost an average of 6.3 ± 4.9 kg (P < 0.001), equivalent to 7.5% of their baseline weight. There were significant reductions in waist circumference (P = 0.001), percent fat mass (P < 0.001), total cholesterol (P = 0.026), and triglycerides (P = 0.002); and improvements in health-related QOL (P = 0.017). Findings suggested that a meal-replacement weight loss approach among ER/PR-negative breast cancer survivors was feasible and was well received.
{"title":"Weight Loss Intervention in Survivors of ER/PR-negative Breast Cancer.","authors":"Mara Z Vitolins, Brandy-Joe Milliron, Judith O Hopkins, Artie Fulmer, Julia Lawrence, Susan Melin, Douglas Case","doi":"10.4137/CMWH.S13955","DOIUrl":"https://doi.org/10.4137/CMWH.S13955","url":null,"abstract":"<p><p>Numerous studies have found that increased body size (weight or body mass index) is a risk factor for breast cancer development, recurrence, and death. The detrimental relationship between body size and breast cancer recurrence may be more pronounced among women with estrogen receptor (ER)/progesterone receptor (PR)-negative breast cancer. Considering the limited availability of treatments, and the association between body size and recurrence, alternative treatments are needed for ER/PR-negative breast cancer survivors, particularly overweight survivors. The objective of this pilot study was to examine the feasibility of a 12-week, multi-component meal-replacement weight loss intervention among overweight or obese ER/PR-negative breast cancer survivors; and to obtain preliminary data on changes in anthropometrics, biomarkers, and health-related quality of life (QOL). The 12-week intervention included a portion-controlled diet (including meal replacements) and a multi-component intervention (including behavioral techniques, diet modification, physical activity, and social support). The goal of the intervention was to help participants lose 5% or more of their initial weight by reducing their caloric intake and increasing their physical activity (to at least 15 minutes each day). Paired t-tests assessed changes in continuous measures. Body weight was measured weekly and mixed-model regression analysis assessed change in weight over time. Nineteen ER/PR-negative breast cancer survivors with a mean age of 59 years participated in the study. All but two of the participants completed the 12-week intervention. Women lost an average of 6.3 ± 4.9 kg (P < 0.001), equivalent to 7.5% of their baseline weight. There were significant reductions in waist circumference (P = 0.001), percent fat mass (P < 0.001), total cholesterol (P = 0.026), and triglycerides (P = 0.002); and improvements in health-related QOL (P = 0.017). Findings suggested that a meal-replacement weight loss approach among ER/PR-negative breast cancer survivors was feasible and was well received. </p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"7 ","pages":"17-24"},"PeriodicalIF":0.0,"publicationDate":"2014-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/CMWH.S13955","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32474349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-05-01eCollection Date: 2014-01-01DOI: 10.4137/CMWH.S13535
Mark Maher, Remon Keriakos
Objective: The aim of this study is to assess women's awareness of the benefit and use of folic acid during pregnancy and to assess whether their knowledge has improved following hospital visits.
Method: This is a prospective survey conducted in a large teaching hospital in the UK. The survey questionnaire consisted of 28 questions about demographic variables, behavioral variables, and knowledge about folic acid and neural tube defects (NTDs).
Result: A total of 603 women participated in this study. Some of them attended for the first time and others had more than one visit, either in their current or previous pregnancies. In about 25% of cases, the pregnancy was not planned. Between 14 and 19% of the women of First and Two+ Visit groups consulted their doctor or other healthcare professional before conception. Nearly 98% of the women stated that they had heard of folic acid, but only 42-52% knew the medical condition it protects against. The main sources of information for women who were aware of folic acid were midwives and general practitioners. Nearly 90% of women who attended their first antenatal visit were taking folic acid. However, only 40% of women knew that they should take it before pregnancy, and only between 36 and 46% knew the dietary sources of folic acid, although about 84% know the foods that should be avoided during pregnancy. This study found that attending antenatal clinic has not increased women's awareness about folic acid.
Conclusion: There is still a high proportion of women who do not know that folic acid should be taken before pregnancy and continued for the first three months of pregnancy. School education, primary care team, and family planning service should take the lead in providing information to women about folic acid.
{"title":"Women's Awareness of Periconceptional Use of Folic Acid Before and After Their Antenatal Visits.","authors":"Mark Maher, Remon Keriakos","doi":"10.4137/CMWH.S13535","DOIUrl":"10.4137/CMWH.S13535","url":null,"abstract":"<p><strong>Objective: </strong>The aim of this study is to assess women's awareness of the benefit and use of folic acid during pregnancy and to assess whether their knowledge has improved following hospital visits.</p><p><strong>Method: </strong>This is a prospective survey conducted in a large teaching hospital in the UK. The survey questionnaire consisted of 28 questions about demographic variables, behavioral variables, and knowledge about folic acid and neural tube defects (NTDs).</p><p><strong>Result: </strong>A total of 603 women participated in this study. Some of them attended for the first time and others had more than one visit, either in their current or previous pregnancies. In about 25% of cases, the pregnancy was not planned. Between 14 and 19% of the women of First and Two+ Visit groups consulted their doctor or other healthcare professional before conception. Nearly 98% of the women stated that they had heard of folic acid, but only 42-52% knew the medical condition it protects against. The main sources of information for women who were aware of folic acid were midwives and general practitioners. Nearly 90% of women who attended their first antenatal visit were taking folic acid. However, only 40% of women knew that they should take it before pregnancy, and only between 36 and 46% knew the dietary sources of folic acid, although about 84% know the foods that should be avoided during pregnancy. This study found that attending antenatal clinic has not increased women's awareness about folic acid.</p><p><strong>Conclusion: </strong>There is still a high proportion of women who do not know that folic acid should be taken before pregnancy and continued for the first three months of pregnancy. School education, primary care team, and family planning service should take the lead in providing information to women about folic acid.</p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"7 ","pages":"9-15"},"PeriodicalIF":0.0,"publicationDate":"2014-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4011717/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32332239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2014-02-13eCollection Date: 2014-01-01DOI: 10.4137/CMWH.S10353
Christopher McConville, Peter Boyd, Ian Major
Human Immunodeficiency Virus (HIV) is a retrovirus that can result in rare opportunistic infections occurring in humans. The onset of these infections is known as Acquired Immune Deficiency Syndrome (AIDS). Sexual transmission is responsible for the majority of infections 1, resulting in transmission of HIV due to infected semen or vaginal and cervical secretions containing infected lymphocytes. HIV microbicides are formulations of chemical or biological agents that can be applied to the vagina or rectum with the intention of reducing the acquisition of HIV. Tenofovir is an NRTI that is phosphorylated by adenylate kinase to tenofovir diphosphate, which in turn competes with deoxyadeosine 5'-triphosphate for incorporation into newly synthesized HIV DNA. Once incorporated, tenofovir diphosphate results in chain termination, thus inhibiting viral replication. Tenofovir has been formulated into a range of vaginal formulations, such as rings, tablets gels and films. It has been shown to safe and effective in numerous animal models, while demonstrating safety and acceptability in numerous human trials. The most encouraging results came from the CAPRISA 004 clinical trial which demonstrated that a 1% Tenofovir vaginal gel reduced HIV infection by approximately 39%.
{"title":"Efficacy of Tenofovir 1% Vaginal Gel in Reducing the Risk of HIV-1 and HSV-2 Infection.","authors":"Christopher McConville, Peter Boyd, Ian Major","doi":"10.4137/CMWH.S10353","DOIUrl":"https://doi.org/10.4137/CMWH.S10353","url":null,"abstract":"<p><p>Human Immunodeficiency Virus (HIV) is a retrovirus that can result in rare opportunistic infections occurring in humans. The onset of these infections is known as Acquired Immune Deficiency Syndrome (AIDS). Sexual transmission is responsible for the majority of infections 1, resulting in transmission of HIV due to infected semen or vaginal and cervical secretions containing infected lymphocytes. HIV microbicides are formulations of chemical or biological agents that can be applied to the vagina or rectum with the intention of reducing the acquisition of HIV. Tenofovir is an NRTI that is phosphorylated by adenylate kinase to tenofovir diphosphate, which in turn competes with deoxyadeosine 5'-triphosphate for incorporation into newly synthesized HIV DNA. Once incorporated, tenofovir diphosphate results in chain termination, thus inhibiting viral replication. Tenofovir has been formulated into a range of vaginal formulations, such as rings, tablets gels and films. It has been shown to safe and effective in numerous animal models, while demonstrating safety and acceptability in numerous human trials. The most encouraging results came from the CAPRISA 004 clinical trial which demonstrated that a 1% Tenofovir vaginal gel reduced HIV infection by approximately 39%. </p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"7 ","pages":"1-8"},"PeriodicalIF":0.0,"publicationDate":"2014-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/CMWH.S10353","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32271057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2013-11-25eCollection Date: 2013-01-01DOI: 10.4137/CMWH.S8213
Hiroki Hamada, Kei Shimoda, Masaharu Seno
Taxol is recognized as one of the most potent anticancer agents used in the treatment of breast and ovarian cancers, which are common cancers in women. To overcome its shortcomings, that is, its low water-solubility that reduces drug loading capacity of DDS carriers when incorporating taxol, chemo-enzymatic synthesis of ester-linked taxol-glucose conjugate, i.e., 7-propionyltaxol 2″-O-α-D-glucoside, as a water soluble taxol prodrug was achieved by using a-glucosidase as a glucosylation catalyst. The water-solubility of 7-propionyltaxol 2″-O-α-D-glucoside (25 mM) was 63 fold higher than that of taxol (0.4 mM). The pre-S1 peptide which displays on the surface of bio-nanocapsules, which are nanoparticles composed of the hepatitis B virus surface antigen, was replaced with the antibody affinity motif of protein A. Conjugation of such bio-nanocapsules with anti-human epidermal growth factor receptor antibody gave hybrid bio-nanocapsules. The hybrid bio-nanocapsules were effective for delivering 7-propionyltaxol 2″-O-α-D-glucoside to human brain glioma cells. 7-Propionyltaxol 2″-O-α-D-glucoside was effectively hydrolyzed to give taxol in 95% by human glioma cells. The drug loading capacity of hybrid bio-nanocapsules incorporating 7-propionyltaxol 2″-O-α-D-glucoside was 120 times higher than that incorporating taxol itself.
紫杉醇被认为是最有效的抗癌药物之一,用于治疗乳腺癌和卵巢癌,这是女性常见的癌症。为克服其水溶性低,掺入紫杉醇时降低DDS载体载药量的缺点,以a-葡萄糖苷酶为糖基化催化剂,化学酶法合成了7-丙基紫杉醇-葡萄糖缀合物7-丙基紫杉醇2″-O-α- d -葡萄糖苷作为水溶性紫杉醇前药。7-丙基紫杉醇2″-O-α- d -葡萄糖苷(25 mM)的水溶性比紫杉醇(0.4 mM)高63倍。将乙型肝炎病毒表面抗原组成的生物纳米胶囊表面显示的前s1肽替换为a蛋白的抗体亲和基序,将这种生物纳米胶囊与抗人表皮生长因子受体抗体偶联得到杂交生物纳米胶囊。混合生物纳米胶囊可有效地将7-丙基紫杉醇2″-O-α- d -糖苷输送到人脑胶质瘤细胞。7-丙基紫杉醇2″-O-α- d -葡萄糖苷被人胶质瘤细胞有效水解为95%的紫杉醇。掺入7-丙基紫杉醇2″-O-α- d -葡萄糖苷的杂化生物纳米胶囊的载药量比掺入紫杉醇的高120倍。
{"title":"Chemo-enzymatic Synthesis of Propionyl-ester-linked Taxol-monosaccharide Conjugate and its Drug Delivery System Using Hybrid-Bio-nanocapsules Targeting Brain Glioma Cells.","authors":"Hiroki Hamada, Kei Shimoda, Masaharu Seno","doi":"10.4137/CMWH.S8213","DOIUrl":"https://doi.org/10.4137/CMWH.S8213","url":null,"abstract":"<p><p>Taxol is recognized as one of the most potent anticancer agents used in the treatment of breast and ovarian cancers, which are common cancers in women. To overcome its shortcomings, that is, its low water-solubility that reduces drug loading capacity of DDS carriers when incorporating taxol, chemo-enzymatic synthesis of ester-linked taxol-glucose conjugate, i.e., 7-propionyltaxol 2″-O-α-D-glucoside, as a water soluble taxol prodrug was achieved by using a-glucosidase as a glucosylation catalyst. The water-solubility of 7-propionyltaxol 2″-O-α-D-glucoside (25 mM) was 63 fold higher than that of taxol (0.4 mM). The pre-S1 peptide which displays on the surface of bio-nanocapsules, which are nanoparticles composed of the hepatitis B virus surface antigen, was replaced with the antibody affinity motif of protein A. Conjugation of such bio-nanocapsules with anti-human epidermal growth factor receptor antibody gave hybrid bio-nanocapsules. The hybrid bio-nanocapsules were effective for delivering 7-propionyltaxol 2″-O-α-D-glucoside to human brain glioma cells. 7-Propionyltaxol 2″-O-α-D-glucoside was effectively hydrolyzed to give taxol in 95% by human glioma cells. The drug loading capacity of hybrid bio-nanocapsules incorporating 7-propionyltaxol 2″-O-α-D-glucoside was 120 times higher than that incorporating taxol itself. </p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"6 ","pages":"71-5"},"PeriodicalIF":0.0,"publicationDate":"2013-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/CMWH.S8213","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32204862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2013-10-20eCollection Date: 2013-01-01DOI: 10.4137/CMWH.S11067
Tiffany M Bohon, Marci A Goolsby
Vitamin D is pivotal to the absorption of calcium and maximizing bone health. Women suffer great morbidity and mortality related to osteoporosis and fractures, which may be decreased by interventions such as vitamin D. In addition, extraskeletal benefits of vitamin D have been postulated including positive effects on cancer. Both the classical and nonclassical functions of vitamin D will be discussed here, with a focus on women.
{"title":"The Role of Vitamin D Supplements in Women's Health.","authors":"Tiffany M Bohon, Marci A Goolsby","doi":"10.4137/CMWH.S11067","DOIUrl":"https://doi.org/10.4137/CMWH.S11067","url":null,"abstract":"<p><p>Vitamin D is pivotal to the absorption of calcium and maximizing bone health. Women suffer great morbidity and mortality related to osteoporosis and fractures, which may be decreased by interventions such as vitamin D. In addition, extraskeletal benefits of vitamin D have been postulated including positive effects on cancer. Both the classical and nonclassical functions of vitamin D will be discussed here, with a focus on women. </p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"6 ","pages":"67-70"},"PeriodicalIF":0.0,"publicationDate":"2013-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/CMWH.S11067","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32204861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2013-09-11eCollection Date: 2013-01-01DOI: 10.4137/CMWH.S11997
Ming-Chien Chyu, Yan Zhang, Jean-Michel Brismée, Raul Y Dagda, Eugene Chaung, Vera Von Bergen, Susan Doctolero, Chwan-Li Shen
Various exercise interventions have been shown to benefit weight control and general health in different populations. However, very few studies have been conducted on martial arts exercise (MAE). The objective of this pilot study is to evaluate the efficacy of 12 weeks of MAE intervention on body composition, serum biomarkers and quality of life (QOL) in overweight/obese premenopausal women. We found that subjects in the MAE group did not lose body weight, while they significantly decreased fat-free mass and muscle mass as compared to those in the control group, who demonstrated an increase in these parameters. The MAE group demonstrated an increase in serum IGF-I concentration, but no change in others. MAE may be a feasible and effective approach to improve body composition and QOL in overweight/obese premenopausal women. Our study underscores the need for further studies using larger samples to establish possible benefits of MAE in various populations.
{"title":"Effects of martial arts exercise on body composition, serum biomarkers and quality of life in overweight/obese premenopausal women: a pilot study.","authors":"Ming-Chien Chyu, Yan Zhang, Jean-Michel Brismée, Raul Y Dagda, Eugene Chaung, Vera Von Bergen, Susan Doctolero, Chwan-Li Shen","doi":"10.4137/CMWH.S11997","DOIUrl":"https://doi.org/10.4137/CMWH.S11997","url":null,"abstract":"<p><p>Various exercise interventions have been shown to benefit weight control and general health in different populations. However, very few studies have been conducted on martial arts exercise (MAE). The objective of this pilot study is to evaluate the efficacy of 12 weeks of MAE intervention on body composition, serum biomarkers and quality of life (QOL) in overweight/obese premenopausal women. We found that subjects in the MAE group did not lose body weight, while they significantly decreased fat-free mass and muscle mass as compared to those in the control group, who demonstrated an increase in these parameters. The MAE group demonstrated an increase in serum IGF-I concentration, but no change in others. MAE may be a feasible and effective approach to improve body composition and QOL in overweight/obese premenopausal women. Our study underscores the need for further studies using larger samples to establish possible benefits of MAE in various populations. </p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"6 ","pages":"55-65"},"PeriodicalIF":0.0,"publicationDate":"2013-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4137/CMWH.S11997","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32204981","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2013-07-23eCollection Date: 2013-01-01DOI: 10.4137/CMWH.S12451
Alexandria J Hill, Thomas H Strong
Background: Bladder flaps are commonly created during routine cesarean deliveries and often require multiple steps that increase operating time and expose the surgeon to inadvertent injury.
Objective: We report a simple method of creating a bladder flap that eliminates the need for multiple instrument handoffs and repositioning.
Conclusion: The simplicity of this method allows the surgeon decreased operative entry time while decreasing exposure to injuries from multiple instrument handoffs during bladder flap development.
{"title":"A new method for creating the bladder flap.","authors":"Alexandria J Hill, Thomas H Strong","doi":"10.4137/CMWH.S12451","DOIUrl":"10.4137/CMWH.S12451","url":null,"abstract":"<p><strong>Background: </strong>Bladder flaps are commonly created during routine cesarean deliveries and often require multiple steps that increase operating time and expose the surgeon to inadvertent injury.</p><p><strong>Objective: </strong>We report a simple method of creating a bladder flap that eliminates the need for multiple instrument handoffs and repositioning.</p><p><strong>Conclusion: </strong>The simplicity of this method allows the surgeon decreased operative entry time while decreasing exposure to injuries from multiple instrument handoffs during bladder flap development.</p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"6 ","pages":"51-4"},"PeriodicalIF":0.0,"publicationDate":"2013-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941185/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32204980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2013-05-06eCollection Date: 2013-01-01DOI: 10.4137/CMWH.S8015
Sandeep Devabhakthuni
The objective of this review was to evaluate the clinical efficacy and safety of remifentanil in the management of labor pain. Although neuraxial analgesia is the best option during labor, alternative analgesic options are needed for patients with contraindications. Using a systematic literature search, clinical outcomes of remifentanil for labor pain have been summarized. Also, comparisons of remifentanil to other options including meperidine, epidural analgesia, fentanyl, and nitrous oxide are provided. Based on the literature review, remifentanil is associated with high overall maternal satisfaction and favorable side-effect profile. However, due to the low reporting of adverse events, large, randomized controlled trials are needed to evaluate maternal and neonatal safety adequately and determine the optimal dosing needed to provide effective analgesia. While remifentanil is a feasible alternative for patients who cannot or do not want to receive epidural analgesia, administration should be monitored closely for potential adverse effects.
{"title":"Efficacy and safety of remifentanil as an alternative labor analgesic.","authors":"Sandeep Devabhakthuni","doi":"10.4137/CMWH.S8015","DOIUrl":"10.4137/CMWH.S8015","url":null,"abstract":"<p><p>The objective of this review was to evaluate the clinical efficacy and safety of remifentanil in the management of labor pain. Although neuraxial analgesia is the best option during labor, alternative analgesic options are needed for patients with contraindications. Using a systematic literature search, clinical outcomes of remifentanil for labor pain have been summarized. Also, comparisons of remifentanil to other options including meperidine, epidural analgesia, fentanyl, and nitrous oxide are provided. Based on the literature review, remifentanil is associated with high overall maternal satisfaction and favorable side-effect profile. However, due to the low reporting of adverse events, large, randomized controlled trials are needed to evaluate maternal and neonatal safety adequately and determine the optimal dosing needed to provide effective analgesia. While remifentanil is a feasible alternative for patients who cannot or do not want to receive epidural analgesia, administration should be monitored closely for potential adverse effects. </p>","PeriodicalId":90142,"journal":{"name":"Clinical medicine insights. Women's health","volume":"6 ","pages":"37-49"},"PeriodicalIF":0.0,"publicationDate":"2013-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941183/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32204979","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}