Standards of Care for the Health of Transsexual, Transgender and Gender Nonconforming People

The World Professional Association for Transgender Health promotes the highest standards of health care for individuals through the articulation of Standards of Care (SOC) for the Health of Transsexual, Transgender, and Gender Nonconforming People. The SOC are based on the best available science and expert professional consensus. The overall goal of the SOC is to provide clinical guidance for health professionals to assist transsexual, transgender, and gender nonconforming people with safe and effective pathways to achieving lasting personal comfort with their gendered selves, in order to maximize their overall health, psychological well-being, and self-fulfillment. This assistance may include primary care, gynecologic and urologic care, reproductive options, voice and communication therapy, mental health services (e.g., assessment, counseling, psychotherapy), and hormonal and surgical treatments. While this is primarily a document for health professionals, the SOC may also be used by individuals, their families, and social institutions to understand how they can assist with promoting optimal health for members of this diverse population. This is the 7th version of the Standards of Care since the original 1979 document. The first six versions were published in 1979, 1980, 1981, 1990, 1998, and 2001. Version 7 of the Standards of Care (SOC) for the Health of Transsexual, Transgender, and Gender Nonconforming People will be available in several additional places for wide distribution and ease of access

Clinical and virological characteristics of hospitalised COVID-19 patients in a German tertiary care centre during the first wave of the SARS-CoV-2 pandemic: a prospective observational study

Purpose: Adequate patient allocation is pivotal for optimal resource management in strained healthcare systems, and requires detailed knowledge of clinical and virological disease trajectories. The purpose of this work was to identify risk factors associated with need for invasive mechanical ventilation (IMV), to analyse viral kinetics in patients with and without IMV and to provide a comprehensive description of clinical course. Methods: A cohort of 168 hospitalised adult COVID-19 patients enrolled in a prospective observational study at a large European tertiary care centre was analysed. Results: Forty-four per cent (71/161) of patients required invasive mechanical ventilation (IMV). Shorter duration of symptoms before admission (aOR 1.22 per day less, 95% CI 1.10-1.37, p < 0.01) and history of hypertension (aOR 5.55, 95% CI 2.00-16.82, p < 0.01) were associated with need for IMV. Patients on IMV had higher maximal concentrations, slower decline rates, and longer shedding of SARS-CoV-2 than non-IMV patients (33 days, IQR 26-46.75, vs 18 days, IQR 16-46.75, respectively, p < 0.01). Median duration of hospitalisation was 9 days (IQR 6-15.5) for non-IMV and 49.5 days (IQR 36.8-82.5) for IMV patients. Conclusions: Our results indicate a short duration of symptoms before admission as a risk factor for severe disease that merits further investigation and different viral load kinetics in severely affected patients. Median duration of hospitalisation of IMV patients was longer than described for acute respiratory distress syndrome unrelated to COVID-19

Intersexuality and Trans-Identities within the Diversity Management Discourse

Within both the scientific discourse on workforce diversity, and diversity management practice, intersexuality and transgender issues have hitherto remained marginalized topics. This chapter gives an overview of the discourses on both phenomena, and proposes starting points for more inclusive organizational diversity management initiatives. It is shown that both topics represent different aspects of the category of "gender". The common practice of conceptually lumping together intersexuality, transgenderism, and sexual orientation can be seen as one important reason that intersexuality and transgenderism are rarely considered in organizational diversity management programs in terms of concrete action. Against this background, a modified, and more integrated approach to structuring the workforce alongside the different dimensions of diversity is proposed. It is shown that the categories of "biological sex and gender", "gender identity", and "sexual orientation" cannot be regarded as being separate from each other. They represent, rather, an interrelated organizational field of action that should be considered as being one interrelated topic for organizational diversity practices. This chapter derives this claim theoretically and discusses the consequences for organizational diversity management practices. For most organizations, this would mean a fundamental rethinking of their goals, in terms of workforce diversity, and the shaping of their diversity management programs

Psychometrische Überprüfung einer Kurzform des Familien-Belastungs-Fragebogens

Dehn L, Korn-Merker E, Pfäfflin M, et al. Erfassung der Belastungen von Eltern anfallskranker Kinder. Zeitschrift für Epileptologie. 2013;26(4):214-222.Hintergrund Die Epilepsie eines Kindes oder Jugendlichen kann zu starken psychosozialen Belastungen bei den Eltern führen. In der vorliegenden Studie wurde untersucht, ob eine Kurzfassung der deutschsprachigen Version der Impact-on-Family Scale [Familien-Belastungs-Fragebogen, FaBel] geeignet ist, diese Belastungen reliabel und valide zu erfassen. Material und Methode An einer Stichprobe von 219 Eltern mit epilepsiekranken Kindern [Mittelwert (M) = 8,7 Jahre; Standardabweichung (SD) ±5,0 Jahre] wurde eine Kurzform des FaBel mit 11 “items“ (FaBel-11) psychometrisch überprüft und mit der Langversion des FaBel (33 Items) verglichen. Angaben zur Epilepsie des Kindes und zu spezifischen Beeinträchtigungen der Eltern wurden mit einem Elternfragenbogen erfasst („PESOS-Elternkurzfragebogen“). Ergebnisse Die Kurzform FaBel-11 wies eine gute Reliabilität (α = 0,91) und faktorielle Validität (exploratorische und konfirmatorische Faktorenanalyse) auf. Die Konstruktvalidität wurde durch erwartungskonforme signifikante Zusammenhänge mit epilepsie-, krankheits- bzw. belastungsbezogenen Variablen (z. B. Anfallshäufigkeit, Schwerbehindertenausweis, Komorbidität und Verhaltensauffälligkeiten des Kindes) nachgewiesen. Schlussfolgerung Der FaBel-11 scheint geeignet, die Belastungen von Eltern mit epilepsiekranken Kindern zuverlässig zu erfassen.Background Epilepsy in a child or adolescent influences the whole family system and can lead to severe psychosocial burden especially for the parents. This study investigated whether a short form of the impact on family scale is appropriate to assess the parental burden. Material and methods In a sample of parents (n = 219) with epileptic children (average age  8.7 years, SD 5.0 years) the psychometric properties of a short form of the impact on family scale (IOF, German FaBel-Fragebogen) with 11 items were examined and compared with the original long version. Epilepsy-specific data of the children and the impairment of the parents were assessed using the PESOS questionnaire for parents of children with epilepsy. Results The short form showed good reliability (α = 0.91) and factorial validity (exploratory and confirmatory factor analysis). Construct validity was demonstrated by a hypothesis-compliant significant correlations with epilepsy, disease and burden-related variables (e.g. seizure frequency, care level, comorbidity and behavioral problems). Conclusion The German IOF short form with 11 items is suitable to reliably determine the burden of parents with epileptic children in research and clinical practice

Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals.

The ileal fatty acid binding protein (FABP6) is known to be involved in enterohepatic bile acid metabolism. We have previously found a significant association between the rare allele of the FABP6 Thr79Met polymorphism and lower type 2 diabetes risk in a small case-control study (192 cases and 384 controls) embedded in the large EPIC-Potsdam cohort. A priori functional implication of the amino acid change was gained from in-silico analysis. In this study, we analysed an independent nested case-cohort including 543 incident type 2 diabetes cases from the EPIC-Potsdam cohort and a case-control study including 939 type 2 diabetes cases from KORA to confirm the association with type 2 diabetes and performed association analyses with quantitative disease-related measures in 2112 non-diabetic individuals. Homozygosity for the Met-allele was associated with lower risk of type 2 diabetes (EPIC-Potsdam: 0.70, P=0.04; KORA: 0.79, P=0.06) if adjusted for age, sex, body mass index (BMI), and waist circumference. The homozygous rare variant showed a significant interaction (P=0.006) with BMI. Relative risks in different categories (BMI &lt;25, 25-30, and &gt;30 kg/m(2)) showed an association exclusively in obese (BMI &gt;30 kg/m(2)) individuals (combined risk ratio: 0.62, 95% CI 0.45-0.86). In non-diabetic individuals from the general adult population, no significant associations were observed with plasma total cholesterol, LDL-, and HDL-cholesterol, triglyceride, insulin and glucose concentration. In summary, we found evidence that the-putative functional-Thr79Met substitution of FABP6 confers a protective effect on type 2 diabetes in obese individuals