OBJETIVO: Os transtornos depressivos constituem um problema de saúde pública devido a sua alta prevalência e impacto psicossocial. Pacientes deprimidos são freqüentadores assíduos de serviços de atendimento primário, porém, muitas vezes, não são diagnosticados como tais. O objetivo do estudo é avaliar a associação entre sintomas depressivos e funcionamento social numa amostra de pacientes que procuraram um serviço de cuidados primários em uma capital brasileira. MÉTODOS: Foram avaliados 2.201 usuários de serviços de cuidados de saúde primários de Porto Alegre quanto à saúde física e emocional. Foi aplicado questionário em entrevista única, com duas questões genéricas de avaliação de qualidade de vida do World Health Organization Quality of Life (WHOQOL-Breve), mais itens do Medical Outcomes Study Short-Forms 12 (SF-12) e MHI 5 (MHI-5), do Centers for Epidemiologic Studies -- Depression (CES-D), além de outras questões referentes a busca de atendimento médico e faltas ao trabalho. Foram realizados testes de Kruska-Wallis e de comparações múltiplas de Tambane. RESULTADOS: Dos indivíduos estudados, 79,5% eram do sexo feminino, com média de idade de 40 anos. A intensidade da sintomatologia depressiva medida pelo CES-D foi de 20,2 para as mulheres e de 16,2 para os homens. Todos os parâmetros avaliados tiveram relação inversa com a intensidade dos sintomas depressivos. CONCLUSÕES: Os resultados reforçam a afirmativa de que a sintomatologia depressiva tem uma alta associação com pior funcionamento social e qualidade de vida e maior utilização de recursos de saúde em pacientes de cuidados primários.

Introduction The 100-item World Health Organization Quality of Life Assessment (WHOQOL-100) evaluates quality of life as a subjective and multidimensional construct. Currently, particularly in Brazil, there are controversies concerning quality of life after sex reassignment surgery (SRS). Aim To assess the impact of surgical interventions on quality of life of 47 Brazilian male-to-female transsexual individuals using the WHOQOL-100. Methods This was a prospective cohort study using the WHOQOL-100 and sociodemographic questions for individuals diagnosed with gender identity disorder according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition. The protocol was used when a transsexual person entered the ambulatory clinic and at least 12 months after SRS. Main Outcome Measures Initially, improvement or worsening of quality of life was assessed using 6 domains and 24 facets. Subsequently, quality of life was assessed for individuals who underwent new surgical interventions and those who did not undergo these procedures 1 year after SRS. Results The participants showed significant improvement after SRS in domains II (psychological) and IV (social relationships) of the WHOQOL-100. In contrast, domains I (physical health) and III (level of independence) were significantly worse after SRS. Individuals who underwent additional surgery had a decrease in quality of life reflected in domains II and IV. During statistical analysis, all results were controlled for variations in demographic characteristics, without significant results. Conclusion The WHOQOL-100 is an important instrument to evaluate the quality of life of male-to-female transsexuals during different stages of treatment. SRS promotes the improvement of psychological aspects and social relationships. However, even 1 year after SRS, male-to-female transsexuals continue to report problems in physical health and difficulty in recovering their independence.

This study examined the impact of sex reassignment surgery on the satisfaction with sexual experience, partnerships, and relationship with family members in a cohort of Brazilian transsexual patients. A group of 19 patients who received sex reassignment between 2000 and 2004 (18 male-to-female, 1 female-to-male) after a two-year evaluation by a multidisciplinary team, and who agreed to participate in the study, completed a written questionnaire. Mean age at entry into the program was 31.21+/-8.57 years and mean schooling was 9.2+/-1.4 years. None of the patients reported regret for having undergone the surgery. Sexual experience was considered to have improved by 83.3% of the patients, and became more frequent for 64.7% of the patients. For 83.3% of the patients, sex was considered to be pleasurable with the neovagina/neopenis. In addition, 64.7% reported that initiating and maintaining a relationship had become easier. The number of patients with a partner increased from 52.6% to 73.7%. Family relationships improved in 26.3% of the cases, whereas 73.7% of the patients did not report a difference. None of the patients reported worse relationships with family members after sex reassignment. In conclusion, the overall impact of sex reassignment surgery on this cohort of patients was positive.

Objective: To provide a description of our transsexual population. Method: This descriptive observational study included 138 patients with a diagnosis of Transsexualism in Brazil, between March 1998 and September 2005. Demographic, clinical and psychiatry data were collected.Results: Age ranged from 16 to 54 years; 88.4% were male. The prevalence of sexually transmitted diseases was 19.5%, and 17.6% were HIV-positive. Hormone therapy was reported by 91.2%, and 47.4% referred drug and alcohol use; 14.2%, attempted suicide; and 12.5%, history of sexual abuse. Self-mutilation was reported by 5.2%s. Fifty-nine patients (42.7%) had at least one currently psychiatric comorbidity (axis I or II).Conclusions: Mental health professionals have a central role in coordinating the multidisciplinary care of transsexuals.