Methods: The study was a focused ethnography conducted over approximately eight months at a single health center. Symbolic interactionism and the theory of culture care diversity and universality were used to guide the design and implementation of the study. Data were collected through passive observations of health care encounters, situational conversations and semi-structured interviews with health care providers, and field notes. Data were analyzed continuously, informed by Leininger’s Phases of Ethnonursing Data Analysis Enabler for Qualitative Data (Wehbe-Alamah & McFarland, 2015).
Results: No specific sexual history taking was observed during 79 health care encounters involving many patients who were homeless and who had concomitant mental health and opioid dependence concerns; this was likely influenced by the characteristics of the patients, communication between patients and health care providers, the prioritization of patients’ basic needs, and time constraints imposed upon encounters. This study provided an in-depth description of a single health center and adds to the evidence that sexual history taking may not routinely occur in the primary care practice setting. To our knowledge this is the only focused ethnography exploring sexual history taking.
Conclusion: The results from this study have implications for education, practice, research, and policy. Education: Exposing, and allowing trainees, to obtain sexual histories from patients across the lifespan and among diverse patient populations is recommended. Practice: The realities of daily clinical practice require adaptation (and at times deviance) from current sexual history taking guidelines. Continuing education for health care providers in sexual history taking and managing patients' sexuality-related needs is recommended. Research: Incorporate data from electronic health records into qualitative data (e.g. exploring data longitudinally to exam if/when sexual histories are documented). Policy: Including sexuality-related quality of care measures that must be reported by health centers who receive federal funding.