Understanding the role of patient communication protocols in sexually transmissible infections point-of-care testing among Aboriginal and Torres Strait Islander peoples in remote communities: a qualitative study

Robert Monaghan, Louise Causer, James Ward, Belinda Hengel, Kirsty Smith, Kelly Andrewartha, Christopher Fairley, Lisa Maher, Donna B. Mak, Caitlyn White, Jessica Leonard, Rebecca Guy, Lise Lafferty, TTANGO2 Collaboration

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Abstract

Background
Untreated sexually transmissible infections (STIs) such as Chlamydia trachomatis and Neisseria gonorrhoeae can lead to serious health issues, including pelvic inflammatory disease, infertility in women, increased HIV risk, and emotional distress. Timely testing and treatment are crucial for reducing transmission. Australia’s STI Management Guidelines recommend regular STI testing every 6–12 months for sexually active individuals aged 15–35 years in high-prevalence, remote areas. However, testing uptake remains low among young Aboriginal and Torres Strait Islander peoples. This analysis explores how healthcare providers engage Aboriginal and Torres Strait Islander peoples in STI testing using point-of-care (POC) diagnostics.

Methods
Semi-structured interviews were conducted with trained STI POC testing operators within the Test Treat ANd GO (TTANGO2) project. Seven clinics involved in TTANGO2 were selected for their ‘high’ and ‘low’ implementation of STI POC testing. Purposive sampling was used to recruit similar personnel from each of the selected clinics. Coding was informed by a patient communication protocol lens.

Results
Twenty healthcare personnel, including Aboriginal Health Workers/Practitioners (n = 8), Registered Nurses (n = 7), Coordinators (n = 2), and Clinical/Practice Managers (n = 3) participated. Key themes related to implementing STI POC testing focused on different stages of identified patient communication protocols, such as offering tests, providing follow-up results, and contact tracing. Concerns about shame and confidentiality were significant factors affecting patient communication protocols throughout the process.

Conclusions
Normalising sexual health discussions in healthcare settings helps reduce feelings of shame and stigma, further encouraging patient participation in sexual health services. Ensuring patient safety and offering culturally appropriate explanations of STI POC testing are essential to reduce barriers, such as shame and stigma. Culturally safe practices can increase patient engagement and provide opportunities for health education. Integrating STI POC testing into routine health care can help normalise testing and boost uptake. However, same-day results may still require patient follow-up to maintain confidentiality. Addressing external factors, such as accessibility, confidentiality, stigma reduction, and community engagement, is crucial for improving STI testing services.
Original languageEnglish
Article numberSH24214
Number of pages8
JournalSexual Health
Volume22
Issue number2
DOIs
Publication statusPublished - 27 Feb 2025

Keywords

  • aboriginal and torres strait islander peoples
  • Sexually transmitted infections (STIs)
  • Point-of-Care (POC) testing
  • qualitative research
  • remote communities

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