Background: Among people living with HIV (PLHIV) enrolled into care, time to anti-retroviral therapy (ART) has not been studied in Myanmar. To inform progress, we conducted this operational research among treatment-naive PLHIV (≥18 years) enrolled during a period of three years (2014–2016) at Pyin Oo Lwin, Myanmar. Objectives: To determine (i) the time from HIV diagnosis to ART initiation (time to ART) and associated factors and (ii) the association between time to ART and attrition (loss to follow-up and death) from ART care. Methods: This was a retrospective cohort study involving a record review of secondary programme data. The PLHIV were followed up to 5 December 2017 for ART initiation and up to 31 March 2018 (date of censoring) for attrition during ART. Results: Of 543 enrolled, 373 (69%) were found to be eligible and initiated on ART. Of 373, 245 (67%) were initiated within 6 weeks of enrolment. The median enrolment delay (from diagnosis) was 4 (IQR: 1, 14) days and median ART initiation delay (from ART eligibility) was 20 (IQR: 13, 36) days. The median time to ART (excluding the time interval in pre-ART care) was 29 (IQR: 18, 55) days and was significantly long in those with prevalent TB and CD4 count ≥ 500/mm3 at enrolment. Among 373, the annual incidence density of attrition was 12.8% (0.95 CI: 10.2, 15.7). Attrition was common in first 100 days. Time to ART (after excluding time interval in pre-ART care) was not significantly associated with attrition. Conclusion: The programme appears to be on track to initiate ART as soon as possible in a ‘test and treat’ scenario (implemented since September 2017) subject to interventions to reduce ART initiation delay.

administration (52%), followed by prescription (30%) and transcription of medications (12%). Most commonly involved medications in MEs were anti-pyretics (33%), those for respiratory conditions (15%) and analgesics (13%). Of the MEs, 9 (9%) were serious errors requiring enhanced monitoring and/ or intervention, while 1 (1%) caused temporary patient harm. Human factors (92%) was the most frequently documented contributing factor, namely failure to comply with established workflows, accurate information provided by guardians, and distractions. Conclusions We have described a low incidence of MEs from 2013 to 2019. Strategies should be developed to ameliorate MEs in the pediatric ED. Areas for focused intervention should include systematic evaluation of drug administration and prescription processes, to enhance compliance with established procedures of checking (amongst the healthcare team and with guardians) and putting safeguards in place to minimize the impact of distractions in the ED setting.