Purpose The goal of 90-90-90 first requires the expansion of access to HIV testing. Our aim was to record frequencies of HIV indicator conditions (ICs) and identify missed opportunities for an early HIV diagnosis.
Methods We retrospectively identified ICs in a population of 231 people living with HIV with known infection dates who attended our clinic. The study population was divided into four groups: (1) those self-tested pre-emptively (47/231, 20.3%), (2) those offered targeted testing based on risk factors (67/231, 29%), (3) those tested after an IC (73/231, 31.6%) and (4) those who were not offered testing after an IC (44/231, 19%). HIV acquisition dates were estimated by molecular clock analysis.
Results A total of 169 healthcare contacts (HCCs) were recorded. The most frequent HCC was mononucleosis-like syndrome (20.1%), unexplained weight loss (10.7%) and STIs (10.1%). AIDS-defining conditions were detected in 11.8%. Only 62.4% (73/117) of those with an IC were offered testing after their first HCC. Patients in group 4 had statistically significant delay in diagnosis compared with group 3 (109.1 weeks (IQR 56.4–238.6) vs 71.6 weeks (IQR 32.3–124.6)). The proportion of patients diagnosed as late presenters in each group was: (1) 16/47 (34%), (2) 37/67 (55.2%), (3) 43/73 (58.9%) and (4) 27/44 (61.4%) (p=0.027).
Conclusions Our study uses a combination of molecular and clinical data and shows evidence that late presentation occurs in a high proportion of patients even in the presence of an IC. Given that risk-based targeted testing has low coverage, IC-guided testing provides a reasonable alternative to facilitate earlier HIV diagnosis and to improve late diagnosis across Europe and globally.
- epidemiology (molecular)
- epidemiology (clinical)
- HIV clinical care
Data availability statement
Data are available at the National and Kapodistrian University of Athens repository, "Pergamos" (https://pergamos.lib.uoa.gr/uoa/dl/object/2934905).
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Handling editor Francesca Ceccherini-Silberstein
Presented at 20th Panhellenic Infectious Diseases Conference, 5–8 March 2020, Athens, Greece; 30th ECCMID, 18–21 April, Paris, France.
Contributors DB performed clinical data collection, statistical analysis and authored the manuscript, EGK and DP performed molecular clock analysis and reviewed the manuscript, AH assisted in statistical analysis, aided in interpreting results, reviewed the manuscript, MP had the original concept and designed the study, reviewed the manuscript and had final supervision.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
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