When community health workers went looking for patients who had started antiretroviral treatment but had stopped showing up for care at 14 clinics across Uganda, Kenya and Tanzania, 13 percent of those sought returned to treatment. That represented a significant, if still small improvement over the 10 percent who returned for care when no effort to find them had been made.
But when researchers didnt include in their count the numbers of patients who couldnt be found, who had died, or who had started receiving treatment elsewhere those, who, as they put it, couldnt, or shouldnt return to the clinic they had attended the value of finding and talking to patients who had begun, but interrupted their treatment became clearer with 22 percent of those who could be found, and not in care elsewhere, returning to care.
The findings, in Clinical Infectious Diseases this week show the benefits that can be gained from an effort widely undertaken in low- and middle-income countries where community health workers and members of patient support groups, play a vital, but often unmeasured and for that matter, often uncompensated or barely compensated role in helping people diagnosed with HIV identify and overcome obstacles that include stigma, transportation challenges, poverty and other life circumstances, to receive and continue to receive the care they need. But, authors led by Anne Bershetyn of the Institute for Disease Modeling in Bellevue, Washington, also note the findings highlight a need to maximize those benefits by seeking data that, in turn, can help community health workers seek the right patients those still living and still nearby.
This excerpt was cross-posted with the permission of Science Speaks. Read the original article.