Evidence map›Paper›PMID 38883973›Full record

ArticleJournal of mixed methods research2021

Integrating Phylogenetic Biomarker Data and Qualitative Approaches: An example of HIV Transmission Clusters as a Sampling Frame for Semistructured Interviews and Implications for the COVID-19 Era.

Shana D Hughes, William J Woods, Kara J O'Keefe, Viva Delgado, Sharon Pipkin, Susan Scheer, Hong-Ha M Truong

Abstract read
In one paragraph

Article in Journal of mixed methods research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Shana D HughesUniversity of California, San Francisco, CA, USA.
William J WoodsUniversity of California, San Francisco, CA, USA.
Kara J O'KeefeSan Francisco Department of Public Health, San Francisco, CA, USA.
Viva DelgadoSan Francisco Department of Public Health, San Francisco, CA, USA.
Sharon PipkinSan Francisco Department of Public Health, San Francisco, CA, USA.
Susan ScheerSan Francisco Department of Public Health, San Francisco, CA, USA.
Hong-Ha M TruongUniversity of California, San Francisco, CA, USA.

Funding

HIV Transmission Cluster Analysis to Inform PreventionR01MH096642 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TRUONG, HONG-HA M · 2012 to 2016
$2.3M
NIMH NIH HHS R01 MH096642
6 · The paper itself

Abstract

Mixed methods studies of human disease that combine surveillance, biomarker, and qualitative data can help elucidate what drives epidemiological trends. Viral genetic data are rarely coupled with other types of data due to legal and ethical concerns about patient privacy. We developed a novel approach to integrate phylogenetic and qualitative methods in order to better target HIV prevention efforts. The overall aim of our mixed methods study was to characterize HIV transmission clusters. We combined surveillance data with HIV genomic data to identify cases whose viruses share enough similarities to suggest a recent common source of infection or participation in linked transmission chains. Cases were recruited through a multi-phase process to obtain consent for recruitment to semi-structured interviews. Through linkage of viral genetic sequences with epidemiological data, we identified individuals in large transmission clusters, which then served as a sampling frame for the interviews. In this article, we describe the multi-phase process and the limitations and challenges encountered. Our approach contributes to the mixed methods research field by demonstrating that phylogenetic analysis and surveillance data can be harnessed to generate a sampling frame for subsequent qualitative data collection, using an explanatory sequential design. The process we developed also respected protections of patient confidentiality. The novel method we devised may offer an opportunity to implement a sampling frame that allows for the recruitment and interview of individuals in high-transmission clusters to better understand what contributes to spread of other infectious diseases, including COVID-19.

Identifiers

PMID38883973
PMCPMC11178346

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.