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. 2020 Oct 27;25(1):27–37. doi: 10.1097/LGT.0000000000000573

TABLE 1.

Characteristics of Study Design, HPV Status, and Persistence Definition for Studies Included in the Current Review

Study characteristics Jaisamrarn et al.42 (2013) Skinner et al.43 (2016) Schiffman et al.2 (2005) and Castle et al.47 (2009) Gage et al.49 (2010) Elfgren et al.48 (2017) Kjaer et al.52 (2010) Kitchener et al.51 (2014) and Gilham et al.50 (2019) Sand et al.53 (2019)
Design PRO; RT PRO; RT PRO; cohort PRO; post hoc; cohort PRO; post hoc; cohort PRO; cohort PRO; RT PRO; cohort
Months of persistent infection 6 6 and 12 12 (range = 9–21) 12 12 (median = 19) 24 36 36
Age, y
 Median nr; >25 37 23 Range = 32–38 28 39.4 31
 Mean 19.7
Recruitment 9,337 2,870 10,049 5,060 12,527 11,088 24,510 40,399
Analysis 4,825 2,838 7,278;a 2,282b 671 6,257 7,482 24,510 5,528
HPV(+) at baseline 3,363 507 542 584 433; 341 1,222 3,813 2,875
Specimen collection dates 2004–2009 2006–2011 1993–1994 2000–2001 1997–2012 1991–1995 2001–2009 2002–2005
Year follow-up ended 2009 2014 nr 2002 2012 2007 2010–2015 2015
Median follow-up 4 y 2 y 5 y 2 y 13 y 12.9 y 6 y; 13 y 8 y
Country Multinational Multinational Costa Rica United States Sweden Denmark England, United Kingdom Denmark
HPV assay DEIA/LiPA25 DEIA/LiPA25 MY09/11 PCR HC2; Line Blot GP5+/6+ PCR HC2; INNO-LiPA LBA; LA; Pap√ of HC2 HC2; INNO-LiPAv2

aTreatment based on colposcopic impression.

bIncluded use of AmpliTaq Gold polymerase.

LA, liner array; OBS, observational study; PCR, polymerase chain reaction; PRO, Prospective design; RETRO, retrospective design; RT, randomized clinical trial.