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. 2016 Oct 26;10(10):e0005080. doi: 10.1371/journal.pntd.0005080

Table 2. Active Trachoma and Chlamydia trachomatis (Ct) infection after the introduction of mass antibiotic treatment.

Country, Year Study design Time Point post 1st MDA Participants Active Trachoma % Ct % Ct+/TF+ Ct+/TF- Comments
Tanzania, 1993, [20, 66] Cross-section survey of randomly selected children one month after the completion of a one month tetracycline treatment course, given as MDA to the entire community. 1 month 1–7 years: 227 1–7 years:
● TF/TI 41.9% (95/227)
● TI 2.6% (6/227)
1–7 years: 23.8% (54/227) Data not available Data not available ● Hyperendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: in-house PCR-EIA for OMP1.
Egypt, 2003, [10, 31] Cross-section population-based survey 14 months after azithromycin MDA. 14 months 1–10 years: 354 1–10 years:
● TF/TI 26.0% (92/354)
1–10 years: 5.1% (18/354) 1–10 years: 9.8% (9/92) 1–10 years: 3.4% (9/262) ● Hyperendemic setting
● Clinical grading: detailed WHO-FPC system
● Chlamydia test: LCR, Abbott Laboratories.
● Only the azithromycin arm is included.
Gambia, 1999, [31] Cross-section population-based survey 12 months after azithromycin MDA. 12 months All ages:
● 675 (exam)
● 540 (tested)
All ages:
● TF/TI 8.6% (58*/675)
● TI 2.2% (15*/675)
All ages: 8.3% (45/540) Data not available Data not available ● Hyperendemic setting, pre treatment
● Clinical grading: detailed WHO-FPC system
● Chlamydia test: LCR, Abbott Laboratories.
● Only the azithromycin arm is included.
Tanzania, 1999, [31] Cross-section population-based survey 12 months after azithromycin MDA. 12 months All ages:
● 1308 (exam)
● 1162 (tested)
All ages:
● TF/TI 24.6% (322*/1308)
● TI 6.3% (83*/1308)
All ages: 7.0% (82/1162) Data not available Data not available ● Hyperendemic setting
● Clinical grading: detailed WHO-FPC system
● Chlamydia test: LCR, Abbott Laboratories.
● Only the azithromycin arm is included.
Nepal, 2001, [23] Cross-section survey of randomly selected normal children and a purposive sample of children with Active Trachoma, 6 months after azithromycin MDA. 6 months 1–7 years:
● 5262 (exam)
● 394 (tested)
1–7 years:
● TF/TI 16% (841*/5262)
Data not available 1–7 years: 11.8% (31/263) 1–7 years: 5.1% (6/118) ● Mesoendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: LCR, Abbott Laboratories.
Tanzania, 2004, [34, 35] Cross-sectional survey of all residents of a sub-village, 24 months after MDA 24 months All ages: 842 All ages:
● TF/TI 5.8% (49/842)
All ages: 0.1% (1/842) All ages: 2.0% (1/49) All ages: 0.0% (0/793) ● Hyperendemic setting, pre-treatment
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Gambia, 2005, [7, 27, 32, 33] Cross-sectional survey of all residents of 14 small villages, 12 months after MDA 12 months ● All ages: 1210
● 1–9 years: 440
All ages:
● TF/TI 3.9% (47/1210)1–9 years:
● TF 6.8% 30/440)
● TI 0.9% (4/440)
All ages: 2.3% (28/1210)1–9 years: 5.4% (24/440) All ages: 29.8% (14/47)1–9 years: 36.7% (11/30) All ages: 1.2% (14/1163)1–9 years: 3.2% (13/410) ● Mesoendemic setting, pre-treatment
● Clinical grading: detailed WHO-FPC system
● Chlamydia test: Amplicor PCR, Roche.
Tanzania, 2005, [27, 3639] Cross-sectional survey of residents of a village, 12 months after MDA 12 months 0–7 years: 287 0–7 years:
● TF/TI 46.8% (134*/287)
0–7 years: 12.8% (37*/287) Data not available Data not available ● Hyperendemic
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Tanzania, 2007, [39] Cross-sectional of population-based survey 5 years after baseline MDA and 3.5 years after a second MDA. 5 years 0–10 years: 464 0–10 years:
● TF 30.2% (140/464)
● TI 10.6% (49/464)
0–10 years: 25.9% (120/464) Data not available Data not available ● Hyperendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Ethiopia, 2008, [67] Cross-sectional population based sample of children from 32 communities. These had received between 1 and 3 rounds of MDA, with the most recent does less than 6 months in about half the communities. Variable 3–9 years: 1459 3–9 years:
● TF 23.6% (345/1459)
3–9 years: 3.0% (44/1459) 3–9 years: 6.1% (21/345) 3–9 years: 6.1% (23/1114) ● Hyperendemic setting
● Heterogeneous treatment history
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Ethiopia, 2009, [47] Cross-sectional population-based sample of 8 randomly selected children (1–5 years) per village from eight villages. The villages had received MDA biannually for 2 years, with the last dose 18 months prior to the survey. 42 months 0–5 years: 120 0–5 years:
● TF/TI 47.5%: (57/120)
● TI 30.0% (36/120)
0–5 years: 15% (18/120) Data not available Data not available ● Hyperendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Ethiopia, 2010, [18, 48] Cross-sectional population-based sample of children (1–5 years) living in 24 villages. Communities had received 4 biannual MDA, the most recent 6 months before survey 24 months 1–5 years: 1234 1–5 years:
● TF/TI 39.2% (mean village prevalence)
1–5 years: 2.0% (mean village prevalence) Data not available Data not available ● Hyperendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
● NB: The data are reported a mean of the prevalence across all 24 villages.
Tanzania, 2011, [15] Cross-sectional population-based sample of children from 71 communities. All communities had received 3 to 7 rounds of MDA. Variable 0–5 years: 7817 0–5 years:
● TF 10.0% (784/7817)
● TI 3.2% (252/7817)
0–5 years: 5.5%% (429/7817) 0–5 years: 23.5% (184/784) 0–5 years: 3.5% (245/7033) ● Mesoendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche Heterogeneous MDA history. Wide range of community level prevalence of infection and disease. Summary data here pools these communities
Ethiopia, 2011, [57] Cross-sectional population-based survey in 24 communities. Both arms of a cluster RCT of latrine provision received a single round of MDA at baseline. 24 months 0–9 years: 1211 0–9 years:
● TF/TI 47.0% (567/1207)
0–9 years: 14.6% (177/1211) Data not available Data not available ● Hyperendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
● Data from both arms combined.
Ethiopia, 2012, [19, 58, 59, 68, 69] Cross-sectional survey of 50 children per village under 10 years in 12 villages. Three annual rounds of MDA were given. The final survey was months after the last MDA. 36 months 0–9 years: 577 0–9 years:
● TF 43.5% (251/577)
0–9 years: 4.3% (25/577) Data not available Data not available ● Hyperendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Gambia, 2013, [25, 70] Cross-sectional population-based sample of children from 48 communities enrolled in an cluster RCT from four districts. 24 communities had 3 annual MDA and 24 communities had a single round of MDA at baseline. Survey was 3 years after the first round of MDA. 36 months 0–5 years:
● District 1: 1128
● District 2: 1199
● District 3: 1243
● District 4: 1246
0–5 years:
● TF 0.2% (2/1128)
● TF 0.3% (3/1199)
● TF 3.8% (47/1243)
● TF 6.4% (80/1246)
0–5 years:
● 0.5% (6/1128)
● 0.1% (1/1198)
● 1.1% (13/1241)
● 0.3% (4/1235)
0–5 years:
● 0.0% (0/2)
● 0.0% (0/3)
● 6.4% (3/47)
● 0.0% (0/80)
0–5 years:
● 0.5% (6/1126)
● 0.1% (1/1196)
● 0.8% (10/1196)
● 0.3% (4/1166)
● Hypoendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche.
● Data from both trial arms were combined, and presented separately for each district.
Tanzania, 2014, [51, 71] Cross-sectional survey of all children under 10 years in four villages. Four annual rounds of MDA were given. The final survey was 6 months after the last MDA. 42 months 0–9 years: 2234 0–9 years:
● TF/TI 7.9% (176/2234)
0–9 years: 5.1% (114/2234) Data not available Data not available ● Hyperendemic setting, pre-treatment
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Tanzania, 2014, [71, 72] Cross-sectional population-based sample of children aged 0–5 years in 32 villages, 100 children per village. Survey was done 12 months after the third MDA. 36 months 0–5 years: 3136 0–5 years:
● TF 7.6% (237/3136)
0–5 years: 4.5% (142*/3136) 0–5 years: 29.5% (70/237) 0–5 years: 2.5% (72*/2899) ● Hyperendemic setting, pre-treatment
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Tanzania,: 2015,[73] Cross-sectional population-based of residents of a village, which had received 2 rounds of MDA 12 and 10 years previously. 12 years ● All ages: 571
● 1–9 years: 200
All ages:
● TF 2.5% (14/571)1–9 years:
● TF 6.5% (13/200)
● TI 1.5% (3/200)
All ages: 0% (0/571)1–9 years: 0% (0/200) Data not available Data not available ● Hyperendemic setting, pre-treatment
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Nepal, 2016,[74] Cross-section survey of 1–9 year olds in 24 randomly selected communities. Four rounds of MDA. The survey was conducted 5 years after the first round. 5 years 1–9 years: 1124 1–9 years:
● TF/TI 0.3% (3/1124)
1–9 years: 0% (0/1124) Data not available Data not available ● Hypoendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Amplicor PCR, Roche
Tanzania, 2016, [75] Random sample of children aged 1–9 years, from 30 hamlets. 50 children were sampled per hamlet. Communities had received variable rounds of MDA, between 4 and seven years previously. 7 years 1–9 years: 1474 1–9 years:
● TF 0.4% (6*/1474)
1–9 years: 1.1% (16/1474) Data not available Data not available ● Hypoendemic setting
● Clinical grading: simplified WHO system
● Chlamydia test: Aptima Combo2, Hologic

* Estimated value inferred from available data in publication.

a Additional data sub-divided by district were provided by the authors of this study.