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Table 2 Mass test and treatment (MTaT) versus no MTaT intervention studies

From: Testing and treatment for malaria elimination: a systematic review

Study

Country

Transmission

Species

TaT method

Proactive or Reactive

Design

Total no. clustersc

Total population

Test

Drug regimen

No. of rounds or events

MTaT coverage

Outcome for MTaT versus no MTaT

Prevalence

Incidence

Follow up (months)

Infection, OR, 95% CIa

Follow up (months)

Symptomatic cases, IRR, 95% CIb

Infection, IRR, 95% CIb

Desai et al. 2020

Kenya

High

Pf

MTaT

Proactive

CRCT

30c

21–50K

RDT/M

DP

6

75–94%

–

–

24

0.79,

0.61–1.02

0.95,

0.87–1.04

Eisele et al. 2016

Zambia

High

Pf

MTaT + fMDA

Proactive

CRCT

20

> 50K

RDT

DP

2

54–63%

12

0.57, 0.13–2.50

5

0.97,

0.73–1.29

0.75,

0.31–1.78

Samuels et al. 2021

Kenya

High

Pf

MTaT

Proactive

CRCT

20

21–50K

RDT

DP

6

75–94%

21

0.92, 0.76–1.10Δ

–

–

–

Tiono et al. 2013

Burkina Faso

High

Pf

MTaT

Proactive

CRCT

18

5–20K

RDT

AL

3

96%

12

0.92, p = 0.3a

12

1.06,

p = 0.3

–

Larsen et al. 2015

Zambia

Moderate

Pf

MTaT

Proactive

CRCT

16

 > 50K

RDT

AL

3

88%

12

0.47, 0.24–0.90a

12

0.83,

0.68–1.01

–

Mlacha et al. 2020

Tanzania

Low/Moderate

Pf

MTaT

Reactive

CQED

4

 > 50K

RDT

DP

85d

Not reported

28

0.34, 0.26–0.44

13

–

–

Bousema et al. 2016

Kenya

Low

Pf

MTaT + fMDA

Proactive

CRCT

10

< 5K

RDT

AL

2

94%

4

difference

1.0,

− 8.3–10.4a

–

–

–

Eisele et al. 2016

Zambia

Low

Pf

MTaT + fMDA

Proactive

CRCT

20

> 50K

RDT

DP

2

54–63%

12

1.28, 0.36–4.60

5

0.80,

0.60–1.08

0.77,

0.22–2.71

Sutanto et al. 2018

Indonesia

Low

Pv > Pf

MTaT

Proactive

CRCT

16c

< 5K

M

DP + PQ

3

89%

–

–

5

–

1.04,

0.36–2.98b

2

87%

0.99,

0.62–1.59b

Cook et al. 2015

Zanzibar

Very Low

Pf

MTaT

Proactive

CQED

10

21–50K

RDT

ASAQ

2

43–54%

–

–

6

No differencee

–

  1. Studies listed in bands from highest to lowest transmission intensity setting, and alphabetically by author within each band
  2. Desai et al. and Samuels et al. were part of the same trial, but presented separately due to different sample sizes used in the two papers
  3. Pf Plasmodium falciparum; Pv Plasmodium vivax; MTaT mass test and treat; fMDA focal mass drug administration; CQED cluster quasi-experimental design; CRCT cluster randomized controlled trial; K thousand; RDT rapid diagnostic test; M microscopy; AL artemether–lumefantrine; DP dihydroartemisinin–piperaquine; PQ primaquine; ASAQ artesunate-amodiaquine; OR odds ratio; CI confidence interval; IRR incidence rate ratio
  4. aAssessed in all ages and by RDT, except for Larsen et al. (in children < 5 years of age and using RDT), Tiono et al. (in children < 5 years of age with parasite density > 5000 p/μL by PCR), and Bousema et al. (all ages, by PCR)
  5. bAssessed in children and by RDT or microscopy, except for Sutanto et al. where also assessed by PCR (results for both studies not statistically significant and not shown) and Tiono et al. where assessed in all ages
  6. cNumbers of intervention and control clusters were equal, except Sutanto et al. (3 rounds of MTaT in 6 clusters, 2 rounds of MTaT in 5 clusters, 5 control clusters) and Desai et al. (10 intervention clusters, 20 control clusters)
  7. dWeekly rounds of MTaT (n = 85 over study period) targeted to villages with the highest recent test positivity rates
  8. eEstimates not provided
  9. fAdjusted ratio of prevalence ratios