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Table 5 Effect of interventions on antimalarial prescribing, RDT use and antibiotic prescribing

From: Prescriber and patient-oriented behavioural interventions to improve use of malaria rapid diagnostic tests in Tanzania: facility-based cluster randomised trial

Outcome

Arm

Number of patients

Prevalence number (%)

Crude RD a (95% CI)

Adjusted RD b (95% CI)

P -value

Patients with fever treated with rAM

Control

9,231

2180 (24%)

0

0

 

HW

9,752

1700 (17%)

0.07 (0.004, 0.13)

0.03 (−0.04, 0.10)

0.44

HWP

7,887

1304 (16%)

0.07 (0.01, 0.14)

0.05 (−0.002, 0.10)

0.06

Patients with no fever treated with rAM

Control

4,863

82 (2%)

0

0

 

HW

6,062

193 (3%)

−0.003 (−0.02, 0.01)

0.002 (−0.01, 0.01)

0.52

HWP

5,984

40 (1%)

0.01 (−0.01, 0.03)

0.002 (−0.01, 0.01)

0.73

RDT uptake

Patients with fever tested with RDT

Control

9,297

4960 (53%)

0

0

 

HW

9,825

5374 (55%)

−0.04 (−0.15, 0.07)

−0.04 (−0.20, 0.10)

0.57

HWP

7,963

5153 (65%)

−0.12 (−0.21, −0.03)

−0.02 (−0.13, 0.09)

0.72

RDT eligible (fever and no obvious alternate diagnosis) not tested

Control

8,241

3697 (45%)

0

0

 

HW

9,064

4000 (44%)

0.04 (−0.07, 0.15)

0.06 (−0.11, 0.23)

0.44

HWP

7,292

2459 (34%)

0.12 (0.04, 0.21)

0.18 (0.05, 0.32)

0.01

RDT ineligible (no fever) tested

Control

4,874

587 (12%)

0

0

 
 

HW

6,083

955 (16%)

−0.01 (−0.07, 0.04)

0.01 (−0.06, 0.07)

0.86

 

HWP

6,000

518 (9%)

0.02 (−0.05, 0.09)

0.02 (−0.04, 0.09)

0.43

Presumptive treatment

RDT eligible treated presumptively for malaria

Control

8,241

471 (6%)

0

0

 

HW

9,064

374 (4%)

0.02 (−0.01, 0.05)

0.01 (−0.02, 0.04)

0.40

HWP

7,292

256 (4%)

0.02 (−0.003, 0.05)

0.02 (−0.004, 0.05)

0.09

RDT ineligible treated presumptively for malaria

Control

4,874

42 (1%)

0

0

 

HW

6,083

47 (1%)

0.004 (−0.001, 0.01)

0.003 (−0.001, 0.01)

0.15

HWP

6,000

12 (0.2%)

0.007 (0.003, 0.01)

0.004 (−0.0001, 0.01)

0.05

Adherence to RDT negative

RDT negative receiving AM

Control

4,015

762 (19%)

0

0

 

HW

4,539

250 (6%)

0.14 (0.08, 0.20)

0.10 (0.03, 0.17)

0.01

HWP

4,330

189 (4%)

0.15 (0.09, 0.21)

0.10 (0.04, 0.16)

0.002

RDT negative receiving AM (among those with fever)

Control

3,488

723 (21%)

0

0

 

HW

3,793

235 (6%)

0.16 (0.08, 0.23)

0.11 (0.03, 0.19)

0.01

HWP

3,897

177 (5%)

0.21 (0.04, 0.17)

0.12 (0.05, 0.19)

0.002

RDT negative receiving AM (among those with no fever)

Control

527

39 (7%)

0

0

 

HW

746

15 (2%)

0.05 (−0.01, 0.10)

0.03 (0.01 0.05)

0.004

HWP

433

12 (3%)

0.04 (−0.01, 0.10)

-

-

Adherence to RDT positive

RDT positive receiving rAM

Control

1,455

1166 (80%)

0

0

 
 

HW

1,696

1402 (83%)

−0.10 (−0.35, 0.15)

−0.13 (−0.45, 0.19)

0.39

 

HWP

1,249

963 (77%)

−0.17 (−0.41, 0.06)

−0.04 (−0.25, 0.17)

0.69

RDT positive receiving rAM (among those with fever)

Control

1,406

1149 (82%)

0

0

 

HW

1,508

1255 (83%)

−0.07 (−0.31, 0.18)

−0.11 (−0.44, 0.22)

0.49

HWP

1,180

942 (79%)

−0.14 (−0.37, 0.09)

−0.01 (−0.23, 0.21)

0.89

RDT positive receiving rAM (among those without fever)

Control

49

17 (35%)

   

HW

188

147 (78%)

-

-

 

HWP

69

21 (30%)

-

-

 

Treatment with antibiotics

Non-malarial illness receiving ABx

Control

8,942

6865 (77%)

0

0

 

HW

10,118

7886 (78%)

0.01 (−0.09, 0.12)

0.02 (−0.22, 0.24)

0.89

HWP

10,163

7525 (74%)

0.01 (−0.04, 0.07)

0.14 (−0.01, 0.29)

0.06

RDT negative receiving ABx

Control

4,015

2977 (74%)

0

0

 

HW

4,539

3527 (78%)

−0.02 (−0.12, 0.09)

0.003 (−0.23, 0.24)

0.98

HWP

4,330

3236 (75%)

−0.004 (−0.07, 0.06)

0.13 (−0.02, 0.27)

0.08

RDT eligible receiving ABx

Control

8,241

5731 (70%)

0

0

 

HW

9,064

6808 (75%)

−0.03 (−0.13, 0.07)

0.01 (−0.21, 0.25)

0.89

HWP

7,292

4,994 (68%)

0.01 (−0.09, 0.10)

0.13 (−0.03, 0.30)

0.09

RDT ineligible receiving ABx

Control

4,863

3774 (78%)

0

0

 

HW

6,062

4531 (75%)

0.07 (−0.07, 0.20)

0.03 (−0.21, 0.28)

0.77

HWP

5,984

4334 (72%)

0.04 (−0.02, 0.10)

0.15 (0.01, 0.30)

0.04

  1. aAdjusted for stratification; effect estimate is risk difference = control – intervention; control is standard RDT training. bAdjusted for facility (stock-out of ACT, stratum, provision of materials), prescriber (age, education, time at facility) and patient (age) characteristics. Treatment outcomes additionally adjusted for facility-level proportion treated with recommended antimalarial (rAM)/any antimalarial (AM) at baseline. Insufficient clusters per stratum and cluster size to conduct a robust analysis. Number of clusters is 12 per arm for all outcomes. ACT, artemisinin-based combination therapies; AM, antimalarial; CI, confidence interval; HW, health worker; HWP, health worker plus patient-oriented; rAM, recommended antimalarial; RD, risk difference; RDT, rapid diagnostic test; SMS, mobile-phone text message.