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Table 1 Quantitative data of responses from key informant consultation on AMR

From: Key informant interview on antimicrobial resistance (AMR) in some countries in the western pacific region

Question

Yes

No

DNK

1. Commit to a comprehensive, financed national plan with accountability and civil society engagement

1a. Does your country have a comprehensive national plan to combat or manage the problem of antimicrobial resistance?

4

28

9

(9.8)

(68.3)

(22.0)

1b. Are local or institutional plans in place for combating or managing antimicrobial resistance even if no national plan?

25

10

5

(62.5)

(25.0)

(12.5)

1c. Is there a reliable estimate of what the financial cost of combating or managing antimicrobial resistance would be in your country?

4

21

16

(9.8)

(51.2)

(21.4)

1d. Is it clear to you who (person or body) is responsible for combating or managing antimicrobial resistance in your country?

17

16

9

(40.5)

(38.1)

(21.4)

1e. Are partners other than the government involved in combating or managing antimicrobial resistance in your country?

19

15

6

 

(47.5)

(37.5)

(11.2)

2. Strengthen surveillance and laboratory capacity

2a. Is there a comprehensive AMR surveillance system in your country?

12

23

7

(28.6)

(54.8)

(16.7)

2b. Are there surveillance systems for AMR in specific organisms such as HIV, malaria, TB, or influenza in your country?

27

5

10

(64.3)

(11.9)

(23.5)

2c. Is it clear to you who is responsible for AMR surveillance in your country?

21

13

8

(50.0)

(31.0)

(19.0)

2d. Is there sufficient laboratory capacity in your country to monitory AMR?

13

23

9

(28.9)

(51.1)

(23.8)

2e. Do you know who is responsible for the laboratory monitoring of AMR?

20

8

12

(50.0)

(20.0)

(30.0)

2 f. Is there a system of monitoring or surveillance for drug consumption in your country?

17

8

12

 

(45.9)

(20.0)

(19.4)

3. Ensure medicines of good quality and regular supply

3a. Does drug quality in your country meet international standards?

27

7

8

(64.3)

(16.7)

(19.0)

3b. Is there a mechanism to halt or control the sale of counterfeit and substandard medicines?

30

7

5

(71.4)

(16.7)

(6.5)

3c. Is there a reliable supply or essential medicines to treat infections?

33

3

6

(78.6)

(7.1)

(14.3)

3d. Is the essential medicine list harmonized or consistent with standard treatment guidelines?

33

2

7

(76.6)

(4.6)

(16.7)

3e. Is there a method for ensuring that expired or improperly stored drugs are not used?

29

4

9

 

(69.0)

(9.5)

(21.4)

4. Regulate and promote rational use of medicines, including in animal husbandry, and ensure proper patient care

4a. Are standard treatment guidelines and continuing education used as part of health provider registration accreditation?

20

14

9

(46.5)

(32.6)

(20.9)

4b. Are antimicrobials available only by prescription from a trained health worker?

23

18

2

(53.5)

(41.9)

(4.7)

4c. Is there a method to ban non-recommended monotherapy with key antimicrobials, such as anti-TB, anti-HIV, and anti-malarial drugs?

21

10

12

(48.8)

(23.3)

(27.9)

4d. Is there legislation to control the inappropriate use of antimicrobials in food animals?

3

20

20

(7.0)

(46.5)

(46.5)

4e. Is there any public education on appropriate use of antimicrobials?

15

24

4

 

(34.9)

(55.8)

(9.3)

5. Enhance infection prevention and control

5a. Do standards for infection prevention and control (IPC) for health care institutions exist?

32

5

4

(78.0)

(12.2)

(9.8)

5b. Is adequate IPC part of health institution accreditation or registration in your country?

13

22

6

(31.7)

(53.7)

(14.6)

5c. Is there a continuing education programme to promote IPC among health workers?

25

9

7

(61.0)

(22.0)

(17.1)

5d. Is there a programme to promote IPC among the general population?

12

23

6

(29.3)

(56.1)

(14.6)

5e. Do you know who is responsible for IPC in your country?

31

6

4

 

(75.6)

(14.6)

(9.8)

6. Foster innovations and research and development of new tools

6a. Is operational research being done to improve the use of existing antimicrobials?

16

14

12

(38.1)

(33.3)

(28.6)

6b. Is research being done to improve the use of existing diagnostic methods for AMR?

13

17

12

(31.0)

(40.5)

(28.6)

6c. Is basic research being done to develop new antimicrobials in your country?

4

27

11

(9.5)

(64.3)

(26.2)

6d. Is basic research being done to develop new diagnostics in your country?

9

19

14

(21.4)

(45.2)

(33.3)

6e. Is there a process to assess whether new antimicrobials and diagnostic should be introduced?

17

14

11

(40.5)

(33.3)

(26.2)

  1. Number (%).