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Session 4: G6PD deficiency in Myanmar
Point-of-care testing for G6PD deficiency to optimize
radical cure of P. vivax
Knowledge sharing
Partnership for Vivax Elimination (PAVE)
Novotel Hotel, Yangon 28 Nov 2022
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Resources
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
G6PD global prevalence
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
G6PD globl prevalence
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Malaria epidemiology
Malaria Morbidity and Mortality in Myanmar (2005-2021)
59,405
62,813
371,612
447,073
384,531
440,208
465,294
481,204
333,871
205,658
182,616
110,146
85,019
76,518
56,411
58,836
79,001
456,636
475,297
149,275
187,207
206,961
252,916
102,158
0
200
400
600
800
1000
1200
1400
1600
1800
-
100,000
200,000
300,000
400,000
500,000
600,000
700,000
800,000
Number
of
Malaria
Deaths
Number
of
Malaria
Cases
Confirmed Malaria Probable Malaria Malaria Death
VBDC Annual
Review Meeting,
2022
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Malaria epidemiology
(VBDC Annual Review Meeting, 2022)
Malaria Situation in States/Regions (2017 to 2021)
0
5
10
15
20
25
Malaria
Cases
Thousands
2017 2018 2019 2020 2021
Annual Parasite Incident by State/ Region (2021)
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Malaria epidemiology
VBDC Annual
Review Meeting,
2022
Monthly Malaria Cases and Proportion by species
(2019-2022 Apr)
0
10
20
30
40
50
60
70
80
90
100
0
2000
4000
6000
8000
10000
12000
14000
Jan-19
Mar-19
May-19
Jul-19
Sep-19
Nov-19
Jan-20
Mar-20
May-20
Jul-20
Sep-20
Nov-20
Jan-21
Mar-21
May-21
Jul-21
Sep-21
Nov-21
Jan-22
Mar-22
Proportion
Total
Number
Axis Title
Total Pf + Mix Total Pv PfMix% Pv%
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Malaria epidemiology
VBDC Annual
Review Meeting,
2022
High malaria burden townships in Myanmar
for implementing Intensification Plan & Acceleration Plan
Sr.
No.
State/
Region
Township Sr. No.
State/
Region
Township
1 Chin Paletwa 13 Mon Ye
2 Kachin Waingmaw 14 Rakhine Buthidaung
3 Kachin Momauk 15 Rakhine Kyauktaw
4 Kachin Shwegu 16 Rakhine Maungdaw
5 Kachin Injangyang 17 Rakhine Minbya
6 Kachin Mansi 18 Rakhine Mrauk U
7 Kachin Sumprabum 19 Sagaing Banmauk
8 Kachin Myitkyina 20 Sagaing Pinlebu
9 Kachin Bhamo 21 Tanintharyi Yebyu
10 Kayin Hpapun 22 Tanintharyi Tanintharyi
11 Kayin Kyainseikgyi 23 Tanintharyi Dawei
12 Kayin Myawaddy 24 Tanintharyi Palaw
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
G6PD Brief for Myanmar
• Several studies estimated Glucose-6-phosphate dehydrogenase (G6PD)
deficiency prevalence in Myanmar, however, no nationwide survey has taken
place to determine overall G6PD deficiency prevalence
• G6PD brief –
• Provide background information on methods to measure G6PD
• Collate all available and accessible data from grey and peer-reviewed
literature on G6PD deficiency
• Inform decision-makers with a comprehensive view of the situation in
Myanmar.
• After collating available data, a draft of this document was shared with members
of the extended Technical Strategy Group for Malaria (TSG) that coordinates
malaria partners in Myanmar.
• Feedback from extended TSG members was incorporated into this document
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
How G6PD was measured
previously in Myanmar
• We identified 17 subnational studies undertaken in nine states in Myanmar
• Nine measured G6PD prevalence with qualitative, or semi-quantitative tests
either the Brewers test, Fluorescent Spot Test (FST), Formazan test.
• Five studies measured G6PD quantitatively using either spectrophotometry or
point-of-care quantitative tests such as the Trinity Biotech® quantitative G6PD or
the G6PD CareStart biosensor.
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
G6PD deficiency
prevalence in Myanmar
 G6PD deficiency prevalence rates varied considerably both between genders and states/ethnic
groups
 Overall prevalence of any G6PD deficiency defined as ‘below normal’ (i.e. either intermediate or
deficient) ranged from 0% (8) - 30.5%.
 Three studies reported quantitative G6PD deficiency estimates by spectrophotometry for males.
Estimates of G6PDd in these studies were 11.7%, 9.4%, and 11.1%. It is expected that G6PD
deficiency prevalence would be half as much in females as the male G6PD deficiency
prevalence rate, and G6PD intermediate prevalence would be twice as much in females.
 Work by the Malaria Atlas Project that collates G6PD data with associated location data
estimates a G6PD deficiency prevalence rate of 6.1% in Myanmar, or over 1.5 million males in
2010 and 880,000 females that year.
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
G6PD deficiency in different
ethnic groups of Myanmar
 The most commonly studied group were Burmese (8 studies), Kachin (5 studies) and
Rakhine (3 studies). Chin, Karen, Mon, and Shan were also participants in two studies
each, while Kayah and Pa-O populations were identified in one study each. Other
ethnicities such as Chinese and Indian were identified in one study.
 The highest prevalence of G6PD deficiency (i.e. either deficient or intermediate) was
reported among Kachin populations with a range of 0% – 30.5% G6PD non-normal
activity.
 In the one study that used quantitative measures, severe G6PD deficiency was
estimated as 2.1% in females and 9.4% in males.
 The population with the next highest prevalence of G6PD non-normal activity were
Burmese with a range from 0 – 21.2 %. In studies using quantitative measures, G6PD
intermediate ranged from 0.9 – 15.8% while G6PD deficient ranged from 0.3 – 11.7%.
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
G6PD deficiency variants in
Myanmar
The most commonly reported mutations identified in Myanmar over the last two
decades were
• Mahidol (>=86% of samples),
• Kaiping (4- 18%) and
• Viangchan (6%).
Others that were identified included
• Mediterranean (4%),
• Union (2%) and
• Canton (2%)
•
G6PD Mahidol is considered a moderately severe variant with varying G6PD
activities which classifies it as WHO class II/III.
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
G6PD deficiency
prevalence in Myanmar
State_Region G6PD intermediate prevalence (%) G6PD deficiency prevalence (%) Total cases (2021)
Ayeyarwady Not available Not available 92
Bago Not available Not available 585
Chin 2.7 - 14.4 0.3 - 12.5
15,961
Kachin 13.2 - 23.4 2.1 - 30
22,449
Kayah 0.14 - 1.3 0 - 1.9 7
Kayin Not available 12.9 - 14.1
21,382
Magway Not available Not available 149
Mandalay 0.9 - 15.8 0.3 - 11.1 411
Mon Not available 0 - 12 2,012
Naypyitaw Not available Not available 7
Rakhine 0.8 - 14.4 0 - 12.5 6,364
Sagaing Not available Not available 1,089
Shan Not available 10.9 - 21.2 707
Tanintharyi Not available 0.3 - 11.1 7,748
Yangon 0 - 14 0.9 - 21 38
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Implications of evidence-based information
to inform policy makers for data-driven
policy adoption
High malaria burden townships (2021) Malaria Atlas Project
estimated G6PD deficiency
allele frequency
12%
0%
6%
G6PDd allele
frequency
Myanmar has an average G6PDd allele
frequency of 6.1%
Annual Parasite Incident by State/ Region (2021)
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
UNOPS-PR
VBDC Annual
Review Meeting,
2022
Sr.
No
.
Sub-
recipients
No. of State/
Region
No. of
townships
covered
No. of
ICMV
Activities
1 MAM Mon, Chin,
Kachin, Kayin,
Sagaing
22 1752 Malaria case
management, Prevention
2 MCC Chin, Kachin 17 529 Malaria case
management, Prevention
3 MHAA Bago East,
Chin
3 141 Malaria case
management, Prevention
4 MMA Ayeyarwady 2 100 Malaria case
management, Prevention,
elimination surveillance
5 MRCS SSS 5 185 Malaria case
management, Prevention
6 SMRU Kayin 4 916 Malaria case
management, Prevention,
Research
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Save the Children Co-PR
VBDC Annual
Review Meeting,
2022
Sr.
No
.
Sub-
recipients
No. of
State/
Region
No. of
townshi
ps
covered
No.
of
ICMV
Activities
1 ARC BagoE,
Kayin,
Mon,
NSS, TYI
23 596 Malaria case management,
Prevention, elimination surveillance
2 HPA Kachin,
NSS, ESS
18 516 Malaria case management,
Prevention
3 IOM Mon,
Sagaing
11 651 Malaria case management,
Prevention, elimination surveillance
4 MI
(Country &
Regional)
Rakhine,
ESS
7 177 Malaria case management,
Prevention
5 PSI
(Country &
Regional)
11 27 759 Malaria case management,
Prevention, elimination surveillance
6 SCI
(Country &
Regional)
Magway,
NSS
7 426 Malaria case management,
Prevention
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
PMI Eliminate Malaria
VBDC Annual
Review Meeting,
2022
Sr.
No
.
Sub-
recipie
nts
No. of
State/
Region
No. of
townshi
ps
covered
NO. of
ICMV
Activities
1 ARC Kayin,
TYI
7 394 Malaria case management,
Prevention, elimination
surveillance
2 MHAA Rakhine 3 231 Malaria case management,
Prevention
3 MNMA Rakhine 2 181 Malaria case management,
Prevention
4 URC Rakhine,
Sagaing,
TYI
24 1338 Malaria case management,
Prevention, elimination
surveillance
Point-of-care testing for G6PD deficiency to optimize
radical cure of P.vivax
Implication of G6PD deficiency prevalence
and variants on NMCP recommendations
 Studies over time, and in several different populations in Myanmar have identified populations with
moderate to high prevalence of G6PD deficiency up to 30.5% prevalence.
 These results strongly support the WHO recommendations to screen G6PD deficiency at health facility
level before the use of primaquine (or any 8-AQ) prior to radical curative regimen for Plasmodium vivax.2
 Given the variability of G6PDd prevalence, patient counselling as to the potential side effects of 8-
aminoquinolines and a strong pharmacovigilance system are important in Myanmar to ensure patient
safety
 Treatment strategies to treat vivax malaria in G6PD deficient patients will be important to achieve malaria
elimination in Myanmar
Session 4: G6PD deficiency in Myanmar
Point-of-care testing for G6PD deficiency to optimize
radical cure of P. vivax
Knowledge sharing
Thank you.

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4. G6PDd_in_Myanmar_final.pptx

  • 1. Session 4: G6PD deficiency in Myanmar Point-of-care testing for G6PD deficiency to optimize radical cure of P. vivax Knowledge sharing Partnership for Vivax Elimination (PAVE) Novotel Hotel, Yangon 28 Nov 2022
  • 2. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Resources
  • 3. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax G6PD global prevalence
  • 4. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax G6PD globl prevalence
  • 5. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Malaria epidemiology Malaria Morbidity and Mortality in Myanmar (2005-2021) 59,405 62,813 371,612 447,073 384,531 440,208 465,294 481,204 333,871 205,658 182,616 110,146 85,019 76,518 56,411 58,836 79,001 456,636 475,297 149,275 187,207 206,961 252,916 102,158 0 200 400 600 800 1000 1200 1400 1600 1800 - 100,000 200,000 300,000 400,000 500,000 600,000 700,000 800,000 Number of Malaria Deaths Number of Malaria Cases Confirmed Malaria Probable Malaria Malaria Death VBDC Annual Review Meeting, 2022
  • 6. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Malaria epidemiology (VBDC Annual Review Meeting, 2022) Malaria Situation in States/Regions (2017 to 2021) 0 5 10 15 20 25 Malaria Cases Thousands 2017 2018 2019 2020 2021 Annual Parasite Incident by State/ Region (2021)
  • 7. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Malaria epidemiology VBDC Annual Review Meeting, 2022 Monthly Malaria Cases and Proportion by species (2019-2022 Apr) 0 10 20 30 40 50 60 70 80 90 100 0 2000 4000 6000 8000 10000 12000 14000 Jan-19 Mar-19 May-19 Jul-19 Sep-19 Nov-19 Jan-20 Mar-20 May-20 Jul-20 Sep-20 Nov-20 Jan-21 Mar-21 May-21 Jul-21 Sep-21 Nov-21 Jan-22 Mar-22 Proportion Total Number Axis Title Total Pf + Mix Total Pv PfMix% Pv%
  • 8. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Malaria epidemiology VBDC Annual Review Meeting, 2022 High malaria burden townships in Myanmar for implementing Intensification Plan & Acceleration Plan Sr. No. State/ Region Township Sr. No. State/ Region Township 1 Chin Paletwa 13 Mon Ye 2 Kachin Waingmaw 14 Rakhine Buthidaung 3 Kachin Momauk 15 Rakhine Kyauktaw 4 Kachin Shwegu 16 Rakhine Maungdaw 5 Kachin Injangyang 17 Rakhine Minbya 6 Kachin Mansi 18 Rakhine Mrauk U 7 Kachin Sumprabum 19 Sagaing Banmauk 8 Kachin Myitkyina 20 Sagaing Pinlebu 9 Kachin Bhamo 21 Tanintharyi Yebyu 10 Kayin Hpapun 22 Tanintharyi Tanintharyi 11 Kayin Kyainseikgyi 23 Tanintharyi Dawei 12 Kayin Myawaddy 24 Tanintharyi Palaw
  • 9. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax G6PD Brief for Myanmar • Several studies estimated Glucose-6-phosphate dehydrogenase (G6PD) deficiency prevalence in Myanmar, however, no nationwide survey has taken place to determine overall G6PD deficiency prevalence • G6PD brief – • Provide background information on methods to measure G6PD • Collate all available and accessible data from grey and peer-reviewed literature on G6PD deficiency • Inform decision-makers with a comprehensive view of the situation in Myanmar. • After collating available data, a draft of this document was shared with members of the extended Technical Strategy Group for Malaria (TSG) that coordinates malaria partners in Myanmar. • Feedback from extended TSG members was incorporated into this document
  • 10. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax How G6PD was measured previously in Myanmar • We identified 17 subnational studies undertaken in nine states in Myanmar • Nine measured G6PD prevalence with qualitative, or semi-quantitative tests either the Brewers test, Fluorescent Spot Test (FST), Formazan test. • Five studies measured G6PD quantitatively using either spectrophotometry or point-of-care quantitative tests such as the Trinity Biotech® quantitative G6PD or the G6PD CareStart biosensor.
  • 11. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax G6PD deficiency prevalence in Myanmar  G6PD deficiency prevalence rates varied considerably both between genders and states/ethnic groups  Overall prevalence of any G6PD deficiency defined as ‘below normal’ (i.e. either intermediate or deficient) ranged from 0% (8) - 30.5%.  Three studies reported quantitative G6PD deficiency estimates by spectrophotometry for males. Estimates of G6PDd in these studies were 11.7%, 9.4%, and 11.1%. It is expected that G6PD deficiency prevalence would be half as much in females as the male G6PD deficiency prevalence rate, and G6PD intermediate prevalence would be twice as much in females.  Work by the Malaria Atlas Project that collates G6PD data with associated location data estimates a G6PD deficiency prevalence rate of 6.1% in Myanmar, or over 1.5 million males in 2010 and 880,000 females that year.
  • 12. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax G6PD deficiency in different ethnic groups of Myanmar  The most commonly studied group were Burmese (8 studies), Kachin (5 studies) and Rakhine (3 studies). Chin, Karen, Mon, and Shan were also participants in two studies each, while Kayah and Pa-O populations were identified in one study each. Other ethnicities such as Chinese and Indian were identified in one study.  The highest prevalence of G6PD deficiency (i.e. either deficient or intermediate) was reported among Kachin populations with a range of 0% – 30.5% G6PD non-normal activity.  In the one study that used quantitative measures, severe G6PD deficiency was estimated as 2.1% in females and 9.4% in males.  The population with the next highest prevalence of G6PD non-normal activity were Burmese with a range from 0 – 21.2 %. In studies using quantitative measures, G6PD intermediate ranged from 0.9 – 15.8% while G6PD deficient ranged from 0.3 – 11.7%.
  • 13. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax G6PD deficiency variants in Myanmar The most commonly reported mutations identified in Myanmar over the last two decades were • Mahidol (>=86% of samples), • Kaiping (4- 18%) and • Viangchan (6%). Others that were identified included • Mediterranean (4%), • Union (2%) and • Canton (2%) • G6PD Mahidol is considered a moderately severe variant with varying G6PD activities which classifies it as WHO class II/III.
  • 14. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax G6PD deficiency prevalence in Myanmar State_Region G6PD intermediate prevalence (%) G6PD deficiency prevalence (%) Total cases (2021) Ayeyarwady Not available Not available 92 Bago Not available Not available 585 Chin 2.7 - 14.4 0.3 - 12.5 15,961 Kachin 13.2 - 23.4 2.1 - 30 22,449 Kayah 0.14 - 1.3 0 - 1.9 7 Kayin Not available 12.9 - 14.1 21,382 Magway Not available Not available 149 Mandalay 0.9 - 15.8 0.3 - 11.1 411 Mon Not available 0 - 12 2,012 Naypyitaw Not available Not available 7 Rakhine 0.8 - 14.4 0 - 12.5 6,364 Sagaing Not available Not available 1,089 Shan Not available 10.9 - 21.2 707 Tanintharyi Not available 0.3 - 11.1 7,748 Yangon 0 - 14 0.9 - 21 38
  • 15. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Implications of evidence-based information to inform policy makers for data-driven policy adoption High malaria burden townships (2021) Malaria Atlas Project estimated G6PD deficiency allele frequency 12% 0% 6% G6PDd allele frequency Myanmar has an average G6PDd allele frequency of 6.1% Annual Parasite Incident by State/ Region (2021)
  • 16. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax UNOPS-PR VBDC Annual Review Meeting, 2022 Sr. No . Sub- recipients No. of State/ Region No. of townships covered No. of ICMV Activities 1 MAM Mon, Chin, Kachin, Kayin, Sagaing 22 1752 Malaria case management, Prevention 2 MCC Chin, Kachin 17 529 Malaria case management, Prevention 3 MHAA Bago East, Chin 3 141 Malaria case management, Prevention 4 MMA Ayeyarwady 2 100 Malaria case management, Prevention, elimination surveillance 5 MRCS SSS 5 185 Malaria case management, Prevention 6 SMRU Kayin 4 916 Malaria case management, Prevention, Research
  • 17. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Save the Children Co-PR VBDC Annual Review Meeting, 2022 Sr. No . Sub- recipients No. of State/ Region No. of townshi ps covered No. of ICMV Activities 1 ARC BagoE, Kayin, Mon, NSS, TYI 23 596 Malaria case management, Prevention, elimination surveillance 2 HPA Kachin, NSS, ESS 18 516 Malaria case management, Prevention 3 IOM Mon, Sagaing 11 651 Malaria case management, Prevention, elimination surveillance 4 MI (Country & Regional) Rakhine, ESS 7 177 Malaria case management, Prevention 5 PSI (Country & Regional) 11 27 759 Malaria case management, Prevention, elimination surveillance 6 SCI (Country & Regional) Magway, NSS 7 426 Malaria case management, Prevention
  • 18. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax PMI Eliminate Malaria VBDC Annual Review Meeting, 2022 Sr. No . Sub- recipie nts No. of State/ Region No. of townshi ps covered NO. of ICMV Activities 1 ARC Kayin, TYI 7 394 Malaria case management, Prevention, elimination surveillance 2 MHAA Rakhine 3 231 Malaria case management, Prevention 3 MNMA Rakhine 2 181 Malaria case management, Prevention 4 URC Rakhine, Sagaing, TYI 24 1338 Malaria case management, Prevention, elimination surveillance
  • 19. Point-of-care testing for G6PD deficiency to optimize radical cure of P.vivax Implication of G6PD deficiency prevalence and variants on NMCP recommendations  Studies over time, and in several different populations in Myanmar have identified populations with moderate to high prevalence of G6PD deficiency up to 30.5% prevalence.  These results strongly support the WHO recommendations to screen G6PD deficiency at health facility level before the use of primaquine (or any 8-AQ) prior to radical curative regimen for Plasmodium vivax.2  Given the variability of G6PDd prevalence, patient counselling as to the potential side effects of 8- aminoquinolines and a strong pharmacovigilance system are important in Myanmar to ensure patient safety  Treatment strategies to treat vivax malaria in G6PD deficient patients will be important to achieve malaria elimination in Myanmar
  • 20. Session 4: G6PD deficiency in Myanmar Point-of-care testing for G6PD deficiency to optimize radical cure of P. vivax Knowledge sharing Thank you.