Severe Falciparum and Vivax Malaria on the Thailand-Myanmar Border: A Review of 1503 Cases

Abstract Background The northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination activities, malaria was a major cause of disease and death. Historically the incidences of symptomatic Plasmodium falciparum and Plasmodium vivax malar...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Clinical infectious diseases Ročník 77; číslo 5; s. 721 - 728
Hlavní autoři: Chu, Cindy S, Stolbrink, Marie, Stolady, Daniel, Saito, Makoto, Beau, Candy, Choun, Kan, Wah, Tha Gay, Mu, Ne, Htoo, Klay, Nu, Be, Keereevijit, Arunrot, Wiladpaingern, Jacher, Carrara, Verena, Phyo, Aung Pyae, Lwin, Khin Maung, Luxemburger, Christine, Proux, Stephane, Charunwatthana, Prakaykaew, McGready, Rose, White, Nicholas J, Nosten, François
Médium: Journal Article
Jazyk:angličtina
Vydáno: US Oxford University Press 05.05.2023
Témata:
ISSN:1058-4838, 1537-6591, 1537-6591
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Abstract Abstract Background The northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination activities, malaria was a major cause of disease and death. Historically the incidences of symptomatic Plasmodium falciparum and Plasmodium vivax malaria were approximately similar. Methods All malaria cases managed in the Shoklo Malaria Research Unit along the Thailand-Myanmar border between 2000 and 2016 were reviewed. Results There were 80 841 consultations for symptomatic P. vivax and 94 467 for symptomatic P. falciparum malaria. Overall, 4844 (5.1%) patients with P. falciparum malaria were admitted to field hospitals, of whom 66 died, compared with 278 (0.34%) with P. vivax malaria, of whom 4 died (3 had diagnoses of sepsis, so the contribution of malaria to their fatal outcomes is uncertain). Applying the 2015 World Health Organization severe malaria criteria, 68 of 80 841 P. vivax admissions (0.08%) and 1482 of 94 467 P. falciparum admissions (1.6%) were classified as severe. Overall, patients with P. falciparum malaria were 15 (95% confidence interval, 13.2–16.8) times more likely than those with P. vivax malaria to require hospital admission, 19 (14.6–23.8) times more likely to develop severe malaria, and ≥14 (5.1–38.7) times more likely to die. Conclusions In this area, both P. falciparum and P. vivax infections were important causes of hospitalization, but life-threatening P. vivax illness was rare. Among 94 467 patients with Plasmodium falciparum and 80 841 with Plasmodium vivax malaria, patients with P. falciparum were 15 times more likely to require hospital admission, 19 times more likely to develop severe malaria, and 14 times more likely to die.
AbstractList Abstract Background The northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination activities, malaria was a major cause of disease and death. Historically the incidences of symptomatic Plasmodium falciparum and Plasmodium vivax malaria were approximately similar. Methods All malaria cases managed in the Shoklo Malaria Research Unit along the Thailand-Myanmar border between 2000 and 2016 were reviewed. Results There were 80 841 consultations for symptomatic P. vivax and 94 467 for symptomatic P. falciparum malaria. Overall, 4844 (5.1%) patients with P. falciparum malaria were admitted to field hospitals, of whom 66 died, compared with 278 (0.34%) with P. vivax malaria, of whom 4 died (3 had diagnoses of sepsis, so the contribution of malaria to their fatal outcomes is uncertain). Applying the 2015 World Health Organization severe malaria criteria, 68 of 80 841 P. vivax admissions (0.08%) and 1482 of 94 467 P. falciparum admissions (1.6%) were classified as severe. Overall, patients with P. falciparum malaria were 15 (95% confidence interval, 13.2–16.8) times more likely than those with P. vivax malaria to require hospital admission, 19 (14.6–23.8) times more likely to develop severe malaria, and ≥14 (5.1–38.7) times more likely to die. Conclusions In this area, both P. falciparum and P. vivax infections were important causes of hospitalization, but life-threatening P. vivax illness was rare. Among 94 467 patients with Plasmodium falciparum and 80 841 with Plasmodium vivax malaria, patients with P. falciparum were 15 times more likely to require hospital admission, 19 times more likely to develop severe malaria, and 14 times more likely to die.
The northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination activities, malaria was a major cause of disease and death. Historically the incidences of symptomatic Plasmodium falciparum and Plasmodium vivax malaria were approximately similar.BACKGROUNDThe northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination activities, malaria was a major cause of disease and death. Historically the incidences of symptomatic Plasmodium falciparum and Plasmodium vivax malaria were approximately similar.All malaria cases managed in the Shoklo Malaria Research Unit along the Thailand-Myanmar border between 2000 and 2016 were reviewed.METHODSAll malaria cases managed in the Shoklo Malaria Research Unit along the Thailand-Myanmar border between 2000 and 2016 were reviewed.There were 80 841 consultations for symptomatic P. vivax and 94 467 for symptomatic P. falciparum malaria. Overall, 4844 (5.1%) patients with P. falciparum malaria were admitted to field hospitals, of whom 66 died, compared with 278 (0.34%) with P. vivax malaria, of whom 4 died (3 had diagnoses of sepsis, so the contribution of malaria to their fatal outcomes is uncertain). Applying the 2015 World Health Organization severe malaria criteria, 68 of 80 841 P. vivax admissions (0.08%) and 1482 of 94 467 P. falciparum admissions (1.6%) were classified as severe. Overall, patients with P. falciparum malaria were 15 (95% confidence interval, 13.2-16.8) times more likely than those with P. vivax malaria to require hospital admission, 19 (14.6-23.8) times more likely to develop severe malaria, and ≥14 (5.1-38.7) times more likely to die.RESULTSThere were 80 841 consultations for symptomatic P. vivax and 94 467 for symptomatic P. falciparum malaria. Overall, 4844 (5.1%) patients with P. falciparum malaria were admitted to field hospitals, of whom 66 died, compared with 278 (0.34%) with P. vivax malaria, of whom 4 died (3 had diagnoses of sepsis, so the contribution of malaria to their fatal outcomes is uncertain). Applying the 2015 World Health Organization severe malaria criteria, 68 of 80 841 P. vivax admissions (0.08%) and 1482 of 94 467 P. falciparum admissions (1.6%) were classified as severe. Overall, patients with P. falciparum malaria were 15 (95% confidence interval, 13.2-16.8) times more likely than those with P. vivax malaria to require hospital admission, 19 (14.6-23.8) times more likely to develop severe malaria, and ≥14 (5.1-38.7) times more likely to die.In this area, both P. falciparum and P. vivax infections were important causes of hospitalization, but life-threatening P. vivax illness was rare.CONCLUSIONSIn this area, both P. falciparum and P. vivax infections were important causes of hospitalization, but life-threatening P. vivax illness was rare.
The northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination activities, malaria was a major cause of morbidity and mortality. Historically the incidences of symptomatic Plasmodium falciparum and Plasmodium vivax malaria were approximately similar. All malaria cases managed in the Shoklo Malaria Research Unit along the Thailand-Myanmar border between 2000 and 2016 were reviewed. There were 80,841 consultations for symptomatic P. vivax and 94,467 for symptomatic P. falciparum malaria. Overall 4,844 (5.1%) patients with P. falciparum malaria were admitted to field hospitals, of whom 66 died, compared with 278 (0.34%) with P. vivax malaria, of whom four died (three were diagnosed with sepsis, so the contribution of malaria to their fatal outcomes is uncertain). Applying the 2015 "World Health Organization severe malaria criteria", 68/80,841 (0.08%) of P. vivax and 1,482/94,467 (1.6%) of P. falciparum admissions were classified as severe. Overall, patients with P. falciparum malaria were 15 (95% CI 13.2-16.8) times more likely than P. vivax to require hospital admission, 19 (95% CI 14.6-23.8) times more likely to develop severe malaria, and at least 14 (95% CI 5.1-38.7) times more likely to die. In this area both P. falciparum and P. vivax infections were important causes of hospitalization, but life-threatening P. vivax illness was rare.
Author Nu, Be
Htoo, Klay
Wiladpaingern, Jacher
Chu, Cindy S
Keereevijit, Arunrot
Stolady, Daniel
Beau, Candy
Saito, Makoto
Carrara, Verena
Lwin, Khin Maung
Stolbrink, Marie
Choun, Kan
White, Nicholas J
Wah, Tha Gay
Charunwatthana, Prakaykaew
Mu, Ne
Phyo, Aung Pyae
McGready, Rose
Luxemburger, Christine
Proux, Stephane
Nosten, François
Author_xml – sequence: 1
  givenname: Cindy S
  surname: Chu
  fullname: Chu, Cindy S
– sequence: 2
  givenname: Marie
  surname: Stolbrink
  fullname: Stolbrink, Marie
– sequence: 3
  givenname: Daniel
  surname: Stolady
  fullname: Stolady, Daniel
– sequence: 4
  givenname: Makoto
  surname: Saito
  fullname: Saito, Makoto
– sequence: 5
  givenname: Candy
  surname: Beau
  fullname: Beau, Candy
– sequence: 6
  givenname: Kan
  surname: Choun
  fullname: Choun, Kan
– sequence: 7
  givenname: Tha Gay
  surname: Wah
  fullname: Wah, Tha Gay
– sequence: 8
  givenname: Ne
  surname: Mu
  fullname: Mu, Ne
– sequence: 9
  givenname: Klay
  surname: Htoo
  fullname: Htoo, Klay
– sequence: 10
  givenname: Be
  surname: Nu
  fullname: Nu, Be
– sequence: 11
  givenname: Arunrot
  surname: Keereevijit
  fullname: Keereevijit, Arunrot
– sequence: 12
  givenname: Jacher
  surname: Wiladpaingern
  fullname: Wiladpaingern, Jacher
– sequence: 13
  givenname: Verena
  surname: Carrara
  fullname: Carrara, Verena
– sequence: 14
  givenname: Aung Pyae
  surname: Phyo
  fullname: Phyo, Aung Pyae
– sequence: 15
  givenname: Khin Maung
  surname: Lwin
  fullname: Lwin, Khin Maung
– sequence: 16
  givenname: Christine
  surname: Luxemburger
  fullname: Luxemburger, Christine
– sequence: 17
  givenname: Stephane
  surname: Proux
  fullname: Proux, Stephane
– sequence: 18
  givenname: Prakaykaew
  surname: Charunwatthana
  fullname: Charunwatthana, Prakaykaew
– sequence: 19
  givenname: Rose
  surname: McGready
  fullname: McGready, Rose
– sequence: 20
  givenname: Nicholas J
  orcidid: 0000-0002-1897-1978
  surname: White
  fullname: White, Nicholas J
  email: nickw@tropmedres.ac
– sequence: 21
  givenname: François
  surname: Nosten
  fullname: Nosten, François
BackLink https://www.ncbi.nlm.nih.gov/pubmed/37144342$$D View this record in MEDLINE/PubMed
BookMark eNo9kMtLAzEQh4NU7ENP3iUn8bKa9ybearEqtAhaPXhZ0iRLU_blplvtf2-k1cMwA7-PYeYbgl5VVw6Ac4yuMVL0xngbS1siyBEYYE7TRHCFe3FGXCZMUtkHwxDWCGEsET8BfZpixigjA_Dx6raudXCqC-Mb3XYl1JWF736rv-FcF7r1GtYV3KwcXKy0L2KazHe6KnUL7-rWuvYWjuGL23r3BescYo4onOjgwik4znUR3Nmhj8Db9H4xeUxmzw9Pk_EsWRPFNomxKUm5zQ01AkusKRfIUomWTKpU8ZSlSObWSOIYEQ6zXBFLjMyV0FKYnNMRuNrvbdr6s3Nhk5U-GFfEU13dhYzIqAlTKVRELw5otyydzZrWxz922Z-PCFzugbpr_lOMsl_RWRSdHUTTH1asbik
ContentType Journal Article
Copyright The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2023
The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
Copyright_xml – notice: The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2023
– notice: The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
DBID TOX
NPM
7X8
DOI 10.1093/cid/ciad262
DatabaseName Oxford Journals Open Access Collection
PubMed
MEDLINE - Academic
DatabaseTitle PubMed
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
PubMed
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: TOX
  name: Oxford Journals Open Access Collection
  url: https://academic.oup.com/journals/
  sourceTypes: Publisher
– sequence: 3
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1537-6591
EndPage 728
ExternalDocumentID 37144342
10.1093/cid/ciad262
Genre Journal Article
GrantInformation_xml – fundername: Wellcome Trust
  grantid: 089179
GroupedDBID ---
..I
.2P
.GJ
.I3
.ZR
08P
0R~
1KJ
1TH
29B
2AX
2WC
36B
3O-
4.4
48X
53G
5GY
5RE
5VS
5WD
6.Y
6J9
70D
AABZA
AACGO
AACZT
AAJKP
AAJQQ
AAMVS
AANCE
AAOGV
AAPGJ
AAPNW
AAPQZ
AAPXW
AAQQT
AARHZ
AASNB
AAUAY
AAUQX
AAVAP
AAWDT
AAYOK
ABBHK
ABEUO
ABIXL
ABJNI
ABKDP
ABLJU
ABNHQ
ABNKS
ABOCM
ABPLY
ABPTD
ABQLI
ABQNK
ABSAR
ABSMQ
ABTLG
ABWST
ABXSQ
ABXVV
ABZBJ
ACFRR
ACGFO
ACGFS
ACMRT
ACPQN
ACPRK
ACUFI
ACUTJ
ACUTO
ACYHN
ACZBC
ADACV
ADBBV
ADEYI
ADGZP
ADHKW
ADHZD
ADIPN
ADJQC
ADOCK
ADQBN
ADRIX
ADRTK
ADULT
ADVEK
ADYVW
ADZXQ
AEGPL
AEGXH
AEJOX
AEKPW
AEKSI
AEMDU
AENEX
AENZO
AEPUE
AETBJ
AEUPB
AEWNT
AEXZC
AFFNX
AFFZL
AFIYH
AFOFC
AFRAH
AFSHK
AFXAL
AFXEN
AFYAG
AGINJ
AGKEF
AGKRT
AGMDO
AGQXC
AGSYK
AGUTN
AHMBA
AHXPO
AI.
AIAGR
AIJHB
AJEEA
ALMA_UNASSIGNED_HOLDINGS
ALUQC
APIBT
APJGH
APWMN
AQDSO
AQKUS
AQVQM
ASPBG
ATGXG
AVNTJ
AVWKF
AXUDD
AZFZN
BAWUL
BAYMD
BCRHZ
BEYMZ
BHONS
BTRTY
BVRKM
BZKNY
C1A
C45
CDBKE
CS3
CZ4
DAKXR
DCCCD
DIK
DILTD
DOOOF
DU5
D~K
E3Z
EBS
EE~
EIHJH
EJD
EMOBN
ENERS
ESX
F5P
F9B
FECEO
FEDTE
FLUFQ
FOEOM
FOTVD
FQBLK
GAUVT
GJXCC
H13
H5~
HAR
HQ3
HTVGU
HVGLF
HW0
HZ~
IOX
IPSME
J21
J5H
JAAYA
JBMMH
JENOY
JHFFW
JKQEH
JLS
JLXEF
JPM
JSG
JSODD
JST
KAQDR
KBUDW
KOP
KSI
KSN
L7B
M49
MBLQV
MHKGH
MJL
ML0
N4W
N9A
NGC
NOMLY
NOYVH
NU-
NVLIB
O0~
O9-
OAUYM
OAWHX
OCZFY
ODMLO
ODZKP
OJQWA
OJZSN
OK1
OPAEJ
OVD
OWPYF
O~Y
P2P
P6G
PAFKI
PB-
PEELM
PQQKQ
Q1.
Q5Y
QBD
RD5
ROX
ROZ
RUSNO
RW1
RXO
SA0
SJN
TCURE
TEORI
TJX
TMA
TOX
TR2
VH1
W8F
X7H
Y6R
YAYTL
YKOAZ
YXANX
ZGI
~91
~S-
ABDFA
ABEJV
ABGNP
ABVGC
AHMMS
NPM
7X8
ABPQP
ADNBA
AEMQT
AHGBF
AJBYB
AJNCP
ALXQX
JXSIZ
ID FETCH-LOGICAL-j294t-cd7275dfc3c6181a3560d380b48979574708fdc82e426e14f92d2c8f96a86cf53
IEDL.DBID TOX
ISICitedReferencesCount 11
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000994522000001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1058-4838
1537-6591
IngestDate Sat Sep 27 21:49:39 EDT 2025
Wed Feb 19 02:23:06 EST 2025
Wed Aug 28 03:18:23 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Keywords epidemiology
severe malaria
Severe malaria
Plasmodium falciparum
Plasmodium vivax
Epidemiology
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-j294t-cd7275dfc3c6181a3560d380b48979574708fdc82e426e14f92d2c8f96a86cf53
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-1897-1978
OpenAccessLink https://dx.doi.org/10.1093/cid/ciad262
PMID 37144342
PQID 2810913869
PQPubID 23479
PageCount 8
ParticipantIDs proquest_miscellaneous_2810913869
pubmed_primary_37144342
oup_primary_10_1093_cid_ciad262
PublicationCentury 2000
PublicationDate 20230505
PublicationDateYYYYMMDD 2023-05-05
PublicationDate_xml – month: 5
  year: 2023
  text: 20230505
  day: 5
PublicationDecade 2020
PublicationPlace US
PublicationPlace_xml – name: US
– name: United States
PublicationTitle Clinical infectious diseases
PublicationTitleAlternate Clin Infect Dis
PublicationYear 2023
Publisher Oxford University Press
Publisher_xml – name: Oxford University Press
SSID ssj0011805
Score 2.478744
Snippet Abstract Background The northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination...
The northwestern border of Thailand is an area of low seasonal malaria transmission. Until recent successful malaria elimination activities, malaria was a...
SourceID proquest
pubmed
oup
SourceType Aggregation Database
Index Database
Publisher
StartPage 721
Title Severe Falciparum and Vivax Malaria on the Thailand-Myanmar Border: A Review of 1503 Cases
URI https://www.ncbi.nlm.nih.gov/pubmed/37144342
https://www.proquest.com/docview/2810913869
Volume 77
WOSCitedRecordID wos000994522000001&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3JTsMwELWgQogL-1KWYiSuEY2dODa3gqg40FKJgioukePYoogmKF0Ef8_YCT0UJLj4FsuaGWXe-I3fIHROEgkoXiWeFVPzoN6gnlDSeCoNqRU8l1y7qSV3UbfLBwPRqxpkx79Q-IJeKPAKnDMl7lfrh9yGc_9-MCcLfO46FQEpuLsxXj3DW_h24QXbDyDpEkp7479H2UTrFWTErdLHW2hJZ9totVOR4jvo-UFDPGrclm-2QbqYjrDMUvw0nMkP3JFQug4lzjMMUA_3X-TQ9jJ6nU-ZjWSBr5z25iVu4ZIlwLnBgN4ovob0Nt5Fj-2b_vWtV41M8F6JCCZgYsAjYWoUVQxyt6QAaFLKm0nARSRCqB2a3KSKEw2ZWfuBESQlihvBJGfKhHQP1bI80wcIU5-yQLHAMOoHkW6KhCdNEYUqYSwlUtXRKdgzfi9FMeKSzKaxnQRcmaiOzr5tHUPQWiZCZjqfjmPCnR4pZ6KO9ksnzDeyEoIBDcjhn_sfoTU7_N21H4bHqDYppvoErajZZDguGmg5GnBYu71Ow8XLFxI5tyg
linkProvider Oxford University Press
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Severe+Falciparum+and+Vivax+Malaria+on+the+Thailand-Myanmar+Border%3A+A+Review+of+1503+Cases&rft.jtitle=Clinical+infectious+diseases&rft.au=Chu%2C+Cindy+S&rft.au=Stolbrink%2C+Marie&rft.au=Stolady%2C+Daniel&rft.au=Saito%2C+Makoto&rft.date=2023-05-05&rft.pub=Oxford+University+Press&rft.issn=1058-4838&rft.eissn=1537-6591&rft.volume=77&rft.issue=5&rft.spage=721&rft.epage=728&rft_id=info:doi/10.1093%2Fcid%2Fciad262&rft.externalDocID=10.1093%2Fcid%2Fciad262
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1058-4838&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1058-4838&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1058-4838&client=summon