Risk of malaria in British residents returning from malarious areas

OBJECTIVES--To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria chemoprophylaxis for preventing P falciparum infections in tropical Africa. DESIGN--Prospective cohort study (case-base linkage) with routine national...

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Published inBMJ Vol. 300; no. 6723; pp. 499 - 503
Main Authors Phillips-Howard, P A, Radalowicz, A, Mitchell, J, Bradley, D J
Format Journal Article
LanguageEnglish
Published London British Medical Journal Publishing Group 24.02.1990
British Medical Association
BMJ Publishing Group LTD
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Abstract OBJECTIVES--To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria chemoprophylaxis for preventing P falciparum infections in tropical Africa. DESIGN--Prospective cohort study (case-base linkage) with routine national surveillance systems. Denominators (base population) were obtained from monitoring a random sample of returning British travellers with the international passenger survey. Numerators (cases) were obtained from reports of malaria infections in British residents, through the Malaria Reference Laboratory network. SETTING--International passenger survey conducted at passport control of international airports in Britain. Malaria reports received nationally were collated centrally in London. SUBJECTS--2948 British residents (0.2%) returning to Britain in 1987 randomly selected and questioned and 1052 British residents with microscopically confirmed malaria infections in 1987, whose case reports were reviewed and on whom additional data were collected by postal survey. MAIN OUTCOME MEASURES--Annual incidence subdivided by categories of risk. Chemoprophylactic efficacy for east and west Africa by principal regimens and compliance. RESULTS--Annual rates of reported infection per 100,000 travellers to Oceania were 4100; to west and east Africa were 375 and 172 respectively; to Latin America, the Far East, and the Middle East were 12, 2, and 1 respectively. Immigrants visiting friends and relatives in Ghana and Nigeria were at greatest risk (1303 and 952 per 100,000 respectively) in west Africa. Business travellers to Kenya experienced the highest attack rates in east Africa (465 per 100,000). Age-sex specific attack rates varied by region. No prophylaxis was reported to have been used by 23% of British visitors to west Africa, 17% to east Africa, 46% to central or southern Africa, and 58% visiting south Asia. The efficacy of chloroquine plus proguanil against P falciparum infection was 73% and 54% in west and east Africa respectively. Lower values were obtained for chloroquine alone and proguanil alone. The efficacy of Maloprim (pyrimethamine-dapsone) was 61% in west Africa, but only 9% in east Africa. Visitors to west Africa who did not comply with their chemoprophylactic regimen were at a 2.5-fold higher risk of infection than fully compliant users. Non-compliant visitors to east Africa had similar rates of infection as non-drug users. CONCLUSIONS--In 1987 chloroquine plus proguanil was the preferred chemoprophylactic regimen for P falciparum infection in Africa; antimalarial drugs must be taken regularly to be effective.
AbstractList OBJECTIVESTo identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria chemoprophylaxis for preventing P falciparum infections in tropical Africa.DESIGNProspective cohort study (case-base linkage) with routine national surveillance systems. Denominators (base population) were obtained from monitoring a random sample of returning British travellers with the international passenger survey. Numerators (cases) were obtained from reports of malaria infections in British residents, through the Malaria Reference Laboratory network.SETTINGInternational passenger survey conducted at passport control of international airports in Britain. Malaria reports received nationally were collated centrally in London.SUBJECTS2948 British residents (0.2%) returning to Britain in 1987 randomly selected and questioned and 1052 British residents with microscopically confirmed malaria infections in 1987, whose case reports were reviewed and on whom additional data were collected by postal survey.MAIN OUTCOME MEASURESAnnual incidence subdivided by categories of risk. Chemoprophylactic efficacy for east and west Africa by principal regimens and compliance.RESULTSAnnual rates of reported infection per 100,000 travellers to Oceania were 4100; to west and east Africa were 375 and 172 respectively; to Latin America, the Far East, and the Middle East were 12, 2, and 1 respectively. Immigrants visiting friends and relatives in Ghana and Nigeria were at greatest risk (1303 and 952 per 100,000 respectively) in west Africa. Business travellers to Kenya experienced the highest attack rates in east Africa (465 per 100,000). Age-sex specific attack rates varied by region. No prophylaxis was reported to have been used by 23% of British visitors to west Africa, 17% to east Africa, 46% to central or southern Africa, and 58% visiting south Asia. The efficacy of chloroquine plus proguanil against P falciparum infection was 73% and 54% in west and east Africa respectively. Lower values were obtained for chloroquine alone and proguanil alone. The efficacy of Maloprim (pyrimethamine-dapsone) was 61% in west Africa, but only 9% in east Africa. Visitors to west Africa who did not comply with their chemoprophylactic regimen were at a 2.5-fold higher risk of infection than fully compliant users. Non-compliant visitors to east Africa had similar rates of infection as non-drug users.CONCLUSIONSIn 1987 chloroquine plus proguanil was the preferred chemoprophylactic regimen for P falciparum infection in Africa; antimalarial drugs must be taken regularly to be effective.
To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria chemoprophylaxis for preventing P falciparum infections in tropical Africa. Prospective cohort study (case-base linkage) with routine national surveillance systems. Denominators (base population) were obtained from monitoring a random sample of returning British travellers with the international passenger survey. Numerators (cases) were obtained from reports of malaria infections in British residents, through the Malaria Reference Laboratory network. International passenger survey conducted at passport control of international airports in Britain. Malaria reports received nationally were collated centrally in London. 2948 British residents (0.2%) returning to Britain in 1987 randomly selected and questioned and 1052 British residents with microscopically confirmed malaria infections in 1987, whose case reports were reviewed and on whom additional data were collected by postal survey. Annual incidence subdivided by categories of risk. Chemoprophylactic efficacy for east and west Africa by principal regimens and compliance. Annual rates of reported infection per 100,000 travellers to Oceania were 4100; to west and east Africa were 375 and 172 respectively; to Latin America, the Far East, and the Middle East were 12, 2, and 1 respectively. Immigrants visiting friends and relatives in Ghana and Nigeria were at greatest risk (1303 and 952 per 100,000 respectively) in west Africa. Business travellers to Kenya experienced the highest attack rates in east Africa (465 per 100,000). Age-sex specific attack rates varied by region. No prophylaxis was reported to have been used by 23% of British visitors to west Africa, 17% to east Africa, 46% to central or southern Africa, and 58% visiting south Asia. The efficacy of chloroquine plus proguanil against P falciparum infection was 73% and 54% in west and east Africa respectively. Lower values were obtained for chloroquine alone and proguanil alone. The efficacy of Maloprim (pyrimethamine-dapsone) was 61% in west Africa, but only 9% in east Africa. Visitors to west Africa who did not comply with their chemoprophylactic regimen were at a 2.5-fold higher risk of infection than fully compliant users. Non-compliant visitors to east Africa had similar rates of infection as non-drug users. In 1987 chloroquine plus proguanil was the preferred chemoprophylactic regimen for P falciparum infection in Africa; antimalarial drugs must be taken regularly to be effective.
To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria chemoprophylaxis for preventing Plasmodium falciparum infections in tropical Africa. Annual rates of reported infection per 100,000 travellers to Oceania were 4100; to west and east Africa were 375 and 172 respectively; to Latin America, the Far East, and the Middle East were 12, 2, and 1 respectively. Immigrants visiting friends and relatives in Ghana and Nigeria were at greatest risk (1303 and 952 per 100,000 respectively) in west Africa. Business travellers to Kenya experienced the highest attack rates in east Africa (465 per 100,000). Age-sex specific attack rates varied by region. No prophylaxis was reported to have been used by 23% of British visitors to west Africa, 17% to east Africa, 46% to central or southern Africa, and 58% visiting south Asia.
Objectives—To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria chemoprophylaxis for preventing P falciparum infections in tropical Africa. Design—Prospective cohort study (case-base linkage) with routine national surveillance systems. Denominators (base population) were obtained from monitoring a random sample of returning British travellers with the international passenger survey. Numerators (cases) were obtained from reports of malaria infections in British residents, through the Malaria Reference Laboratory network. Setting—International passenger survey conducted at passport control of international airports in Britain. Malaria reports received nationally were collated centrally in London. Subjects—2948 British residents (0.2%) returning to Britain in 1987 randomly selected and questioned and 1052 British residents with microscopically confirmed malaria infections in 1987, whose case reports were reviewed and on whom additional data were collected by postal survey. Main outcome measures—Annual incidence subdivided by categories of risk. Chemoprophylactic efficacy for east and west Africa by principal regimens and compliance. Results—Annual rates of reported infection per 100 000 travellers to Oceania were 4100; to west and east Africa were 375 and 172 respectively; to Latin America, the Far East, and the Middle East were 12, 2, and 1 respectively. Immigrants visiting friends and relatives in Ghana and Nigeria were at greatest risk (1303 and 952 per 100 000 respectively) in west Africa. Business travellers to Kenya experienced the highest attack rates in east Africa (465 per 100 000). Age-sex specific attack rates varied by region. No prophylaxis was reported to have been used by 23% of British visitors to west Africa, 17% to east Africa, 46% to central or southern Africa, and 58% visiting south Asia. The efficacy of chloroquine plus proguanil against P falciparum infection was 73% and 54% in west and east Africa respectively. Lower values were obtained for chloroquine alone and proguanil alone. The efficacy of Maloprim (pyrimethamine-dapsone) was 61% in west Africa, but only 9% in east Africa. Visitors to west Africa who did not comply with their chemoprophylactic regimen were at a 2.5-fold higher risk of infection than fully compliant users. Non-compliant visitors to east Africa had similar rates of infection as non-drug users. Conclusions—In 1987 chloroquine plus proguanil was the preferred chemoprophylactic regimen for P falciparum infection in Africa; antimalarial drugs must be taken regularly to be effective.
Author Bradley, D J
Phillips-Howard, P A
Mitchell, J
Radalowicz, A
AuthorAffiliation Department of Epidemiology and Population Sciences, London School of Hygiene and Tropical Medicine
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https://www.ncbi.nlm.nih.gov/pubmed/2107927$$D View this record in MEDLINE/PubMed
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Infection
Prevention
Protozoa
Plasmodium falciparum
Protozoal disease
Malaria
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Parasitosis
Sporozoa
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PublicationDate_xml – month: 02
  year: 1990
  text: 1990-02-24
  day: 24
PublicationDecade 1990
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationTitle BMJ
PublicationTitleAlternate BMJ
PublicationYear 1990
Publisher British Medical Journal Publishing Group
British Medical Association
BMJ Publishing Group LTD
Publisher_xml – name: British Medical Journal Publishing Group
– name: British Medical Association
– name: BMJ Publishing Group LTD
References Pthillips-Howard, P.A.; Mitchell, J.; Bradley, D.J. (ref_5) press,).; 12
Kirkwoud, B. (ref_6); 1988
D)J, Bradley (ref_1) 1989; 82
Lobel, H.O. (ref_3); 7
(ref_7) 1989; 299
lEA, Peto; CF, Gilks (ref_2) 1986; i
Harrics Al), Forcshav (C. J Friedti HM (ref_4) 1988; 82
References_xml – volume: 299
  start-page: 1087
  year: 1989
  ident: ref_7
  article-title: Prophylaxis agaitist malaria for travcllcrs from the United Kingdiom
  publication-title: lr.lli-dj
– volume: i:
  start-page: 1256
  year: 1986
  ident: ref_2
  article-title: Stratcgies for the prevention of malaria in travellers: comparisoni ot' drug regimens hv mcans of risk henefit analysis. LIancet'
  contributor:
    fullname: lEA, Peto; CF, Gilks
– volume: 7
  start-page: 820
  issue: 1988
  ident: ref_3
  article-title: Phillips-Howard 1'A, Brandling-Bcnnctt AD, ei al. Malaria incidencc and prevention among huro ati and North American trav, cllcrs to Kcnya
  publication-title: Br Med; Nalaria chemoproph\ylaxis in travcllers to cast Af'rica: a comparative prospective study of chloroquicte pltis progtianil with chloroquine ptiis sulfadoxinc-pyrimethaminc
  contributor:
    fullname: Lobel, H.O.
– volume: 82
  start-page: 69
  year: 1988
  ident: ref_4
  article-title: Malaria prophylaxis atnoligst British residtits of Lilonigwc and Kastingit districts, Mialawi. Irans R Soc Trop
  contributor:
    fullname: Harrics Al), Forcshav (C. J Friedti HM
– volume: 1988
  start-page: 366
  ident: ref_6
  article-title: IEssentials of medical sailisuics. Oxfiord: Blackw, cll Scicntilic Publications, 1988: 174-S. 14 Phillips-Howard I'A. [h'le cpidcmiologv of' malaria in Britaill lI'hl) thesis]. Lontidon: Univcrsitv oif
  publication-title: Londoti
  contributor:
    fullname: Kirkwoud, B.
– volume: 82
  start-page: 17
  year: 1989
  ident: ref_1
  article-title: Current trends in malaria in Britain..7 R
  publication-title: Soc. Aled
  contributor:
    fullname: D)J, Bradley
– volume: 12
  start-page: 1
  year: press,).
  ident: ref_5
  article-title: Validation ol malaria stirvillaticc rcports: implicatiotis fuor sttdies of' malaria risk. j I.pidemlo/ (Couluniiltvis'
  publication-title: Health in; Shnrt tcrm travel to toalariotis arcas; malaria risk in UK travellers. lravel, M1dicinti
  contributor:
    fullname: Pthillips-Howard, P.A.; Mitchell, J.; Bradley, D.J.
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Snippet OBJECTIVES--To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria...
Objectives—To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria...
To identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria chemoprophylaxis for...
OBJECTIVESTo identify which British residents travelling abroad are at greatest risk of malaria infection, and to determine the efficacy of malaria...
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StartPage 499
SubjectTerms Adolescent
Adult
Africa - epidemiology
Aged
Animals
Antimalarials
Antimalarials - therapeutic use
Asia, Southeastern - epidemiology
Biological and medical sciences
Case-Control Studies
Chemoprevention
Child
Child, Preschool
Confidence interval
Female
Holiday travel
Humans
Infant
Infant, Newborn
Infections
Infectious diseases
Malaria
Malaria - epidemiology
Malaria - prevention & control
Male
Medical sciences
Medication adherence
Middle Aged
Parasitic diseases
Passengers
Patient Compliance
Plasmodium falciparum
Prescription drugs
Prospective Studies
Risk Factors
Travel
United Kingdom - epidemiology
Title Risk of malaria in British residents returning from malarious areas
URI http://dx.doi.org/10.1136/bmj.300.6723.499
https://api.istex.fr/ark:/67375/NVC-0XT444HF-V/fulltext.pdf
https://www.jstor.org/stable/29707021
https://www.ncbi.nlm.nih.gov/pubmed/2107927
https://www.proquest.com/docview/1776427808/abstract/
https://search.proquest.com/docview/15610129
https://search.proquest.com/docview/79686007
https://pubmed.ncbi.nlm.nih.gov/PMC1662322
Volume 300
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