Randomized Trial of Piperaquine with Sulfadoxine-Pyrimethamine or Dihydroartemisinin for Malaria Intermittent Preventive Treatment in Children 英文参考文献.docVIP
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Randomized Trial of Piperaquine with Sulfadoxine-Pyrimethamine or Dihydroartemisinin for Malaria Intermittent Preventive Treatment in Children 英文参考文献
RandomizedTrialofPiperaquinewithSulfadoxine-
PyrimethamineorDihydroartemisininforMalaria
IntermittentPreventiveTreatmentinChildren
BadaraCisse1,2,MatthewCairns2,ErnestFaye1,OusmaneNDiaye3,BabacarFaye1,CecileCames3 ,Yue
Cheng4,MaguetteNDiaye2,AminataColle′Lo?2,KirstenSimondon3,Jean-FrancoisTrape3,OumarFaye2,5,
JeanLouisNDiaye1,OumarGaye1,BrianGreenwood2,PaulMilligan2*
1DepartmentofParasitologyandMycology,UniversiteCheikhAntaDiop,Dakar,Senegal,2LondonSchoolofHygieneandTropicalMedicine,London,UnitedKingdom,
3InstitutdeRecherchepourleDeveloppement,Dakar,Senegal,4Xi’anJiaotongUniversityCollegeofMedicine,Xi’an,China,5MinisteredelaSante,Senegal
Abstract
Background:Thelongterminalhalflifeofpiperaquinemakesitsuitableforintermittentpreventivetreatmentformalaria
butnostudiesofitsuseforpreventionhavebeendoneinAfrica.Wedidaclusterrandomizedtrialtodeterminewhether
piperaquineincombinationwitheitherdihydroartemisin(DHA)orsulfadoxine-pyrimethamine(SP)isaseffective,andbetter
tolerated, than SP plus amodiaquine (AQ), when used for intermittent preventive treatment in children delivered by
communityhealthworkersinaruralareaofSenegal.
Methods: Treatments were delivered to children 3–59 months of age in their homes once per month during the
transmissionseasonbycommunityhealthworkers.33healthworkers,eachcoveringabout60children,wererandomizedto
deliver either SP+AQ, DHA+PQ or SP+PQ. Primary endpoints were the incidence of attacks of clinical malaria, and the
incidenceofadverseevents.
Results: 1893 children were enrolled. Coverage of monthly rounds and compliance with daily doses was similar in all
groups;90%ofchildrenreceived atleast2monthlydoses.PiperaquinecombinationswerebettertoleratedthanSP+AQ
withasignificantlylowerriskofcommon,mildadverseevents.103episodesofclinicalmalariawererecordedduringthe
courseofthetrial.68childrenhadmalariawithparasitaemia.3000/mL,29/671(4.3%)intheSP+AQgroup,comparedwith
22/604(3.6%)intheDHA+PQgroup(riskdifference0.47%,95%CI22.3%,+3.3%),and17/618(2.8%)int
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