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ORE Open Research Exeter TITLE Dietary interventions for recurrent abdominal pain in childhood AUTHORS Newlove-Delgado, TV; Martin, AE; Abbott, RA; et al. JOURNAL Cochrane Database of Systematic Reviews DEPOSITED IN ORE 07 June 2017 This version available at http://hdl.handle.net/10871/27846 COPYRIGHT AND REUSE Open Research Exeter makes this work available in accordance with publisher policies. A NOTE ON VERSIONS The version presented here may differ from the published version. If citing, you are advised to consult the published version for pagination, volume/issue and date of publication CochraneDatabaseofSystematicReviews Dietary interventions for recurrent abdominal pain in childhood (Review) Newlove-DelgadoTV,MartinAE,AbbottRA,BethelA,Thompson-CoonJ,WhearR,LoganS Newlove-DelgadoTV,MartinAE,AbbottRA,BethelA,Thompson-CoonJ,WhearR,LoganS. Dietaryinterventionsforrecurrentabdominalpaininchildhood. CochraneDatabaseofSystematicReviews2017,Issue3.Art.No.:CD010972. DOI:10.1002/14651858.CD010972.pub2. www.cochranelibrary.com Dietaryinterventionsforrecurrentabdominalpaininchildhood(Review) Copyright©2017TheCochraneCollaboration.PublishedbyJohnWiley&Sons,Ltd. TABLE OF CONTENTS HEADER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 ABSTRACT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 PLAINLANGUAGESUMMARY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 SUMMARYOFFINDINGSFORTHEMAINCOMPARISON . . . . . . . . . . . . . . . . . . . 4 BACKGROUND . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 OBJECTIVES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 METHODS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 RESULTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 Figure1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 Figure2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 Figure3. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17 Figure4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 Figure5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 ADDITIONALSUMMARYOFFINDINGS . . . . . . . . . . . . . . . . . . . . . . . . . . 24 DISCUSSION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27 AUTHORS’CONCLUSIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 ACKNOWLEDGEMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29 REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29 CHARACTERISTICSOFSTUDIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35 DATAANDANALYSES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60 Analysis 1.1. Comparison 1 Probiotics versus placebo, Outcome 1 Change in pain frequency: 0 to 3 months’ postintervention. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61 Analysis 1.2. Comparison 1 Probiotics versus placebo, Outcome 2 Change in pain frequency: 0 to 3 months’ postintervention.Sensitivityanalysis. . . . . . . . . . . . . . . . . . . . . . . . . . . 62 Analysis 1.3. Comparison 1 Probiotics versus placebo, Outcome 3 Change in pain intensity: 0 to 3 months’ postintervention. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63 Analysis1.4.Comparison1Probioticsversusplacebo,Outcome4Changeinpainintensity:0to3months’postintervention. Sensitivityanalysis. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64 Analysis1.5.Comparison1Probioticsversusplacebo,Outcome5Improvementinpain:0to3months’postintervention. 65 Analysis1.6.Comparison1Probioticsversusplacebo,Outcome6Improvementinpain:0to3months’postintervention. Sensitivityanalysis. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66 Analysis1.7.Comparison1Probioticsversusplacebo,Outcome7Improvementinpain:0to3months’postintervention. Subgroupanalysis(irritablebowelsyndrome). . . . . . . . . . . . . . . . . . . . . . . . 67 Analysis1.8.Comparison1Probioticsversusplacebo,Outcome8Improvementinpain:3to6months’postintervention. 68 Analysis2.1.Comparison2Fibreversusplacebo,Outcome1Changeinpainintensity:0to3months’postintervention. 68 Analysis2.2.Comparison2Fibreversusplacebo,Outcome2Improvementinpain:0to3months’postintervention. 69 ADDITIONALTABLES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69 APPENDICES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71 WHAT’SNEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85 CONTRIBUTIONSOFAUTHORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85 DECLARATIONSOFINTEREST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86 SOURCESOFSUPPORT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86 DIFFERENCESBETWEENPROTOCOLANDREVIEW . . . . . . . . . . . . . . . . . . . . . 87 NOTES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87 Dietaryinterventionsforrecurrentabdominalpaininchildhood(Review) i Copyright©2017TheCochraneCollaboration.PublishedbyJohnWiley&Sons,Ltd. [InterventionReview] Dietary interventions for recurrent abdominal pain in childhood TamsinVNewlove-Delgado1,AliceEMartin2,RebeccaAAbbott1,AlisonBethel1,JoannaThompson-Coon1,RebeccaWhear1,Stuart Logan1 1NIHRCLAHRCSouthWestPeninsula(PenCLAHRC),UniversityofExeterMedicalSchool,Exeter,UK.2Paediatrics,RoyalDevon andExeterHospital,Exeter,UK Contactaddress:TamsinVNewlove-Delgado,NIHRCLAHRCSouthWestPeninsula(PenCLAHRC),UniversityofExeterMedical School,StLuke’sCampus,Exeter,England,EX12LU,[email protected],[email protected]. Editorialgroup:CochraneDevelopmental,PsychosocialandLearningProblemsGroup. Publicationstatusanddate:New,publishedinIssue3,2017. Citation: Newlove-DelgadoTV,MartinAE,Abbott RA,BethelA,Thompson-Coon J,WhearR,Logan S.Dietary interventions for recurrent abdominal pain in childhood. Cochrane Database of Systematic Reviews 2017, Issue 3. Art. No.: CD010972. DOI: 10.1002/14651858.CD010972.pub2. Copyright©2017TheCochraneCollaboration.PublishedbyJohnWiley&Sons,Ltd. ABSTRACT Background ThisisanupdateoftheoriginalCochranereview,lastpublishedin2009(Huertas-Ceballos2009).Recurrentabdominalpain(RAP), includingchildrenwithirritablebowelsyndrome,isacommonproblemaffectingbetween4%and25%ofschool-agedchildren.For themajorityofsuchchildren,noorganiccausefortheirpaincanbefoundonphysicalexaminationorinvestigation. Manydietary inventions havebeensuggested toimprovethesymptomsofRAP.Thesemayinvolveeitherexcludingingredients fromthedietor addingsupplementssuchasfibreorprobiotics. Objectives ToexaminetheeffectivenessofdietaryinterventionsinimprovingpaininchildrenofschoolagewithRAP. Searchmethods WesearchedCENTRAL,OvidMEDLINE,Embase,eightotherdatabases,andtwotrialsregisters,togetherwithreferencechecking, citationsearchingandcontactwithstudyauthors,inJune2016. Selectioncriteria Randomisedcontrolledtrials(RCTs)comparingdietaryinterventionswithplaceboornotreatmentinchildrenagedfiveto18years withRAPoranabdominalpain-related,functionalgastrointestinaldisorder,asdefinedbytheRomeIIIcriteria(Rasquin2006). Datacollectionandanalysis WeusedstandardmethodologicalproceduresexpectedbyCochrane.Wegroupeddietaryinterventionstogetherbycategoryforanalysis. Wecontactedstudyauthorstoaskformissinginformationandclarification,whenneeded.Weassessedthequalityoftheevidencefor eachoutcomeusingtheGRADEapproach. Dietaryinterventionsforrecurrentabdominalpaininchildhood(Review) 1 Copyright©2017TheCochraneCollaboration.PublishedbyJohnWiley&Sons,Ltd. Mainresults Weincluded19RCTs,reportedin27paperswithatotalof1453participants.Fifteenofthesestudieswerenotincludedintheprevious review. All19RCTs hadfollow-upranging fromonetofivemonths. Participantswereagedbetweenfour and18yearsfromeight differentcountriesandwererecruitedlargelyfrompaediatricgastroenterologyclinics.Themeanageatrecruitmentrangedfrom6.3 yearsto13.1years.Girlsoutnumberedboysinmosttrials.Fourteentrialsrecruitedchildrenwithadiagnosisunderthebroadumbrella ofRAPorfunctionalgastrointestinaldisorders;fivetrialsspecificallyrecruitedonlychildrenwithirritablebowelsyndrome.Thestudies fellintofourcategories:trialsofprobiotic-basedinterventions(13studies),trialsoffibre-basedinterventions(fourstudies),trialsof lowFODMAP(fermentableoligosaccharides, disaccharides, monosaccharides andpolyols)diets(onestudy), andtrialsoffructose- restricteddiets(onestudy). Wefoundthatchildrentreatedwithprobioticsreportedagreaterreductioninpainfrequencyatzerotothreemonthspostintervention than those given placebo (standardised mean difference (SMD) -0.55, 95% confidence interval (CI) -0.98 to -0.12; 6 trials; 523 children).Therewasalsoadecreaseinpainintensityintheinterventiongroupatthesametimepoint(SMD-0.50,95%CI-0.85 to-0.15;7studies;575children).However,wejudgedtheevidencefortheseoutcomestobeoflowqualityusingGRADEduetoan unclearriskofbiasfromincompleteoutcomedataandsignificantheterogeneity. Wefoundthatchildrentreatedwithprobioticsweremorelikelytoexperienceimprovementinpainatzerotothreemonthspostin- terventionthanthosegivenplacebo(oddsratio(OR)1.63,95%CI1.07to2.47;7studies;722children).Theestimatednumber neededtotreatforanadditionalbeneficialoutcome(NNTB)waseight,meaningthateightchildrenwouldneedtoreceiveprobiotics foronetoexperienceimprovementinpaininthistimescale.Wejudgedtheevidenceforthisoutcometobeofmoderatequalitydue tosignificantheterogeneity. Childrenwithasymptomprofiledefinedasirritablebowelsyndrometreatedwithprobioticsweremorelikelytoexperienceimprovement inpainatzerotothreemonthspostinterventionthanthosegivenplacebo(OR3.01,95%CI1.77to5.13;4studies;344children). Childrentreatedwithprobioticsweremorelikelytoexperienceimprovementinpainatthreetosixmonthspostinterventioncompared tothosereceivingplacebo(OR1.94,95%CI1.10to3.43;2studies;224children).Wejudgedtheevidenceforthesetwooutcomes tobeofmoderatequalityduetosmallnumbersofparticipantsincludedinthestudies. Wefoundthatchildrentreatedwithfibre-basedinterventionswerenotmorelikelytoexperienceanimprovementinpainatzeroto threemonthspostinterventionthanchildrengivenplacebo(OR1.83,95%CI0.92to3.65;2studies;136children).Therewasalsono reductioninpainintensitycomparedtoplaceboatthesametimepoint(SMD-1.24,95%CI-3.41to0.94;2studies;135children). Wejudgedtheevidencefortheseoutcomestobeoflowqualityduetoanunclearriskofbias,imprecision,andsignificantheterogeneity. We found only one study of low FODMAP dietsand only one trial of fructose-restricteddiets, meaning no pooled analyseswere possible. Wewereunabletoperformanymeta-analysesforthesecondaryoutcomesofschoolperformance,socialorpsychologicalfunctioning, orqualityofdailylife,asnotenoughstudiesincludedtheseoutcomesorusedcomparablemeasurestoassessthem. Withtheexceptionofonestudy,allstudiesreportedmonitoringchildrenforadverseevents;nomajoradverseeventswerereported. Authors’conclusions Overall,wefoundmoderate-tolow-qualityevidencesuggestingthatprobioticsmaybeeffectiveinimprovingpaininchildrenwith RAP.Cliniciansmaythereforeconsiderprobioticinterventionsaspartofaholisticmanagementstrategy.However,furthertrialsare neededtoexaminelonger-termoutcomesandtoimproveconfidenceinestimatingthesizeoftheeffect,aswellastodeterminethe optimalstrainanddosage.Futureresearchshouldalsoexploretheeffectivenessofprobioticsinchildrenwithdifferentsymptomprofiles, suchasthosewithirritablebowelsyndrome. Wefoundonlyasmallnumberoftrialsoffibre-basedinterventions,withoveralllow-qualityevidencefortheoutcomes.Therewas thereforenoconvincingevidencethatfibre-basedinterventionsimprovepaininchildrenwithRAP.Furtherhigh-qualityRCTsoffibre supplementsinvolvinglargernumbersofparticipantsarerequired.FuturetrialsoflowFODMAPdietsandotherdietaryinterventions arealsorequiredtofacilitateevidence-basedrecommendations. PLAIN LANGUAGE SUMMARY Dietaryinterventionsforrecurrentabdominalpaininchildren Dietaryinterventionsforrecurrentabdominalpaininchildhood(Review) 2 Copyright©2017TheCochraneCollaboration.PublishedbyJohnWiley&Sons,Ltd. Reviewquestion Wereviewedtheevidenceontheeffectsofdietaryinterventionsonpaininchildrenagedbetweenfiveand18yearswithrecurrent abdominalpain(RAP). Background Recurrentabdominalpain,orRAP,isatermusedforunexplainedepisodesofstomachacheorabdominalpaininchildren.Recurrent abdominalpainisacommoncondition,andmostchildrenarelikelytobehelpedbysimplemeasures.However,arangeoftreatments havebeenrecommendedtorelieveabdominalpain,includingmakingchangestothechild’seatinghabitsbyaddingsupplementsor excludingcertainfoods. Studycharacteristics ThisevidenceiscurrenttoJune2016. Nineteenstudiesmetourinclusioncriteria,including13studiesofprobioticsandfourstudiesoffibreinterventions.Wealsofound onestudyofadietlowinsubstancesknownasFODMAPs(fermentableoligosaccharides,disaccharides,monosaccharidesandpolyols) andonestudyofafructose-restricteddiet. Allofthestudiescompareddietaryinterventionstoaplaceboorcontrol.Thetrialswerecarriedoutineightcountriesandincludeda totalof1453participants,agedbetweenfiveand18years.Mostchildrenwererecruitedfromoutpatientclinics.Mostinterventions lastedfourtosixweeks. Keyresults Probiotics Wefoundevidencefrom13studiessuggestingthatprobioticsmightbeeffectiveinimprovingpainintheshorterterm.Moststudies didnotreportonotherareassuchasqualityofdailylife.Noharmfuleffectswerereported,otherthandrymouthinonestudy.We judgedthisevidencetobeofmoderateorlowqualitybecausesomestudiesweresmall,showedvaryingresults,orwereatriskofbias. Fibresupplements Wefoundnoclearevidenceofimprovementofpainfromfourstudiesoffibresupplements.Moststudiesdidnotreportonotherareas suchasqualityofdailylife.Noharmfuleffectswerereported.Therewerefewstudiesoffibresupplements,andsomeofthesestudies wereatriskofbias.Wejudgedthisevidencetobeoflowquality. LowFODMAPdiets WefoundonlyonestudyevaluatingtheeffectivenessoflowFODMAPdietsinchildrenwithRAP. Fructose-restricteddiets Wefoundonlyonestudyevaluatingtheeffectivenessoffructose-restricteddietsinchildrenwithRAP. Conclusion WefoundsomeevidencesuggestingthatprobioticsmaybehelpfulinrelievingpaininchildrenwithRAPintheshortterm.Clinicians maythereforeconsiderprobioticinterventionsaspartofthemanagementstrategyforRAP.Furthertrialsareneededtofindouthow effectiveprobioticsareoverlongerperiodsoftimeandwhichprobioticsmightworkbest. WedidnotfindconvincingevidencethatfibresupplementsareeffectiveinimprovingpaininchildrenwithRAP.Futurelarger,high- qualitystudiesareneededtotesttheeffectivenessoffibreandlowFODMAPdiettreatments. Dietaryinterventionsforrecurrentabdominalpaininchildhood(Review) 3 Copyright©2017TheCochraneCollaboration.PublishedbyJohnWiley&Sons,Ltd. CopyrigDietary SUMMARY OF FINDINGS FOR THE MAIN COMPARISON [Explanation] ht©inte 20rve Probioticscomparedtoplaceboforrecurrentabdominalpaininchildhood 1n 7Ttio hn es Patientorpopulation:Childrenwithrecurrentabdominalpain Cfo ochrre Settings:Mixedsettings,includingpaediatricgastroenterologyclinics racu Intervention:Probiotics nerre Comparison:Placebo Cn ot llaab bodo Outcomes Illustrativecomparativerisks* (95%CI) Relativeeffect Numberofparticipants Qualityoftheevidence Comments rm atioina (95%CI) (studies) (GRADE) nl .p Pa uin Assumedrisk Correspondingrisk blisin hc eh dbyildho Placebo Probiotics Johod Change in pain fre- - The mean change in - 523 ⊕⊕(cid:13)(cid:13) As a rule of thumb, n(R We quency:0to3 months’ pain frequency: 0 to (6studies) Low1,2 0.2 SD represents a v ileyiew postintervention 3months’postinterven- smalldifference,0.5SD &) Different measures tionscores intheinter- a moderate difference, S o n were used to assess vention groups was 0. and 0.8 SD a large dif- s , L pain frequency, such 55 SDs lower (0.98 to ference td . as a visual analogue 0.12lower). scale and the Wong- Baker FACESPain Rat- ing Scale (McGrath 1996;Wong1988). Change in pain inten- - The mean change in - 575 ⊕⊕(cid:13)(cid:13) As a rule of thumb, sity: 0 to 3 months’ pain intensity: 0 to 3 (7studies) Low1,2 0.2 SD represents a postintervention months’ postinterven- smalldifference,0.5SD Different mea- tionscores intheinter- a moderate difference, sures were used to as- vention groups was 0. and 0.8 SD a large dif- sess pain intensity, as 50 SDs lower (0.85 to ference above 0.15lower). 4 CD opyrigietary ht©inte Improvementinpain:0 421per10003 542per1000 OR1.63 722 ⊕⊕⊕(cid:13) - 20rve to3months’postinter- (438to642) (1.07to2.47) (7studies) Moderate4 1n 7Ttio vention NNTB=8 hens Differentmeasuresand Cofor definitions were used chrarecu for improvement in nerre pain, such as Likert Cn ot scale, visual analogue llababd scale, and Subject’s oo ratiomina GRelolibeafl SAcsasleess(MmceGntraothf nl .p Pa 1996; Muller-Lissner uin blisin 2003). hc eh dbyildho Improvementinpain:0 359per1000 627per1000 OR3.01 344 ⊕⊕⊕(cid:13) - Johod to3months’postinter- (498to742) (1.77to5.13) (4studies) Moderate5 nW(Re ventionSubgroup(irri- NNTB=4 v ileyiew tablebowelsyndrome) &) Different S on measureswereusedto s ,L assessimprovement in td. pain,asabove Improvementinpain:3 589per1000 736per1000 OR1.94 224 ⊕⊕⊕(cid:13) - to6months’postinter- (612to831) (1.10to3.43) (2studies) Moderate5 vention NNTB=7 Different measureswereusedto assessimprovement in pain,asabove *The basis for the assumedrisk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95%confidence interval) is basedontheassumedriskinthecomparisongroupandtherelativeeffectof theintervention(andits95%CI). CI:confidenceinterval;NNTB:numberneeded to treat for anadditional beneficialoutcome,basedon theabsoluterisk reduction betweentheintervention and comparison groupprobableoutcomes;OR:oddsratio;SD:standarddeviation. 5 CD opyrigietary ht©inte GRADEWorkingGroupgradesof evidence 20rve Highquality:Furtherresearchisveryunlikelytochangeourconfidenceintheestimateof effect. 1n 7Ttio Moderatequality:Furtherresearchislikelytohaveanimportantimpactonourconfidenceintheestimateof effectandmaychangetheestimate. hens Lowquality:Furtherresearchisverylikelytohaveanimportantimpactonourconfidenceintheestimateof effectandislikelytochangetheestimate. Cofor Verylowquality:Weareveryuncertainabouttheestimate. chre ranecurre 1Downgradedonelevelduetoincompleteoutcomedatainanumberof includedstudiesleadingtoanunclearorhighriskof Cn bias. ot llaab 2Downgradedonelevelforevidenceof significantheterogeneity(I²>70%;Chi²P<0.001). bd orom 3Assumedriskisbasedonthemeanoutcomeof thecontrolgroupsinallincludedstudies. atioina 4Downgradedonelevelduetoevidenceof heterogeneity(I²=45%;Chi²P=0.09). nl .Ppa 5Downgradedonelevelforimprecision. uin blisin xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx hc eh dbyildho Johod n(R We v ileyiew &) S o n s , L td . 6 BACKGROUND egoriesforpaediatricpresentations(Rasquin2006).Throughout thisreview we have thereforeusedRAP asan umbrellatermto refertothefivesubcategoriesincludedwithintheRomeIIIcat- Descriptionofthecondition egory of childhood abdominal pain-related functional gastroin- testinaldisorders,whichare:functionaldyspepsia,irritablebowel This review is an update of a previously published review in syndrome,abdominalmigraine,functionalabdominalpain,and the Cochrane Library on ’Psychosocial interventions for recur- functionalabdominalpainsyndrome.Itshouldbenotedthatthe rentabdominalpainandirritablebowelsyndromeinchildhood’ painclassificationforeachoftheRomeIIIdiagnosesisdefinedby (Huertas-Ceballos 2009). Recurrent abdominal pain (RAP) is a atleastoneepisodeperweekforatleasttwomonths;thisvaries common problem in paediatric practice. It has been suggested fromApley’soriginaldefinitionofRAP(Apley1958).TheRome that4%to25%ofschool-agedchildrenwillatsomepointsuf- IV criteria were produced in spring 2016; in this new iteration ferfromrecurrentorchronicabdominalpainthatinterfereswith thecategoryofchildhoodfunctionalabdominalpaindisordersin- theiractivitiesofdailyliving(Konijnenberg2005;Williams1996; cludesfunctionaldyspepsia,irritablebowelsyndrome,abdominal Youssef2006),witharecentmeta-analysisestimatingthat13.5% migraine,andfunctionalabdominalpainnototherwisespecified ofchildrenworldwidemaybeaffected(Korterink2015).Recur- (Drossman2016).However,theRomeclassificationisnotbased rentabdominalpainisoftenregardedasarelativelybenigncon- onknownpathophysiologicaldifferencesbetweentheconditions, dition, butitisimportanttonotetheassociated morbidity and butratherontheconstellationofclinicalfeatures.Itisunclearthe theanxietyitcausesforchildrenandcaregivers(Paul2013).The extenttowhichseparatingchildrenintothesecategoriesdefines conditionisassociatedwithschoolabsences,hospitaladmissions, groupsthataredistinctclinicalentitiesthatarelikelytorespond emotional disorders and, on occasion, unnecessary surgical in- differentlytotreatment. tervention (Scharff 1997; Stickler 1979; Størdal 2005; Walker There is no consensus about which of the numerous proposed 1998;Youssef2008).Theabdominalpainisalsocommonlyas- causal pathways result in the heterogeneous presentations of sociated with other symptoms, including headaches, recurrent chronic abdominal pain, although it is suggested that physical, limbpains,pallor,andvomiting(Abu-Arafeh1995;Devanarayana emotional,andenvironmentalfactorsmaycontributetotheman- 2011;Hyams1995).Symptomssometimescontinueintoadult- ifestationofunexplainedabdominalpain.Whenconsideringthe hood;childhoodRAPisassociatedwithahigherriskofanxiety diverseproposedmechanisms,itisunsurprisingthatavarietyof disordersinadults(Horst2014;Shelby2013). treatmentshavebeensuggested.Thetreatmentapproachescanbe Apleyfirstsoughttodefinetheconditioninthe1950sandsug- groupedaspharmacological,dietary,orpsychosocial(psycholog- gestedthatthediagnostic labelshouldbebasedonthepresence ical or behavioural, or both). Thisreview focusedonany inter- of at least three episodes of severe abdominal pain (often, but ventionwithdietarychangesintendedtoimprovethesymptoms not necessarily, with associated systemic symptoms) over three ofRAP,andhencedietary approachesonly arediscussed below. months(Apley1958),withnoestablishedorganiccause.Histor- Updated companion reviews of pharmacological interventions, icallydiversetermshavesincebeenusedtodescribethesecondi- Martin2014a,andpsychosocialinterventions,Abbott2017,for tions, some implying causation. Theseinclude: “abdominal mi- RAPhavebeenpublished. graine”(Bain1974;Farquar1956;Hockaday1992;Symon1986), “abdominal epilepsy” (Stowens 1970), “the irritable bowel syn- dromeinchildhood”(Stone1970),“allergic-tension-fatiguesyn- drome” (Sandberg 1973; Speer 1954), “neurovegetative dysto- Descriptionoftheintervention nia” (Peltonen 1970; Rubin 1967), “functional gastrointestinal disorder”(Drossman1995),and“theirritatedcolonsyndrome” Dietary interventions mayinvolveexcluding orreducingafood (Harvey1973;Painter1964). grouporspecificingredientfromthedietorsupplementingitand It is now generally accepted that RAP in children represents a thereforeincreasingitsintake.Suchdietaryinterventionsinclude groupoffunctionalgastrointestinaldisordersthathaveanunclear eliminatingorrestrictingfoodgroupsorfoodcomponents,such aetiology.ThelatestRomeFoundationcriteriastatethatsuchdis- as dairy products or fructose (Bain 1974; Bayless 1971; Wirth ordersaredefinedbysymptomsrelatedtomotilitydisturbance; 2014),andtakingfibresupplements(Horvath2013).Probiotics, visceral hypersensitivity; alteredmucosal andimmune function; whicharelivingmicro-organismssuchasLactobacillus,havealso alteredgutmicrobiota;andalteredcentralnervoussystemprocess- beenusedinmanagingchildrenwithRAP(Wilhelm2008).More ing, and are “theproductof ...interactions of psychosocial fac- recentlytherehasbeeninterestintheuseoflowFODMAP(fer- torsandalteredgutphysiologyviathebrain-gutaxis”(Drossman mentable oligosaccharides, disaccharides, monosaccharides and 2016).TheRomeFoundationhasproducedcriteriaforthisgroup polyols)dietsinthemanagementofirritablebowelsyndrome,al- ofconditionssince1994byinternationalconsensus.Moststudies though themajority of studies have included adult populations includedinthisreviewusetheRomeIIIcriteriafrom2006,which (Rao2015),withonerecentrandomisedcontrolledtrialinchil- includedasymptom-basedclassificationsystemwithspecificcat- dren(Chumpitazi2015). Dietaryinterventionsforrecurrentabdominalpaininchildhood(Review) 7 Copyright©2017TheCochraneCollaboration.PublishedbyJohnWiley&Sons,Ltd.

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1NIHR CLAHRC South West Peninsula (PenCLAHRC), University of Exeter Medical School, Exeter, UK. 2Paediatrics, Royal Devon These may involve either excluding ingredients from the diet or . vention Subgroup (irri- Guy W. ECDEU Assessment Manual for Psychopharmacology. Rockville
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