{"doc_desc":{"title":"Treatment as Prevention ANRS 12249 - datasets for Lancet HIV pain paper","idno":"DDI.ANRS12249.lancet.hiv.main.paper","producers":[{"name":"Kobus Herbst","abbreviation":"","affiliation":"Africa Centre for Health and Population Studies","role":"Dataset production"},{"name":"Joseph Larmarange","abbreviation":"","affiliation":"Ceped (UMR 196 Paris Descartes IRD) / Africa Centre for Health and Population Studies","role":"Data documentation"},{"name":"Jaco Dreyer","abbreviation":"","affiliation":"Africa Centre for Health and Population Studies","role":"Data documentation"}],"prod_date":"2017-06-13","version_statement":{"version":"11.3.0","version_date":"2017-06-13","version_notes":"1.0.0 Intitial version (2 May 2014)\n1.0.1 Labels and missing values added to IQs dataset (7 May 2014)\n1.0.2 Labels and missing values added to CBCs, HIV Drug Treatments, ARTemis patients and ARTemis Lab results dataset (8 May 2014)\n1.0.3 Value labels of ShouldTestWhenRegHowOften in IQs dataset fixed (12 May 2014)\n1.1.0 IndividualId in IQs dataset fixed (12 May 2014)\n1.1.1 Typo fixed in trial statuses value labels in Individuals dataset (14 May 2014)\n2.0.0 Initial release of version 2 (15 July 2014)\n--- Generated from a new snapshot of the database, dated 22 May 2014\n--- New datasets: HHIs, CHE Adverse events, CHE Action Plans, SCBs SCCs, SCIs, Specimens, Individual Consents, iDART\n--- Individuals dataset: AgeGroupAtRegistration has been fixed\n--- IQs dataset:\n------ Health Care expenditure section has been added\n------ Variables CurrentCluster, CurrentClusterType, ClusterAtRegistration, ClusterTypeAtRegistration, FormType added\n------ Deprecated value fixed for variables ShouldTestWhenFeelSick to ShouldTestWhenRefused , KnowsPosMyself to KnowsPosCommunity\n------ Not applicable value fixed for variables WhyNotHIVTestTodayPos to WhyNotHIVTestTodayRefused\n------ Some duplicates removed\n--- CBCs dataset: variables CurrentCluster, CurrentClusterType, ClusterAtRegistration, ClusterTypeAtRegistration added\n--- CHEs dataset:\n------ Variables CurrentCluster, CurrentClusterType, ClusterAtRegistration, ClusterTypeAtRegistration added\n------ PrevTB1DateStarted, PrevTB2DateStarted and CurrTBDateStarted  variables fixed\n--- Lab Test Results dataset: VisitId added\n--- ARTemis Patients dataset: \n------ DateOfViralLoadNear6m DateOfViralLoadNear24m and DateOfViralLoadNear36m added\n------ AreaOfResidenceCode recoded\n3.0.0 Initial release of version 3 (25 September 2014)\n--- Generated from a new snapshot of the database, dated 19 September 2014\n--- End of data collection for phase 1 is now fixed to 31st May 2014 (included)\n--- Locations dataset: ConstructionState and MappedOnDevice variables have been removed\n--- Individuals dataset:\n------ Trial statuses have been removed from that file and are now provided in a separate Trial Statuses dataset\n------ 85 new pre-calculated variables have been added, following the TasP definitions document\n--- IQs dataset: Issue of missing IQs fixed\n--- Lab Tests Reults dataset: Some PIMA CD4 count documented initialy only in CHEs have been added to the dataset\n3.1.0 Distance variables added to Locations dataset (30 Sep 2014)\n3.2.0 Locations datatset: duplicates bug introduced in version 3.1.0 of the dataset is now fixed (7 Oct 2014)\n3.3.0 All datasets have been regenerated (9 Oct 2014)\n--- A bug with LocationId and HouseholdId has been fixed\n--- Cluster dataset has been added\n--- Individuals dataset:\n------ BaselineClinicVisitDate and LastClinicVisitDate definition has been updated (see TasP definitions do)\n------ 100 new pre-calculated variables added on retention in TasP clinics\n--- Trial Statuses dataset: details of Exits have been added\n--- Visits dataset: CBCcomputed, CHEcomputed, BaselineClinicVisitDate, onART, NextAppointmentDateComputed and PreviousClinicVisitDate added\n--- HHIs dataset: ClusterId, CalendarRound, AssetsScore and AssetsScoreCat added\n--- CBCs dataset: EarliestHIVDrugRegStartDate updated (new definition) and ARTInitiationDate removed\n3.4.0 (23 Oct 2014)\n--- Lab Test Results: duplicates (PIMA CD4 count) removed (23 Oct 2014)\n--- 2 new datasets: CFUs and CFU Pill Tests\n--- Shapefiles added on the repository\n--- Individuals dataset\n------ minor fix of variable TasPBaselineARTUse\n------ 3 variables added: FirstReferralTS, EverEnteredCareAR and NewlyDiagnosedAtReferral\n3.5.0 (19 Jan 2015)\n--- New datasets: \n------ SAE Initial Notifications, SAE Initial Notifications - Events details, SAE Initial Notifications - Medications, SAE Complementary Notifications & SAE Complementary Notifications - Medications\n--- Individuals dataset:\n------ AgeAtRegistration has been updated (now exact age and missig if year of birth is unknown)\n------ New variables about age: \n            AgeAtReferral, AgeAtBaselineClinicVisit\n------ New variables derived from IQs: \n            BaselineHighestEducationLevel, BaselineMaritalStatus, BaselineProfessionalStatus, BaselineEmployed & BaselineActiveStatus\n------ New variables derived from iDART: \n            LinkedToIDART, iDARTLastEpisodeStartDateBR, iDARTLastPackageCollectionDateBR, iDARTFirstEpisodeStartDateAR, \n            iDARTFirstPackageCollectionDateAR, iDARTLastEpisodeStartDateBHSBT, iDARTLastPackageCollectionDateBH, iDARTFirstEpisodeStartDate, \n            iDARTLastEpisodeStartDate, iDARTFirstPackageCollectionDate, iDARTLastPackageCollectionDate\n------ Other new variables: \n            NbTasPClinicVisits, InCareAtBeginning, TasPLCVDate, TasPLCVAppointmentDate, EverInCare, EverDiagnosedHIVPositive,\n            InCareAtEndPhase1, InTasPCareAtEndPhase1, ARTemisLastVL, ARTemisLastVLDate, TasPLastVL, TasPLastVLDate,\n            LastVL, LastVLDate, UndetectableVLAtEndPhase1\n------ Variable updated due to changes in TasP definitions document: \n            SeenInTasPClinic, TasPInitiatedART, CareAtReferral, InCareAtEndPhase1, OnARTAtBeginning, OnARTAtReferral & OnARTAtEndPhase1\n--- IQs dataset\n------ New variables:\n            AgeAtIQ, NonEmploymentTypeRecoded, HighestEducationLevel2, CurrentMaritalStatus2, Employed, ProfessionalStatus, ActiveStatus\n--- Visits dataset\n------ Variable PreviousClinicVisitDate fixed\n4.0.0 Initial release of version 4 (02 Sep 2015)\n--- Inclusion of data collected up to the 15th of July 2015\n--- New datasets:\n------ Local Areas, Census Rounds, Exits\n--- Exits\n------ Introduction of distinction between Population and Clinic Exit.\n------ Manual recoding has been performed for phase 1 exit forms. Cf. *Computed variables\n--- Individuals dataset:\n------ ExitedEndDataCollection and ExitTypeEndDataCollection now refers only to Population exit. (cf. Exits dataset)\n------ CR* variables (per calendar round) have been replaced by CC* variables (per data collection cycle). Cf. Census Rounds dataset\n------ Retention in TasP Care variables have been extended up to M36\n--- Trial Statuses datasets:\n------ Exit details have been removed and are now provided in Exits datasets.\n------ Duplicated Trial Statuses (same visit date / same trial status) have been removed.\n------ Exit Trial Statuses have been re-created from the Exits datasets importing only Population Exits.\n------ Logical rounds are not used any more.\n------ Introduction of the concepts of Census Rounds and Data Collection Cycles. (cf. Census Rounds dataset)\n--- HHIs Dataset: \n------ New variable: DataCollectionCycle\n--- IQs dataset:\n------ New variables in sexual behaviors component: MRPWillShareTheirStatus, MRPPartnerStatus, MRPLocalAreaCode, MRPIntercouseNTimesLast3Months, PP1WillShareTheirStatus, PP1PartnerStatus, PP1LocalAreaCode, PP1IntercouseNTimesLast3Months, PP2WillShareTheirStatus, PP2PartnerStatusPP2LocalAreaCode, PP2LocalAreaCode, PP2IntercouseNTimesLast3Months, HIVStatusWillingToShare, HIVStatusWhatIS\n--- DBS results dataset:\n------ New variables: DBSRank, ValidDBSRank, CalendarRound, DataCollectionCycle\n--- CBCs dataset:\n------ New variables: BaselineARTProviderOthSpec, WhyNoLongerOnARTOthSpec, HIVDrugRegimen\n--- SCIs dataset:\n------ New variables in sexual behaviors component: MRPWillShareTheirStatus, MRPPartnerStatus, MRPLocalAreaCode, MRPIntercouseNTimesLast3Months, PP1WillShareTheirStatus, PP1PartnerStatus, PP1LocalAreaCode, PP1IntercouseNTimesLast3Months, PP2WillShareTheirStatus, PP2PartnerStatusPP2LocalAreaCode, PP2LocalAreaCode, PP2IntercouseNTimesLast3Months\n--- Individuals Consents dataset\n------ Individual Consents has been reformatted to vertical layout where each consent given is visible as a row on its own and no longer be displayed in one row per individual with different items representing each consent given. \n------ New variables includes: FormId, VisitId, VisitDate, IndividualResponse\n--- SAEs Initial Notifications dataset:\n------ New variables: VisitDate, NotificationDate, LastWeightDate, LastCD4CountDate, LastViralLoadDate, SerCritDateOfDeath, SAEOutcomeRecoverDate\n--- SAEs Initial Notifications - Event details dataset:\n------ New variables: DateInvestigatorAware, DateOfOnset, DateResolved\n--- SAEs Initial Notifications - Medications dataset:\n------ New variables: DateStarted, DateStopped\n--- SAEs Complementary Notifications dataset:\n------ New variables: VisitDate, NotificationDate, DateOfOnset, DateOfNewDiagnosis, DateDiscontinued, DateReintroduced, SAEOutcomeDeathDate, SAEOutcomeRecoverDate\n--- SAEs Complementary Notifications - Medications dataset\n------ New variables: VisitDate, DateStarted, DateStopped\n4.1.0 Updated release of version 4 (16 Oct 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning that includes re-entry of EXIT forms\n--- Initial release of Sequence Genomics dataset\n4.2.0 Updated release of version 4 (25 Nov 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning\n--- Initial release of Next Generation Sequence (NGS) datasets: NgsGenomics and MinorityVariants\n--- All IQP forms are now also exported after a bug was fixed in the Pentaho transfromation\n------ New items exported: MRPCondomOccasions, PP1CondomOccasions, PP2CondomOccasions\n4.3.0 Updated release of version 4 (10 Dec 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning\n------ Contains omitted Trial Statuses that has been recaptured from the fieldworker diaries\n4.3.1 Updated release of version 4 (10 Dec 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning\n------ Contains omitted Trial Statuses that has been recaptured from the fieldworker diaries\n--- Trial Statuses\n------ New variable: Source\n5.0.0 Initial release of version 5 (09 Mar 2016)\n--- Inclusion of data collected up to the 30th of December 2015\n--- Contains changes to data as result of ongoing data cleaning\n--- New datasets:\n------ BMQ Survey, Refusals, NgsAssembQuality\n---SampleGenomics:\n------ New Variable: ResistanceType\n6.0.0 Initial release of version 6 (22 Apr 2016)\n--- Inclusion of data collected up to the 20th of April 2016\n--- Contains changes to data as result of ongoing data cleaning\n--- Individuals:\n------ New Variables: CC7* variables, TasPBaselinePrevARTuse, TasPBaselineARTStatus\n6.1.0 Updated release of version 6 (26 Apr 2016)\n--- Inclusion of data collected up to the 26th of April 2016\n--- Contains changes to data as result of ongoing data cleaning\n6.1.1 Updated release of version 6 (26 Apr 2016)\n--- Released new dataset LinkToCareTracker\n7.0.0 Initial release of version 7 (27 Jun 2016)\n--- Inclusion of data collected up to the 23rd of June 2016\n--- Contains changes to data as result of ongoing data cleaning\n--- Trial Statuses:\n------ New Variables: ClosestID, ClosestIQWithin7Days\n7.0.1 Updated release of version 7 data (27 Jun 2016)\n--- Correct issues with Trial Status dataset\n8.0.0 Initial release of version 8 (05 Jul 2016)\n--- Inclusion of data collected up to the 5th of July 2016\n--- Contains changes to data as result of ongoing data cleaning\n9.0.0  Initial release of version 9 (06 Sep 2016)\n--- Inclusion of data collected up to the 6th of September 2016\n--- Contains changes to data as result of ongoing data cleaning\n--- Changes to datasets:\n------ Exits dataset:\n--------- Updates to variables:DTHDateComputed,ExitDateComputed, TRODateComputed, LFUDateComputed, NMCDateComputed, OUTDateCompued\n--------- New variable added: ExitDateComputedEstimated\n------ Individuals dataset: \n--------- Updates to variables: DateOfBirth \n------ HIV Drug Treatments dataset:\n--------- This dataset has been cleaned and treatments re-aligned by Dr Collins Iwuji\n------ SampleGenomics dataset:\n--------- New variable added: SeqId\n9.0.1 Updated release of version 9 (06 Sep 2016)\n--- Correction made to Visits dataset\n--- Correction was made to the Exits dataset\n10.0.0  Initial release of version 10 (29 Nov 2016)\n--- Inclusion of data collected from the field and clinics\n--- Contains changes to data as result of data cleaning\n--- Lab data:\n------ All Lab data have been reconcilled\n------ All discordant serology results has been resolved\n------ Missing ARTemis VL and CD4 from Feb 2016 till end of July 2016 has now been uploaded\n10.1.0  Updated release of version 10 (29 Nov2016)\n--- New datasets:\n------ ACCDB Encounters, ACCDB Encouter Therapies\n10.1.1  Updated release of version 10 (29 Nov2016)\n--- Distance measurements updated in Locations dataset\n--- Errors fixed on the HIV Drug Treatments dataset\n10.2.0  Updated release of version 10 (29 Nov2016)\n--- Corrected HIVDrugTreatments dataset\n10.2.1  Updated release of version 10 (29 Nov2016)\n--- Corrected Date formats for SAE datasets\n11.0.0  Initial release of version 11 (27 Jan 2017)\n--- Inclusion of data collected from the field and clinics\n--- Contains changes to data as result of data cleaning\n--- Changes to datasets:\n------ Individuals:\n--------- Pre-computed variables were removed namely:\n------------ End of Phase 1 variables\n------------ End of Data collection variables\n------------ ART coverage in DoH is estimated only at the beginning of the trial (the estimates at all other dates will be done through the production of the cascade datasets, in order to harmonize all the computation)\n------------ The computation of the cascade is not anymore developed in the Definition document (as it is now developed separately).\n------------ Variables related to iDART\n------------ Includes data clearing by Collins Iwuji\n------ ExitFormDetails:\n--------- Forms were removed for individuals exiting more than once with no contact visit in-between the exits.\n------ iDART\n--------- Dataset has been dropped from the list of analytical datasets\n--- All data collected after a person was reported as being of No Mental Capacity (NMC) was removed\n11.2.0  Updated release of version 11 (15 Feb 2017)\n--- Updates to Exits dataset\n11.3.0  Updated release of version 11 (13 Jun 2017)\n--- Excluded under age individuals"}},"study_desc":{"title_statement":{"idno":"ANRS12249TasP.3ie.main.paper","title":"Treatment as Prevention ANRS 12249 - datasets for Lancet HIV pain paper","alt_title":"TasP - Lancet HIV Main Paper","translated_title":"Ukuphila kwami, ukuphila kwethu (my health for our health)"},"authoring_entity":[{"name":"Dabis, Fran\u00e7ois","affiliation":"Inserm Unit\u00e9 897, ISPED"},{"name":"Newell, Marie-Louise","affiliation":"Faculty of Medicine, Faculty of Social and Human Sciences, University of Southampton"},{"name":"Pillay, Deenan","affiliation":"Africa Centre for Health and Population Studies"}],"production_statement":{"producers":[{"name":"Africa Centre for Health and Population Studies","affiliation":"UKZN","role":""}],"prod_date":"2017-06-13","prod_place":"Somkhele, South Africa","funding_agencies":[{"name":"Agence Nationale de Recherche sur le Sida et les h\u00e9patites virales","abbreviation":"ANRS","role":"Sponsor and funder"},{"name":"Deutsche Gesellschaft f\u00fcr Internationale Zusammenarbeit","abbreviation":"GIZ","role":"Funder"},{"name":"MERCK & Co. Inc and Gilead Sciences","abbreviation":"","role":"Drugs supply"},{"name":"Wellcome Trust","abbreviation":"","role":"Core funding of Africa Centre"},{"name":"International Initiative for Impact Evaluation","abbreviation":"3ie","role":"Funder"}],"grant_no":"ANRS 12249 2010.2048.6-003.00"},"distribution_statement":{"distributors":[{"name":"Africa Centre for Health and Population Studies","abbreviation":"AC","affiliation":"UKZN","uri":"http://data.africacentre.ac.za/"}]},"version_statement":{"version":"11.2","version_date":"2017-02-15","version_notes":"1.0.0 Intitial version (2 May 2014)\n1.0.1 Labels and missing values added to IQs dataset (7 May 2014)\n1.0.2 Labels and missing values added to CBCs, HIV Drug Treatments, ARTemis patients and ARTemis Lab results dataset (8 May 2014)\n1.0.3 Value labels of ShouldTestWhenRegHowOften in IQs dataset fixed (12 May 2014)\n1.1.0 IndividualId in IQs dataset fixed (12 May 2014)\n1.1.1 Typo fixed in trial statuses value labels in Individuals dataset (14 May 2014)\n2.0.0 Initial release of version 2 (15 July 2014)\n--- Generated from a new snapshot of the database, dated 22 May 2014\n--- New datasets: HHIs, CHE Adverse events, CHE Action Plans, SCBs SCCs, SCIs, Specimens, Individual Consents, iDART\n--- Individuals dataset: AgeGroupAtRegistration has been fixed\n--- IQs dataset:\n------ Health Care expenditure section has been added\n------ Variables CurrentCluster, CurrentClusterType, ClusterAtRegistration, ClusterTypeAtRegistration, FormType added\n------ Deprecated value fixed for variables ShouldTestWhenFeelSick to ShouldTestWhenRefused , KnowsPosMyself to KnowsPosCommunity\n------ Not applicable value fixed for variables WhyNotHIVTestTodayPos to WhyNotHIVTestTodayRefused\n------ Some duplicates removed\n--- CBCs dataset: variables CurrentCluster, CurrentClusterType, ClusterAtRegistration, ClusterTypeAtRegistration added\n--- CHEs dataset:\n------ Variables CurrentCluster, CurrentClusterType, ClusterAtRegistration, ClusterTypeAtRegistration added\n------ PrevTB1DateStarted, PrevTB2DateStarted and CurrTBDateStarted  variables fixed\n--- Lab Test Results dataset: VisitId added\n--- ARTemis Patients dataset: \n------ DateOfViralLoadNear6m DateOfViralLoadNear24m and DateOfViralLoadNear36m added\n------ AreaOfResidenceCode recoded\n3.0.0 Initial release of version 3 (25 September 2014)\n--- Generated from a new snapshot of the database, dated 19 September 2014\n--- End of data collection for phase 1 is now fixed to 31st May 2014 (included)\n--- Locations dataset: ConstructionState and MappedOnDevice variables have been removed\n--- Individuals dataset:\n------ Trial statuses have been removed from that file and are now provided in a separate Trial Statuses dataset\n------ 85 new pre-calculated variables have been added, following the TasP definitions document\n--- IQs dataset: Issue of missing IQs fixed\n--- Lab Tests Reults dataset: Some PIMA CD4 count documented initialy only in CHEs have been added to the dataset\n3.1.0 Distance variables added to Locations dataset (30 Sep 2014)\n3.2.0 Locations datatset: duplicates bug introduced in version 3.1.0 of the dataset is now fixed (7 Oct 2014)\n3.3.0 All datasets have been regenerated (9 Oct 2014)\n--- A bug with LocationId and HouseholdId has been fixed\n--- Cluster dataset has been added\n--- Individuals dataset:\n------ BaselineClinicVisitDate and LastClinicVisitDate definition has been updated (see TasP definitions do)\n------ 100 new pre-calculated variables added on retention in TasP clinics\n--- Trial Statuses dataset: details of Exits have been added\n--- Visits dataset: CBCcomputed, CHEcomputed, BaselineClinicVisitDate, onART, NextAppointmentDateComputed and PreviousClinicVisitDate added\n--- HHIs dataset: ClusterId, CalendarRound, AssetsScore and AssetsScoreCat added\n--- CBCs dataset: EarliestHIVDrugRegStartDate updated (new definition) and ARTInitiationDate removed\n3.4.0 (23 Oct 2014)\n--- Lab Test Results: duplicates (PIMA CD4 count) removed (23 Oct 2014)\n--- 2 new datasets: CFUs and CFU Pill Tests\n--- Shapefiles added on the repository\n--- Individuals dataset\n------ minor fix of variable TasPBaselineARTUse\n------ 3 variables added: FirstReferralTS, EverEnteredCareAR and NewlyDiagnosedAtReferral\n3.5.0 (19 Jan 2015)\n--- New datasets: \n------ SAE Initial Notifications, SAE Initial Notifications - Events details, SAE Initial Notifications - Medications, SAE Complementary Notifications & SAE Complementary Notifications - Medications\n--- Individuals dataset:\n------ AgeAtRegistration has been updated (now exact age and missig if year of birth is unknown)\n------ New variables about age: \n            AgeAtReferral, AgeAtBaselineClinicVisit\n------ New variables derived from IQs: \n            BaselineHighestEducationLevel, BaselineMaritalStatus, BaselineProfessionalStatus, BaselineEmployed & BaselineActiveStatus\n------ New variables derived from iDART: \n            LinkedToIDART, iDARTLastEpisodeStartDateBR, iDARTLastPackageCollectionDateBR, iDARTFirstEpisodeStartDateAR, \n            iDARTFirstPackageCollectionDateAR, iDARTLastEpisodeStartDateBHSBT, iDARTLastPackageCollectionDateBH, iDARTFirstEpisodeStartDate, \n            iDARTLastEpisodeStartDate, iDARTFirstPackageCollectionDate, iDARTLastPackageCollectionDate\n------ Other new variables: \n            NbTasPClinicVisits, InCareAtBeginning, TasPLCVDate, TasPLCVAppointmentDate, EverInCare, EverDiagnosedHIVPositive,\n            InCareAtEndPhase1, InTasPCareAtEndPhase1, ARTemisLastVL, ARTemisLastVLDate, TasPLastVL, TasPLastVLDate,\n            LastVL, LastVLDate, UndetectableVLAtEndPhase1\n------ Variable updated due to changes in TasP definitions document: \n            SeenInTasPClinic, TasPInitiatedART, CareAtReferral, InCareAtEndPhase1, OnARTAtBeginning, OnARTAtReferral & OnARTAtEndPhase1\n--- IQs dataset\n------ New variables:\n            AgeAtIQ, NonEmploymentTypeRecoded, HighestEducationLevel2, CurrentMaritalStatus2, Employed, ProfessionalStatus, ActiveStatus\n--- Visits dataset\n------ Variable PreviousClinicVisitDate fixed\n4.0.0 Initial release of version 4 (02 Sep 2015)\n--- Inclusion of data collected up to the 15th of July 2015\n--- New datasets:\n------ Local Areas, Census Rounds, Exits\n--- Exits\n------ Introduction of distinction between Population and Clinic Exit.\n------ Manual recoding has been performed for phase 1 exit forms. Cf. *Computed variables\n--- Individuals dataset:\n------ ExitedEndDataCollection and ExitTypeEndDataCollection now refers only to Population exit. (cf. Exits dataset)\n------ CR* variables (per calendar round) have been replaced by CC* variables (per data collection cycle). Cf. Census Rounds dataset\n------ Retention in TasP Care variables have been extended up to M36\n--- Trial Statuses datasets:\n------ Exit details have been removed and are now provided in Exits datasets.\n------ Duplicated Trial Statuses (same visit date / same trial status) have been removed.\n------ Exit Trial Statuses have been re-created from the Exits datasets importing only Population Exits.\n------ Logical rounds are not used any more.\n------ Introduction of the concepts of Census Rounds and Data Collection Cycles. (cf. Census Rounds dataset)\n--- HHIs Dataset: \n------ New variable: DataCollectionCycle\n--- IQs dataset:\n------ New variables in sexual behaviors component: MRPWillShareTheirStatus, MRPPartnerStatus, MRPLocalAreaCode, MRPIntercouseNTimesLast3Months, PP1WillShareTheirStatus, PP1PartnerStatus, PP1LocalAreaCode, PP1IntercouseNTimesLast3Months, PP2WillShareTheirStatus, PP2PartnerStatusPP2LocalAreaCode, PP2LocalAreaCode, PP2IntercouseNTimesLast3Months, HIVStatusWillingToShare, HIVStatusWhatIS\n--- DBS results dataset:\n------ New variables: DBSRank, ValidDBSRank, CalendarRound, DataCollectionCycle\n--- CBCs dataset:\n------ New variables: BaselineARTProviderOthSpec, WhyNoLongerOnARTOthSpec, HIVDrugRegimen\n--- SCIs dataset:\n------ New variables in sexual behaviors component: MRPWillShareTheirStatus, MRPPartnerStatus, MRPLocalAreaCode, MRPIntercouseNTimesLast3Months, PP1WillShareTheirStatus, PP1PartnerStatus, PP1LocalAreaCode, PP1IntercouseNTimesLast3Months, PP2WillShareTheirStatus, PP2PartnerStatusPP2LocalAreaCode, PP2LocalAreaCode, PP2IntercouseNTimesLast3Months\n--- Individuals Consents dataset\n------ Individual Consents has been reformatted to vertical layout where each consent given is visible as a row on its own and no longer be displayed in one row per individual with different items representing each consent given. \n------ New variables includes: FormId, VisitId, VisitDate, IndividualResponse\n--- SAEs Initial Notifications dataset:\n------ New variables: VisitDate, NotificationDate, LastWeightDate, LastCD4CountDate, LastViralLoadDate, SerCritDateOfDeath, SAEOutcomeRecoverDate\n--- SAEs Initial Notifications - Event details dataset:\n------ New variables: DateInvestigatorAware, DateOfOnset, DateResolved\n--- SAEs Initial Notifications - Medications dataset:\n------ New variables: DateStarted, DateStopped\n--- SAEs Complementary Notifications dataset:\n------ New variables: VisitDate, NotificationDate, DateOfOnset, DateOfNewDiagnosis, DateDiscontinued, DateReintroduced, SAEOutcomeDeathDate, SAEOutcomeRecoverDate\n--- SAEs Complementary Notifications - Medications dataset\n------ New variables: VisitDate, DateStarted, DateStopped\n4.1.0 Updated release of version 4 (16 Oct 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning that includes re-entry of EXIT forms\n--- Initial release of Sequence Genomics dataset\n4.2.0 Updated release of version 4 (25 Nov 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning\n--- Initial release of Next Generation Sequence (NGS) datasets: NgsGenomics and MinorityVariants\n--- All IQP forms are now also exported after a bug was fixed in the Pentaho transfromation\n------ New items exported: MRPCondomOccasions, PP1CondomOccasions, PP2CondomOccasions\n4.3.0 Updated release of version 4 (10 Dec 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning\n------ Contains omitted Trial Statuses that has been recaptured from the fieldworker diaries\n4.3.1 Updated release of version 4 (10 Dec 2015)\n--- Cut off point for datasets is still 15-Jul-2015 as with version 4.0.0\n--- Contains changes to data as result of ongoing data cleaning\n--- Trial Statuses\n------ New variable: Source\n--- Trial Statuses\n------ New variable: Source\n5.0.0 Initial release of version 5 (09 Mar 2016)\n--- Inclusion of data collected up to the 30th of December 2015\n--- Contains changes to data as result of ongoing data cleaning\n--- New datasets:\n------ BMQ Survey, Refusals, NgsAssembQuality\n---SampleGenomics:\n------ New Variable: ResistanceType\n6.0.0 Initial release of version 6 (22 Apr 2016)\n--- Inclusion of data collected up to the 20th of April 2016\n--- Contains changes to data as result of ongoing data cleaning\n--- Individuals:\n------ New Variables: CC7* variables, TasPBaselinePrevARTuse, TasPBaselineARTStatus\n6.1.0 Updated release of version 6 (26 Apr 2016)\n--- Inclusion of data collected up to the 26th of April 2016\n--- Contains changes to data as result of ongoing data cleaning\n6.1.1 Updated release of version 6 (26 Apr 2016)\n--- Released new dataset LinkToCareTracker\n7.0.0 Initial release of version 7 (27 Jun 2016)\n--- Inclusion of data collected up to the 23rd of June 2016\n--- Contains changes to data as result of ongoing data cleaning\n--- Trial Statuses:\n------ New Variables: ClosestID, ClosestIQWithin7Days\n7.0.1 Updated release of version 7 data (27 Jun 2016)\n--- Correct issues with Trial Status dataset\n8.0.0 Initial release of version 8 (05 Jul 2016)\n--- Inclusion of data collected up to the 5th of July 2016\n--- Contains changes to data as result of ongoing data cleaning\n9.0.0  Initial release of version 9 (06 Sep 2016)\n--- Inclusion of data collected up to the 6th of September 2016\n--- Contains changes to data as result of ongoing data cleaning\n--- Changes to datasets:\n------ Exits dataset:\n--------- Updates to variables:DTHDateComputed,ExitDateComputed, TRODateComputed, LFUDateComputed, NMCDateComputed, OUTDateCompued\n--------- New variable added: ExitDateComputedEstimated\n------ Individuals dataset: \n--------- Updates to variables: DateOfBirth \n------ HIV Drug Treatments dataset:\n--------- This dataset has been cleaned and treatments re-aligned by Dr Collins Iwuji\n------ SampleGenomics dataset:\n--------- New variable added: SeqId\n9.0.1 Updated release of version 9 (06 Sep 2016)\n--- Correction made to Visits dataset\n--- Correction was made to the Exits dataset\n10.0.0  Initial release of version 9 (06 Sep 2016)\n--- Inclusion of data collected from the field and clinics\n--- Contains changes to data as result of data cleaning\n--- Lab data:\n------ All Lab data have been reconcilled\n------ All discordant serology results has been resolved\n------ Missing ARTemis VL and CD4 from Feb 2016 till end of July 2016 has now been uploaded\n10.0.0  Initial release of version 10 (29 Nov 2016)\n--- Inclusion of data collected from the field and clinics\n--- Contains changes to data as result of data cleaning\n--- Lab data:\n------ All Lab data have been reconcilled\n------ All discordant serology results has been resolved\n------ Missing ARTemis VL and CD4 from Feb 2016 till end of July 2016 has now been uploaded\n10.1.0  Updated release of version 10 (29 Nov2016)\n--- New datasets:\n------ ACCDB Encounters, ACCDB Encouter Therapies\n10.1.1  Updated release of version 10 (29 Nov2016)\n--- Distance measurements updated in Locations dataset\n--- Errors fixed on the HIV Drug Treatments dataset\n10.2.0  Updated release of version 10 (29 Nov2016)\n--- Corrected HIVDrugTreatments dataset\n10.2.1  Updated release of version 10 (29 Nov2016)\n--- Corrected Date formats for SAE datasets\n11.0.0  Initial release of version 11 (27 Jan 2017)\n--- Inclusion of data collected from the field and clinics\n--- Contains changes to data as result of data cleaning\n--- Changes to datasets:\n------ Individuals:\n--------- Pre-computed variables were removed namely:\n------------ End of Phase 1 variables\n------------ End of Data collection variables\n------------ ART coverage in DoH is estimated only at the beginning of the trial (the estimates at all other dates will be done through the production of the cascade datasets, in order to harmonize all the computation)\n------------ The computation of the cascade is not anymore developed in the Definition document (as it is now developed separately).\n------------ Variables related to iDART\n------------ Includes data clearing by Collins Iwuji\n------ ExitFormDetails:\n--------- Forms were removed for individuals exiting more than once with no contact visit in-between the exits.\n------ iDART\n--------- Dataset has been dropped from the list of analytical datasets\n--- All data collected after a person was reported as being of No Mental Capacity (NMC) was removed\n11.1.0  Updated release of version 11 (02 Feb 2017)\n--- Rerun of all transformations\n11.2.0  Updated release of version 11 (15 Feb 2017)\n--- Updates to Exits dataset\n11.3.0  Updated release of version 11 (13 Jun 2017)\n--- Excluded under age individuals"},"study_notes":"A dataset containing GPS coordinates of homesteads has been released on the internal data repository of Africa Centre. Access conditions for this dataset are specific (cf. internal AC data repository).","study_info":{"topics":[{"topic":"","vocab":" ","uri":" "}],"abstract":"Background: Thirty years after the discovery of the human immunodeficiency virus (HIV), prevention is difficult to achieve and the pandemic does not show any sign of abating. Antiretroviral therapy (ART) is now rolled out at a large scale in lower-income countries. ART with fully suppressive antiretroviral (ARV) drugs combinations lowers HIV viral load (VL) in all body compartments and decreases the risk of transmission to a low level. It is thus legitimate to raise the following question: Could ART contribute to reducing transmission at individual and population level? Not only may earlier treatment reduce HIV incidence (acquisition of new cases of HIV infection through sexual or mother-to-child transmission), it may also benefit the individual. The long-term benefits of starting ART earlier would likely be of particular importance in settings where the incidence of life-threatening HIV-related diseases occurring at relatively high CD4 levels (tuberculosis, invasive bacterial diseases, and possibly malaria) is substantial, a typical situation in most sub-Saharan Africa including South Africa.\n\nResearch hypothesis: HIV testing of all adult members of a community, followed by immediate ART initiation of all, or nearly all, HIV-infected participants regardless of immunological or clinical staging will prevent onward transmission and reduce HIV incidence in this population.\n\nObjectives: To estimate the effect of ART initiated immediately after HIV diagnosis, irrespective of CD4 count criteria, on the reduction in incidence of new HIV infections in the general population in the same setting. \nSetting: The trial will be conducted in Hlabisa sub-district, Umkhanyakude district, Northern KwaZulu-Natal, South Africa. This rural setting of 1430 km2 in size has a population of approximately 220 000 Zulu-speaking people. In this sub-district, the Africa Centre for Health and Population studies, a research institute at the University of KwaZulu-Natal (<http://www.africacentre.com>) carries out socio-demographic and HIV surveillance and clinical research. The KwaZulu-Natal Department of Health and the Africa Centre established in 2004 the Hlabisa HIV Treatment and Care Programme, devolved to all 17 primary health care clinics in the sub-district. By mid-2013, over 28 000 HIV-infected people eligible for treatment had been initiated on ART; patients' treatment eligibility is determined by South African guidelines. \n\nDesign: A cluster-randomised trial with 22 (2\u00d711) clusters will be conducted within the Hlabisa sub-district, covering a total population of approximately 22 000 inhabitants aged 16 years and above, of whom an estimated 17 600 will be HIV-negative. A full prevention and HIV testing strategy will be provided in both the intervention and control arms, consisting of the current range of community and clinic testing options plus the implementation of 6-monthly rounds of home-based HIV testing. The adult HIV-infected population residing in the intervention clusters will be offered immediate ART initiation upon HIV diagnosis whereas the HIV-infected population in the control clusters will be offered ART according to national guidelines (CD4 less than 350 cells/ml, WHO stage 3 or 4 disease or MDR/XDR TB). The protocol outlines the overall trial design, which has HIV incidence as primary outcome. The first phase of the trial (24 months) will take place in ten (2\u00d75) clusters, with two to three rounds of home-based HIV testing and surveillance according to the trial protocol, and has as main outcome acceptability and feasibility rather than HIV incidence. If results from the first phase indicate acceptability and feasibility, the trial will be rolled-out to the other 12 clusters during the second phase. Possible amendments to the trial for phase 2 will be based on the advice from the Data Safety Monitoring Board and the Scientific Advisory Board.\n\nTrial eligibility criteria: To be aged 16 years and above and a member of a household in the designated cluster (head of household defines membership status in KwaZulu culture).\n\nTreatment eligibility criteria: Those already on ART from the Hlabisa HIV Treatment and Care Programme may opt to transfer their care to the trial; the few (if any) people already on ART from private/other HIV treatment providers will be encouraged to take part in the trial monitoring procedures, and be given the opportunity to change ART provider to the Hlabisa HIV Treatment and Care Programme trial. \n\nTrial treatment: The standard first-line drug regimen will be the combination of tenofovir (TDF) + emtricitabine (FTC) + efavirenz (EFV) once daily, i.e. Atripla\u00ae. This will also be applicable to pregnant women irrespective of the trimester of pregnancy.","time_periods":[{"start":"2012-03-09","end":"2014-05-31","cycle":"Phase 1"},{"start":"2014-06-01","end":"2016-07-30","cycle":"Phase 2"}],"coll_dates":[{"start":"2012-03-09","end":"2016-07-30","cycle":"Data Collection"}],"nation":[{"name":"South Africa","abbreviation":"ZA"}],"geog_coverage":"Twenty Two survey clusters located in Hlabisa sub-district, Umkhanyakude district, of northern KwaZulu-Natal, South Africa.\nThe Hlabisa health sub-district is a rural setting of 1 430 km2 in size, with a population of approximately 220 000 Zulu-speaking people of whom 3.3% are located in a formal urban township (KwaMsane), 19.9% in peri-urban areas and the remainder (76.8%) classified as living in a rural area. The rural population lives in scattered homesteads that are not concentrated into villages or compounds (as would be the case in many other parts of Africa).","analysis_unit":"Clusters, Households, Individuals","universe":"Clusters: the trial area consists of 150 local areas (neighbourhoods). These were aggregated into 34 clusters of between one and six contiguous neighbourhoods, each cluster comprising an average of 1 000 individuals >15 years of age. Clusters were designed to encompass social networks based on earlier studies. TasP phase 1 has been implemented in 10 geographic clusters (5 control and 5 intervention). Twelve additional clusters have been opened in June 2014.\n\nLocations: corresponds to physical locations. There are two types of locations: homesteads and TasP clinics.\n\nHomesteads: the population lives in scattered homesteads that are not concentrated into villages or compounds. All usable and occupied homesteads were eligible for trial participation.\n\nHouseholds: each homestead coul be composed of one or several households. An household remains always attached to the same homestead.\n\nEligible individuals : all 16 years or older and resident household members. Each individuals is attached to an household. In case of internal migration, an individual could move to another household.\n\nTasP clinics: dedicated trial clinics implemented in each survey cluster."},"method":{"data_collection":{"data_collectors":[{"name":"Africa Centre for Health and Population Studies","abbreviation":"AC","affiliation":"UKZN"}],"frequency":"A calendar round refers to the time period it took to implement one home-based HIV testing round in all the clusters. During the first phase of the trial, three calendar rounds were conducted in four clusters (first group, 8 months, 4 months, 4 months duration) and two calendar rounds in six clusters (second group, 6 months and 6 months). In Phase 2 Calendar rounds were implemented every 6 months.\n\nClinical data of HIV-infected patients followed in TasP clinics has been collected on a day-to-day basis.","sampling_procedure":"Randomisation (control clusters vs intervention clusters) was performed by the trial statisticians at the start of the trial for all clusters. \n\nAll individuals 16 years or older and resident member of a local household are eligible.","coll_mode":"Face to face interviews"}},"data_access":{"dataset_use":{"conditions":"To access these datasets, an analysis proposal needs to be discussed with one of the TasP working groups and approved by TasP's principal investigators.\n\nPlease contact Collins Iwuj <ciwuji@africacentre.ac.za> and/or Joanna Orne-Gliemann <Joanna.Orne-Gliemann@isped.u-bordeaux2.fr> for further details and the model of form for submitting an analysis proposal.\n\nThis form must be filled and submitted by the Lead Researcher. Lead Researcher refers to the person who serves as the main point of contact for all communications involving this agreement. Access to licensed datasets will only be granted when the Lead Researcher is an employee of a legally registered receiving agency (university, company, research centre, national or international organization, etc.) on behalf of which access to the data is requested. The Lead Researcher assumes all responsibility for compliance with all terms of this Data Access Agreement by employees of the receiving organization."}}},"schematype":"survey","type":"survey","data_files":[{"file_id":"F22","file_name":"HIV Drug Treatments","description":"HIV drug treatment for TasP patients in care in TasP clinics. One row per regimen and per patient.\nEach time a patient switched from one regimen to another regimen, a new record was stored in that dataset.","case_count":"52237","var_count":"9","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F24","file_name":"Households","description":"This dataset contains one row per registered households.","case_count":"7814","var_count":"7","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F29","file_name":"CHEs","description":"This dataset corresponds to Clinical History and Examination forms (CHE) completed by nurses in tasP clinics. The following sections of the questionnaire are provided in separate datasets:\n- 11. Concomitant medication not recorded in ART or TB regimen -> HIV Drug Treatments dataset\n- 12. Adverse Events -> Adverse Events dataset\n- 24. Drug Prescriptions -> HIV Drug Treatments dataset\n- 25. Action Plan -> Action Plans dataset","case_count":"53274","var_count":"151","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F30","file_name":"Lab Test Results","description":"This dataset contains the resuts of the clinical tests done for patients in care in TasP clinics. It contains one row per test date and per individual.","case_count":"41508","var_count":"33","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F31","file_name":"ARTemis Lab Results","description":"This dataset contains all ARTemis Lab test results (in particular CD4 counts and viral loads) for TasP registered individuals linked to ARTemis.","case_count":"27498","var_count":"16","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F32","file_name":"ARTemis Patients","description":"This file contains data from ARTemis database for each registered TasP individual linked to ARTemis. One row per individual.\n\nThe data collated here is obtained from patients' records completed during routine HIV clinical care within the Hlabisa Treatment and Care Programme. The HIV treatment and Care programme was implemented as a joint initiative by the Department of Health (DoH) and the Africa Centre for Health and Population Studies (http://www.africacentre.ac.za) in response to the Comprehensive HIV and AIDS Care Management and Treatment Plan in 2004. HIV treatment and care is offered in 17 nurse-led primary health-care (PHC) clinics and 1 district hospital. The data comprises HIV positive patients pre- and post- ART initiation. However for patients pre-ART only the personal identifiers (name, sex and South African ID number) and the CD4 counts measured for assessment of ART eligibility are recorded. All patients within ARTemis are HIV positive and all patients are aware of their HIV status. This database was initially set up for monitoring and evaluating (M&E) patients and programme performance and outcomes. Over time in addition to M&E, these data are used to answer research questions to better understand issues related to HIV and ART in HIV positive patients. \n\nRoutine data collection schedule is summarized below:\n\nBasic details \n\nAge, sex, address, ID number, contact details, treatment clinic (collected at ART initiation only or when need arises during follow-up)\n\nSocio-demographic details \n\nGrants received, employment, school attendance, number of dependents (collected at ART initiation only)\n\nTuberculosis (TB) record\n\nTuberculosis (TB) record\n\nPrevious history of TB, TB treatment at initiation, new episodes of TB (collected only in those receiving ART)\n\nART record \n\nWHO clinical stage, Previous ART and/or PMTCT, ART regimen at initiation, changes in ART regimen during treatment\n\nLaboratory data \n\nFor patients on ART\n\nBaseline and 6-monthly CD4 and HIV viral load, baseline haematology and biochemistry\n\nFor patients pre-ART\n\nAll pre-ART CD4 cell counts routinely done in accordance with the South African ART guidelines are recorded","case_count":"5362","var_count":"121","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F34","file_name":"CHE Adverse Events","description":"This dataset corresponds to the Adverse Events section of the CHE (clinical history examination) forms. It contains one row per recorded adverse event.","case_count":"695","var_count":"7","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F39","file_name":"SCBs SCCs","description":"This dataset contains SCBs and SCCs forms (clinic-based survey, ART consellor administered), one row per form.","case_count":"7072","var_count":"97","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F44","file_name":"CHE Action Plans","description":"This dataset corresponds to the Action Plans section of the CHE (clinical history examination) forms. It contains one row per recordedaction plan.","case_count":"151477","var_count":"6","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F46","file_name":"Clusters","description":"Trial clusters","case_count":"22","var_count":"5","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F49","file_name":"Visits","description":"This table contains one row per visit. There are two sorts of visits: homestead visits and TasP clinic visits, that can be identified through the variable LocationType.\n\nLocationId refers to a homestead or to a TasP visit, according to the sort of visit.\n\nSeveral individuals could be surveyed for a same homestead visit while a TasP clinic visit always concerns only one individual.","case_count":"257410","var_count":"20","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F50","file_name":"HHIs","description":"This dataset contains Household Information / Assets forms. One row per form.","case_count":"18819","var_count":"50","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F52","file_name":"CFUs","description":"This file contains one row per Clinic Follow-Up form (CFU) completed by Trial Counsellor. Data from question 3.5 (Adherence Pill Identification Test) are provided in a seperate dataset (CFU Pill tests).","case_count":"50392","var_count":"21","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F53","file_name":"CFU Pill Tests","description":"This file contains data from question 3.5 (Adherence Pill Identification Test), one row per pill. You can link data with CFUs dataset using CVIntId.","case_count":"56726","var_count":"11","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F70","file_name":"Local Areas","description":"This dataset contains one row per Local Area. Local Areas are used in sexual behaviours questionnaires.","case_count":"314","var_count":"5","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F71","file_name":"Census Rounds","description":"This dataset contains one row per Census Round, i.e. one row per survey round and per cluster. That dataset provides the corresponding Calendar Rounds and Data Collection Cycles, please refer to TasP Definition document for details.","case_count":"133","var_count":"6","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F72","file_name":"SCIs","description":"This dataset contains SCI forms (clinic-based survey, independent interwiever administered), one row per form.","case_count":"3619","var_count":"280","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F73","file_name":"Individual Consents","description":"This dataset contains individual consents. One row per individual.","case_count":"186017","var_count":"5","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F74","file_name":"SAEs Initial Notifications","description":"Serious Adverse Events - Initial Notifications. This dataset contains one row per SAE notification.","case_count":"244","var_count":"31","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F75","file_name":"SAEs Initial Notifications - Events details","description":"One row per event.","case_count":"294","var_count":"9","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F76","file_name":"SAEs Initial Notifications - Medications","description":"One row per drug","case_count":"588","var_count":"12","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F77","file_name":"SAEs Complementary Notifications","description":"One row per complementary form","case_count":"101","var_count":"27","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F78","file_name":"SAEs Complementary Notifications - Medications","description":"One row per drug","case_count":"86","var_count":"15","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F81","file_name":"CBCs","description":"This dataset corresponds to Clinic Baseline Visit (CBC) forms completed by ART counsellors in TasP clinics.","case_count":"3010","var_count":"30","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F83","file_name":"Specimens","description":"This dataset indicates specimens collected within TasP (at home or in TasP clinics), one row per specimen.","case_count":"90607","var_count":"6","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F85","file_name":"IQs","description":"This dataset contains Individual Questionnaires (IQ1, IQ2, IQ3 and IQP) completed at home by fieldworkers.\n\nThe database doesn't allow the completion of more than one IQ1, one IQ2 and one IQ3 per individual.\n\nThe database does however allow the completion of more than one IQP per individual.\n\nAccording to the protocol, an IQ3 should be completed only if an IQ2 has been previously completed. However, there are few cases of individuals having completed an IQ3 without having completed an IQ2.\nAlso, an individual should normally complete a maximum of one IQ per calendar round, but some individuals have completed two IQs during the same calendar round (at different dates).\nFinally, although definition of logical rounds is based on IQ completion, there are some inconsistencies between logical rounds as recorded in the individuals file and completion of IQs.\n\nIQ1 and IQ3 are identical (they have the same questionnaire), while IQ2 is a shorter questionnaire with specific questions.","case_count":"78355","var_count":"169","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F87","file_name":"Minority Variants","description":"Dataset contains multiple rows per individual sequence analysed with the Next Generation Sequencing method and include information about drug resistance minority variants","case_count":"8594","var_count":"11","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F88","file_name":"BMQ Surveys","description":"This dataset corresponds to Beliefs about medicines questionnaire (BMQ) forms completed by ART counsellors in TasP clinics.","case_count":"282","var_count":"31","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F89","file_name":"NGS Genomics","description":"Dataset contains 1 row per individual sequence analysed. All sequences contained in this dataset has been analysed with the Next Generation Sequencing method.","case_count":"1541","var_count":"16","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F90","file_name":"Refusals","description":"This dataset corresponds to reasons why a household refused participantion in the study. Colleced by fieldworkers","case_count":"285","var_count":"17","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F91","file_name":"NgsAssembQuality","description":"Dataset contains 1 row per individual Next Generation Sequencing (NGS) sequence analysed. Dataset provided details of the Sequence assembly quality for each sample analysed.","case_count":"1426","var_count":"22","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F92","file_name":"Sample Genomics","description":"Dataset contains 1 row per individual sequence analysed. All sequences contained in this dataset has been analysed with the Sanger method.","case_count":"502","var_count":"11","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F94","file_name":"Locations","description":"Locations, i.e Homesteads and TasP clinics","case_count":"12167","var_count":"15","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F98","file_name":"LinkToCareTracker","description":"This dataset corresponds to the Linkage to Care Tracking forms completed by the TasP Linkage to Care Team.","case_count":"5074","var_count":"7","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F100","file_name":"Exits","description":"This dataset contains one row per exit form completed, including both population and clinic exits.\nIn Phase 1 (before 31st of May 2014), there were no formal distinction between population and clinic exits, only one form being used in the field (EXI). Since June 2014 two exit forms are used (EXIH and EXIC). Phase 1 forms have been manually recoded (using all available information, including field notes) to identify properly population and clinic exits. Please refer to variables PopulationExitComputed, ClinicExitComputed and PopulationExitTypeComputed.\nVariables: DTHDateComputed, ExitDateComputed, NMCDateComputed, OUTDateComputed, TRODateComputed, LFUDateComputed have been populating by taking into account the following corrections: (i) if exit date was missing or (ii) the year of the exit date was unknown or (iii) exit date was after VisitDate, then VisitDate (the date the exit from has been completed) was used instead of the exit date.","case_count":"12632","var_count":"43","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F101","file_name":"ACCDB Encounters","description":"Dataset contains one record per Individual visit (encounter) in the Africa Centre Clinical Database (ACCDB)","case_count":"126209","var_count":"9","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F102","file_name":"ACCDB Encounter Therapies","description":"Dataset contains multiple records per Individual for each Therapy received in the Africa Centre Clinical Database (ACCDB)","case_count":"348890","var_count":"11","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F103","file_name":"Individuals","description":"Registered individuals.\n\nAn individual is registered during the first calendar round he/she is eligible, i.e. all individuals who have been eligible at least once are registered and all registered individuals have been eligible at least once. Individuals could be registered only in a fully contacted household where the household head or another key informant accepted to participate.","case_count":"28419","var_count":"298","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F105","file_name":"Trial Statuses","description":"These file contains individual trial statuses, one row per trial status.\n\nDuplicated Trial Statuses (same visit date / same trial status) have been removed. Exit Trial Statuses have been re-created from the Exits datasets importing only Population Exits.","case_count":"118259","var_count":"27","producer":null,"data_checks":null,"missing_data":null,"version":null,"notes":null,"metadata":null},{"file_id":"F106","file_name":"DBS results expanded","description":"This file contains the results of HIV tests performed on Dried Blood Spots (DBS) collected during the home-based survey. 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TB highly prevalant in subdistrict","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Had Menorrhagra dummy the last Menstrual period.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Has been I Tasp on Atripla  sine 2013 withat   prior advvese  events . Deranged  LFT  likely due to an extenal case .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"High risk of malnutrition due to immunosuppression","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"High viral load despite prolong ARV use , amotype slims resistance  to EFV and 3TC  .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Hiluly to be related  to alcohol  consumption","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"History Incomplete","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Iron deficiency anaemia, cause not yet identified.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Known HPT/CCF/Chronic renal failure","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"LFT's including GGT with grade 3 abnormalities at baseline due to alcohol abuse.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"LT Upper  Zone PNeumonia , To Exclude Pulmonary TB Peptic ulcer  disease .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"LTS's abnormal at baseline synerstic synergistic toxiaty from Atripla + Alcohol + herbal remedies","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Likely to be worsering  curonic kidney Disease due to Hypertension  but coud Also be HIV - Associated Nepuropathy .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Lower Respiratory Trect  Infection","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Most likely cause of deranged LFT is alcohol.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Multiple ART defaults, cannot exlude bone narrow suppression from Cotrimaxazole","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Multy-Drug resistant treatment.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Normocytic anaemia, requires further investigation.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Not enough information","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Not on ART in Control cluster and not eligible for ART but returned after 6months and found eligible under new guidelines. Currently not on ART.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant already had TB symptoms at baseline.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant default ed flucconazole, at rist of recurrent cryptococcal meningitis","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant defaulted anti - epileptic treatment and thus had siezures","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant diagnosis with throat cancer","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant found to be Anaemia at baseline visit.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant had dirrhoea, admitted use of herbal medicines and had been nephrotoxic medication.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant had stroke at a young age.  She is still undergoing investigation.  HIV stroke may be contributing","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant has Malnutrion and severe wasting with low CD4 count. He is highly susceptible to infections","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant has cervical cancer","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant has history of alcohol abuse which is likely to account for raised liver enzymes.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant is hypertensive - risk of renal failure is high.  Nephrotoxic treatment also may add to severity","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant most likely has iron deficiency anaemia","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant newly diagnosed with PTb May have disseminated TB strong hstory of cannibis use","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant severely immunosuppressed with PTB. Exact cause of death not yet known.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant surely immunocompromised upon enrolment. Supected TB IRIS.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant susceptible to TB due to immunosuppression.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant unknown with Bipoal mood disorder - is prone to relapsed acute episodes.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant using herbal medicines for Sangoma initiation. At risk of nephiotoxity","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant was assaulted","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant will longstanding history of severe illness, failed to go to hospital with cormobid HIV and extrapulmonary TB.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant with advances HIV and TB. Needs to be invesitgated to exclude dissiminated or resistant TB.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant with declining CD4 count very suscetible to oppotunistic infections.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant with evidence of treatment failure, no clinical improvement. Has co-morbid TB and HIV. Very ill.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant with history of incorrect dosing of ART. Also previously on NVP which may caused liver toxicity.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant with uncontrolled diabetes  , at risk of renal failure","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participant with very low CD4, not on ART, developed acute renal failure from diarrhoea.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participants was injured","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Participantwith very low CD4 succeptable to oppotunisic infections.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Partiocipant succestible to TB due to immunosuppresion.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient ART na\u00efve and not prescribed any drugs within trial","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient LFT's are demaged at baseline entry into TasP","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient at risk of cancer regardless of participation in research","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient at risk of diarrhoea as imnosuppressed and on Aluvia. Unrelated to research","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient committed suicide, the reason for thi is unknown.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient complained of weight loss and dry cough recently .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient developed panariatitis most likely from an acute which is still being investigated.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient developes severe diarrhoea and Acute renal failure prior to Atripla Reveles by blood test done on same day started Atripla. Atripla could have exacerbated the acute renal failuere","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient did not go to hospital when referred. She most likely had TB.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient died in his sleep cause unknown.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient extremely immunosuppressed","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient had been on ART fkor long period of time before having psychotic episode.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient had breast cancer the trial unfortunately it has progressed","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient had deranged LFT prior 0to TasP likely alcohol is the main contributor","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient had longstanding history of abdnormal bleeding and had defaulted ART.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient had longstanding history of undiagnored depression which complicated with psychosis","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient had variable blood sugar readings over time at Tasp clinics. Was at risk of type 2 diabetes.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient has been to Tasp for 9 months. Only returned now as he is sick.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient has multiple myeloma + on naproxen","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient has multiple risk factors for derange LFT's.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient immuno","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient immunocompromised . At rish of multiple causes of confusion .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient immunosuppressed, prone to apportunities infections.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is HIV POSITIVE WITH CHRONIC ANAEMIA. Need amement","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is HIV positive, on ART prior to Tasp. Came of LFT deranged unclear ar present.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is diabetic,hypertensive and HIV positive which mascles him susceptible to multiple infections.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is imiunocompromised +atrisk of infection","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is immcompromised with incresed risk of gastroentritis. Risk of dehydration is high with gastroentrities","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is immnocompromised. At risk of TB","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is immnosupressed, At risk of GE","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient is severely  immunocompromised + at risk of abcsess","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient most likely had prostate cancer. PSA was 57 and patient was symptomatic","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient must have suffered from dehydrated to vomiting exacerbated by tenofavir + hydrocithorothiazide","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient must likely  had cervical  cancer","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient newly diagnosed with TB. She is","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient severely ill with co-morbid MDR-TB and advanced AIDS desease","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient transfered in at baseline with Hb 6.1","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient transferred in with this problem.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was already on TDF which could be a cause orcontributing factor to this renal failure, fixed doze ARV's stopped.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was already on antiretroviral drug before joining the research .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was immnocompromised + side at entry into the trial","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was immunocompromised  and known to Abuse alcohol .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was immunoconipromised with a possible TB ccontact, so was high risk of TB","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was known with congestive cardiac failure. He had defaulted treatment and not disclosed to trail clinic","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was on long term asprin prior to Tasp study.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient was severely immunocompromised. Alluvia can cause diarrhoea, but patient was complinity of diarrhoea before switching to Alluvia.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient with PTB, succeptable to superimposed bacterial infection","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patient with advances HIV, poor compliance and pulmonary TB","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Patients age and immune status are risk factors fo cancer.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pelvic inflammatory disease","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Physical /Sexual  Assault","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pnevious TB Episodes ( 2007/2008 )","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Poor adherence to ART mth multiple stops restarts possibly IRIS","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Possibly a combination of Stavudine treatment , Alcohol  and Hepatitis  B .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Possibly related to Advanced HIV infection. Patient also anemic with weight loss.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pre - existing abnormality in YGT, Whilst on D4T/3TC/EFV. Need to obtain alcohol history.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Predated the reseach .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Present at baseline with renal failure. Post discharge drug will be ratranalised","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Present at baseline.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Previous TB,possibly bronchiectasis.Alcohol abuse.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probable Iron deficiency Anaemia","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probable Iron deficiency anemia present at baseline","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probable Pulmonary TB","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probable iron Defigency Anaemia","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probable iron deficiency.Anaemia","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probable iron definancy anaemia presental  baseline","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probably Haemorrhoids","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probably alcohol abuse although HAART can cause elevate GT .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probably alcohol abuse.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probably alcohol related elevation of gamma glutamyl transference.Efavirenz was prescribed before participation in reseach.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probably iron  deficientcy Anaemia","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probably iron deficiency anaemia.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Probably related  to Alcohol  abuse","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Propable TB,L Presented of baseline","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pt had familly CD4 count and cough she may have had TB which was not investigated. She also had social stressor.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pt on ART for a long time. Confusion is acute with PTB being diagnosed. C7 brain is important to exclude space occupying lesion in the brain","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pt with multiple episode pulmonary TB susceptible to dyspnoea due to lung fibrosis","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pt with underlying autommune disease . She recovered quickly from psychosisdespite not being on treatment & is still on Atripla .","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Pulmonary TB","labl":null,"is_missing":null,"stats":[{"value":"4","type":"freq","wgtd":null}]},{"value":"Rirely due to taking tenofovir , which she commenced prior to enrolling at TASP . No previus renal past medlet history","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Severe diarrhoea  and renal failure pre - dated baseline clinic visit. Severe diarrhoea must have resulted in Pre renal failure with additional neuphrotixicty from Tinofavir","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Severe gastroenteritis resulting in acute renal failure exacerbated bytenofovir prescribed before joining trisil","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Stabbed abdomen","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Stroke","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"Tdhis patient is Immnocompromised would have been at risk of pneumonia / sepsis regarden of participant in Tasp.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The parent had proven pulmonary tuberculosis","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient died of a presumed urinary truck infetion cammy sepsis,although she was not referred for past- mortem","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient has HIV and is at risk of opportunistic infections.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient is at risk of gastroentertis due to immunoconipromise","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient was already on TB treatment prior to enrolment in TasP.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient was imminospprened and at risk of oppotunistic infection.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient was immonoscomposed and at risk of aopportunist infection.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient was immunosuppressed and at risk of infection","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient was on D4T prior to Tasp but started TDF April 2013 + was stable until this point","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The patient was pregnant + at risk of complaications in research.","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"The putient was aneemia before entry into Tasp. Women with HIV are at high risk of cervical cancer","labl":null,"is_missing":null,"stats":[{"value":"1","type":"freq","wgtd":null}]},{"value":"This patient had HIV and hypertension. 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