Identifying Pain Trajectories In Sickle Cell Disease Using Latent Class Analysis
Identifying Pain Trajectories In Sickle Cell Disease Using Latent Class Analysis
批准号:
9299186
负责人:
Angie Mae Rodday
金额:
$26.25万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-05-23 至 2019-01-31
关键词:
Academic Medical CentersAccountingAcuteAdmission activityAdultAffectAfricanAfrican AmericanAnti-Inflammatory AgentsAnti-inflammatoryAsian IndianAvascular necrosis of boneClinicalCommunicationDiseaseEmergency department visitErythrocytesEthnic OriginEuropeanFutureGoalsHealth Care CostsHealth Services AccessibilityHealthcareHematological DiseaseHemolytic AnemiaHeritabilityHispanicsHome environmentHospitalizationIndividualInpatientsInsurance CoverageInterventionLow incomeMeasuresMethodologyMinority GroupsMorbidity - disease rateNumeric Rating ScaleOpioidOutcomeOutpatientsOverdosePainPain MeasurementPain intensityPain managementPatient Outcomes AssessmentsPatient riskPatientsPatternPerceptionPharmaceutical PreparationsPneumoniaPostoperative PainPrevalenceProspective StudiesProviderRaceRecruitment ActivityReportingRetrospective cohortRiskSepticemiaSeverity of illnessSickle CellSickle Cell AnemiaSignal TransductionStatistical MethodsTechniquesVariantacute chest syndromeaddictionbody systemcancer painclinical caredrug addictethnic minority populationexhaustexperiencehealth care disparityhealth care service utilizationhealth related quality of lifehigh riskimprovedinnovationmortalitypatient home careprospectiveracial and ethnic disparitiesracial minoritytreatment strategy
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英文摘要
PROJECT SUMMARY/ABSTRACT
Sickle cell disease (SCD) is a group of heritable red blood cell disorders that primarily affect individuals who
identify as Black or African-American. Other affected groups include those of Hispanic, southern European,
Middle Eastern, and Asian Indian descent. The hallmark of SCD is the painful vaso-occlusive crisis (VOC),
which is still not well understood or managed. This may result in delays in treatment, undertreatment, and
unnecessary suffering. Because SCD primarily affects African-Americans and other minority groups, mistrust
between patients and providers may put patients with SCD at increased risk of healthcare disparities, including
reduced access to necessary pain management. For most patients, pain is managed at home, further
contributing to underestimation by healthcare practitioners of the prevalence and impact of SCD pain.
However, when patients in VOC present acutely, they have usually exhausted home care and outpatient
therapies, thereby signaling the need for parenteral opioids. Using a retrospective cohort of 150 patients with
SCD hospitalized at one urban academic medical center, the overall goal of this study is to develop
methodology to characterize the sickle cell pain trajectory. Specifically, the aims are to (1) use latent class
analysis to identify different patterns of pain trajectories during hospitalizations for sickle cell pain crisis and
determine socio-demographic and clinical factors associated with the different pain trajectories; (2) describe
the relationship between treatment management strategies and sickle cell pain scores during hospitalization;
and (3) assess the relationship between different patterns of sickle cell pain trajectories and future readmission
for sickle cell pain crisis. Results from the proposed study can then be used to develop prospective studies to
better measure pain during hospitalizations or to identify factors that affect the pain trajectory, which can be
used to target interventions or pain management approaches. In addition, better characterization of the pain
trajectory and treatment of pain in SCD are especially urgent as efforts are made nationally to restrict access to
opioids given the current crisis of abuse, addiction, and overdose. Patients experiencing severe and
devastating pain, such as those with SCD, should not be made to suffer because they are denied necessary
treatment.
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