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    <Citation xmlns="ddi:reusable:3_1">
        <Title>Metadata record for Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatment (SUPPORT) and Hospitalized Elderly Longitudinal Project (HELP), 1989-1997</Title>
        <Creator>ICPSR</Creator>
        <Copyright>
        ICPSR metadata records are licensed under a Creative Commons Attribution-Noncommercial 
        3.0 United States License (http://creativecommons.org/licenses/by-nc/3.0/us/).
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    <StudyUnit xmlns="ddi:studyunit:3_1" id="StudyUnit02957" versionDate="2006-01-12">
        <Citation xmlns="ddi:reusable:3_1">
            <Title>Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatment (SUPPORT) and Hospitalized Elderly Longitudinal Project (HELP), 1989-1997</Title>
 				
	    	
				<Creator xmlns="ddi:reusable:3_1" affiliation="George Washington University">Knaus, William</Creator>
	    	
				<Creator xmlns="ddi:reusable:3_1" affiliation="George Washington University">Lynn, Joanne</Creator>
	    	
	    	<Publisher>Inter-university Consortium for Political and Social Research</Publisher>
  			<Contributor role="distributor">ICPSR</Contributor>
   			<PublicationDate>
    			<SimpleDate>2006-01-12</SimpleDate>
   			</PublicationDate>
   			<InternationalIdentifier xmlns="ddi:reusable:3_1" type="ICPSR Number">2957</InternationalIdentifier>
   			<InternationalIdentifier xmlns="ddi:reusable:3_1" type="DOI">doi://10.3886/ICPSR02957.v1</InternationalIdentifier>
        </Citation>

        <Abstract isIdentifiable="true" id="Abstract02957">
            <Content xmlns="ddi:reusable:3_1">
            <div xmlns="http://www.w3.org/1999/xhtml" id="Summary02957">The objective of the SUPPORT and HELP projects was to
improve decision-making in order to address the growing national
concern over the loss of control that patients have near the end of
life and to reduce the frequency of a mechanical, painful, and
prolonged process of dying. SUPPORT comprised a two-year prospective
observational study (Phase I) followed by a two-year controlled
clinical trial (Phase II). Phase I of SUPPORT collected data from
patients accessioned during 1989-1991 to characterize the care,
treatment preferences, and patterns of decision-making among
critically ill patients. It also served as a preliminary step for
devising an intervention strategy for improving critically-ill
patients' care and for the construction of statistical models for
predicting patient prognosis and functional status. An intervention
was implemented in Phase II of SUPPORT, which accessioned patients
during 1992-1994. The Phase II intervention provided physicians with
accurate predictive information on future functional ability, survival
probability to six months, and patients' preferences for end-of-life
care. Additionally, a skilled nurse was provided as part of the
intervention to elicit patient preferences, provide prognoses, enhance
understanding, enable palliative care, and facilitate advance
planning. The intervention was expected to increase communication,
resulting in earlier decisions to have orders against resuscitation,
decrease time that patients spent in undesirable states (e.g., in the
Intensive Care Unit, on a ventilator, and in a coma), increase
physician understanding of patients' preferences for care, decrease
patient pain, and decrease hospital resource use. Data collection in
both phases of SUPPORT consisted of questionnaires administered to
patients, their surrogates, and physicians, plus chart reviews for
abstracting clinical, treatment, and decision information. Phase II
also collected information regarding the implementation of the
intervention, such as patient-specific logs maintained by nurses
assigned to patients as part of the intervention. SUPPORT patients
were followed for six months after inclusion in the study. Those who
did not die within six months or were lost to follow-up were matched
against the National Death Index to identify deaths through 1997. The
HELP study was conducted in 1993 concomitantly with Phase II of
SUPPORT and collected data to characterize the care, treatment
preferences, and patterns of decision-making among hospitalized
patients who were at least 80 years old. HELP data were also intended
for use in adapting existing mortality and functional status models of
elderly hospitalized patients. Data collection methods of HELP were
essentially the same as those of SUPPORT. HELP patients were followed
for 12 months after inclusion in the study. Patients who did not die
within one year or were lost to follow-up were matched against the
National Death Index to identify deaths through 1997.</div>
             </Content>
        </Abstract>
        
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  		</UniverseReference>

 				
 				<FundingInformation xmlns="ddi:reusable:3_1">
    				
  						<AgencyOrganizationReference>
							 <ID>Organization02957_1</ID>
   						</AgencyOrganizationReference>
  						
   							<GrantNumber>23715, 20856</GrantNumber>
   						
    				
    				</FundingInformation>
				
        <Purpose id="Purpose02957">
            <Content xmlns="ddi:reusable:3_1">
            
           </Content>
        </Purpose>
        
        
        
          <Coverage xmlns="ddi:reusable:3_1">

   <TopicalCoverage xmlns="ddi:reusable:3_1" id="TopicalCoverage02957">
		
      		<Subject codeListAgency="NACDA">NACDA.VI</Subject>
      	
      		<Subject codeListAgency="ICPSR">ICPSR.IX</Subject>
      	
      		<Subject codeListAgency="HMCA">HMCA.IV</Subject>
      	
		
      		<Keyword>attitudes toward death</Keyword>
      	
      		<Keyword>decision making</Keyword>
      	
      		<Keyword>dying</Keyword>
      	
      		<Keyword>informed consent</Keyword>
      	
      		<Keyword>intervention</Keyword>
      	
      		<Keyword>intervention strategies</Keyword>
      	
      		<Keyword>patient care</Keyword>
      	
      		<Keyword>right to die</Keyword>
      	
      		<Keyword>terminal care</Keyword>
      	
      		<Keyword>terminal illnesses</Keyword>
      	
      		<Keyword>treatment</Keyword>
      	
   </TopicalCoverage>
 

	
   <SpatialCoverage id="SpatialCoverage02957">
		<Description>
			
				United States
			
		</Description>
    <TopLevelReference>
     <LevelName> </LevelName>
    </TopLevelReference>
    <LowestLevelReference>
     <LevelName> </LevelName>
    </LowestLevelReference>
   </SpatialCoverage>
   


	

   <TemporalCoverage id="TemporalCoverage02957">

		
    <ReferenceDate>
		
				
      		<StartDate>1989</StartDate>
      		<EndDate>1997</EndDate>
			
			
      		
    </ReferenceDate>
    
     
   </TemporalCoverage>
 
 
 
         </Coverage>
 


	    	
	    		<KindOfData>administrative records data</KindOfData>
	    	
	    		<KindOfData>clinical data</KindOfData>
	    	
	    		<KindOfData>survey data</KindOfData>
	    	


        
   <ConceptualComponent xmlns="ddi:conceptualcomponent:3_1" id="ConceptualComponent02957">
   <UniverseScheme id="UniverseScheme02957">
	    	
    <Universe id="Universe02957_1">
     <HumanReadable>SUPPORT: Critically ill patients admitted to United States
hospitals with advanced stages of serious illness. HELP: Patients 80
years of age or older admitted to United States hospitals.</HumanReadable>
    </Universe>
    
    
   </UniverseScheme>
   
   
   
   
  </ConceptualComponent>
        
  <DataCollection xmlns="ddi:datacollection:3_1" id="DataCollection02957">
  			



   <Methodology id="Methodology02957">


    <SamplingProcedure id="SamplingProcedure02957">
     <Content xmlns="ddi:reusable:3_1">SUPPORT: All patients in five United States medical
 centers who met inclusion and exclusion criteria for nine disease
 categories: acute respiratory failure, chronic obstructive pulmonary
 disease, congestive heart failure, liver disease, coma, colon cancer,
 lung cancer, multiple organ system failure with malignancy, and
 multiple organ system failure with sepsis. Phase I of SUPPORT
 accessioned 4,301 patients from June 12, 1989, through June 11, 1991,
 and in Phase II, 4,804 patients were accessioned from January 7, 1992,
 through January 24, 1994. HELP: A random sample of 1,176 patients at
 least 80 years old who were admitted to four United States hospitals
 from January 21, 1993, through November 21, 1993. Patients meeting the
 HELP age criterion were excluded if they were admitted electively for
 surgery or invasive radiographic procedures, were not
 English-speaking, were admitted for trauma except falls, were admitted
 to hospice care, were foreign nationals whose purpose for entry in the
 United States was medical treatment or who became ill while visiting
 the United States, had an AIDS diagnosis, had a planned discharge of
 less than 72 hours, transferred from another hospital to a
 nonintensive unit, were admitted to psychiatry, or were discharged or
 died within 48 hours of admission. All patients admitted into SUPPORT
 were automatically screened for the HELP project. As a result of this
 screening, 90 SUPPORT patients were enrolled in HELP as well as
SUPPORT, yielding a total of 1,266 HELP patients.</Content>
    </SamplingProcedure>
  
   </Methodology>
   
 
		
   <CollectionEvent id="CollectionEvent02957_1">
    
    <DataSource>
     <SourceDescription>
     
    		medical records, personal interviews, and the National
Death Index
    	
    </SourceDescription>
    </DataSource>
    
		<DataCollectionDate>
 		
				
      		<StartDate xmlns="ddi:reusable:3_1">1989</StartDate>
      		<EndDate xmlns="ddi:reusable:3_1">1997</EndDate>
			
			
      		
      		</DataCollectionDate>

    


   </CollectionEvent>
      	
 
 
 
    
   <ProcessingEvent id="ProcessingEvent02957">
 
   

   

    
   </ProcessingEvent>
  </DataCollection>

  			

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   <ArchiveSpecific>




    <ArchiveOrganizationReference>
     <ID xmlns="ddi:reusable:3_1">ICPSR</ID>
    </ArchiveOrganizationReference>




    <DefaultAccess id="DefaultAccess02957">
     
                <Restrictions>
                	<div xmlns="http://www.w3.org/1999/xhtml" id="Restrictions02957">
                		As explained in the ICPSR Processing Note in the codebook, some variables are restricted from general dissemination for reasons of confidentiality. Users interested in obtaining these data must complete an Agreement for the Use of Confidential Data, specify the reasons for the request, and obtain IRB approval or notice of exemption for their research. Apply for access to these data through the ICPSR restricted data contract portal, which can be accessed via the <a href="http://dx.doi.org/10.3886/ICPSR02957">study home page</a>.
                	</div>
                </Restrictions>
                
     <AccessConditions>
     
        
      <div xmlns="http://www.w3.org/1999/xhtml" id="AccessConditions02957">

 			
                
					AVAILABLE.  This study is freely available to the general public.
                
                  
                

</div>

</AccessConditions>
<AccessConditions>
      <div xmlns="http://www.w3.org/1999/xhtml" id="AccessConditions02957-disclaimer">
The original collector of the data, ICPSR, and the relevant funding agency bear no 
                responsibility for use of the data or for interpretations or inferences based upon such uses.
                </div>

                </AccessConditions>

			
       



    </DefaultAccess>
   
   
   </ArchiveSpecific>
   
   <OrganizationScheme id="OrganizationScheme02957">
    <Organization id="ICPSR" xmlns="ddi:archive:3_1">
     <OrganizationName xmlns="ddi:archive:3_1">Inter-university Consortium for Political and Social Rearch</OrganizationName>
     <Nickname>ICPSR</Nickname>
     <Location id="LocationICPSR">
      <Address>
       <City>Ann Arbor</City>
       <State>MI</State>
      </Address>
     </Location>
     <URL>http://www.icpsr.umich.edu/</URL>
     <Email>netmail@icpsr.umich.edu</Email>
    </Organization>

 				
    				
						<Organization xmlns="ddi:archive:3_1" id="Organization02957_1">
   							<OrganizationName xmlns="ddi:archive:3_1">Robert Wood Johnson Foundation</OrganizationName>
  						</Organization>
    				
				


   </OrganizationScheme>
  
 
   <LifecycleInformation xmlns="ddi:reusable:3_1">
 
 
    	
           
<LifecycleEvent id="LifecyleEvent02957-2006-01-12">
             <Date>
             <SimpleDate>2006-01-12</SimpleDate>
             </Date>
     <AgencyOrganizationReference>
      <ID>ICPSR</ID>
     </AgencyOrganizationReference>
             <Description>2006-01-12 All files were removed from dataset 16 and flagged as study-level files, so that they will accompany all downloads.</Description>
           </LifecycleEvent>
    	
 
 
    
 
   </LifecycleInformation>


    
    <Note type="Comment" xmlns="ddi:reusable:3_1" id="Note02957_1">
   <Relationship>
    <RelatedToReference>
     <ID>StudyUnit02957</ID>
    </RelatedToReference>
   </Relationship>
   <Content>
		<div xmlns="http://www.w3.org/1999/xhtml">
			This data collection comprises a subset of all the
variables generated by the SUPPORT and HELP projects.
		</div>
	</Content>
  </Note>
  
    <Note type="Comment" xmlns="ddi:reusable:3_1" id="Note02957_2">
   <Relationship>
    <RelatedToReference>
     <ID>StudyUnit02957</ID>
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   <Content>
		<div xmlns="http://www.w3.org/1999/xhtml">
			Part 15, SAS
Transport Library Comprising Input Control Datasets, contains
information that the SAS FORMAT procedure can use to construct
formats.
		</div>
	</Content>
  </Note>
  
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   <Content>
		<div xmlns="http://www.w3.org/1999/xhtml">
			The SAS transport files were created using the SAS XPORT
engine.
		</div>
	</Content>
  </Note>
  

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