Loading…

PD54 Associated Factors Renal Graft Loss Using Real-World Evidence In Brazil

Introduction:Renal transplantation is considered a cost-effective treatment compared to dialysis and represents a significant percentage of public health resources. Post-transplant treatment requires the use of three immunosuppressive drugs. The immunosuppressive regimens consists of a corticosteroi...

Full description

Saved in:
Bibliographic Details
Published in:International journal of technology assessment in health care 2018, Vol.34 (S1), p.148-149
Main Authors: Gomes, Rosângela Maria, Barbosa, Wallace Breno, de Assis Acurcio, Francisco, Guerra, Augusto Afonso
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 149
container_issue S1
container_start_page 148
container_title International journal of technology assessment in health care
container_volume 34
creator Gomes, Rosângela Maria
Barbosa, Wallace Breno
de Assis Acurcio, Francisco
Guerra, Augusto Afonso
description Introduction:Renal transplantation is considered a cost-effective treatment compared to dialysis and represents a significant percentage of public health resources. Post-transplant treatment requires the use of three immunosuppressive drugs. The immunosuppressive regimens consists of a corticosteroid, a calcineurin inhibitor (cyclosporine or tacrolimus) and an antiproliferative agent (azathioprine or mycophenolate) and also by sirolimus or everolimus. In Brazil, the Unified Health System (as known as Sistema Único de Saúde - SUS) is responsible for 95 percent of all kidney transplants performed, as well as ensuring access to immunosuppressive drugs. Therefore, there is a huge and growing economic impact caused by the distribution of these drugs in SUS. We evaluated the factors associated with kidney graft loss in patients who received deceased donor organ and used maintenance immunosuppressive regimens in SUS, in fifteen years.Methods:We analyzed a nationwide cohort of kidney transplant recipients from January 2000 to December 2015 developed through deterministic-probabilistic linkage of SUS administrative databases: Hospital Information System (SIH/SUS); Subsystem for High Complexity Procedures (SIA/SUS) and the Mortality Information System (SIM). Graft loss was defined as death or dialysis for more than three months. All regimens included corticosteroid. We used Cox proportional hazards model to evaluate the factors associated with progression to graft loss.Results:In total, 18,333 patients were included; 58.5 percent used tracolimus+mycophenolate, 11.7 percent cyclosporine+mycophenolate, 8.9 percent tacrolimus+azathyoprine, 5.5 percent cyclosporine+azathyoprine and 15.4 percent received other immunosuppressive regimens (sirolimus+mycophenolate, everolimus+mycophenolate, tacrolimus, mycophenolate, cyclosporine, azathyoprine) . Most patients were male with a median age of 46 years. A higher risk of graft loss was associated with the use of tracolimus+mycophenolate (HR = 1.069; 95% CI, 0.999–1.146), sirolimus+mycophenolate (HR1.395;95% CI, 1 .150–1.692), tracolimus (monotherapy) (1.468;1.239–1.739); mycophenolate (monotherapy) (1.297;1.126–1.493), male gender (1.144; 1.072–1.221), an additional year of age (1.010; 1.007–1.013), a median dialysis period greater than 38 months (1.266; 1.182–1.356), a diagnosis of diabetes (1.211; 1.071–1.367) and a diagnosis of arterial hypertension (1.209; 1.134–1.288) (HR=1.468;95% CI,1.239 −1.739); mycophenolate (monother
doi_str_mv 10.1017/S0266462318003173
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2338905536</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cupid>10_1017_S0266462318003173</cupid><sourcerecordid>2338905536</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1146-924197ab4b134a459b936a32d5c77be8b73cdd3f6a5cc0b1f1aa11b0f96a91b3</originalsourceid><addsrcrecordid>eNp1kEFLw0AQhRdRsFZ_gLcFz9GdzGaTPdba1kJB0YrHMLvZlJQ0qbupoL_elBY8iKeBee97PB5j1yBuQUB69ypipaSKETIhEFI8YQOQKUQKZXbKBns52uvn7CKEtRCAQosBWzw_JJKPQmhtRZ0r-JRs1_rAX1xDNZ95Kju-aEPgb6FqVv2b6ui99XXBJ59V4Rrr-Lzh956-q_qSnZVUB3d1vEO2nE6W48do8TSbj0eLyAJIFelYgk7JSAMoSSbaaFSEcZHYNDUuMynaosBSUWKtMFACEYARpVakweCQ3Rxit7792LnQ5et25_u6IY8RMy2SBFXvgoPL-r6-d2W-9dWG_FcOIt9vlv_ZrGfwyNDG-KpYud_o_6kfQWFrkw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2338905536</pqid></control><display><type>article</type><title>PD54 Associated Factors Renal Graft Loss Using Real-World Evidence In Brazil</title><source>ABI/INFORM Global</source><source>Cambridge University Press</source><creator>Gomes, Rosângela Maria ; Barbosa, Wallace Breno ; de Assis Acurcio, Francisco ; Guerra, Augusto Afonso</creator><creatorcontrib>Gomes, Rosângela Maria ; Barbosa, Wallace Breno ; de Assis Acurcio, Francisco ; Guerra, Augusto Afonso</creatorcontrib><description>Introduction:Renal transplantation is considered a cost-effective treatment compared to dialysis and represents a significant percentage of public health resources. Post-transplant treatment requires the use of three immunosuppressive drugs. The immunosuppressive regimens consists of a corticosteroid, a calcineurin inhibitor (cyclosporine or tacrolimus) and an antiproliferative agent (azathioprine or mycophenolate) and also by sirolimus or everolimus. In Brazil, the Unified Health System (as known as Sistema Único de Saúde - SUS) is responsible for 95 percent of all kidney transplants performed, as well as ensuring access to immunosuppressive drugs. Therefore, there is a huge and growing economic impact caused by the distribution of these drugs in SUS. We evaluated the factors associated with kidney graft loss in patients who received deceased donor organ and used maintenance immunosuppressive regimens in SUS, in fifteen years.Methods:We analyzed a nationwide cohort of kidney transplant recipients from January 2000 to December 2015 developed through deterministic-probabilistic linkage of SUS administrative databases: Hospital Information System (SIH/SUS); Subsystem for High Complexity Procedures (SIA/SUS) and the Mortality Information System (SIM). Graft loss was defined as death or dialysis for more than three months. All regimens included corticosteroid. We used Cox proportional hazards model to evaluate the factors associated with progression to graft loss.Results:In total, 18,333 patients were included; 58.5 percent used tracolimus+mycophenolate, 11.7 percent cyclosporine+mycophenolate, 8.9 percent tacrolimus+azathyoprine, 5.5 percent cyclosporine+azathyoprine and 15.4 percent received other immunosuppressive regimens (sirolimus+mycophenolate, everolimus+mycophenolate, tacrolimus, mycophenolate, cyclosporine, azathyoprine) . Most patients were male with a median age of 46 years. A higher risk of graft loss was associated with the use of tracolimus+mycophenolate (HR = 1.069; 95% CI, 0.999–1.146), sirolimus+mycophenolate (HR1.395;95% CI, 1 .150–1.692), tracolimus (monotherapy) (1.468;1.239–1.739); mycophenolate (monotherapy) (1.297;1.126–1.493), male gender (1.144; 1.072–1.221), an additional year of age (1.010; 1.007–1.013), a median dialysis period greater than 38 months (1.266; 1.182–1.356), a diagnosis of diabetes (1.211; 1.071–1.367) and a diagnosis of arterial hypertension (1.209; 1.134–1.288) (HR=1.468;95% CI,1.239 −1.739); mycophenolate (monotherapy) (HR = 1.297; 95% CI, 1.126–1.493), male gender (HR = 1.144; 95% CI 1.072–1.221), an additional year of age (HR = 1.010; 95% CI, 1.007–1.013), a median dialysis period greater than 38 months (HR = 1.266; 95% CI, 1.182–1.356), a diagnosis of diabetes (HR = 1.211; 95% CI, 1.071–1.367) and a diagnosis of arterial hypertension (HR = 1.209; 95% CI, 1.134–1.288)as the primary cause of chronic kidney disease.Conclusions:In Brazil, the use of regimens mycophenolate, tacrolimus, tacrolimus+mycophenolate was associated a higher risk of graft loss, among other factors. The choice of drug therapy is one of the few factors that influence survival amenable to direct action by health professionals. Therefore, the results of this study are important and should be disseminated aiming to better outcomes for kidney transplant patients.</description><identifier>ISSN: 0266-4623</identifier><identifier>EISSN: 1471-6348</identifier><identifier>DOI: 10.1017/S0266462318003173</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><subject>Age ; Azathioprine ; Calcineurin ; Calcineurin inhibitors ; Chemotherapy ; Corticosteroids ; Cyclosporins ; Diabetes ; Diabetes mellitus ; Diagnosis ; Dialysis ; Drug development ; Drug therapy ; Drugs ; Economic impact ; Grafting ; Hemodialysis ; Hypertension ; Immunosuppressive agents ; Impact analysis ; Information systems ; Kidney diseases ; Kidney transplantation ; Kidney transplants ; Medical personnel ; Mycophenolic acid ; Patients ; Poster Display Presentations ; Public health ; Rapamycin ; Statistical models ; Steroids ; Subsystems ; Tacrolimus ; Transplantation ; Transplants ; Transplants &amp; implants</subject><ispartof>International journal of technology assessment in health care, 2018, Vol.34 (S1), p.148-149</ispartof><rights>Copyright © Cambridge University Press 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2338905536/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2338905536?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,4009,11668,27902,27903,27904,36039,44342,72706,74641</link.rule.ids></links><search><creatorcontrib>Gomes, Rosângela Maria</creatorcontrib><creatorcontrib>Barbosa, Wallace Breno</creatorcontrib><creatorcontrib>de Assis Acurcio, Francisco</creatorcontrib><creatorcontrib>Guerra, Augusto Afonso</creatorcontrib><title>PD54 Associated Factors Renal Graft Loss Using Real-World Evidence In Brazil</title><title>International journal of technology assessment in health care</title><addtitle>Int J Technol Assess Health Care</addtitle><description>Introduction:Renal transplantation is considered a cost-effective treatment compared to dialysis and represents a significant percentage of public health resources. Post-transplant treatment requires the use of three immunosuppressive drugs. The immunosuppressive regimens consists of a corticosteroid, a calcineurin inhibitor (cyclosporine or tacrolimus) and an antiproliferative agent (azathioprine or mycophenolate) and also by sirolimus or everolimus. In Brazil, the Unified Health System (as known as Sistema Único de Saúde - SUS) is responsible for 95 percent of all kidney transplants performed, as well as ensuring access to immunosuppressive drugs. Therefore, there is a huge and growing economic impact caused by the distribution of these drugs in SUS. We evaluated the factors associated with kidney graft loss in patients who received deceased donor organ and used maintenance immunosuppressive regimens in SUS, in fifteen years.Methods:We analyzed a nationwide cohort of kidney transplant recipients from January 2000 to December 2015 developed through deterministic-probabilistic linkage of SUS administrative databases: Hospital Information System (SIH/SUS); Subsystem for High Complexity Procedures (SIA/SUS) and the Mortality Information System (SIM). Graft loss was defined as death or dialysis for more than three months. All regimens included corticosteroid. We used Cox proportional hazards model to evaluate the factors associated with progression to graft loss.Results:In total, 18,333 patients were included; 58.5 percent used tracolimus+mycophenolate, 11.7 percent cyclosporine+mycophenolate, 8.9 percent tacrolimus+azathyoprine, 5.5 percent cyclosporine+azathyoprine and 15.4 percent received other immunosuppressive regimens (sirolimus+mycophenolate, everolimus+mycophenolate, tacrolimus, mycophenolate, cyclosporine, azathyoprine) . Most patients were male with a median age of 46 years. A higher risk of graft loss was associated with the use of tracolimus+mycophenolate (HR = 1.069; 95% CI, 0.999–1.146), sirolimus+mycophenolate (HR1.395;95% CI, 1 .150–1.692), tracolimus (monotherapy) (1.468;1.239–1.739); mycophenolate (monotherapy) (1.297;1.126–1.493), male gender (1.144; 1.072–1.221), an additional year of age (1.010; 1.007–1.013), a median dialysis period greater than 38 months (1.266; 1.182–1.356), a diagnosis of diabetes (1.211; 1.071–1.367) and a diagnosis of arterial hypertension (1.209; 1.134–1.288) (HR=1.468;95% CI,1.239 −1.739); mycophenolate (monotherapy) (HR = 1.297; 95% CI, 1.126–1.493), male gender (HR = 1.144; 95% CI 1.072–1.221), an additional year of age (HR = 1.010; 95% CI, 1.007–1.013), a median dialysis period greater than 38 months (HR = 1.266; 95% CI, 1.182–1.356), a diagnosis of diabetes (HR = 1.211; 95% CI, 1.071–1.367) and a diagnosis of arterial hypertension (HR = 1.209; 95% CI, 1.134–1.288)as the primary cause of chronic kidney disease.Conclusions:In Brazil, the use of regimens mycophenolate, tacrolimus, tacrolimus+mycophenolate was associated a higher risk of graft loss, among other factors. The choice of drug therapy is one of the few factors that influence survival amenable to direct action by health professionals. Therefore, the results of this study are important and should be disseminated aiming to better outcomes for kidney transplant patients.</description><subject>Age</subject><subject>Azathioprine</subject><subject>Calcineurin</subject><subject>Calcineurin inhibitors</subject><subject>Chemotherapy</subject><subject>Corticosteroids</subject><subject>Cyclosporins</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diagnosis</subject><subject>Dialysis</subject><subject>Drug development</subject><subject>Drug therapy</subject><subject>Drugs</subject><subject>Economic impact</subject><subject>Grafting</subject><subject>Hemodialysis</subject><subject>Hypertension</subject><subject>Immunosuppressive agents</subject><subject>Impact analysis</subject><subject>Information systems</subject><subject>Kidney diseases</subject><subject>Kidney transplantation</subject><subject>Kidney transplants</subject><subject>Medical personnel</subject><subject>Mycophenolic acid</subject><subject>Patients</subject><subject>Poster Display Presentations</subject><subject>Public health</subject><subject>Rapamycin</subject><subject>Statistical models</subject><subject>Steroids</subject><subject>Subsystems</subject><subject>Tacrolimus</subject><subject>Transplantation</subject><subject>Transplants</subject><subject>Transplants &amp; implants</subject><issn>0266-4623</issn><issn>1471-6348</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>M0C</sourceid><recordid>eNp1kEFLw0AQhRdRsFZ_gLcFz9GdzGaTPdba1kJB0YrHMLvZlJQ0qbupoL_elBY8iKeBee97PB5j1yBuQUB69ypipaSKETIhEFI8YQOQKUQKZXbKBns52uvn7CKEtRCAQosBWzw_JJKPQmhtRZ0r-JRs1_rAX1xDNZ95Kju-aEPgb6FqVv2b6ui99XXBJ59V4Rrr-Lzh956-q_qSnZVUB3d1vEO2nE6W48do8TSbj0eLyAJIFelYgk7JSAMoSSbaaFSEcZHYNDUuMynaosBSUWKtMFACEYARpVakweCQ3Rxit7792LnQ5et25_u6IY8RMy2SBFXvgoPL-r6-d2W-9dWG_FcOIt9vlv_ZrGfwyNDG-KpYud_o_6kfQWFrkw</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Gomes, Rosângela Maria</creator><creator>Barbosa, Wallace Breno</creator><creator>de Assis Acurcio, Francisco</creator><creator>Guerra, Augusto Afonso</creator><general>Cambridge University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7U5</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88C</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>H94</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>KB0</scope><scope>L.-</scope><scope>L7M</scope><scope>M0C</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>2018</creationdate><title>PD54 Associated Factors Renal Graft Loss Using Real-World Evidence In Brazil</title><author>Gomes, Rosângela Maria ; Barbosa, Wallace Breno ; de Assis Acurcio, Francisco ; Guerra, Augusto Afonso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1146-924197ab4b134a459b936a32d5c77be8b73cdd3f6a5cc0b1f1aa11b0f96a91b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Age</topic><topic>Azathioprine</topic><topic>Calcineurin</topic><topic>Calcineurin inhibitors</topic><topic>Chemotherapy</topic><topic>Corticosteroids</topic><topic>Cyclosporins</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diagnosis</topic><topic>Dialysis</topic><topic>Drug development</topic><topic>Drug therapy</topic><topic>Drugs</topic><topic>Economic impact</topic><topic>Grafting</topic><topic>Hemodialysis</topic><topic>Hypertension</topic><topic>Immunosuppressive agents</topic><topic>Impact analysis</topic><topic>Information systems</topic><topic>Kidney diseases</topic><topic>Kidney transplantation</topic><topic>Kidney transplants</topic><topic>Medical personnel</topic><topic>Mycophenolic acid</topic><topic>Patients</topic><topic>Poster Display Presentations</topic><topic>Public health</topic><topic>Rapamycin</topic><topic>Statistical models</topic><topic>Steroids</topic><topic>Subsystems</topic><topic>Tacrolimus</topic><topic>Transplantation</topic><topic>Transplants</topic><topic>Transplants &amp; implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomes, Rosângela Maria</creatorcontrib><creatorcontrib>Barbosa, Wallace Breno</creatorcontrib><creatorcontrib>de Assis Acurcio, Francisco</creatorcontrib><creatorcontrib>Guerra, Augusto Afonso</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database (ProQuest)</collection><collection>Immunology Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>ABI/INFORM Collection</collection><collection>ABI/INFORM Global (PDF only)</collection><collection>Health &amp; Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ABI/INFORM Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>Business Premium Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Business Premium Collection (Alumni)</collection><collection>Health Research Premium Collection</collection><collection>ABI/INFORM Global (Corporate)</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Business Collection (Alumni Edition)</collection><collection>ProQuest Business Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ABI/INFORM Professional Advanced</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ABI/INFORM Global</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Business</collection><collection>ProQuest One Business (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>International journal of technology assessment in health care</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomes, Rosângela Maria</au><au>Barbosa, Wallace Breno</au><au>de Assis Acurcio, Francisco</au><au>Guerra, Augusto Afonso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PD54 Associated Factors Renal Graft Loss Using Real-World Evidence In Brazil</atitle><jtitle>International journal of technology assessment in health care</jtitle><addtitle>Int J Technol Assess Health Care</addtitle><date>2018</date><risdate>2018</risdate><volume>34</volume><issue>S1</issue><spage>148</spage><epage>149</epage><pages>148-149</pages><issn>0266-4623</issn><eissn>1471-6348</eissn><abstract>Introduction:Renal transplantation is considered a cost-effective treatment compared to dialysis and represents a significant percentage of public health resources. Post-transplant treatment requires the use of three immunosuppressive drugs. The immunosuppressive regimens consists of a corticosteroid, a calcineurin inhibitor (cyclosporine or tacrolimus) and an antiproliferative agent (azathioprine or mycophenolate) and also by sirolimus or everolimus. In Brazil, the Unified Health System (as known as Sistema Único de Saúde - SUS) is responsible for 95 percent of all kidney transplants performed, as well as ensuring access to immunosuppressive drugs. Therefore, there is a huge and growing economic impact caused by the distribution of these drugs in SUS. We evaluated the factors associated with kidney graft loss in patients who received deceased donor organ and used maintenance immunosuppressive regimens in SUS, in fifteen years.Methods:We analyzed a nationwide cohort of kidney transplant recipients from January 2000 to December 2015 developed through deterministic-probabilistic linkage of SUS administrative databases: Hospital Information System (SIH/SUS); Subsystem for High Complexity Procedures (SIA/SUS) and the Mortality Information System (SIM). Graft loss was defined as death or dialysis for more than three months. All regimens included corticosteroid. We used Cox proportional hazards model to evaluate the factors associated with progression to graft loss.Results:In total, 18,333 patients were included; 58.5 percent used tracolimus+mycophenolate, 11.7 percent cyclosporine+mycophenolate, 8.9 percent tacrolimus+azathyoprine, 5.5 percent cyclosporine+azathyoprine and 15.4 percent received other immunosuppressive regimens (sirolimus+mycophenolate, everolimus+mycophenolate, tacrolimus, mycophenolate, cyclosporine, azathyoprine) . Most patients were male with a median age of 46 years. A higher risk of graft loss was associated with the use of tracolimus+mycophenolate (HR = 1.069; 95% CI, 0.999–1.146), sirolimus+mycophenolate (HR1.395;95% CI, 1 .150–1.692), tracolimus (monotherapy) (1.468;1.239–1.739); mycophenolate (monotherapy) (1.297;1.126–1.493), male gender (1.144; 1.072–1.221), an additional year of age (1.010; 1.007–1.013), a median dialysis period greater than 38 months (1.266; 1.182–1.356), a diagnosis of diabetes (1.211; 1.071–1.367) and a diagnosis of arterial hypertension (1.209; 1.134–1.288) (HR=1.468;95% CI,1.239 −1.739); mycophenolate (monotherapy) (HR = 1.297; 95% CI, 1.126–1.493), male gender (HR = 1.144; 95% CI 1.072–1.221), an additional year of age (HR = 1.010; 95% CI, 1.007–1.013), a median dialysis period greater than 38 months (HR = 1.266; 95% CI, 1.182–1.356), a diagnosis of diabetes (HR = 1.211; 95% CI, 1.071–1.367) and a diagnosis of arterial hypertension (HR = 1.209; 95% CI, 1.134–1.288)as the primary cause of chronic kidney disease.Conclusions:In Brazil, the use of regimens mycophenolate, tacrolimus, tacrolimus+mycophenolate was associated a higher risk of graft loss, among other factors. The choice of drug therapy is one of the few factors that influence survival amenable to direct action by health professionals. Therefore, the results of this study are important and should be disseminated aiming to better outcomes for kidney transplant patients.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><doi>10.1017/S0266462318003173</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0266-4623
ispartof International journal of technology assessment in health care, 2018, Vol.34 (S1), p.148-149
issn 0266-4623
1471-6348
language eng
recordid cdi_proquest_journals_2338905536
source ABI/INFORM Global; Cambridge University Press
subjects Age
Azathioprine
Calcineurin
Calcineurin inhibitors
Chemotherapy
Corticosteroids
Cyclosporins
Diabetes
Diabetes mellitus
Diagnosis
Dialysis
Drug development
Drug therapy
Drugs
Economic impact
Grafting
Hemodialysis
Hypertension
Immunosuppressive agents
Impact analysis
Information systems
Kidney diseases
Kidney transplantation
Kidney transplants
Medical personnel
Mycophenolic acid
Patients
Poster Display Presentations
Public health
Rapamycin
Statistical models
Steroids
Subsystems
Tacrolimus
Transplantation
Transplants
Transplants & implants
title PD54 Associated Factors Renal Graft Loss Using Real-World Evidence In Brazil
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T23%3A07%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=PD54%20Associated%20Factors%20Renal%20Graft%20Loss%20Using%20Real-World%20Evidence%20In%20Brazil&rft.jtitle=International%20journal%20of%20technology%20assessment%20in%20health%20care&rft.au=Gomes,%20Ros%C3%A2ngela%20Maria&rft.date=2018&rft.volume=34&rft.issue=S1&rft.spage=148&rft.epage=149&rft.pages=148-149&rft.issn=0266-4623&rft.eissn=1471-6348&rft_id=info:doi/10.1017/S0266462318003173&rft_dat=%3Cproquest_cross%3E2338905536%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1146-924197ab4b134a459b936a32d5c77be8b73cdd3f6a5cc0b1f1aa11b0f96a91b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2338905536&rft_id=info:pmid/&rft_cupid=10_1017_S0266462318003173&rfr_iscdi=true