Mechanical circulatory support as a bridge to transplantation
From December 1985 through April 1988, 11 patients (three female and eight males), 33.1 ± 3.9 (±SEM) years of age (range, 15 to 50 years), underwent heart transplantation preceded by the use of mechanical circulatory support. The causes of cardiac failure were ischemic (four), viral cardiomyopathy (...
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Veröffentlicht in: | The Journal of thoracic and cardiovascular surgery 1989-11, Vol.98 (5), p.935-941 |
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creator | Joyce, L.D. Emery, R.W. Eales, F. Von Rueden, T.J. Kiser, J.C. Hoffman, F.M. Johnson, K.E. Toninato, C.J. Kersten, T.E. Nicoloff, D.M. Pritzker, M.R. |
description | From December 1985 through April 1988, 11 patients (three female and eight males), 33.1 ± 3.9 (±SEM) years of age (range, 15 to 50 years), underwent heart transplantation preceded by the use of mechanical circulatory support. The causes of cardiac failure were ischemic (four), viral cardiomyopathy (three), idiopathic cardiomyopathy (two), congenital heart disease (one), and valvular heart disease (one). All patients were preterminal. Mechanical circulatory support consisted of intra-aortic balloon pump (eight), the total artificial heart (seven), biventricular assist (three), and left ventricular assist (two). Seven patients had more than one form of support. The duration of mechanical circulatory support was 12.2 ±4.1 days (range, 1 to 44 days). Once listed for transplantation, patients waited for 8.1 ± 2.4 days for a donor. Seven patients received OKT3 monoclonal antibody as prophylaxis, in addition to triple-drug immunosuppression. There were four rejection episodes and 12 serious infections. In addition, eight patients suffered a major posttransplant complication of a distant organ system: central nervous system (three), renal (two), and respiratory (three). Post transplant hospitalizaton was 48 ± 22 days (range, 15 to 248 days). Two patients (18%) died after transplant, one of severe acute rejection (29 days) and one of multisystem failure (248 days). All patients surviving transplant hospitalization are alive 6 to 34 months after the transplant procedure. Eight patients are in functional class I and and 1 patient class II. This patient attends school full-time but has a premechanical support system neurologic defect. In follow-up of 163 patient-months except for yearly catheterization, these nine patients required only 5 hospital days. Although the use of the mechanical circulatory support as a bridge to transplantation can result in a prolonged, complicated hospitalization after transplant, the long-term results are gratifying. |
doi_str_mv | 10.1016/S0022-5223(19)34274-6 |
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The causes of cardiac failure were ischemic (four), viral cardiomyopathy (three), idiopathic cardiomyopathy (two), congenital heart disease (one), and valvular heart disease (one). All patients were preterminal. Mechanical circulatory support consisted of intra-aortic balloon pump (eight), the total artificial heart (seven), biventricular assist (three), and left ventricular assist (two). Seven patients had more than one form of support. The duration of mechanical circulatory support was 12.2 ±4.1 days (range, 1 to 44 days). Once listed for transplantation, patients waited for 8.1 ± 2.4 days for a donor. Seven patients received OKT3 monoclonal antibody as prophylaxis, in addition to triple-drug immunosuppression. There were four rejection episodes and 12 serious infections. In addition, eight patients suffered a major posttransplant complication of a distant organ system: central nervous system (three), renal (two), and respiratory (three). Post transplant hospitalizaton was 48 ± 22 days (range, 15 to 248 days). Two patients (18%) died after transplant, one of severe acute rejection (29 days) and one of multisystem failure (248 days). All patients surviving transplant hospitalization are alive 6 to 34 months after the transplant procedure. Eight patients are in functional class I and and 1 patient class II. This patient attends school full-time but has a premechanical support system neurologic defect. In follow-up of 163 patient-months except for yearly catheterization, these nine patients required only 5 hospital days. 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The causes of cardiac failure were ischemic (four), viral cardiomyopathy (three), idiopathic cardiomyopathy (two), congenital heart disease (one), and valvular heart disease (one). All patients were preterminal. Mechanical circulatory support consisted of intra-aortic balloon pump (eight), the total artificial heart (seven), biventricular assist (three), and left ventricular assist (two). Seven patients had more than one form of support. The duration of mechanical circulatory support was 12.2 ±4.1 days (range, 1 to 44 days). Once listed for transplantation, patients waited for 8.1 ± 2.4 days for a donor. Seven patients received OKT3 monoclonal antibody as prophylaxis, in addition to triple-drug immunosuppression. There were four rejection episodes and 12 serious infections. In addition, eight patients suffered a major posttransplant complication of a distant organ system: central nervous system (three), renal (two), and respiratory (three). Post transplant hospitalizaton was 48 ± 22 days (range, 15 to 248 days). Two patients (18%) died after transplant, one of severe acute rejection (29 days) and one of multisystem failure (248 days). All patients surviving transplant hospitalization are alive 6 to 34 months after the transplant procedure. Eight patients are in functional class I and and 1 patient class II. This patient attends school full-time but has a premechanical support system neurologic defect. In follow-up of 163 patient-months except for yearly catheterization, these nine patients required only 5 hospital days. Although the use of the mechanical circulatory support as a bridge to transplantation can result in a prolonged, complicated hospitalization after transplant, the long-term results are gratifying.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Bacterial Infections - etiology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Graft Rejection</subject><subject>Heart Transplantation - adverse effects</subject><subject>Heart Transplantation - mortality</subject><subject>Heart-Assist Devices</subject><subject>Humans</subject><subject>Immunosuppression - methods</subject><subject>Length of Stay</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Quality of Life</subject><subject>Retrospective Studies</subject><subject>Time Factors</subject><issn>0022-5223</issn><issn>1097-685X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLw0AUhQdRaq3-hEJWoovovNNZiEjxBRUXKrgbJpMbO5ImcWai9N-bPqhLV3fznXMPH0Jjgi8IJvLyBWNKU0EpOyPqnHGa8VTuoSHBKkvlRLzvo-EOOURHIXxijDNM1AAN6IQQTvkQXT2BnZvaWVMl1nnbVSY2fpmErm0bHxMTEpPk3hUfkMQmid7Uoa1MHU10TX2MDkpTBTjZ3hF6u7t9nT6ks-f7x-nNLLWcTWJKS8FLRRhglZekyEHZEvLC8lwwaQRgIzNGmco5MCEF41JCRlkhMVMlpSUbodNNb-ubrw5C1AsXLFT9EGi6oDNFlaSS9aDYgNY3IXgodevdwvilJlivtOm1Nr1yoonSa21a9rnx9kGXL6DYpbae_gbM3cf8x3nQYWGqqqeJ_ow2qIkWWjHRg9cbEHod3w68DtZBbaHoQzbqonH_TPkFfdeJyg</recordid><startdate>19891101</startdate><enddate>19891101</enddate><creator>Joyce, L.D.</creator><creator>Emery, R.W.</creator><creator>Eales, F.</creator><creator>Von Rueden, T.J.</creator><creator>Kiser, J.C.</creator><creator>Hoffman, F.M.</creator><creator>Johnson, K.E.</creator><creator>Toninato, C.J.</creator><creator>Kersten, T.E.</creator><creator>Nicoloff, D.M.</creator><creator>Pritzker, M.R.</creator><general>Elsevier Inc</general><general>AATS/WTSA</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19891101</creationdate><title>Mechanical circulatory support as a bridge to transplantation</title><author>Joyce, L.D. ; Emery, R.W. ; Eales, F. ; Von Rueden, T.J. ; Kiser, J.C. ; Hoffman, F.M. ; Johnson, K.E. ; Toninato, C.J. ; Kersten, T.E. ; Nicoloff, D.M. ; Pritzker, M.R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-2f54f913e09bf1dbe9cfebdc4b536a5e0a673239b4e35653466e723d6039f22f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Bacterial Infections - etiology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Graft Rejection</topic><topic>Heart Transplantation - adverse effects</topic><topic>Heart Transplantation - mortality</topic><topic>Heart-Assist Devices</topic><topic>Humans</topic><topic>Immunosuppression - methods</topic><topic>Length of Stay</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Quality of Life</topic><topic>Retrospective Studies</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joyce, L.D.</creatorcontrib><creatorcontrib>Emery, R.W.</creatorcontrib><creatorcontrib>Eales, F.</creatorcontrib><creatorcontrib>Von Rueden, T.J.</creatorcontrib><creatorcontrib>Kiser, J.C.</creatorcontrib><creatorcontrib>Hoffman, F.M.</creatorcontrib><creatorcontrib>Johnson, K.E.</creatorcontrib><creatorcontrib>Toninato, C.J.</creatorcontrib><creatorcontrib>Kersten, T.E.</creatorcontrib><creatorcontrib>Nicoloff, D.M.</creatorcontrib><creatorcontrib>Pritzker, M.R.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joyce, L.D.</au><au>Emery, R.W.</au><au>Eales, F.</au><au>Von Rueden, T.J.</au><au>Kiser, J.C.</au><au>Hoffman, F.M.</au><au>Johnson, K.E.</au><au>Toninato, C.J.</au><au>Kersten, T.E.</au><au>Nicoloff, D.M.</au><au>Pritzker, M.R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanical circulatory support as a bridge to transplantation</atitle><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle><addtitle>J Thorac Cardiovasc Surg</addtitle><date>1989-11-01</date><risdate>1989</risdate><volume>98</volume><issue>5</issue><spage>935</spage><epage>941</epage><pages>935-941</pages><issn>0022-5223</issn><eissn>1097-685X</eissn><abstract>From December 1985 through April 1988, 11 patients (three female and eight males), 33.1 ± 3.9 (±SEM) years of age (range, 15 to 50 years), underwent heart transplantation preceded by the use of mechanical circulatory support. The causes of cardiac failure were ischemic (four), viral cardiomyopathy (three), idiopathic cardiomyopathy (two), congenital heart disease (one), and valvular heart disease (one). All patients were preterminal. Mechanical circulatory support consisted of intra-aortic balloon pump (eight), the total artificial heart (seven), biventricular assist (three), and left ventricular assist (two). Seven patients had more than one form of support. The duration of mechanical circulatory support was 12.2 ±4.1 days (range, 1 to 44 days). Once listed for transplantation, patients waited for 8.1 ± 2.4 days for a donor. Seven patients received OKT3 monoclonal antibody as prophylaxis, in addition to triple-drug immunosuppression. There were four rejection episodes and 12 serious infections. In addition, eight patients suffered a major posttransplant complication of a distant organ system: central nervous system (three), renal (two), and respiratory (three). Post transplant hospitalizaton was 48 ± 22 days (range, 15 to 248 days). Two patients (18%) died after transplant, one of severe acute rejection (29 days) and one of multisystem failure (248 days). All patients surviving transplant hospitalization are alive 6 to 34 months after the transplant procedure. Eight patients are in functional class I and and 1 patient class II. This patient attends school full-time but has a premechanical support system neurologic defect. In follow-up of 163 patient-months except for yearly catheterization, these nine patients required only 5 hospital days. Although the use of the mechanical circulatory support as a bridge to transplantation can result in a prolonged, complicated hospitalization after transplant, the long-term results are gratifying.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>2811424</pmid><doi>10.1016/S0022-5223(19)34274-6</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Antibodies, Monoclonal - therapeutic use Bacterial Infections - etiology Female Follow-Up Studies Graft Rejection Heart Transplantation - adverse effects Heart Transplantation - mortality Heart-Assist Devices Humans Immunosuppression - methods Length of Stay Male Middle Aged Quality of Life Retrospective Studies Time Factors |
title | Mechanical circulatory support as a bridge to transplantation |
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