Salvage of Pacemakers and Automatic Implantable Cardioverter-Defibrillators Using Dermis Grafts

Background Thin patients with thoracic pacemakers and automatic implantable cardioverter-defibrillators often have minimal tissue over the devices, with erosion through the surface a major concern. This erosion can lead to device infection and need for removal, or primary device infection can, in tu...

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Veröffentlicht in:The Annals of thoracic surgery 2011-02, Vol.91 (2), p.452-456
Hauptverfasser: Rudolph, Ross, MD, Smith, Michael R., MD, Curtis, Guy P., MD, PhD
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container_title The Annals of thoracic surgery
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creator Rudolph, Ross, MD
Smith, Michael R., MD
Curtis, Guy P., MD, PhD
description Background Thin patients with thoracic pacemakers and automatic implantable cardioverter-defibrillators often have minimal tissue over the devices, with erosion through the surface a major concern. This erosion can lead to device infection and need for removal, or primary device infection can, in turn, lead to erosion. Even worse is exposure and infection of the leads to the heart, with fatalities having occurred. Pressure symptoms, as with shoulder seatbelt straps, can occur, and the visible deformity may be objectionable. Methods To correct these problems without device removal, we used a novel surgical approach. Thirteen patients had 15 grafts, of either the acellular dermal graft AlloDerm (LifeCell Corp, Branchburg, NJ [n = 13 for threatened exposure or pressure symptoms, including two repeats]) or autogenous dermis (n = 2 for existing open wounds with chronic drainage) placed over the devices. Results After all graft procedures, there was no skin breakdown; exposure and extrusion were completely prevented. Follow-up was 3 to 68 months (mean 36.8). The 2 open wound patients treated with dermis autografts had no recurrence of wound breakdown. Most patients with pressure symptoms had reduction in tenderness and pain. Patients liked the visible softening of the device contour, but not the subtly increased forward projection. The only immediate complication was one rapidly expanding hematoma leading to graft removal. One late complication was a mild infection, treated successfully. Conclusions Acellular human dermal allografts, or live dermis autografts, provided significant protection over cardiac pacing devices in 13 patients with 15 grafts, with no subsequent surface exposures or extrusions.
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This erosion can lead to device infection and need for removal, or primary device infection can, in turn, lead to erosion. Even worse is exposure and infection of the leads to the heart, with fatalities having occurred. Pressure symptoms, as with shoulder seatbelt straps, can occur, and the visible deformity may be objectionable. Methods To correct these problems without device removal, we used a novel surgical approach. Thirteen patients had 15 grafts, of either the acellular dermal graft AlloDerm (LifeCell Corp, Branchburg, NJ [n = 13 for threatened exposure or pressure symptoms, including two repeats]) or autogenous dermis (n = 2 for existing open wounds with chronic drainage) placed over the devices. Results After all graft procedures, there was no skin breakdown; exposure and extrusion were completely prevented. Follow-up was 3 to 68 months (mean 36.8). The 2 open wound patients treated with dermis autografts had no recurrence of wound breakdown. Most patients with pressure symptoms had reduction in tenderness and pain. Patients liked the visible softening of the device contour, but not the subtly increased forward projection. The only immediate complication was one rapidly expanding hematoma leading to graft removal. One late complication was a mild infection, treated successfully. Conclusions Acellular human dermal allografts, or live dermis autografts, provided significant protection over cardiac pacing devices in 13 patients with 15 grafts, with no subsequent surface exposures or extrusions.</description><identifier>ISSN: 0003-4975</identifier><identifier>EISSN: 1552-6259</identifier><identifier>DOI: 10.1016/j.athoracsur.2010.10.004</identifier><identifier>PMID: 21256289</identifier><identifier>CODEN: ATHSAK</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Aged ; Aged, 80 and over ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Cardiology. Vascular system ; Cardiothoracic Surgery ; Cell-Free System ; Defibrillators, Implantable - adverse effects ; Dermis - transplantation ; Electrodes, Implanted - adverse effects ; Female ; Follow-Up Studies ; Hematoma - etiology ; Humans ; Male ; Medical sciences ; Middle Aged ; Pacemaker, Artificial - adverse effects ; Pain - etiology ; Pain - prevention &amp; control ; Pneumology ; Prosthesis-Related Infections - etiology ; Prosthesis-Related Infections - prevention &amp; control ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. 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This erosion can lead to device infection and need for removal, or primary device infection can, in turn, lead to erosion. Even worse is exposure and infection of the leads to the heart, with fatalities having occurred. Pressure symptoms, as with shoulder seatbelt straps, can occur, and the visible deformity may be objectionable. Methods To correct these problems without device removal, we used a novel surgical approach. Thirteen patients had 15 grafts, of either the acellular dermal graft AlloDerm (LifeCell Corp, Branchburg, NJ [n = 13 for threatened exposure or pressure symptoms, including two repeats]) or autogenous dermis (n = 2 for existing open wounds with chronic drainage) placed over the devices. Results After all graft procedures, there was no skin breakdown; exposure and extrusion were completely prevented. Follow-up was 3 to 68 months (mean 36.8). The 2 open wound patients treated with dermis autografts had no recurrence of wound breakdown. Most patients with pressure symptoms had reduction in tenderness and pain. Patients liked the visible softening of the device contour, but not the subtly increased forward projection. The only immediate complication was one rapidly expanding hematoma leading to graft removal. One late complication was a mild infection, treated successfully. Conclusions Acellular human dermal allografts, or live dermis autografts, provided significant protection over cardiac pacing devices in 13 patients with 15 grafts, with no subsequent surface exposures or extrusions.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Cardiology. Vascular system</subject><subject>Cardiothoracic Surgery</subject><subject>Cell-Free System</subject><subject>Defibrillators, Implantable - adverse effects</subject><subject>Dermis - transplantation</subject><subject>Electrodes, Implanted - adverse effects</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hematoma - etiology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pacemaker, Artificial - adverse effects</subject><subject>Pain - etiology</subject><subject>Pain - prevention &amp; control</subject><subject>Pneumology</subject><subject>Prosthesis-Related Infections - etiology</subject><subject>Prosthesis-Related Infections - prevention &amp; control</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Reoperation</subject><subject>Salvage Therapy - methods</subject><subject>Skin - pathology</subject><subject>Skin Transplantation - adverse effects</subject><subject>Skin Transplantation - methods</subject><subject>Surgery</subject><subject>Transplantation, Homologous - methods</subject><issn>0003-4975</issn><issn>1552-6259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1r3DAQQEVpabZp_0LxpfTkrSRLa-tSSDdtEgg0kAR6E2N5lGpjW1tJXsi_r5zdJpBTT0Izbz54DCEFo0tG2erLZgnptw9g4hSWnD6Gl5SKV2TBpOTlikv1miwopVUpVC2PyLsYN_nLc_otOeKMyxVv1ILoa-h3cIeFt8UVGBzgHkMsYOyKkyn5AZIzxcWw7WFM0PZYrCF0zu8wJAzlKVrXBtf3kHyuuo1uvCtOMQwuFmcBbIrvyRsLfcQPh_eY3P74frM-Ly9_nl2sTy5LI2mTStYqq1opQAgJrK5z1EBXCSWF4iBQUktbmqFmxSrFOwEta5mCzkqbQVsdk8_7vtvg_0wYk847GMybjeinqBtR81qximey2ZMm-BgDWr0NboDwoBnVs1290c929Wx3zmS7ufTjYcjUDtg9Ff7TmYFPBwCigd4GGI2Lz1zVMCWqOnPf9hxmJTuHQUfjcDTYuYAm6c67_9nm64smpnejy3Pv8QHjxk9hzMo105Frqq_na5iPgeUz4Lz6Vf0FaF-zyw</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>Rudolph, Ross, MD</creator><creator>Smith, Michael R., MD</creator><creator>Curtis, Guy P., MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>20110201</creationdate><title>Salvage of Pacemakers and Automatic Implantable Cardioverter-Defibrillators Using Dermis Grafts</title><author>Rudolph, Ross, MD ; Smith, Michael R., MD ; Curtis, Guy P., MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-1b9f9b54a445a177c50cad3495492a4e50f0b0b9f861392d4ab1b19adf5fcadf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Cardiology. Vascular system</topic><topic>Cardiothoracic Surgery</topic><topic>Cell-Free System</topic><topic>Defibrillators, Implantable - adverse effects</topic><topic>Dermis - transplantation</topic><topic>Electrodes, Implanted - adverse effects</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hematoma - etiology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pacemaker, Artificial - adverse effects</topic><topic>Pain - etiology</topic><topic>Pain - prevention &amp; control</topic><topic>Pneumology</topic><topic>Prosthesis-Related Infections - etiology</topic><topic>Prosthesis-Related Infections - prevention &amp; control</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Reoperation</topic><topic>Salvage Therapy - methods</topic><topic>Skin - pathology</topic><topic>Skin Transplantation - adverse effects</topic><topic>Skin Transplantation - methods</topic><topic>Surgery</topic><topic>Transplantation, Homologous - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rudolph, Ross, MD</creatorcontrib><creatorcontrib>Smith, Michael R., MD</creatorcontrib><creatorcontrib>Curtis, Guy P., MD, PhD</creatorcontrib><collection>Pascal-Francis</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 Annals of thoracic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rudolph, Ross, MD</au><au>Smith, Michael R., MD</au><au>Curtis, Guy P., MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salvage of Pacemakers and Automatic Implantable Cardioverter-Defibrillators Using Dermis Grafts</atitle><jtitle>The Annals of thoracic surgery</jtitle><addtitle>Ann Thorac Surg</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>91</volume><issue>2</issue><spage>452</spage><epage>456</epage><pages>452-456</pages><issn>0003-4975</issn><eissn>1552-6259</eissn><coden>ATHSAK</coden><abstract>Background Thin patients with thoracic pacemakers and automatic implantable cardioverter-defibrillators often have minimal tissue over the devices, with erosion through the surface a major concern. 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Most patients with pressure symptoms had reduction in tenderness and pain. Patients liked the visible softening of the device contour, but not the subtly increased forward projection. The only immediate complication was one rapidly expanding hematoma leading to graft removal. One late complication was a mild infection, treated successfully. Conclusions Acellular human dermal allografts, or live dermis autografts, provided significant protection over cardiac pacing devices in 13 patients with 15 grafts, with no subsequent surface exposures or extrusions.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>21256289</pmid><doi>10.1016/j.athoracsur.2010.10.004</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Aged, 80 and over
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Cardiology. Vascular system
Cardiothoracic Surgery
Cell-Free System
Defibrillators, Implantable - adverse effects
Dermis - transplantation
Electrodes, Implanted - adverse effects
Female
Follow-Up Studies
Hematoma - etiology
Humans
Male
Medical sciences
Middle Aged
Pacemaker, Artificial - adverse effects
Pain - etiology
Pain - prevention & control
Pneumology
Prosthesis-Related Infections - etiology
Prosthesis-Related Infections - prevention & control
Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
Reoperation
Salvage Therapy - methods
Skin - pathology
Skin Transplantation - adverse effects
Skin Transplantation - methods
Surgery
Transplantation, Homologous - methods
title Salvage of Pacemakers and Automatic Implantable Cardioverter-Defibrillators Using Dermis Grafts
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