Prevalence and timing of bend relief disconnection in patients supported by the late version HeartMate II left ventricular assist device

Melana Yuzefpolskaya, Nir Uriel, Daniel S. Chow, Susan W. Restaino, Donna M. Mancini, Margaret Flannery, Rosie Te-Frey, Joanne Chichetti, Takeyoshi Ota, Hyonah Kim, Drew D. Dano, Gregory D. Pearson, Hiroo Takayama, Yoshifumi Naka, Ulrich P. Jorde

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Background: On April 4, 2012, the U.S. Food and Drug Administration issued a Class 1R recall of the HeartMate II (Thoratec Corporation, Pleasanton, CA) left ventricular assist device (LVAD) due to spontaneous detachment of the bend relief from its intended position in patients implanted with the most recent version of the HM II. This study examined the incidence and timing of outflow graft bend relief disconnection in patients implanted with the HM II LVAD. Methods: All patients supported with the modified version of the HM II LVAD were asked to report for dedicated abdominal X-ray imaging to assess the position of the bend relief. Also performed was a retrospective review of X-ray images of all patients who had previously been supported with this version but had since received a transplant, undergone LVAD explant, or died. Results: Between March 9, 2011, and April 9, 2012, 59 patients underwent primary implant with the modified version HM II. Follow up X-ray images were available for 56 patients (95%). The bend relief was found fully disconnected in 6 of 56 (11%) and partially disconnected in 13 (23%). Two of 6 patients (33%) with full bend relief disconnection and 1 of 13 of the initially partially disconnected patients (7.7%) required urgent surgical intervention due to symptoms of hemolysis and/or heart failure. Conclusions: Bend relief disconnection is common and may be observed immediately after implant but may also develop over time. Full bend relief disconnect may present with hemolysis and/or heart failure symptoms and often requires surgical revision. Surveillance abdominal X-ray imaging should be performed routinely on all patients who were implanted with the modified version HM II.

Original languageEnglish (US)
Pages (from-to)320-325
Number of pages6
JournalJournal of Heart and Lung Transplantation
Volume32
Issue number3
DOIs
StatePublished - Mar 2013
Externally publishedYes

Fingerprint

Heart-Assist Devices
X-Rays
Hemolysis
Heart Failure
Transplants
United States Food and Drug Administration
Reoperation
Cohort Studies

Keywords

  • bend relief disconnection
  • Heart Mate II
  • left ventricular assist device
  • outflow graft

ASJC Scopus subject areas

  • Transplantation
  • Cardiology and Cardiovascular Medicine
  • Pulmonary and Respiratory Medicine
  • Surgery

Cite this

Prevalence and timing of bend relief disconnection in patients supported by the late version HeartMate II left ventricular assist device. / Yuzefpolskaya, Melana; Uriel, Nir; Chow, Daniel S.; Restaino, Susan W.; Mancini, Donna M.; Flannery, Margaret; Te-Frey, Rosie; Chichetti, Joanne; Ota, Takeyoshi; Kim, Hyonah; Dano, Drew D.; Pearson, Gregory D.; Takayama, Hiroo; Naka, Yoshifumi; Jorde, Ulrich P.

In: Journal of Heart and Lung Transplantation, Vol. 32, No. 3, 03.2013, p. 320-325.

Research output: Contribution to journalArticle

Yuzefpolskaya, M, Uriel, N, Chow, DS, Restaino, SW, Mancini, DM, Flannery, M, Te-Frey, R, Chichetti, J, Ota, T, Kim, H, Dano, DD, Pearson, GD, Takayama, H, Naka, Y & Jorde, UP 2013, 'Prevalence and timing of bend relief disconnection in patients supported by the late version HeartMate II left ventricular assist device', Journal of Heart and Lung Transplantation, vol. 32, no. 3, pp. 320-325. https://doi.org/10.1016/j.healun.2012.11.016
Yuzefpolskaya, Melana ; Uriel, Nir ; Chow, Daniel S. ; Restaino, Susan W. ; Mancini, Donna M. ; Flannery, Margaret ; Te-Frey, Rosie ; Chichetti, Joanne ; Ota, Takeyoshi ; Kim, Hyonah ; Dano, Drew D. ; Pearson, Gregory D. ; Takayama, Hiroo ; Naka, Yoshifumi ; Jorde, Ulrich P. / Prevalence and timing of bend relief disconnection in patients supported by the late version HeartMate II left ventricular assist device. In: Journal of Heart and Lung Transplantation. 2013 ; Vol. 32, No. 3. pp. 320-325.
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abstract = "Background: On April 4, 2012, the U.S. Food and Drug Administration issued a Class 1R recall of the HeartMate II (Thoratec Corporation, Pleasanton, CA) left ventricular assist device (LVAD) due to spontaneous detachment of the bend relief from its intended position in patients implanted with the most recent version of the HM II. This study examined the incidence and timing of outflow graft bend relief disconnection in patients implanted with the HM II LVAD. Methods: All patients supported with the modified version of the HM II LVAD were asked to report for dedicated abdominal X-ray imaging to assess the position of the bend relief. Also performed was a retrospective review of X-ray images of all patients who had previously been supported with this version but had since received a transplant, undergone LVAD explant, or died. Results: Between March 9, 2011, and April 9, 2012, 59 patients underwent primary implant with the modified version HM II. Follow up X-ray images were available for 56 patients (95{\%}). The bend relief was found fully disconnected in 6 of 56 (11{\%}) and partially disconnected in 13 (23{\%}). Two of 6 patients (33{\%}) with full bend relief disconnection and 1 of 13 of the initially partially disconnected patients (7.7{\%}) required urgent surgical intervention due to symptoms of hemolysis and/or heart failure. Conclusions: Bend relief disconnection is common and may be observed immediately after implant but may also develop over time. Full bend relief disconnect may present with hemolysis and/or heart failure symptoms and often requires surgical revision. Surveillance abdominal X-ray imaging should be performed routinely on all patients who were implanted with the modified version HM II.",
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T1 - Prevalence and timing of bend relief disconnection in patients supported by the late version HeartMate II left ventricular assist device

AU - Yuzefpolskaya, Melana

AU - Uriel, Nir

AU - Chow, Daniel S.

AU - Restaino, Susan W.

AU - Mancini, Donna M.

AU - Flannery, Margaret

AU - Te-Frey, Rosie

AU - Chichetti, Joanne

AU - Ota, Takeyoshi

AU - Kim, Hyonah

AU - Dano, Drew D.

AU - Pearson, Gregory D.

AU - Takayama, Hiroo

AU - Naka, Yoshifumi

AU - Jorde, Ulrich P.

PY - 2013/3

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N2 - Background: On April 4, 2012, the U.S. Food and Drug Administration issued a Class 1R recall of the HeartMate II (Thoratec Corporation, Pleasanton, CA) left ventricular assist device (LVAD) due to spontaneous detachment of the bend relief from its intended position in patients implanted with the most recent version of the HM II. This study examined the incidence and timing of outflow graft bend relief disconnection in patients implanted with the HM II LVAD. Methods: All patients supported with the modified version of the HM II LVAD were asked to report for dedicated abdominal X-ray imaging to assess the position of the bend relief. Also performed was a retrospective review of X-ray images of all patients who had previously been supported with this version but had since received a transplant, undergone LVAD explant, or died. Results: Between March 9, 2011, and April 9, 2012, 59 patients underwent primary implant with the modified version HM II. Follow up X-ray images were available for 56 patients (95%). The bend relief was found fully disconnected in 6 of 56 (11%) and partially disconnected in 13 (23%). Two of 6 patients (33%) with full bend relief disconnection and 1 of 13 of the initially partially disconnected patients (7.7%) required urgent surgical intervention due to symptoms of hemolysis and/or heart failure. Conclusions: Bend relief disconnection is common and may be observed immediately after implant but may also develop over time. Full bend relief disconnect may present with hemolysis and/or heart failure symptoms and often requires surgical revision. Surveillance abdominal X-ray imaging should be performed routinely on all patients who were implanted with the modified version HM II.

AB - Background: On April 4, 2012, the U.S. Food and Drug Administration issued a Class 1R recall of the HeartMate II (Thoratec Corporation, Pleasanton, CA) left ventricular assist device (LVAD) due to spontaneous detachment of the bend relief from its intended position in patients implanted with the most recent version of the HM II. This study examined the incidence and timing of outflow graft bend relief disconnection in patients implanted with the HM II LVAD. Methods: All patients supported with the modified version of the HM II LVAD were asked to report for dedicated abdominal X-ray imaging to assess the position of the bend relief. Also performed was a retrospective review of X-ray images of all patients who had previously been supported with this version but had since received a transplant, undergone LVAD explant, or died. Results: Between March 9, 2011, and April 9, 2012, 59 patients underwent primary implant with the modified version HM II. Follow up X-ray images were available for 56 patients (95%). The bend relief was found fully disconnected in 6 of 56 (11%) and partially disconnected in 13 (23%). Two of 6 patients (33%) with full bend relief disconnection and 1 of 13 of the initially partially disconnected patients (7.7%) required urgent surgical intervention due to symptoms of hemolysis and/or heart failure. Conclusions: Bend relief disconnection is common and may be observed immediately after implant but may also develop over time. Full bend relief disconnect may present with hemolysis and/or heart failure symptoms and often requires surgical revision. Surveillance abdominal X-ray imaging should be performed routinely on all patients who were implanted with the modified version HM II.

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