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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2024The safety and feasibility of same-day discharge after subcutaneous implantable cardioverter defibrillator implantationcitations
  • 2024Outcomes of subcutaneous implantable cardioverter defibrillators: UK tertiary centre experiencecitations
  • 2015Modelling the properties of pigment-printed polypropylene nonwoven fabric using the Box-Behnken technique11citations

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Chart of shared publication
Toon, L. T.
2 / 2 shared
Patil, R.
2 / 4 shared
Roberts, P. R.
2 / 2 shared
Hudson, J.
2 / 2 shared
Elrefai, M.
2 / 2 shared
Bates, A.
2 / 2 shared
Masood, R.
1 / 1 shared
Areeb, T.
1 / 1 shared
Ullah, A.
1 / 3 shared
Umar, Muhammad
1 / 10 shared
Hussain, T.
1 / 14 shared
Chart of publication period
2024
2015

Co-Authors (by relevance)

  • Toon, L. T.
  • Patil, R.
  • Roberts, P. R.
  • Hudson, J.
  • Elrefai, M.
  • Bates, A.
  • Masood, R.
  • Areeb, T.
  • Ullah, A.
  • Umar, Muhammad
  • Hussain, T.
OrganizationsLocationPeople

article

The safety and feasibility of same-day discharge after subcutaneous implantable cardioverter defibrillator implantation

  • Toon, L. T.
  • Zubair, Z.
  • Patil, R.
  • Roberts, P. R.
  • Hudson, J.
  • Elrefai, M.
  • Bates, A.
Abstract

<jats:title>Abstract</jats:title><jats:sec><jats:title>Introduction</jats:title><jats:p>Subcutaneous Implantable cardioverter defibrillators (S-ICDs) are now progressively administered as a day-case procedure. While existing data supports the feasibility and safety of same-day discharge after transvenous ICD implantation, comparable evidence for S-ICDs is not well established. This study addresses this by presenting data from the most extensive population documented in the medical literature. We seek to evaluate the feasibility and safety of same-day discharge after S-ICD implantation.</jats:p></jats:sec><jats:sec><jats:title>Purpose</jats:title><jats:p>To investigate the feasibility and safety of same-day discharge following S-ICD implantation.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>A retrospective analysis was conducted, encompassing data from all patients who underwent S-ICD implantation at our institution between January 2011 to April 2023 (n=240). The cohort was stratified into two groups: those discharged on the same day of the procedure (SD, n=124) and those subject to at least overnight hospital observation (OD, n=116). The medical records were reviewed during this period aiming to identify potential complications. Complications were categorized as device-related complications or inappropriate shock. Specific events, such as inappropriate shocks; lead revision; infection necessitating lead or generator extraction; pocket hematoma requiring drainage, blood transfusion, or prolongation of hospitalization; and other complications related to the lead or generator prompting medical or surgical intervention were documented. An inappropriate shock was defined as one delivered for any rhythm other than ventricular fibrillation or ventricular tachycardia.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Among the 240 patients included in the study, 123 were scheduled for a day case procedure, while the remaining 117 underwent S-ICD implantation as in-patients. Notably, 112(91%) out of 123 planned-day patients and 12 in-patients (SD, total n=124) were successfully discharged on the same day. A substantial proportion (84%) of SD group had undergone the procedure for primary prevention. Patients with congenital heart disease were predominantly observed overnight.</jats:p><jats:p>Defibrillation testing (DFT) is routine in our practice to ensure S-ICD integrity and was conducted in all S-ICD patients unless contraindicated. The success rate of DFT among attempted patients was high, standing at 72% and 78% in the SD and OD groups, respectively.</jats:p><jats:p>The incidence of device-related complications was comparable between the two groups. The SD group displayed a slightly higher superficial infection rate but the incidence of inappropriate shocks was lower in the SD groups.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Based on our findings, same-day discharge following S-ICD implantation emerges as an appropriate practice. Our data strongly supports the assertion that same-day discharge in this context is safe and feasible, offering valuable insights into the optimal post-procedural management of S-ICD patients.Table 1ComplicationsTable 2Defibrillation Test</jats:p></jats:sec>

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