Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study
Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and e...
Ausführliche Beschreibung
Autor*in: |
Vos, Dagmar I [verfasserIn] |
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E-Artikel |
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Englisch |
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2012 |
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Anmerkung: |
© Vos et al.; licensee BioMed Central Ltd. 2012 |
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Übergeordnetes Werk: |
Enthalten in: BMC musculoskeletal disorders - London : BioMed Central, 2000, 13(2012), 1 vom: 15. Aug. |
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Übergeordnetes Werk: |
volume:13 ; year:2012 ; number:1 ; day:15 ; month:08 |
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DOI / URN: |
10.1186/1471-2474-13-147 |
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Katalog-ID: |
SPR028020146 |
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520 | |a Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 | ||
650 | 4 | |a Implant removal |7 (dpeaa)DE-He213 | |
650 | 4 | |a Metal implants |7 (dpeaa)DE-He213 | |
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650 | 4 | |a Complications |7 (dpeaa)DE-He213 | |
650 | 4 | |a Complaints |7 (dpeaa)DE-He213 | |
700 | 1 | |a Verhofstad, Michael HJ |4 aut | |
700 | 1 | |a Hanson, Beate |4 aut | |
700 | 1 | |a van der Graaf, Yolanda |4 aut | |
700 | 1 | |a van der Werken, Chris |4 aut | |
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10.1186/1471-2474-13-147 doi (DE-627)SPR028020146 (SPR)1471-2474-13-147-e DE-627 ger DE-627 rakwb eng Vos, Dagmar I verfasserin aut Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Vos et al.; licensee BioMed Central Ltd. 2012 Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 Implant removal (dpeaa)DE-He213 Metal implants (dpeaa)DE-He213 Fracture healing (dpeaa)DE-He213 Fracture surgery (dpeaa)DE-He213 Osteosynthesis (dpeaa)DE-He213 Complications (dpeaa)DE-He213 Complaints (dpeaa)DE-He213 Verhofstad, Michael HJ aut Hanson, Beate aut van der Graaf, Yolanda aut van der Werken, Chris aut Enthalten in BMC musculoskeletal disorders London : BioMed Central, 2000 13(2012), 1 vom: 15. Aug. (DE-627)326643745 (DE-600)2041355-5 1471-2474 nnns volume:13 year:2012 number:1 day:15 month:08 https://dx.doi.org/10.1186/1471-2474-13-147 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1 15 08 |
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10.1186/1471-2474-13-147 doi (DE-627)SPR028020146 (SPR)1471-2474-13-147-e DE-627 ger DE-627 rakwb eng Vos, Dagmar I verfasserin aut Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Vos et al.; licensee BioMed Central Ltd. 2012 Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 Implant removal (dpeaa)DE-He213 Metal implants (dpeaa)DE-He213 Fracture healing (dpeaa)DE-He213 Fracture surgery (dpeaa)DE-He213 Osteosynthesis (dpeaa)DE-He213 Complications (dpeaa)DE-He213 Complaints (dpeaa)DE-He213 Verhofstad, Michael HJ aut Hanson, Beate aut van der Graaf, Yolanda aut van der Werken, Chris aut Enthalten in BMC musculoskeletal disorders London : BioMed Central, 2000 13(2012), 1 vom: 15. Aug. (DE-627)326643745 (DE-600)2041355-5 1471-2474 nnns volume:13 year:2012 number:1 day:15 month:08 https://dx.doi.org/10.1186/1471-2474-13-147 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1 15 08 |
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10.1186/1471-2474-13-147 doi (DE-627)SPR028020146 (SPR)1471-2474-13-147-e DE-627 ger DE-627 rakwb eng Vos, Dagmar I verfasserin aut Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Vos et al.; licensee BioMed Central Ltd. 2012 Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 Implant removal (dpeaa)DE-He213 Metal implants (dpeaa)DE-He213 Fracture healing (dpeaa)DE-He213 Fracture surgery (dpeaa)DE-He213 Osteosynthesis (dpeaa)DE-He213 Complications (dpeaa)DE-He213 Complaints (dpeaa)DE-He213 Verhofstad, Michael HJ aut Hanson, Beate aut van der Graaf, Yolanda aut van der Werken, Chris aut Enthalten in BMC musculoskeletal disorders London : BioMed Central, 2000 13(2012), 1 vom: 15. Aug. (DE-627)326643745 (DE-600)2041355-5 1471-2474 nnns volume:13 year:2012 number:1 day:15 month:08 https://dx.doi.org/10.1186/1471-2474-13-147 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1 15 08 |
allfieldsGer |
10.1186/1471-2474-13-147 doi (DE-627)SPR028020146 (SPR)1471-2474-13-147-e DE-627 ger DE-627 rakwb eng Vos, Dagmar I verfasserin aut Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Vos et al.; licensee BioMed Central Ltd. 2012 Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 Implant removal (dpeaa)DE-He213 Metal implants (dpeaa)DE-He213 Fracture healing (dpeaa)DE-He213 Fracture surgery (dpeaa)DE-He213 Osteosynthesis (dpeaa)DE-He213 Complications (dpeaa)DE-He213 Complaints (dpeaa)DE-He213 Verhofstad, Michael HJ aut Hanson, Beate aut van der Graaf, Yolanda aut van der Werken, Chris aut Enthalten in BMC musculoskeletal disorders London : BioMed Central, 2000 13(2012), 1 vom: 15. Aug. (DE-627)326643745 (DE-600)2041355-5 1471-2474 nnns volume:13 year:2012 number:1 day:15 month:08 https://dx.doi.org/10.1186/1471-2474-13-147 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1 15 08 |
allfieldsSound |
10.1186/1471-2474-13-147 doi (DE-627)SPR028020146 (SPR)1471-2474-13-147-e DE-627 ger DE-627 rakwb eng Vos, Dagmar I verfasserin aut Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Vos et al.; licensee BioMed Central Ltd. 2012 Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 Implant removal (dpeaa)DE-He213 Metal implants (dpeaa)DE-He213 Fracture healing (dpeaa)DE-He213 Fracture surgery (dpeaa)DE-He213 Osteosynthesis (dpeaa)DE-He213 Complications (dpeaa)DE-He213 Complaints (dpeaa)DE-He213 Verhofstad, Michael HJ aut Hanson, Beate aut van der Graaf, Yolanda aut van der Werken, Chris aut Enthalten in BMC musculoskeletal disorders London : BioMed Central, 2000 13(2012), 1 vom: 15. Aug. (DE-627)326643745 (DE-600)2041355-5 1471-2474 nnns volume:13 year:2012 number:1 day:15 month:08 https://dx.doi.org/10.1186/1471-2474-13-147 kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2012 1 15 08 |
language |
English |
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clinical outcome of implant removal after fracture healing. design of a prospective multicentre clinical cohort study |
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Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study |
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Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 © Vos et al.; licensee BioMed Central Ltd. 2012 |
abstractGer |
Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 © Vos et al.; licensee BioMed Central Ltd. 2012 |
abstract_unstemmed |
Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297 © Vos et al.; licensee BioMed Central Ltd. 2012 |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR028020146</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519065839.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201007s2012 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1186/1471-2474-13-147</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR028020146</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)1471-2474-13-147-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Vos, Dagmar I</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Clinical outcome of implant removal after fracture healing. Design of a prospective multicentre clinical cohort study</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2012</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Vos et al.; licensee BioMed Central Ltd. 2012</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Background The clinical results of removal of metal implants after fracture healing are unknown and the question whether to remove or to leave them in is part of discussion worldwide. We present the design of a prospective clinical multicentre cohort study to determine the main indications for and expectations of implant removal, the influence on complaints, the incidence of surgery related complications and the socio-economic consequences of implant removal. Methods/Design In a prospective multicentre clinical cohort study at least 200 patients with a healed fracture after osteosynthesis with a metal implant are included for analyzing the outcome after removal. Six hospitals in the Netherlands are participating. Special questionnaires are designed. The follow up after surgery will be at least six months. The primary endpoint is the incidence of surgery related complications. Secondary endpoints are the influence of removal on preoperative symptoms and complaints and the socio-economic consequences. Discussion By performing this study we hope to find profound arguments to remove or not to remove metal implants after fracture healing that can help to develop clear guidelines for daily practice. Trial registration NTR1297, http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1297</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Implant removal</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Metal implants</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Fracture healing</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Fracture surgery</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Osteosynthesis</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Complications</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Complaints</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Verhofstad, Michael HJ</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hanson, Beate</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">van der Graaf, Yolanda</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">van der Werken, Chris</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">BMC musculoskeletal disorders</subfield><subfield code="d">London : BioMed Central, 2000</subfield><subfield code="g">13(2012), 1 vom: 15. 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