Implantable port thrombosis in cancer patients: a monocentric experience

<b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cance...
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Gespeichert in:

Autor*in:	Manel Dridi [verfasserIn] Nesrine Mejri [verfasserIn] Soumaya Labidi [verfasserIn] Mehdi Afrit [verfasserIn] Houda El Benna [verfasserIn] Khaoula Ben Miled [verfasserIn] Hamouda Boussen [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2016

Schlagwörter:	Implantable port cancer patients thrombosis

Übergeordnetes Werk:	In: Cancer Biology & Medicine - China Anti-Cancer Association, 2019, 13(2016), 3, Seite 384-388
Übergeordnetes Werk:	volume:13 ; year:2016 ; number:3 ; pages:384-388

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.20892/j.issn.2095-3941.2016.0057

Katalog-ID:	DOAJ002717255

Internformat


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520			\|a <b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation.
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653		0	\|a Neoplasms. Tumors. Oncology. Including cancer and carcinogens
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allfields	10.20892/j.issn.2095-3941.2016.0057 doi (DE-627)DOAJ002717255 (DE-599)DOAJ7bdc7cf19fa4455caad51de25d060600 DE-627 ger DE-627 rakwb eng RC254-282 Manel Dridi verfasserin aut Implantable port thrombosis in cancer patients: a monocentric experience 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation. Implantable port cancer patients thrombosis Neoplasms. Tumors. Oncology. Including cancer and carcinogens Nesrine Mejri verfasserin aut Soumaya Labidi verfasserin aut Mehdi Afrit verfasserin aut Houda El Benna verfasserin aut Khaoula Ben Miled verfasserin aut Hamouda Boussen verfasserin aut In Cancer Biology & Medicine China Anti-Cancer Association, 2019 13(2016), 3, Seite 384-388 (DE-627)72193739X (DE-600)2676322-9 20953941 nnns volume:13 year:2016 number:3 pages:384-388 https://doi.org/10.20892/j.issn.2095-3941.2016.0057 kostenfrei https://doaj.org/article/7bdc7cf19fa4455caad51de25d060600 kostenfrei http://www.cancerbiomed.org/index.php/cocr/article/view/958 kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 2016 3 384-388
spelling	10.20892/j.issn.2095-3941.2016.0057 doi (DE-627)DOAJ002717255 (DE-599)DOAJ7bdc7cf19fa4455caad51de25d060600 DE-627 ger DE-627 rakwb eng RC254-282 Manel Dridi verfasserin aut Implantable port thrombosis in cancer patients: a monocentric experience 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation. Implantable port cancer patients thrombosis Neoplasms. Tumors. Oncology. Including cancer and carcinogens Nesrine Mejri verfasserin aut Soumaya Labidi verfasserin aut Mehdi Afrit verfasserin aut Houda El Benna verfasserin aut Khaoula Ben Miled verfasserin aut Hamouda Boussen verfasserin aut In Cancer Biology & Medicine China Anti-Cancer Association, 2019 13(2016), 3, Seite 384-388 (DE-627)72193739X (DE-600)2676322-9 20953941 nnns volume:13 year:2016 number:3 pages:384-388 https://doi.org/10.20892/j.issn.2095-3941.2016.0057 kostenfrei https://doaj.org/article/7bdc7cf19fa4455caad51de25d060600 kostenfrei http://www.cancerbiomed.org/index.php/cocr/article/view/958 kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 2016 3 384-388
allfields_unstemmed	10.20892/j.issn.2095-3941.2016.0057 doi (DE-627)DOAJ002717255 (DE-599)DOAJ7bdc7cf19fa4455caad51de25d060600 DE-627 ger DE-627 rakwb eng RC254-282 Manel Dridi verfasserin aut Implantable port thrombosis in cancer patients: a monocentric experience 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation. Implantable port cancer patients thrombosis Neoplasms. Tumors. Oncology. Including cancer and carcinogens Nesrine Mejri verfasserin aut Soumaya Labidi verfasserin aut Mehdi Afrit verfasserin aut Houda El Benna verfasserin aut Khaoula Ben Miled verfasserin aut Hamouda Boussen verfasserin aut In Cancer Biology & Medicine China Anti-Cancer Association, 2019 13(2016), 3, Seite 384-388 (DE-627)72193739X (DE-600)2676322-9 20953941 nnns volume:13 year:2016 number:3 pages:384-388 https://doi.org/10.20892/j.issn.2095-3941.2016.0057 kostenfrei https://doaj.org/article/7bdc7cf19fa4455caad51de25d060600 kostenfrei http://www.cancerbiomed.org/index.php/cocr/article/view/958 kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 2016 3 384-388
allfieldsGer	10.20892/j.issn.2095-3941.2016.0057 doi (DE-627)DOAJ002717255 (DE-599)DOAJ7bdc7cf19fa4455caad51de25d060600 DE-627 ger DE-627 rakwb eng RC254-282 Manel Dridi verfasserin aut Implantable port thrombosis in cancer patients: a monocentric experience 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation. Implantable port cancer patients thrombosis Neoplasms. Tumors. Oncology. Including cancer and carcinogens Nesrine Mejri verfasserin aut Soumaya Labidi verfasserin aut Mehdi Afrit verfasserin aut Houda El Benna verfasserin aut Khaoula Ben Miled verfasserin aut Hamouda Boussen verfasserin aut In Cancer Biology & Medicine China Anti-Cancer Association, 2019 13(2016), 3, Seite 384-388 (DE-627)72193739X (DE-600)2676322-9 20953941 nnns volume:13 year:2016 number:3 pages:384-388 https://doi.org/10.20892/j.issn.2095-3941.2016.0057 kostenfrei https://doaj.org/article/7bdc7cf19fa4455caad51de25d060600 kostenfrei http://www.cancerbiomed.org/index.php/cocr/article/view/958 kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 2016 3 384-388
allfieldsSound	10.20892/j.issn.2095-3941.2016.0057 doi (DE-627)DOAJ002717255 (DE-599)DOAJ7bdc7cf19fa4455caad51de25d060600 DE-627 ger DE-627 rakwb eng RC254-282 Manel Dridi verfasserin aut Implantable port thrombosis in cancer patients: a monocentric experience 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation. Implantable port cancer patients thrombosis Neoplasms. Tumors. Oncology. Including cancer and carcinogens Nesrine Mejri verfasserin aut Soumaya Labidi verfasserin aut Mehdi Afrit verfasserin aut Houda El Benna verfasserin aut Khaoula Ben Miled verfasserin aut Hamouda Boussen verfasserin aut In Cancer Biology & Medicine China Anti-Cancer Association, 2019 13(2016), 3, Seite 384-388 (DE-627)72193739X (DE-600)2676322-9 20953941 nnns volume:13 year:2016 number:3 pages:384-388 https://doi.org/10.20892/j.issn.2095-3941.2016.0057 kostenfrei https://doaj.org/article/7bdc7cf19fa4455caad51de25d060600 kostenfrei http://www.cancerbiomed.org/index.php/cocr/article/view/958 kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei https://doaj.org/toc/2095-3941 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 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_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 2016 3 384-388
language	English
source	In Cancer Biology & Medicine 13(2016), 3, Seite 384-388 volume:13 year:2016 number:3 pages:384-388
sourceStr	In Cancer Biology & Medicine 13(2016), 3, Seite 384-388 volume:13 year:2016 number:3 pages:384-388
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Implantable port cancer patients thrombosis Neoplasms. Tumors. Oncology. Including cancer and carcinogens
isfreeaccess_bool	true
container_title	Cancer Biology & Medicine
authorswithroles_txt_mv	Manel Dridi @@aut@@ Nesrine Mejri @@aut@@ Soumaya Labidi @@aut@@ Mehdi Afrit @@aut@@ Houda El Benna @@aut@@ Khaoula Ben Miled @@aut@@ Hamouda Boussen @@aut@@
publishDateDaySort_date	2016-01-01T00:00:00Z
hierarchy_top_id	72193739X
id	DOAJ002717255
language_de	englisch
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callnumber-first	R - Medicine
author	Manel Dridi
spellingShingle	Manel Dridi misc RC254-282 misc Implantable port misc cancer patients misc thrombosis misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens Implantable port thrombosis in cancer patients: a monocentric experience
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topic_title	RC254-282 Implantable port thrombosis in cancer patients: a monocentric experience Implantable port cancer patients thrombosis
topic	misc RC254-282 misc Implantable port misc cancer patients misc thrombosis misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens
topic_unstemmed	misc RC254-282 misc Implantable port misc cancer patients misc thrombosis misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens
topic_browse	misc RC254-282 misc Implantable port misc cancer patients misc thrombosis misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens
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title	Implantable port thrombosis in cancer patients: a monocentric experience
ctrlnum	(DE-627)DOAJ002717255 (DE-599)DOAJ7bdc7cf19fa4455caad51de25d060600
title_full	Implantable port thrombosis in cancer patients: a monocentric experience
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journal	Cancer Biology & Medicine
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author_browse	Manel Dridi Nesrine Mejri Soumaya Labidi Mehdi Afrit Houda El Benna Khaoula Ben Miled Hamouda Boussen
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author-letter	Manel Dridi
doi_str_mv	10.20892/j.issn.2095-3941.2016.0057
author2-role	verfasserin
title_sort	implantable port thrombosis in cancer patients: a monocentric experience
callnumber	RC254-282
title_auth	Implantable port thrombosis in cancer patients: a monocentric experience
abstract	<b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation.
abstractGer	<b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation.
abstract_unstemmed	<b<Objective: </b< Implantable port thrombosis (IPT) in cancer patients is a relatively rare but severe complication. Several factors are reportedly associated with the occurrence of thrombosis. We aimed to describe the prevalence and the anatomoclinical features of IPT observed in cancer patients who were treated in a medical oncology department in Tunisia. <b<Methods: </b< A total of 600 cancer patients who had port implantation from January 2013 to December 2015 were retrospectively identified. Cases with symptomatic/incidental IPT (radiologically confirmed) were further identified. Epidemiological and anatomoclinical features were collected from patient records and the department database. <b<Results</title<: <p<We observed that 33 of the 600 patients had IPT; thus, the prevalence was 5.5%. The median age was 57 years, and the gender ratio was 0.43. Overweight or obesity was observed in 73% of the patients. IPT occurred mainly in patients with breast (36.4%) and colorectal (33.3%) cancers, which were mostly nonmetastatic (79%). At least one identified classical thromboembolic risk factor was found in 13 patients (smoking in 9, tamoxifen in 2). IPT was symptomatic in 93% of the cases, occurring within an average time of 56 days. Implantable ports were removed because of infection in 2 cases and nonfunctionality in 3 cases. IPT treatment was based on low-molecular-weight heparins (94%) and antivitamin K (6%) for an average of 130 days. Four patients had post-therapy complications: one thrombosis recurrence and three infections.<b<Conclusions: </b< IPT cases in the 600 patients were observed to occur in obese nonmetastatic cancer patients within the first 3 months after IP implantation.
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title_short	Implantable port thrombosis in cancer patients: a monocentric experience
url	https://doi.org/10.20892/j.issn.2095-3941.2016.0057 https://doaj.org/article/7bdc7cf19fa4455caad51de25d060600 http://www.cancerbiomed.org/index.php/cocr/article/view/958 https://doaj.org/toc/2095-3941
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