A comparison between distal and proximal port device insertion in head and neck cancer

被引:27
作者
Marcy, P. -Y. [1 ]
Chamorey, E. [2 ]
Amoretti, N. [1 ]
Benezery, K. [3 ]
Bensadoun, R. J. [3 ]
Bozec, A. [4 ]
Poissonnet, G. [4 ]
Dassonville, O. [4 ]
Rame, A. [5 ]
Italiano, A. [6 ]
Peyrade, F. [6 ]
Brenac, F. [7 ]
Gallard, J. C. [7 ]
机构
[1] Antoine Lacassagne Anticanc Res Inst, Dept Radiodiagnost & Intervent Radiol, F-06189 Nice 1, France
[2] Antoine Lacassagne Anticanc Res Inst, Biostat & Clin Res Unit, F-06189 Nice 1, France
[3] Antoine Lacassagne Anticanc Res Inst, Dept Radiat Therapy, F-06189 Nice 1, France
[4] Antoine Lacassagne Anticanc Res Inst, Dept Head & Neck Surg, F-06189 Nice 1, France
[5] Francois Baclesse Anticanc Res Inst, Dept Head & Neck Surg, F-14076 Caen 05, France
[6] Antoine Lacassagne Anticanc Res Inst, Dept Oncol, F-06189 Nice 1, France
[7] Francois Baclesse Anticanc Res Inst, Dept Radiodiagnost & Intervent Radiol, F-14076 Caen 05, France
来源
EJSO | 2008年 / 34卷 / 11期
关键词
Catheter and catheterization; Cephalic vein cutdown; Totally implantable central venous access devices; Veins; Interventional procedures; Head and neck neoplasm; Peripheral venous catheterization;
D O I
10.1016/j.ejso.2007.09.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: To compare technical feasibility and complications of radiologically arm port device implantation using arm venography exclusively (API-Group B) with chestport placement using cephalic vein cutdown (CVC-Group A), in advanced consecutive head and neck cancer patients (HNP). Methods: Port device placement was attempted in 225 consecutive HNP. Decision for inclusion in Group A or B was made first by the availability of the surgeon/radiologist to perform the procedure, second by contraindications of each technique. Patient transfer from one group to the other was recorded as well as technical feasibility, complications and device specific duration in this retrospective study. Results: Technical success was statistically higher in Arm Port Group (99.1%) compared to Chest Port Group (75.2%). Device specific duration rate of the whole population was 53% (95%CI) [0.47-0.60] at 6 months, 44.1% (95%CI) [24.4-37.8] at 12 months and 8% (95%CI) [4.4-14.5] at 24 months. Median follow-up was 5.55 months (range: 0.032-9.6] in Group A versus 5.90 months [range: 0.06-27.6] (p = ns) in Group B. Complication rate was 15.9% in Group A versus 8.9% in Group B corresponding to a complication rate per patient-implantation-days of 0.66/1000 patient-days (A) versus 0.42/1000 patient-days (B). Premature port device explantation rate was 4.4% (A) versus 5.4% (B). Axillary and subclavian venous thrombosis was the main complication and occurred in 12 Group A patients and three Group B patients. Venous thrombosis rate was 0.37/1000 patient-days (A) and 0.13/1000 patient-days (B) (p = 0.03). Conclusions: A few data exist about device insertion in HNP in whom venous cervical access is contraindicated. This comparative study demonstrates that both implantation techniques are safe and effective. The higher technical success rate with 0% heavy sedation, the lower venous thrombosis rate in the API group, and the 5.3% (A-B) patient transfer rate argue in favour of arm port placement in HNP. Indications for API include patients with an ipsilateral major pectoralis-myocutaneous flap, with radiodermatitis, tumour recurrence in the neck and upper chest, or with respiratory impairment. (C) 2007 Published by Elsevier Ltd.
引用
收藏
页码:1262 / 1269
页数:8
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