Comparison between microcatheter and nebulizer for generating Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC)

被引:5
|
作者
Toussaint, Laura [1 ,2 ]
Sautkin, Yaroslav [1 ]
Illing, Barbara [1 ]
Weinreich, Frank-Juergen [3 ,4 ]
Nadiradze, Giorgi [1 ,4 ]
Koenigsrainer, Alfred [1 ,4 ]
Wichmann, Doerte [4 ,5 ]
机构
[1] Univ Hosp Tubingen, Natl Ctr Pleura & Peritoneum, Tubingen, Germany
[2] Univ Hosp Lausanne, Dept Gastrointestinal Surg, Lausanne, Switzerland
[3] Univ Hosp Tubingen, Inst Pathol & Neuropathol, Tubingen, Germany
[4] Univ Hosp Tubingen, Dept Gen & Transplant Surg, Tubingen, Germany
[5] Univ Hosp Tubingen, Interdisciplinary Endoscopy Unit, Hoppe Seyler Str 3, D-72076 Tubingen, Germany
关键词
Intraperitoneal chemotherapy; Aerosol; Doxorubicin; Cisplatin; Peritoneal metastasis; Medical devices; PIPAC; PERITONEAL CARCINOMATOSIS; 1ST EVIDENCE;
D O I
10.1007/s00464-020-07546-z
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background This study compares an endoscopic microcatheter and a nebulizer for delivering Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC). Methods This is an in vitro and ex vivo study in an established model (inverted bovine urinary bladder). Four parameters were compared to determine the performance of a micro-perforated endoscopic spray catheter vs. state-of-the art, nozzle technology: (1) surface coverage and pattern with methylene blue on blotting paper at three different distances; (2) median aerodynamic diameter (MAD) of aerosol droplets with three different solutions (H2O, Glc 5% and silicon oil); (3) depth of tissue penetration of doxorubicin (DOX) and (4) tissue concentration of cisplatin (CIS) and DOX using standard clinical solutions. Results The spray area covered by the microcatheter was larger (p < 0.001) but its pattern was inhomogenous than with the nozzle technology. We found that aerosol droplets were larger in the test group than in the control group for all three solutions tested. Median tissue penetration of DOX was lower (980 mu m) with the microcatheter than with the nebulizer (1235 mu m) and distribution was more heterogeneous ( = 0.003) with the microcatheter. The median tissue concentration of DOX and CIS was lower and concentration of DOX was more heterogeneous with the microcatheter (p = 0.002). Conclusions This investigation has revealed that microcatheter technology generates larger aerosol droplet size, less drug tissue penetration and lower drug tissue concentration than the current nozzle technology. In the absence of clinical studies, use of microcatheters for delivering PIPAC can not be recommended at this stage.
引用
收藏
页码:1636 / 1643
页数:8
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