Platelet and leukocyte activation and design consequences for thoracic artificial lungs

被引:15
作者
Cook, KE
Maxhimer, J
Leonard, DJ
Mavroudis, C
Backer, CL
Mockros, LF
机构
[1] Childrens Mem Hosp, Div Cardiovasc Thorac Surg, Chicago, IL 60614 USA
[2] Northwestern Univ, Evanston, IL USA
关键词
D O I
10.1097/00002480-200211000-00008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Blood contact with the prosthetic surfaces of artificial lungs causes extensive activation of molecular and cellular mediators of coagulation and inflammation that can lead to patient morbidity and mortality. To determine the effects of artificial lung fiber bundle shear stress and surface area on blood activation, porcine blood was recirculated for 4 hours through circuits containing mock artificial lungs with bundle shear stresses of 11.6, 7.3, and 3.9 dynes/cm' and surface areas of 5.2, 3.5, and 1.7 cm(2)/ml of circuit volume. Blood from these circuits was assayed for platelet and leukocyte counts, soluble P-selectin concentrations, and lactoferrin concentrations to determine the level of platelet and leukocyte adherence to the circuit, platelet activation, and leukocyte activation, respectively. Neither platelet nor leukocyte counts were significantly affected by shear stress or surface area. P-selectin and lactoferrin concentrations were significantly greater at a fiber bundle shear stress of 11.6 dynes/cm(2). P-selectin and lactoferrin concentrations were significantly greater at a fiber bundle surface area of 5.2 cm(2)/ml of circuit volume. Artificial lungs, therefore, should be designed with average bundle shear stresses < 11.6 dynes/cm(2) and with surface areas < 5.2 cm(2)/ml of circuit volume. Current thoracic artificial lungs meet both these requirements.
引用
收藏
页码:620 / 630
页数:11
相关论文
共 39 条
[1]  
Abbas A.K., 1994, Cellular and molecular immunology
[2]  
ADDONIZIO VP, 1985, J THORAC CARDIOV SUR, V89, P926
[3]  
ALTIERI DC, 1988, J BIOL CHEM, V263, P7007
[4]   ADHESIVE RECEPTOR MAC-1 COORDINATES THE ACTIVATION OF FACTOR-X ON STIMULATED CELLS OF MONOCYTIC AND MYELOID DIFFERENTIATION - AN ALTERNATIVE INITIATION OF THE COAGULATION PROTEASE CASCADE [J].
ALTIERI, DC ;
MORRISSEY, JH ;
EDGINGTON, TS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (20) :7462-7466
[5]   ILOPROST AND ECHISTATIN PROTECT PLATELETS DURING SIMULATED EXTRACORPOREAL-CIRCULATION [J].
BERNABEI, A ;
GIKAKIS, N ;
KOWALSKA, MA ;
NIEWIAROWSKI, S ;
EDMUNDS, LH .
ANNALS OF THORACIC SURGERY, 1995, 59 (01) :149-153
[6]   HEMOLYTIC EFFECTS OF ENERGY DISSIPATION IN FLOWING BLOOD [J].
BLUESTEI.M ;
MOCKROS, LF .
MEDICAL & BIOLOGICAL ENGINEERING, 1969, 7 (01) :1-&
[7]   HYDROPHOBIC POLYMER SURFACES AND THEIR INTERACTIONS WITH BLOOD [J].
BRASH, JL .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1977, 283 (FEB10) :356-371
[8]  
BRASH JL, 1988, BLOOD, V71, P932
[9]   ADSORPTION ON GLASS AND POLYETHYLENE FROM SOLUTIONS OF FIBRINOGEN AND ALBUMIN [J].
BRASH, JL ;
DAVIDSON, VJ .
THROMBOSIS RESEARCH, 1976, 9 (03) :249-259
[10]  
CHOW TW, 1992, BLOOD, V80, P113