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PMID: 840277 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Complement and leukocyte-mediated pulmonary dysfunction in hemodialysis.

The New England journal of medicine ·Vol. 296 ·No. 14 ·1977-04-07 ·Pages 769-74

Craddock PR, Fehr J, Brigham KL, Kronenberg RS, Jacob HS

Abstract

During hemodialysis, cardiopulmonary decompensation may appear in uremic patients, possibly caused by plugging of pulmonary vessels by leukocytes. In 34 patients we noted leukopenia (20% of initial levels) during hemodialysis that in 15 was associated with impaired pulmonary function. When we infused autologous plasma, incubated with dialyzer cellophane, into rabbits and sheep, sudden leukopenia and hypoxia occurred, with doubling of pulmonary-artery pressures and quintupling of pulmonary-lymph effluent. Histologic examination showed severe pulmonary-vessel-leukostasis and interstitial edema. The syndrome was prevented by preinactivation of complement but was reproduced by infusions of plasma in which complement was activated by zymosan. Thus, acute pulmonary dysfunction from complement-mediated leukostasis may play a major part in the acute cardiopulmonary complications of cellophane-membrane hemodialysis.

MeSH Terms
Adolescent Adult Aged Agranulocytosis/etiology Animals Carbon Dioxide/blood Cellophane/adverse effects Complement System Proteins/physiology Humans Hypoxia/etiology Kidney Failure, Chronic/therapy Leukocyte Count Lung/physiopathology Lung Diseases/etiology,physiopathology Middle Aged Neutropenia/etiology Pulmonary Diffusing Capacity Rabbits Recurrence Renal Dialysis/adverse effects Sheep Time Factors
Chemicals
Carbon Dioxide Cellophane Complement System Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Craddock P R
Fehr J
Brigham K L
Kronenberg R S
Jacob H S
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
Published
1977-04-07
Pages
769-74
Language
English
Region
United States
NLM ID
0255562
Subset
IM
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