dc.contributor.author |
Kertai, Miklos D |
|
dc.contributor.author |
Cheruku, Sreekanth |
|
dc.contributor.author |
Qi, Wenjing |
|
dc.contributor.author |
Li, Yi-Ju |
|
dc.contributor.author |
Hughes, G Chad |
|
dc.contributor.author |
Mathew, Joseph P |
|
dc.contributor.author |
Karhausen, Jörn A |
|
dc.coverage.spatial |
United States |
|
dc.date.accessioned |
2017-01-03T15:31:19Z |
|
dc.date.issued |
2017-01 |
|
dc.identifier |
http://www.ncbi.nlm.nih.gov/pubmed/27697359 |
|
dc.identifier |
S0022-5223(16)31100-X |
|
dc.identifier.uri |
https://hdl.handle.net/10161/13338 |
|
dc.description.abstract |
OBJECTIVE: Aortic surgeries requiring hypothermic circulatory arrest evoke systemic
inflammatory responses that often manifest as vasoplegia and hypotension. Because
mast cells can rapidly release vasoactive and proinflammatory effectors, we investigated
their role in intraoperative hypotension. METHODS: We studied 31 patients undergoing
proximal aortic repair with hypothermic circulatory arrest between June 2013 and April
2015 at Duke University Medical Center. Plasma samples were obtained at different
intraoperative time points to quantify chymase, interleukin-6, interleukin-8, tumor
necrosis factor alpha, and white blood cell CD11b expression. Hypotension was defined
as the area (minutes × millimeters mercury) below a mean arterial pressure of 55 mm
Hg. Biomarker responses and their association with intraoperative hypotension were
analyzed by 2-sample t test and Wilcoxon rank sum test. Multivariable logistic regression
analysis was used to examine the association between clinical variables and elevated
chymase levels. RESULTS: Mast cell-specific chymase increased from a median 0.97 pg/mg
(interquartile range [IQR], 0.01-1.84 pg/mg) plasma protein at baseline to 5.74 pg/mg
(IQR, 2.91-9.48 pg/mg) plasma protein after instituting cardiopulmonary bypass, 6.16 pg/mg
(IQR, 3.60-9.41 pg/mg) plasma protein after completing circulatory arrest, and 7.64
pg/mg (IQR, 4.63-12.71 pg/mg) plasma protein after weaning from cardiopulmonary bypass
(each P value < .0001 vs baseline). Chymase was the only biomarker associated with
hypotension during (P = .0255) and after (P = .0221) cardiopulmonary bypass. Increased
temperatures at circulatory arrest and low presurgical hemoglobin levels were independent
predictors of increased chymase responses. CONCLUSIONS: Mast cell activation occurs
in cardiac surgery requiring cardiopulmonary bypass and hypothermic circulatory arrest
and is associated with intraoperative hypotension.
|
|
dc.language |
eng |
|
dc.publisher |
Elsevier BV |
|
dc.relation.ispartof |
J Thorac Cardiovasc Surg |
|
dc.relation.isversionof |
10.1016/j.jtcvs.2016.05.063 |
|
dc.subject |
blood pressure |
|
dc.subject |
cardiac surgical procedures |
|
dc.subject |
inflammation mediators |
|
dc.subject |
mast cell |
|
dc.title |
Mast cell activation and arterial hypotension during proximal aortic repair requiring
hypothermic circulatory arrest.
|
|
dc.type |
Journal article |
|
duke.contributor.id |
Kertai, Miklos D|0544354 |
|
duke.contributor.id |
Li, Yi-Ju|0271809 |
|
duke.contributor.id |
Hughes, G Chad|0066100 |
|
duke.contributor.id |
Mathew, Joseph P|0215327 |
|
duke.contributor.id |
Karhausen, Jörn A|0493854 |
|
pubs.author-url |
http://www.ncbi.nlm.nih.gov/pubmed/27697359 |
|
pubs.begin-page |
68 |
|
pubs.end-page |
76.e2 |
|
pubs.issue |
1 |
|
pubs.organisational-group |
Anesthesiology |
|
pubs.organisational-group |
Anesthesiology, Cardiothoracic |
|
pubs.organisational-group |
Basic Science Departments |
|
pubs.organisational-group |
Biostatistics & Bioinformatics |
|
pubs.organisational-group |
Clinical Science Departments |
|
pubs.organisational-group |
Duke |
|
pubs.organisational-group |
Duke Molecular Physiology Institute |
|
pubs.organisational-group |
Institutes and Centers |
|
pubs.organisational-group |
School of Medicine |
|
pubs.organisational-group |
Surgery |
|
pubs.organisational-group |
Surgery, Cardiovascular and Thoracic Surgery |
|
pubs.publication-status |
Published |
|
pubs.volume |
153 |
|
dc.identifier.eissn |
1097-685X |
|
duke.contributor.orcid |
Mathew, Joseph P|0000-0002-3815-4131 |
|