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dc.contributor.authorWiswell, Thomas E.
dc.contributor.authorSmith, Robert M.
dc.contributor.authorKatz, Laurence B.
dc.contributor.authorMastroianni, Lisa
dc.contributor.authorWong, Davies Y.
dc.contributor.authorWillms, David
dc.contributor.authorHeard, Stephen O.
dc.contributor.authorWilson, Mark M.
dc.contributor.authorHite, R. Duncan
dc.contributor.authorAnzueto, Antonio
dc.contributor.authorRevak, Susan D.
dc.contributor.authorCochrane, Charles G.
dc.date2022-08-11T08:07:58.000
dc.date.accessioned2022-08-23T15:37:47Z
dc.date.available2022-08-23T15:37:47Z
dc.date.issued1999-10-01
dc.date.submitted2012-08-01
dc.identifier.citation<p>Am J Respir Crit Care Med. 1999 Oct;160(4):1188-95.</p>
dc.identifier.issn1073-449X (Linking)
dc.identifier.doi10.1056/NEJM199901073400101
dc.identifier.pmid10508806
dc.identifier.urihttp://hdl.handle.net/20.500.14038/25794
dc.description.abstractWe performed a trial to assess the safety and tolerability of sequential bronchopulmonary segmental lavage with a dilute synthetic surfactant (Surfaxin) in 12 adults with ARDS. Patients received one of three dosing regimens in which aliquots of Surfaxin were administered via a wedged bronchoscope to each of the 19 bronchopulmonary segments. Suctioning was performed 10-30 s after instillation of individual aliquots. Group 1 patients (n = 3) received one 30-ml aliquot of a 2.5-mg/ml concentration of Surfaxin in each segment, followed by a second 30-ml aliquot with a 10-mg/ml concentration. Group 2 patients (n = 4) received two 30-ml aliquots of the 2.5-mg/ml concentration followed by a third lavage with the 10-mg/ml concentration. Group 3 patients (n = 5) received therapy identical to that received by patients in Group 2 and were eligible for repeat dosing 6 to 24 h later. All patients tolerated the procedure. There were no serious adverse experiences ascribed to either the procedure or the surfactant. In the 96 h after treatment initiation, FI(O(2)) decreased from 0.80 to 0.52 and PEEP decreased from 10.3 to 7.6 cm H(2)O. Bronchoscopic "cleansing" of the lungs with dilute Surfaxin may offer a safe and feasible approach to improving outcomes in patients with ARDS. Wiswell TE, Smith RM, Katz LB, Mastroianni L, Wong DY, Willms D, Heard S, Wilson M, Hite RD, Anzueto A, Revak SD, Cochrane CG. Bronchopulmonary segmental lavage with Surfaxin (KL(4)-surfactant) for acute respiratory distress syndrome.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=10508806&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1056/NEJM199901073400101
dc.subject*Bronchoalveolar Lavage
dc.subjectBronchoalveolar Lavage Fluid
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectPeptides
dc.subjectPositive-Pressure Respiration
dc.subjectProteins
dc.subjectPulmonary Gas Exchange
dc.subjectPulmonary Surfactants
dc.subjectRespiratory Distress Syndrome, Adult
dc.subjectAnesthesiology
dc.subjectRespiratory Tract Diseases
dc.subjectTherapeutics
dc.titleBronchopulmonary segmental lavage with Surfaxin (KL(4)-surfactant) for acute respiratory distress syndrome
dc.typeJournal Article
dc.source.journaltitleAmerican journal of respiratory and critical care medicine
dc.source.volume160
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/anesthesiology_pubs/36
dc.identifier.contextkey3168570
html.description.abstract<p>We performed a trial to assess the safety and tolerability of sequential bronchopulmonary segmental lavage with a dilute synthetic surfactant (Surfaxin) in 12 adults with ARDS. Patients received one of three dosing regimens in which aliquots of Surfaxin were administered via a wedged bronchoscope to each of the 19 bronchopulmonary segments. Suctioning was performed 10-30 s after instillation of individual aliquots. Group 1 patients (n = 3) received one 30-ml aliquot of a 2.5-mg/ml concentration of Surfaxin in each segment, followed by a second 30-ml aliquot with a 10-mg/ml concentration. Group 2 patients (n = 4) received two 30-ml aliquots of the 2.5-mg/ml concentration followed by a third lavage with the 10-mg/ml concentration. Group 3 patients (n = 5) received therapy identical to that received by patients in Group 2 and were eligible for repeat dosing 6 to 24 h later. All patients tolerated the procedure. There were no serious adverse experiences ascribed to either the procedure or the surfactant. In the 96 h after treatment initiation, FI(O(2)) decreased from 0.80 to 0.52 and PEEP decreased from 10.3 to 7.6 cm H(2)O. Bronchoscopic "cleansing" of the lungs with dilute Surfaxin may offer a safe and feasible approach to improving outcomes in patients with ARDS. Wiswell TE, Smith RM, Katz LB, Mastroianni L, Wong DY, Willms D, Heard S, Wilson M, Hite RD, Anzueto A, Revak SD, Cochrane CG. Bronchopulmonary segmental lavage with Surfaxin (KL(4)-surfactant) for acute respiratory distress syndrome.</p>
dc.identifier.submissionpathanesthesiology_pubs/36
dc.contributor.departmentDepartment of Medicine, Division of Pulmonary, Allergy And Critical Care Medicine
dc.contributor.departmentDepartment of Surgery
dc.contributor.departmentDepartment of Anesthesiology
dc.source.pages1188-95


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