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Lipid emulsion therapy during management of the critically-ill poisoned patient: a prospective cohort study.
Levine, Michael; Brent, Jeffrey; Wiegand, Timothy; Maguire, Bryan; Cohen, Neta; Vaerrier, David; Beuhler, Michael; Leikin, Jerrold B; Ganetsky, Michael; Stellpflug, Samuel; Ruha, Anne-Michelle; Carey, Jennifer; Geib, Ann-Jeannette; Cao, Dazhe James; Kleinschmidt, Kurt; Vohra, Rais; Riley, Brad D; Moore, Phillip; Schwarz, Evan; Neavyn, Mark; Rusyniak, Daniel E; Greene, Spencer; Nogar, Joshua; Manini, Alex; Wermuth, Mary; Pizon, Anthony; Hendrickson, Robert G; Griswold, Matthew; Aldy, Kim; Wax, Paul; Spyres, Meghan Beth; Campleman, Sharan; Macdonald, Erin; Finkelstein, Yaron.
Afiliação
  • Levine M; Department of Emergency Medicine, University of California, Los Angeles, CA, USA.
  • Brent J; University of Colorado Boulder, Denver, CO, USA.
  • Wiegand T; Department of Emergency Medicine, Division of Medical Toxicology, University of Rochester, Rochester, NY, USA.
  • Maguire B; The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Cohen N; The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Vaerrier D; Department of Emergency Medicine, University of Mississippi Medical Center, Jackson, MS, USA.
  • Beuhler M; NC Poison Control Center, Charlotte, NC, USA.
  • Leikin JB; Division of Environmental and Occupational Health Science and the Occupational and Environmental Medicine Service of UI Health, University of Illinois Chicago, Chicago, IL, USA.
  • Ganetsky M; Department of Emergency Medicine, Division of Medical Toxicology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Stellpflug S; Department of Emergency Medicine, Regions Hospital, St. Paul, MN, USA.
  • Ruha AM; Department of Medical Toxicology, Banner University Medical Center, Phoenix, AZ, USA.
  • Carey J; Department of Emergency Medicine, University of Massachusetts, Worchester, MA, USA.
  • Geib AJ; Antrum Health, Carolinas Medical Center, Charlotte, NC, USA.
  • Cao DJ; Department of Emergency Medicine, Division of Medical Toxicology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Kleinschmidt K; Department of Emergency Medicine, Division of Medical Toxicology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Vohra R; Department of Emergency Medicine, Division of Medical Toxicology, University of California San Francisco-Fresno Medical Center, Fresno, CA, USA.
  • Riley BD; Michigan State University College of Human Medicine, Grand Rapids, MI, USA.
  • Moore P; Department of Emergency Medicine, Penn State University College of Medicine, Hershey, PA, USA.
  • Schwarz E; Department of Emergency Medicine, University of California, Los Angeles, CA, USA.
  • Neavyn M; Department of Emergency Medicine, Division of Medical Toxicology, Washington University, St. Louis, MO, USA.
  • Rusyniak DE; Department of Emergency Medicine, Hartford Hospital, Hartford, CT, USA.
  • Greene S; Department of Emergency Medicine, Division of Medical Toxicology, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Nogar J; Department of Emergency Medicine, HCA Houston Healthcare - Kingwood, University of Houston College of Medicine, Houston, TX, USA.
  • Manini A; Department of Emergency Medicine, North Shore University, Manhasset, NY, USA.
  • Wermuth M; Department of Emergency Medicine, Division of Medical Toxicology, Icahn School of Medicine at Mount Sinai, Elmhurst Hospital Center, New York, NY, USA.
  • Pizon A; Department of Emergency Medicine, Division of Medical Toxicology, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Hendrickson RG; Department of Emergency Medicine, Division of Medical Toxicology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Griswold M; Department of Emergency Medicine, Division of Medical Toxicology, Oregon Health Science University, Portland, OR, USA.
  • Aldy K; Department of Emergency Medicine, Connecticut Children's Medical Center, Hartford, CT, USA.
  • Wax P; American College of Medical Toxicology, Phoenix, AZ, USA.
  • Spyres MB; American College of Medical Toxicology, Phoenix, AZ, USA.
  • Campleman S; Department of Medical Toxicology, Banner University Medical Center, Phoenix, AZ, USA.
  • Macdonald E; American College of Medical Toxicology, Phoenix, AZ, USA.
  • Finkelstein Y; The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Clin Toxicol (Phila) ; 61(8): 584-590, 2023 08.
Article em En | MEDLINE | ID: mdl-37655788
ABSTRACT

BACKGROUND:

Despite conflicting data, intravenous lipid emulsion has emerged as a potential antidote. The "lipid sink" theory suggests that following intravenous administration of lipid, lipophilic drugs are sequestered in the vascular compartment, thereby reducing their tissue concentrations. This study sought to determine if survival is associated with the intoxicant's degree of lipophilicity.

METHODS:

We reviewed all cases in the Toxicology Investigators Consortium's lipid sub-registry between May 2012 through December 2018. Information collected included demographics, exposure circumstances, clinical course, management, disposition, and outcome. The primary outcome was survival after lipid emulsion therapy. Survival was stratified by the log of the intoxicant's octanol-water partition coefficient. We also assessed the association between intoxicant lipophilicity and an increase in systolic blood pressure after lipid emulsion administration.

RESULTS:

We identified 134 patients, including 81 (60.4%) females. The median age was 40 years (interquartile range 21-75). One hundred and eight (80.6%) patients survived, including 45 (33.6%) with cardiac arrest during their intoxication. Eighty-two (61.2%) were hypotensive, and 98 (73.1%) received mechanical ventilation. There was no relationship between survival and the log of the partition coefficient of the intoxicant on linear analysis (P = 0.89) or polynomial model (P = 0.10). Systolic blood pressure increased in both groups. The median (interquartile range) systolic blood pressure before lipid administration was 68 (60-78) mmHg for those intoxicants with a log partition coefficient < 3.6 compared with 89 (76-104) mmHg after lipid administration. Among those drugs with a log partition coefficient > 3.6, the median (interquartile range) was 69 (60-84) mmHg before lipid and 89 (80-96) mmHg after lipid administration.

CONCLUSION:

Most patients in this cohort survived. Lipophilicity was not correlated with survival or the observed changes in blood pressure. The study did not address the efficacy of lipid emulsion.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Intoxicação / Emulsões Gordurosas Intravenosas Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Toxicol (Phila) Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Intoxicação / Emulsões Gordurosas Intravenosas Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Toxicol (Phila) Ano de publicação: 2023 Tipo de documento: Article