Ketamine administration for acute painful sickle cell crisis: A randomized controlled trial-Reference-Cited by-同舟云学术

Ketamine administration for acute painful sickle cell crisis: A randomized controlled trial

Published:2021-09-21 Issue: Volume: Page:
ISSN:1069-6563
Container-title:Academic Emergency Medicine
language:en
Short-container-title:Acad Emerg Med

Author:

Alshahrani Mohammed S.¹^ORCID,AlSulaibikh Amal H.²^ORCID,ElTahan Mohamed R.³^ORCID,AlFaraj Sukayna Z.²,Asonto Laila P.¹^ORCID,AlMulhim Abdullah A.²,AlAbbad Murad F.²,Almaghraby Nisreen²,AlJumaan Mohammed A.²^ORCID,AlJunaid Thamir O.²,Darweesh Moath N.²,AlHawaj Faisal M.²,Mahmoud Alaa M.²,Alossaimi Bader K.²,Alotaibi Shaikhah K.²,AlMutairi Talal M.²,AlSulaiman PharmD Duaa A.⁴,Alfaraj Dunya²,Alhawwas Reem²,Mbuagbaw Lawrence⁵^ORCID,Lewis Kim⁶,Verhovsek Madeleine⁶^ORCID,Crowther Mark⁶,Guyatt Gordon⁵,Alhazzani Waleed⁵^ORCID,

Affiliation:

1. Emergency and Critical Care Departments King Fahad Hospital of the University‐Imam Abdulrahman Bin Faisal University Dammam Kingdom of Saudi Arabia

2. Emergency Department King Fahad Hospital of the University‐Imam Abdulrahman Bin Faisal University Dammam Kingdom of Saudi Arabia

3. Anesthesiology Department King Fahad Hospital of the University‐Imam Abdulrahman Bin Faisal University Dammam Kingdom of Saudi Arabia

4. Pharmacy Department King Fahad Hospital of the University‐Imam Abdulrahman Bin Faisal University Dammam Kingdom of Saudi Arabia

5. Department of Health Research Methods, Evidence and Impact McMaster University Hamilton Ontario Canada

6. Department of Medicine McMaster University Hamilton Ontario Canada

Publisher

Wiley

Subject

Emergency Medicine,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/acem.14382

Reference45 articles.

1. Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significance

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4. Sickle cell disease: a new era

5. Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease

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