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Evaluation of inhaled nitric oxide (iNO) treatment for moderate-to-severe ARDS in critically ill patients with COVID-19: a multicenter cohort study.
Al Sulaiman, Khalid; Korayem, Ghazwa B; Altebainawi, Ali F; Al Harbi, Shmeylan; Alissa, Abdulrahman; Alharthi, Abdullah; Kensara, Raed; Alfahed, Amjaad; Vishwakarma, Ramesh; Al Haji, Hussain; Almohaimid, Naif; Al Zumai, Omar; Alrubayan, Fahad; Asiri, Abdulmajid; Alkahtani, Nasser; Alolayan, Abdulaziz; Alsohimi, Samiah; Melibari, Nawal; Almagthali, Alaa; Aljahdali, Seba; Alenazi, Abeer A; Alsaeedi, Alawi S; Al Ghamdi, Ghassan; Al Faris, Omar; Alqahtani, Joud; Al Qahtani, Jalal; Alshammari, Khalid A; Alshammari, Khalil I; Aljuhani, Ohoud.
  • Al Sulaiman K; Pharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia. alsulaimankh@hotmail.com.
  • Korayem GB; College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia. alsulaimankh@hotmail.com.
  • Altebainawi AF; King Abdullah International Medical Research Center, King Abdulaziz Medical City (KAMC), Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia. alsulaimankh@hotmail.com.
  • Al Harbi S; Department of Pharmacy Practice, College of Pharmacy, Princess Nourah Bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia. alsulaimankh@hotmail.com.
  • Alissa A; Saudi Critical Care Pharmacy Research (SCAPE) Platform, Riyadh, Saudi Arabia. alsulaimankh@hotmail.com.
  • Alharthi A; Department of Pharmacy Practice, College of Pharmacy, Princess Nourah Bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia.
  • Kensara R; Pharmaceutical Care Services, King Salman Specialist Hospital, Hail Health Cluster, Hail, Saudi Arabia.
  • Alfahed A; Pharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Vishwakarma R; College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Al Haji H; King Abdullah International Medical Research Center, King Abdulaziz Medical City (KAMC), Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Almohaimid N; Pharmaceutical Care Services, King Abdullah bin Abdulaziz University Hospital, Riyadh, Saudi Arabia.
  • Al Zumai O; Pharmaceutical Care Department, King Abdulaziz Medical City, Jeddah, Saudi Arabia.
  • Alrubayan F; Pharmaceutical Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Asiri A; College of Pharmacy, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Alkahtani N; King Abdullah International Medical Research Center, King Abdulaziz Medical City (KAMC), Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Alolayan A; Department of Pharmacy Practice, College of Pharmacy, Princess Nourah Bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia.
  • Alsohimi S; Statistics Department, European Organization for Research and Treatment of Cancer (EORTC) Headquarters, Brussels, Belgium.
  • Melibari N; Respiratory Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Almagthali A; Respiratory Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Aljahdali S; Respiratory Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Alenazi AA; King Abdullah International Medical Research Center, King Abdulaziz Medical City (KAMC), Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Alsaeedi AS; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Al Ghamdi G; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Al Faris O; King Abdullah International Medical Research Center, King Abdulaziz Medical City (KAMC), Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.
  • Alqahtani J; Intensive Care Department, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
  • Al Qahtani J; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Alshammari KA; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Alshammari KI; Pharmaceutical Services Department, King Abdulaziz University Hospital, Jeddah, Saudi Arabia.
  • Aljuhani O; Phamacy Department, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
Crit Care ; 26(1): 304, 2022 10 03.
Article in English | MEDLINE | ID: covidwho-2053942
ABSTRACT

BACKGROUND:

Inhaled nitric oxide (iNO) is used as rescue therapy in patients with refractory hypoxemia due to severe COVID-19 acute respiratory distress syndrome (ARDS) despite the recommendation against the use of this treatment. To date, the effect of iNO on the clinical outcomes of critically ill COVID-19 patients with moderate-to-severe ARDS remains arguable. Therefore, this study aimed to evaluate the use of iNO in critically ill COVID-19 patients with moderate-to-severe ARDS.

METHODS:

This multicenter, retrospective cohort study included critically ill adult patients with confirmed COVID-19 treated from March 01, 2020, until July 31, 2021. Eligible patients with moderate-to-severe ARDS were subsequently categorized into two groups based on inhaled nitric oxide (iNO) use throughout their ICU stay. The primary endpoint was the improvement in oxygenation parameters 24 h after iNO use. Other outcomes were considered secondary. Propensity score matching (12) was used based on the predefined criteria.

RESULTS:

A total of 1598 patients were screened, and 815 were included based on the eligibility criteria. Among them, 210 patients were matched based on predefined criteria. Oxygenation parameters (PaO2, FiO2 requirement, P/F ratio, oxygenation index) were significantly improved 24 h after iNO administration within a median of six days of ICU admission. However, the risk of 30-day and in-hospital mortality were found to be similar between the two groups (HR 1.18; 95% CI 0.77, 1.82; p = 0.45 and HR 1.40; 95% CI 0.94, 2.11; p= 0.10, respectively). On the other hand, ventilator-free days (VFDs) were significantly fewer, and  ICU and hospital LOS were significantly longer in the iNO group. In addition, patients who received iNO had higher odds of acute kidney injury (AKI) (OR (95% CI) 2.35 (1.30, 4.26), p value = 0.005) and hospital/ventilator-acquired pneumonia (OR (95% CI) 3.2 (1.76, 5.83), p value = 0.001).

CONCLUSION:

In critically ill COVID-19 patients with moderate-to-severe ARDS, iNO rescue therapy is associated with improved oxygenation parameters but no mortality benefits. Moreover, iNO use is associated with higher odds of AKI, pneumonia, longer LOS, and fewer VFDs.
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Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Acute Kidney Injury / COVID-19 / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Limits: Adult / Humans Language: English Journal: Crit Care Year: 2022 Document Type: Article Affiliation country: S13054-022-04158-y

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Respiratory Distress Syndrome / Acute Kidney Injury / COVID-19 / COVID-19 Drug Treatment Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Limits: Adult / Humans Language: English Journal: Crit Care Year: 2022 Document Type: Article Affiliation country: S13054-022-04158-y