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. 2023 Jun 22;15(6):e40789. doi: 10.7759/cureus.40789

Table 1. Summary of included studies.

PaO2, partial pressure of oxygen in arterial blood; FiO2, fraction of inspiratory oxygen concentration; SpO2, oxygen saturation; T0, prior to ketamine use; T1, 1 h after ketamine infusion; TW, when the ketamine was discontinued; CAS, clinical asthma score

Author Year Study design Number of patients Age Mean age (years) Ketamine dose Duration Intubation Measures of improvement Results Adverse effects
Petrillo et al. [10] 2001 Prospective observational study 10 5-16 years 8 IV bolus 1 mg/kg followed by a continuous infusion of 0.75 mg/kg/h (12.5 mcg/kg/min). 1 h No CAS, peak expiratory flow, and vital signs The study showed a significant decrease in the asthma score, improved peak expiratory flow, reduced respiratory rate, and enhanced oxygen saturation Mild side effects (hallucinations, flushing, hypertension) in four patients were resolved with medication or discontinuation.
Youssef et al. [11] 1996 Retrospective chart review 17 5 months-17 years 6 +/- 5.7 IV bolus 2 mg/kg, followed by continuous infusions of 20-60 mcg/kg per minute (32 +/- 10 mcg/kg per minute) 40 h (12-96) Yes PaO2/FIO2, and dynamic compliance PaO2/FIO2 ratio significantly increased after ketamine infusion at 1, 8, and 24 h. Dynamic compliance also improved. One patient required glycopyrrolate for airway secretions, while another needed diazepam for ketamine-related hallucinations
Kshirsagar et al. [12] 2013 Prospective observational study 20 2 months-2 years - IV bolus 1 mg/kg followed by a continuous infusion of 10 mcg/kg/min (continuous infusion was given in 14 pts) Average 15 h No Uyan score and SpO2 Uyan score significantly improved (T0: 13.14 ± 1.17, T1: 9.82 ± 1.21, TW: 0.5 ± 0.65). SpO2 also showed significant improvement (T0: 87.71% ± 2.05%, T1: 92.64% ± 2.46%, TW: 99.5% ± 0.51%). None
Allen and Macias [13] 2005 Double-blinded, randomized, placebo-controlled trial 68 2-18 years 6.1 +/- 4.0 IV bolus 0.2 mg/kg followed by a 2-h ketamine infusion at 0.5 mg/kg/h 2 h No Pulmonary Index Score No significant difference between groups None
Tiwari et al. [14] 2016 Randomized, open-label, controlled trial 48 16 months-12 years 4 0.5 mg/kg bolus over 20 min, followed by continuous infusion of 0.6 mg/kg/h for 3 h 3 h No PRAM score Similar primary outcomes were observed in both groups: ketamine (4.00 ± 1.25) and aminophylline (4.17 ± 1.68) with respect to PRAM score changes.   In the ketamine group, two patients experienced hypertension. Tachycardia was observed in both groups at enrollment and persisted after 3 h. Aside from one episode of vomiting in a patient from the ketamine group, no other adverse effects were reported in either group