Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Treston G 2004 Australia | 272 consecutive children undergoing ketamine sedation in the emergency department. Results available on 257. Authors examined the relationship between fasting time and incidence of vomiting. Patients were given IV ketamine | Prospective cohort study | Incidence of vomiting in children fasted less than one hour | 2/30 (6%) | Patients fasted more than 3 hours are grouped together rather than discriminated at 6 hours. Further information was sought from the original author but data differentiating patients at 6 hours was not available. |
Incidence of vomiting in children fasted 1-3 hours | 14/100 (14%) | ||||
Incidence of vomiting in children fasted more than 3 hours | 20/127 (15.7%) | ||||
Statistical trend of vomiting rates | Non significant trend towards increased vomiting with increased fasting time. p=0.08 | ||||
Effect of age on vomiting rates | More common in older age groups | ||||
Incidence of aspiration pneumonitis | There was no evidence of aspiration in any patients | ||||
Roback MG 2004 USA | Database of 2085 children undergoing procedural sedation by emergency physicians. Age range 19 days to 32.1 years in database. Median age was 6.7 years. Fasting time documented in 1555 patients. Analysis of complication rates was divided into 0 to 2, 2 to 4, 4 to 6, 6 to 8 and greater than 8 and not documented. Sedation options were ketamine (IV or IM), midazolam/ketamine, midazolam/fentanyl, midazolam, midazolam/morphine, other. | Prospective cohort | Overall incidence of serious adverse events | 172/2085 (8.2%) of all patients had a respiratory adverse event (hypoxia, desaturation, apnea, laryngospasm, aspiration) | Incomplete data collection (a quarter of charts were not completed). Specific influence of fasting time on ketamine patients unknown as all agents reported as a group. No differentiation of food vs fluids fasting. |
Use of ketamine | 57% of patients (1199) had ketamine as the sole sedative agent. | ||||
Adverse events when ketamine used alone | 70/1199 (5.8%) had respiratory adverse event. 129/1199 vomited. | ||||
Influence of fasting time to adverse events | 7.3% for 0-2 hours; 7.7% for 2-4 hours; 7.2% for 4-6 hours; 9.6% for 6-8 hours; 6.3% for >8 hours. p=NS | ||||
Respiratory adverse events for different agents | At 5.8% ketamine had the lowest incidence of respiratory complications. | ||||
Vomiting with ketamine | 129/1199 (10.8%) of patients vomited with ketamine (highest incidence between agents range 0.9-10.8%) | ||||
IM or IV ketamine? | 1022 had IV ketamine, 177 had IM ketamine | ||||
Agrawal D, et al. 2003 USA | 1014 patients undergoing procedural sedation in a paediatric emergency department. A variety of different agents were used but 474 (47%) had ketamine. Fasting time against established guidelines was recorded (<6 months 4- 6 hours, 6-36 months 6 hours, >36 months 6-8 hours). Or 2 hours for clear liquids in all age groups. | Prospective case series | Data collection standards | 905 (98%) had fasting status recorded. | Less than 14 patients aged less than 6 months in the study. 11% of patients did not have fasting time documented. Numerous agents used so difficult to determine if there are drug specific differences. |
Number of minor adverse events (e.g. desaturation, emesis, aspiration, hypotension, laryngospasm) | 75 events in 66 patients. All succesfully treated with minor intervention (e.g. airway repositioning, suction etc.) | ||||
No of patients with evidence of pulmonary aspiration | No events (1 sided 97.5% confidence interval 0-0.4%) | ||||
No of patients requiring admission | 2 patients admitted following sedation. One had multiple medical problems and received pentobarbital. One had a generalised fit with ketamine 2 hours post injection. | ||||
Fasting status | 396/905 (44%) of patients met fasting status. 509/905 (56%) did not | ||||
Adverse events in relation to fasting status | 32/396 (8.1%, 95CI 5.6% to 11.2%) of fasted patients vs. 35/509 (6.9%, 95% CI 4.8% to 9.4%) for those not fasted. p=0.49 | ||||
Adverse events in relation to time of fasting | Median fasting duration in patients with adverse events was 7.3 hours for solids and 6.6 hours for fluids vs. 6.8 hours and 6.0 hours for those without. p=0.13 | ||||
Emesis in relation to time of fasting | Median duration fasting in patients with emesis was 6.8 hours for solids and 5.8 hours for fluids vs. 6.8 hours and 6.0 hours p=0.70 |