Considerations for physicians using ketamine for sedation of children in emergency departments
Ketamine use in emergency departments (EDs) for procedural sedation and analgesia is becoming increasingly common. However, few studies have examined patient factors related to adverse events associated with ketamine. This study investigated factors for consideration when using ketamine to sedate pe...
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| Published in | Clinical and experimental emergency medicine Vol. 4; no. 4; pp. 244 - 249 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Korea (South)
The Korean Society of Emergency Medicine
01.12.2017
대한응급의학회 |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2383-4625 2383-4625 |
| DOI | 10.15441/ceem.16.155 |
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| Abstract | Ketamine use in emergency departments (EDs) for procedural sedation and analgesia is becoming increasingly common. However, few studies have examined patient factors related to adverse events associated with ketamine. This study investigated factors for consideration when using ketamine to sedate pediatric ED patients.
The study included pediatric patients receiving ketamine for laceration repair in the ED. Before sedation, information was collected about upper respiratory tract infection symptoms, allergy history, and fasting time. Patients received 2 mg/kg ketamine intravenously or 4 mg/kg ketamine intramuscularly. The primary outcomes were adverse events due to ketamine.
We studied 116 patients aged 8 months to 7 years (2.8±1.5 years). The group with adverse events was significantly younger on average than the group without adverse events (2.5±1.5 vs. 3.1±1.5, P=0.028). Upper respiratory tract infection symptoms were not significant variables affecting ketamine sedation (48.9% vs. 43.7%, P=0.719). There was no significant association between duration of fasting and adverse events (P=0.073 and P=0.897, respectively), or between food type and adverse events (P=0.734). However, the number of attempts to sedate and ketamine dose correlated with adverse events (P<0.001 and P=0.022, respectively). In multiple logistic regression analysis, intravenous injection and ketamine dose were significant factors (odds ratio, 16.77; 95% confidence interval, 1.78 to 498.54; odds ratio, 4.37; 95% confidence interval, 1.59 to 22.9, respectively).
Emergency medicine physicians should consider injection type and ketamine dose when using ketamine sedation while suturing lacerations. |
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| AbstractList | Ketamine use in emergency departments (EDs) for procedural sedation and analgesia is becoming increasingly common. However, few studies have examined patient factors related to adverse events associated with ketamine. This study investigated factors for consideration when using ketamine to sedate pediatric ED patients.
The study included pediatric patients receiving ketamine for laceration repair in the ED. Before sedation, information was collected about upper respiratory tract infection symptoms, allergy history, and fasting time. Patients received 2 mg/kg ketamine intravenously or 4 mg/kg ketamine intramuscularly. The primary outcomes were adverse events due to ketamine.
We studied 116 patients aged 8 months to 7 years (2.8±1.5 years). The group with adverse events was significantly younger on average than the group without adverse events (2.5±1.5 vs. 3.1±1.5, P=0.028). Upper respiratory tract infection symptoms were not significant variables affecting ketamine sedation (48.9% vs. 43.7%, P=0.719). There was no significant association between duration of fasting and adverse events (P=0.073 and P=0.897, respectively), or between food type and adverse events (P=0.734). However, the number of attempts to sedate and ketamine dose correlated with adverse events (P<0.001 and P=0.022, respectively). In multiple logistic regression analysis, intravenous injection and ketamine dose were significant factors (odds ratio, 16.77; 95% confidence interval, 1.78 to 498.54; odds ratio, 4.37; 95% confidence interval, 1.59 to 22.9, respectively).
Emergency medicine physicians should consider injection type and ketamine dose when using ketamine sedation while suturing lacerations. Ketamine use in emergency departments (EDs) for procedural sedation and analgesia is becoming increasingly common. However, few studies have examined patient factors related to adverse events associated with ketamine. This study investigated factors for consideration when using ketamine to sedate pediatric ED patients.OBJECTIVEKetamine use in emergency departments (EDs) for procedural sedation and analgesia is becoming increasingly common. However, few studies have examined patient factors related to adverse events associated with ketamine. This study investigated factors for consideration when using ketamine to sedate pediatric ED patients.The study included pediatric patients receiving ketamine for laceration repair in the ED. Before sedation, information was collected about upper respiratory tract infection symptoms, allergy history, and fasting time. Patients received 2 mg/kg ketamine intravenously or 4 mg/kg ketamine intramuscularly. The primary outcomes were adverse events due to ketamine.METHODSThe study included pediatric patients receiving ketamine for laceration repair in the ED. Before sedation, information was collected about upper respiratory tract infection symptoms, allergy history, and fasting time. Patients received 2 mg/kg ketamine intravenously or 4 mg/kg ketamine intramuscularly. The primary outcomes were adverse events due to ketamine.We studied 116 patients aged 8 months to 7 years (2.8±1.5 years). The group with adverse events was significantly younger on average than the group without adverse events (2.5±1.5 vs. 3.1±1.5, P=0.028). Upper respiratory tract infection symptoms were not significant variables affecting ketamine sedation (48.9% vs. 43.7%, P=0.719). There was no significant association between duration of fasting and adverse events (P=0.073 and P=0.897, respectively), or between food type and adverse events (P=0.734). However, the number of attempts to sedate and ketamine dose correlated with adverse events (P<0.001 and P=0.022, respectively). In multiple logistic regression analysis, intravenous injection and ketamine dose were significant factors (odds ratio, 16.77; 95% confidence interval, 1.78 to 498.54; odds ratio, 4.37; 95% confidence interval, 1.59 to 22.9, respectively).RESULTSWe studied 116 patients aged 8 months to 7 years (2.8±1.5 years). The group with adverse events was significantly younger on average than the group without adverse events (2.5±1.5 vs. 3.1±1.5, P=0.028). Upper respiratory tract infection symptoms were not significant variables affecting ketamine sedation (48.9% vs. 43.7%, P=0.719). There was no significant association between duration of fasting and adverse events (P=0.073 and P=0.897, respectively), or between food type and adverse events (P=0.734). However, the number of attempts to sedate and ketamine dose correlated with adverse events (P<0.001 and P=0.022, respectively). In multiple logistic regression analysis, intravenous injection and ketamine dose were significant factors (odds ratio, 16.77; 95% confidence interval, 1.78 to 498.54; odds ratio, 4.37; 95% confidence interval, 1.59 to 22.9, respectively).Emergency medicine physicians should consider injection type and ketamine dose when using ketamine sedation while suturing lacerations.CONCLUSIONEmergency medicine physicians should consider injection type and ketamine dose when using ketamine sedation while suturing lacerations. Objective Ketamine use in emergency departments (EDs) for procedural sedation and analgesia is becoming increasingly common. However, few studies have examined patient factors related to adverse events associated with ketamine. This study investigated factors for consideration when using ketamine to sedate pediatric ED patients. Methods The study included pediatric patients receiving ketamine for laceration repair in the ED. Before sedation, information was collected about upper respiratory tract infection symptoms, allergy history, and fasting time. Patients received 2 mg/kg ketamine intravenously or 4 mg/kg ketamine intramuscularly. The primary outcomes were adverse events due to ketamine. Results We studied 116 patients aged 8 months to 7 years (2.8±1.5 years). The group with adverse events was significantly younger on average than the group without adverse events (2.5±1.5 vs. 3.1±1.5, P=0.028). Upper respiratory tract infection symptoms were not significant variables affecting ketamine sedation (48.9% vs. 43.7%, P=0.719). There was no significant association between duration of fasting and adverse events (P=0.073 and P=0.897, respectively), or between food type and adverse events (P=0.734). However, the number of attempts to sedate and ketamine dose correlated with adverse events (P<0.001 and P=0.022, respectively). In multiple logistic regression analysis, intravenous injection and ketamine dose were significant factors (odds ratio, 16.77; 95% confidence interval, 1.78 to 498.54; odds ratio, 4.37; 95% confidence interval, 1.59 to 22.9, respectively). Conclusion Emergency medicine physicians should consider injection type and ketamine dose when using ketamine sedation while suturing lacerations. KCI Citation Count: 0 Objective Ketamine use in emergency departments (EDs) for procedural sedation and analgesia is becoming increasingly common. However, few studies have examined patient factors related to adverse events associated with ketamine. This study investigated factors for consideration when using ketamine to sedate pediatric ED patients. Methods The study included pediatric patients receiving ketamine for laceration repair in the ED. Before sedation, information was collected about upper respiratory tract infection symptoms, allergy history, and fasting time. Patients received 2 mg/kg ketamine intravenously or 4 mg/kg ketamine intramuscularly. The primary outcomes were adverse events due to ketamine. Results We studied 116 patients aged 8 months to 7 years (2.8±1.5 years). The group with adverse events was significantly younger on average than the group without adverse events (2.5±1.5 vs. 3.1±1.5, P=0.028). Upper respiratory tract infection symptoms were not significant variables affecting ketamine sedation (48.9% vs. 43.7%, P=0.719). There was no significant association between duration of fasting and adverse events (P=0.073 and P=0.897, respectively), or between food type and adverse events (P=0.734). However, the number of attempts to sedate and ketamine dose correlated with adverse events (P<0.001 and P=0.022, respectively). In multiple logistic regression analysis, intravenous injection and ketamine dose were significant factors (odds ratio, 16.77; 95% confidence interval, 1.78 to 498.54; odds ratio, 4.37; 95% confidence interval, 1.59 to 22.9, respectively). Conclusion Emergency medicine physicians should consider injection type and ketamine dose when using ketamine sedation while suturing lacerations. |
| Author | Lee, Bora Choi, Hanbyul Kim, Woo Sung Kim, Ho Jung Choi, Hyo Jeong Ku, Ji Yeon |
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| Keywords | Ketamine Adverse events Emergency service, hospital Pediatric sedation Monitoring |
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| References_xml | – start-page: 247 volume-title: Clinical policy: procedural sedation and analgesia in the emergency department year: 2014 ident: ref11 – start-page: 10 volume-title: Ketamine: review of its pharmacology and its use in pediatric anesthesia year: 1999 ident: ref27 – start-page: 460 volume-title: Clinical practice guideline for emergency department ketamine dissociative sedation in children year: 2004 ident: ref6 – start-page: 557 volume-title: Does ondansetron have an effect on intramuscular ketamine-associated vomiting in children? A prospective, randomised, open, controlled study year: 2014 ident: ref20 – start-page: 740 volume-title: Pulse oximetry in pediatric practice year: 2011 ident: ref16 – start-page: 178 volume-title: Is local anesthesia necessary in ketamine sedation for pediatric facial laceration repair? A double-blind, randomized, controlled study year: 2014 ident: ref4 – start-page: 483 volume-title: Adverse events of procedural sedation and analgesia in a pediatric emergency department year: 1999 ident: ref22 – start-page: 1004 volume-title: Practice guidelines for sedation and analgesia by non-anesthesiologists year: 2002 ident: ref8 – start-page: 636 volume-title: Preprocedural fasting state and adverse events in children undergoing procedural sedation and analgesia in a pediatric emergency department year: 2003 ident: ref9 – start-page: 766 volume-title: Procedural sedation and analgesia in children year: 2006 ident: ref1 – start-page: 938 volume-title: Sedation and analgesia for procedures in children year: 2000 ident: ref5 – start-page: 688 volume-title: Intramuscular ketamine for pediatric sedation in the emergency department: safety profile in 1,022 cases year: 1998 ident: ref25 – year: 2004 ident: ref2 – start-page: 1011 volume-title: Normal ranges of heart rate and respiratory rate in children from birth to 18 years of age: a systematic review of observational studies year: 2011 ident: ref17 – start-page: 42 volume-title: Epilepsy in the accident and emergency department year: 1994 ident: ref26 – start-page: 492 volume-title: Inadvertent ketamine overdose in children: clinical manifestations and outcome year: 1999 ident: ref23 – start-page: 495 volume-title: Ketamine sedation after administration of oral contrast: a retrospective cohort study year: 2015 ident: ref10 – start-page: 1128 volume-title: Adjunctive atropine versus metoclopramide: can we reduce ketamine-associated vomiting in young children? a prospective, randomized, open, controlled study year: 2012 ident: ref7 – start-page: 303 volume-title: Korean guidelines for pediatric procedural sedation and analgesia year: 2012 ident: ref3 – start-page: e20161212 volume-title: Guidelines for monitoring and management of pediatric patients before, during, and after sedation for diagnostic and therapeutic procedures: update 2016 year: 2016 ident: ref12 – start-page: 145 volume-title: Prolonged pre-procedure fasting time is unnecessary when using titrated intravenous ketamine for paediatric procedural sedation year: 2004 ident: ref19 – start-page: 651 volume-title: Members of task force on prolonged apnea: reports of the task force on prolonged apnea of the American Academy of Pediatrics year: 1978 ident: ref18 – start-page: 705 volume-title: Comparison of adverse events and satisfaction between iv and im routes for ketamine sedation in pediatric facial laceration repair in the emergency department year: 2012 ident: ref15 – start-page: 309 volume-title: Is prophylactic atropine necessary during ketamine sedation in children? year: 2013 ident: ref21 – start-page: 239 volume-title: Morbidity and mortality in pediatric anesthesia year: 1994 ident: ref24 – start-page: 913 volume-title: The Vancouver sedative recovery scale for children: validation and reliability of scoring based on videotaped instruction year: 1994 ident: ref13 – start-page: 339 volume-title: Ketamine use of pediatric sedation in emergency room year: 2000 ident: ref14 |
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| SubjectTerms | adverse events emergency service, hospital ketamine monitoring Original pediatric sedation 응급의학 |
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| Title | Considerations for physicians using ketamine for sedation of children in emergency departments |
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