Intravenous ketamine sedation for painful oncology procedures

Summary Background:  The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for painful procedures. Methods:  A single‐agent, procedural sedation protocol using titrated doses of ketamine i.v. (maximum...

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Published inPediatric anesthesia Vol. 15; no. 2; pp. 131 - 138
Main Authors EVANS, DAN, TURNHAM, LUCY, BARBOUR, KATHRYN, KOBE, JEFF, WILSON, LAURA, VANDEBEEK, CHRISTINE, J. MONTGOMERY, CAROLYNE, ROGERS, PAUL
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.02.2005
Blackwell
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Online AccessGet full text
ISSN1155-5645
1460-9592
DOI10.1111/j.1460-9592.2005.01407.x

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Abstract Summary Background:  The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for painful procedures. Methods:  A single‐agent, procedural sedation protocol using titrated doses of ketamine i.v. (maximum 2 mg·kg−1) was conducted in outpatient pediatric oncology patients undergoing lumbar puncture (LP), bone marrow biopsy/aspiration (BMBx/A) or combination (LP/BMBx/A) in a tertiary care setting. The efficacy of analgesia and sedation (ability to perform the procedure), procedure duration, recovery time and the occurrence of adverse events are described. Results:  Fifty‐eight subjects of a median age of 5 years (1–13) and median weight of 20 kg (10.5–68) underwent 119 sedations. An LP was performed in 73% of cases, a BMBx/A in 13% and LP/BMBx/A in 13%. Efficacy was 100% and the mean dose of ketamine was 1.3 mg·kg−1 (0.4). The mean duration of the procedure was 6.6 min (4.2) and the recovery time was 11 min (4–45). Two subjects (1.7%) had a hypoxemia (SpO2 of <94%). No major airway complications occurred. The prevalence of hypertension (systolic > 20% at 5 min) was 54%. The median pain visual analogue score (VAS) for an observer was 0 (range 0–3) and caregiver was 0 (range 0–4). The median VAS for satisfaction (observer) was 10 (range 7–10) and caregiver VAS was also 10 (range 5–10). At 24 h after discharge, the incidence of bad dreams was 3.3%; vomiting, 10.8%; and abnormal behavior, 4.2%. Conclusion:  Ketamine i.v. up to 2 mg·kg−1 is an effective sedative for oncology procedures using a defined protocol.
AbstractList The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for painful procedures. A single-agent, procedural sedation protocol using titrated doses of ketamine i.v. (maximum 2 mg.kg(-1)) was conducted in outpatient pediatric oncology patients undergoing lumbar puncture (LP), bone marrow biopsy/aspiration (BMBx/A) or combination (LP/BMBx/A) in a tertiary care setting. The efficacy of analgesia and sedation (ability to perform the procedure), procedure duration, recovery time and the occurrence of adverse events are described. Fifty-eight subjects of a median age of 5 years (1-13) and median weight of 20 kg (10.5-68) underwent 119 sedations. An LP was performed in 73% of cases, a BMBx/A in 13% and LP/BMBx/A in 13%. Efficacy was 100% and the mean dose of ketamine was 1.3 mg.kg(-1) (0.4). The mean duration of the procedure was 6.6 min (4.2) and the recovery time was 11 min (4-45). Two subjects (1.7%) had a hypoxemia (SpO2 of <94%). No major airway complications occurred. The prevalence of hypertension (systolic > 20% at 5 min) was 54%. The median pain visual analogue score (VAS) for an observer was 0 (range 0-3) and caregiver was 0 (range 0-4). The median VAS for satisfaction (observer) was 10 (range 7-10) and caregiver VAS was also 10 (range 5-10). At 24 h after discharge, the incidence of bad dreams was 3.3%; vomiting, 10.8%; and abnormal behavior, 4.2%. Ketamine i.v. up to 2 mg.kg(-1) is an effective sedative for oncology procedures using a defined protocol.
The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for painful procedures.BACKGROUNDThe aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for painful procedures.A single-agent, procedural sedation protocol using titrated doses of ketamine i.v. (maximum 2 mg.kg(-1)) was conducted in outpatient pediatric oncology patients undergoing lumbar puncture (LP), bone marrow biopsy/aspiration (BMBx/A) or combination (LP/BMBx/A) in a tertiary care setting. The efficacy of analgesia and sedation (ability to perform the procedure), procedure duration, recovery time and the occurrence of adverse events are described.METHODSA single-agent, procedural sedation protocol using titrated doses of ketamine i.v. (maximum 2 mg.kg(-1)) was conducted in outpatient pediatric oncology patients undergoing lumbar puncture (LP), bone marrow biopsy/aspiration (BMBx/A) or combination (LP/BMBx/A) in a tertiary care setting. The efficacy of analgesia and sedation (ability to perform the procedure), procedure duration, recovery time and the occurrence of adverse events are described.Fifty-eight subjects of a median age of 5 years (1-13) and median weight of 20 kg (10.5-68) underwent 119 sedations. An LP was performed in 73% of cases, a BMBx/A in 13% and LP/BMBx/A in 13%. Efficacy was 100% and the mean dose of ketamine was 1.3 mg.kg(-1) (0.4). The mean duration of the procedure was 6.6 min (4.2) and the recovery time was 11 min (4-45). Two subjects (1.7%) had a hypoxemia (SpO2 of <94%). No major airway complications occurred. The prevalence of hypertension (systolic > 20% at 5 min) was 54%. The median pain visual analogue score (VAS) for an observer was 0 (range 0-3) and caregiver was 0 (range 0-4). The median VAS for satisfaction (observer) was 10 (range 7-10) and caregiver VAS was also 10 (range 5-10). At 24 h after discharge, the incidence of bad dreams was 3.3%; vomiting, 10.8%; and abnormal behavior, 4.2%.RESULTSFifty-eight subjects of a median age of 5 years (1-13) and median weight of 20 kg (10.5-68) underwent 119 sedations. An LP was performed in 73% of cases, a BMBx/A in 13% and LP/BMBx/A in 13%. Efficacy was 100% and the mean dose of ketamine was 1.3 mg.kg(-1) (0.4). The mean duration of the procedure was 6.6 min (4.2) and the recovery time was 11 min (4-45). Two subjects (1.7%) had a hypoxemia (SpO2 of <94%). No major airway complications occurred. The prevalence of hypertension (systolic > 20% at 5 min) was 54%. The median pain visual analogue score (VAS) for an observer was 0 (range 0-3) and caregiver was 0 (range 0-4). The median VAS for satisfaction (observer) was 10 (range 7-10) and caregiver VAS was also 10 (range 5-10). At 24 h after discharge, the incidence of bad dreams was 3.3%; vomiting, 10.8%; and abnormal behavior, 4.2%.Ketamine i.v. up to 2 mg.kg(-1) is an effective sedative for oncology procedures using a defined protocol.CONCLUSIONKetamine i.v. up to 2 mg.kg(-1) is an effective sedative for oncology procedures using a defined protocol.
Summary Background:  The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for painful procedures. Methods:  A single‐agent, procedural sedation protocol using titrated doses of ketamine i.v. (maximum 2 mg·kg−1) was conducted in outpatient pediatric oncology patients undergoing lumbar puncture (LP), bone marrow biopsy/aspiration (BMBx/A) or combination (LP/BMBx/A) in a tertiary care setting. The efficacy of analgesia and sedation (ability to perform the procedure), procedure duration, recovery time and the occurrence of adverse events are described. Results:  Fifty‐eight subjects of a median age of 5 years (1–13) and median weight of 20 kg (10.5–68) underwent 119 sedations. An LP was performed in 73% of cases, a BMBx/A in 13% and LP/BMBx/A in 13%. Efficacy was 100% and the mean dose of ketamine was 1.3 mg·kg−1 (0.4). The mean duration of the procedure was 6.6 min (4.2) and the recovery time was 11 min (4–45). Two subjects (1.7%) had a hypoxemia (SpO2 of <94%). No major airway complications occurred. The prevalence of hypertension (systolic > 20% at 5 min) was 54%. The median pain visual analogue score (VAS) for an observer was 0 (range 0–3) and caregiver was 0 (range 0–4). The median VAS for satisfaction (observer) was 10 (range 7–10) and caregiver VAS was also 10 (range 5–10). At 24 h after discharge, the incidence of bad dreams was 3.3%; vomiting, 10.8%; and abnormal behavior, 4.2%. Conclusion:  Ketamine i.v. up to 2 mg·kg−1 is an effective sedative for oncology procedures using a defined protocol.
Background:  The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for painful procedures. Methods:  A single‐agent, procedural sedation protocol using titrated doses of ketamine i.v. (maximum 2 mg·kg −1 ) was conducted in outpatient pediatric oncology patients undergoing lumbar puncture (LP), bone marrow biopsy/aspiration (BMBx/A) or combination (LP/BMBx/A) in a tertiary care setting. The efficacy of analgesia and sedation (ability to perform the procedure), procedure duration, recovery time and the occurrence of adverse events are described. Results:  Fifty‐eight subjects of a median age of 5 years (1–13) and median weight of 20 kg (10.5–68) underwent 119 sedations. An LP was performed in 73% of cases, a BMBx/A in 13% and LP/BMBx/A in 13%. Efficacy was 100% and the mean dose of ketamine was 1.3 mg·kg −1 (0.4). The mean duration of the procedure was 6.6 min (4.2) and the recovery time was 11 min (4–45). Two subjects (1.7%) had a hypoxemia (SpO 2 of <94%). No major airway complications occurred. The prevalence of hypertension (systolic > 20% at 5 min) was 54%. The median pain visual analogue score (VAS) for an observer was 0 (range 0–3) and caregiver was 0 (range 0–4). The median VAS for satisfaction (observer) was 10 (range 7–10) and caregiver VAS was also 10 (range 5–10). At 24 h after discharge, the incidence of bad dreams was 3.3%; vomiting, 10.8%; and abnormal behavior, 4.2%. Conclusion:  Ketamine i.v. up to 2 mg·kg −1 is an effective sedative for oncology procedures using a defined protocol.
Author EVANS, DAN
ROGERS, PAUL
TURNHAM, LUCY
WILSON, LAURA
J. MONTGOMERY, CAROLYNE
KOBE, JEFF
VANDEBEEK, CHRISTINE
BARBOUR, KATHRYN
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Issue 2
Keywords lumbar puncture
Intravenous administration
bone marrow biopsy
procedural sedation
Glutamate receptor
Sedation
Pain
Ketamine
General anesthetic
Biopsy
Bone marrow
Anesthesia
Antagonist
NMDA receptor
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Snippet Summary Background:  The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by...
Background:  The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist...
The aim of the study was to determine the efficacy and adverse effects of intravenous (i.v.) ketamine sedation administered by nonanesthetist physicians for...
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StartPage 131
SubjectTerms Adolescent
Analgesics - administration & dosage
Analgesics - adverse effects
Analgesics - therapeutic use
Anesthesia
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Anesthetics, Local - therapeutic use
Biological and medical sciences
Biopsy, Needle - adverse effects
bone marrow biopsy
Bone Marrow Examination - adverse effects
Child
Child, Preschool
Dose-Response Relationship, Drug
Female
Humans
Infant
Injections, Intravenous - methods
ketamine
Ketamine - administration & dosage
Ketamine - adverse effects
Ketamine - therapeutic use
Lidocaine - therapeutic use
lumbar puncture
Male
Medical sciences
Pain - etiology
Pain - prevention & control
Pain Measurement - methods
Patient Satisfaction
Prilocaine - therapeutic use
procedural sedation
Spinal Puncture - adverse effects
Tetracaine - therapeutic use
Treatment Outcome
Title Intravenous ketamine sedation for painful oncology procedures
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https://www.ncbi.nlm.nih.gov/pubmed/15675930
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Volume 15
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