Received 25 November 2015; accepted 10 January 2016; published 13 January 2016
Pain remains one of the most common chief complaints for adults presenting to emergency departments (ED) nationwide. Chest pain, abdominal pain, back pain, headache and injuries are cited as the top five reasons for ED presentation based on national ED survey data from 2006 and 2011   . These same data report that approximately half of all patients presenting to the ED describe their pain as moderate (25%) or severe (20.4%)  . Depending on the nature and severity of pain, the standard of care for initial treatment of pain in the ED involves using non-specific analgesics such as a non-steroidal anti-inflammatory agent or an opioid  .
For some patients, complex past medical histories and concomitant disease states render standard approaches inadequate to treat their pain. In such cases, an alternative analgesic agent such as ketamine should be considered. Ketamine has been shown to be a beneficial analgesic agent in the ED, particularly in patients with opioid-resistant pain (sickle-cell crisis, chronic pain such as cancer and palliative care) or trauma patients who are hemodynamically unstable   . The use of ketamine in the ED has been viewed as favorable by both patients and ED physicians  .
Ketamine is a potent noncompetitive N-methyl-D-aspartate (NMDA) antagonist, best known for its anesthetic properties. At standard doses, it produces profound and rapid anesthesia and analgesia with minimal to no respiratory or hemodynamic compromise and has a predictable duration of action with a relatively short elimination half-life   . At subdissociative doses of 0.1 - 0.5 mg/kg, ketamine provides effective analgesic properties, when used alone or as an adjunct to opioid analgesics, with less pronounced psychoactive effects   . Additionally, ketamine has a wide margin of safety minimizing the concern for accidental overdose  . For these reasons, low-dose ketamine has gained favor as an option for pain management in the ED as reflected by the increased volume of research published in emergency medicine literature over recent years.
At our institution, intravenous (IV) ketamine use is restricted by indication and service, and may be ordered and administered by ED attending physicians for analgesia associated with uncontrolled, incident pain  . The purpose of this study was to evaluate current practices and prescribing patterns of ketamine in our ED and to describe clinical outcomes associated with the use of low-dose ketamine for acute pain in the ED.
This was a single-center, retrospective, descriptive analysis of clinical practice of adult patients admitted to our ED who received ketamine for acute pain. Our institutional review board reviewed and approved the study protocol prior to data collection.
Patients were identified between March 1, 2012 and March 31, 2013 via a report generated from the ED Order Entry system. To be included in the analysis, patients had to be >18 years of age and received at least one dose of ketamine for acute pain. Patients were excluded if they received ketamine in the ED for a non-pain indication or if ketamine was ordered but not administered.
Investigators collected data retrospectively, and demographic data collected included age, gender, ethnicity, comorbidities, ketamine indication, home opioid use, and baseline vitals. Outcomes assessed included doses administered, total cumulative doses, concurrent opioid administration, additional therapies used for the treatment of acute pain, and any documented efficacy and safety endpoints in patient charts. Efficacy endpoints were defined as documentation of decreased pain scores and patient reported pain relief after ketamine administration. We assessed safety endpoints by reviewing notes in the patient chart for documentation of patient reported events directly related to ketamine administration as well as medication records for the use of benzodiazepines post ketamine administration as a surrogate for serious behavioral disturbance.
During the study timeframe, 46 patients were evaluated for inclusion. Twenty-one patients were excluded: ketamine was ordered and discontinued (7 patients); ketamine was used during rapid sequence intubation (8 patients); ketamine was used for deep procedural sedation (6 patients). A total of 25 patients (54.3%) were included in the final analysis. Demographic information is outlined in Table 1. The majority of our patients was opioid tolerant (80%) and presented to the ED with a chief complaint of pain (92%). The top three pain presentations were traumatic pain related to motor vehicle crash or fall (30.4%), abdominal pain (21.7%) and oncology pain (17.4%). Ketamine was prescribed by 10 different emergency medicine attendings.
The mean initial ketamine dose was 0.12 ± 0.06 mg/kg and 8 patients (32%) received multiple doses of ketamine (1.5 ± 0.8 doses per patient). Dosing regimens are outlined in Table 2. Ketamine was used as the initial therapy in 5 patients (20%). Ketamine was used concomitantly with opioids in 23 patients (92%).
Table 1. Patient demographics.
*Mean ± SD; **n (%).
Table 2. Ketamine therapy.
*Mean ± SD; **n (%); ‡ Median (IQR); ﬡDiphenhydramine, tizanidine administered; ^1 patient received post ketamine.
In terms of efficacy, 11 patients (44%) reported adequate pain relief and 5 patients (20%) reported partial pain relief, and 3 patients (12%) reported no pain relief. Efficacy was not documented in 3 patients (12%), and the remaining 3 patients (12%) reported tolerable relief (Figure 1).
Subsequent reports of anxiety and agitation were documented on 2 patients (8%) and 1 patient received a benzodiazepine post ketamine administration. There was no documentation of adverse outcomes in 84% of patients (Figure 2). Of the 5 patient self-reported adverse events documented, there was 1 instance of feeling weird, 1 instance of feeling anxious, and 1 patient was still in pain. Although there was no documentation of unstable vital signs, there were 2 documented cases of stable vital signs. Of the 25 patients treated with ketamine for pain, 10 patients were discharged from the ED to home (40%).
The mainstay of treatment for severe acute pain in the ED is IV opioids, and although opioids can provide effective and rapid pain relief, doses needed to achieve adequate pain relief may result in over sedation and respiratory depression  . Ketamine is a recognized anesthetic and short-acting analgesic that has been in use for over 30 years  . It has a remarkable safety profile and is one of the world’s most commonly used agents for procedural sedation and general anesthesia  . Since ketamine is an NMDA receptor antagonist, it is a logical choice for controlling pain as well as inducing anesthesia   . At subdissociative doses of 0.1 - 0.5 mg/kg, ketamine provides effective analgesic properties with little to no dissociative effects   . Studies evaluating the benefit of low-dose ketamine for acute pain have produced favorable results for this indication, however, optimal dosing, specific patient populations, and additional efficacy and safety outcomes (e.g. single bolus vs. repeat dosing, need for rescue analgesia) have not been evaluated     -  .
Low-dose ketamine therapy was studied by Beaudoin, et al.  , evaluating 60 adult patients with acute pain who presented to the ED. Patients were randomized to receive low-dose ketamine as an adjunct to morphine versus standard care with morphine alone. The dosing for ketamine was either 0.15 mg/kg or 0.3 mg/kg. The investigators of the study found that low-dose ketamine is a viable analgesic adjunct to morphine for the treatment of moderate to severe acute pain based on patient-reported pain scores, and that the dosing of 0.3 mg/kg is possibly more effective than 0.15 mg/kg, but may be associated with minor adverse events, such as dysphoria and dizziness.
Figure 1. Efficacy data.
Figure 2. Safety data.
Our study is similar to the study by Beaudoin, et al. in that an improvement in patients’ pain scores with minimal adverse events was noted. Our analysis contributes to the literature by further discussing the practice of low-dose ketamine administration at a tertiary academic medical center and describes the prescribing practices at this institution. In our experience, ketamine is not used as a first line agent and is typically used after opioid therapy has been ineffective. The patient population that received ketamine included those who were opioid tolerant. Despite the limited number of patients who received ketamine as a first line therapy, this population may benefit from receiving ketamine as a first line treatment option or earlier in their treatment plan. Our analysis differs from the Beaudoin, et al. since the mean ketamine dose used in our analysis was lower than the ketamine dose used in the Beaudoin, et al. study, which reflects the current practice of our prescribers and may optimize pain control with a lower incidence of adverse effects. Further studies are needed to determine the ideal dose of ketamine.
We acknowledge several limitations in our study; this was a single center, descriptive, retrospective study and has the associated limitations of this design. The retrospective nature of this study may have caused some data to be missed due to inconsistent documentation that was retrospectively reviewed. The sample size is small, and there was inconsistent documentation between the ED Order Entry system and paper medical record documentation and lack of documented safety outcomes.
Ketamine, administered at low doses, resulted in an improvement of patients’ pain scores while maintaining vital signs. When taking into account the minimal amount of documented adverse outcomes in this patient cohort, ketamine has shown to be a safe and effective option for acute pain relief in the emergency department either as first line therapy or as rescue therapy after opioid administration.
This research was presented in part at the 2014 Society of Critical Care Medicine’s Annual Congress in Phoenix, AZ.
ED: Emergency Department.
SD: Standard Deviation.
IQR: Interquartile Range.
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