This article reports a rare case of the use of low-dose
ketamine infusion as an adjuvant to
opioids to treat
pain in
sickle cell disease. A 31-year-old African-American male with history of
sickle cell disease presented to the emergency department with complaints of chest tightness, multiple
joint pain, and
headache for 1 week. His vital signs and physical examination were unremarkable. His admission lab included
hemoglobin of 8.4 g/dl, reticulocyte count of 16.3%,
bilirubin of 1.7 mg/dl, and LDH of 1,267 U/l. Chest X-ray showed middle and lower lobe opacity and interstitial thickening. He was treated for
acute pain crisis and community-acquired
pneumonia with intravenous fluids, supplemental
oxygen, and intravenous
levofloxacin. He was placed on
fentanyl patient-controlled analgesia (PCA),
oxycodone,
ketorolac, and
methadone with co-
analgesic gabapentin and
venlafaxine. Over the course of his hospitalization, his
chest pain resolved, but the
joint pains continued. He was then transferred to the ICU and was discharged a day later after 7 days of
ketamine infusion.
Ketamine is a noncompetitive antagonist at the
N-methyl-D-aspartate (
NMDA) receptor. This property has been shown to modulate
opioid tolerance and
opioid-induced
hyperalgesia. There have been a very few published reports on the use of low-dose
ketamine in sickle cell
pain management. A PubMed search revealed four published articles (Table 1). Fourteen out of the 17 cases (82.35%) who received
ketamine infusion showed improvement in self-reported
pain intensity and significant reduction in
opioid dosage. Only one patient (5.9%) developed serious side effect leading to discontinuation of the
drug. A low-dose
ketamine can be an option for
pain control in
sickle cell disease. Randomized trial is required to establish this benefit of
ketamine over currently available
therapies.