Citations

The clinical courses of 51 patients with postherpetic pain who were referred to the Pain Clinic were reviewed. Twenty-three patients were treated on a trial basis with an intensive series of sensory and sympathetic blocks, whereas 28 control patients, who were seen before the initiation of this study, were treated with other modalities. Fifteen control patients (54%) were disabled by postherpetic neuralgia, as compared with four patients (17%) in the trial group.

Background and Objectives Epinephrine-containing test doses for detection of intravascular injection during epidural anesthesia may be unreliable or hazardous in beta-blocked, elderly, or pregnant patients. Subtoxic injections of lidocaine have been used as an alternative marker of intravascular injection in unpremedicated patients. We studied two groups of premedicated patients and unpremedicated subjects to evaluate the reliability of the local anesthetics bupivacaine (B) and 2-chloroprocaine (2-CP) as test dose injections. Methods Thirty ASA I and II subjects received blinded randomized injections of 2-CP, B, or normal saline via a peripheral vein. Results In group I, 10 healthy unpremedicated volunteers universally recognized injection of 90 mg 2-CP or 25 mg B, but did not reliably detect the injection of 60 mg 2-CP. In group II, 20 patients premedicated with 1 μg/kg fentanyl and 30 μg/kg midazolam could not reliably detect similar injections. Sixteen responded to the injection of 90 mg 2-CP, while 13 detected the 25 mg B test dose. A blinded observer rated only 12 of the subjective reports as conclusive of detection of intravascular injection after each drug. There were no false-positive reports in any group. Conclusions While 90 mg 2-CP or 25 mg B may be reliable alternatives to epinephrine test doses in unpremedicated subjects, they are unreliable indicators of intravascular injection in the premedicated patient.

Morphine sulfate, a narcotic analgesic, possesses the undesirable side effects of central depression, tolerance, and dependency. Opiate receptors have been found in the brain and the spinal cord. Intrathecally applied opiates produce potent analgesia that can be antagonized by naloxone. The time-response study with tail-flick response after intrathecal injections of a small dosage of morphine (25 μg) demonstrated a long-lasting analgesia. Intrathecal injections of morphine or opiate-like peptides may become a predictable modality of pain relief without attendant loss of other neurologic function.

During a 3-year period, 51 patients with upperextremity reflex sympathetic dystrophy were studied. Of 20 patients managed by conservative methods, nine (45%) showed signs of improvement 3 years after onset of the syndrome. Of 31 patients treated with repeated stellate ganglion blocks, 23 (74%) had improved at the 3-year evaluation. Management of both the potential causes and the symptoms of reflex sympathetic dystrophy is necessary. Although sympathetic blocks failed to improve all cases, they should be considered as one of the important methods for the management of reflex sympathetic dystrophy.