AI Article Synopsis

  • Optimal symptom control in patients with advanced cancer requiring pain management may involve interventional procedures like paravertebral blockade (PVB) with local anesthetics, as demonstrated in a case study of a 71-year-old patient with complex pain issues.
  • The administration of bupivacaine through lumbar PVB provided effective pain relief and reduced the need for opioids without significant side effects, despite the patient's existing health conditions that raised toxicity concerns.
  • Bupivacaine was more effectively eliminated when administered in boluses compared to continuous infusion, but both methods maintained safe drug serum concentrations throughout the treatment, highlighting bolus administration as a preferable option for this patient's pain management.

Article Abstract

Optimal symptoms control in advanced cancer disease, with refractory to conventional pain treatment, needs an interventional procedure. This paper presents coadministration of local anesthetic (LA) via paravertebral blockade (PVB) as the alternative to an unsuccessful subcutaneous fentanyl pain control in a 71-year old cancer patient with pathological fracture of femoral neck, bone metastases, and contraindications to morphine. Bupivacaine in continuous infusion (0.25%, 5 mL · hour(-1)) or in boluses (10 mL of 0.125%-0.5% solution), used for lumbar PVB, resulted in pain relief, decreased demand for opioids, and led to better social interactions. The factors contributing to an increased risk of systemic toxicity from LA in the patient were: renal impairment; heart failure; hypoalbuminemia; hypocalcemia; and a complex therapy with possible drug-drug interactions. These factors were taken into consideration during treatment. Bupivacaine's side effects were absent. Coadministered drugs could mask LA's toxicity. Elevated plasma α1-acid glycoprotein levels were a protective factor. To evaluate the benefit-risk ratio of the PVB treatment in boluses and in constant infusion, bupivacaine serum levels were determined and the drug plasma half-lives were calculated. Bupivacaine's elimination was slower when administered in constant infusion than in boluses (t½ = 7.80 hours versus 2.64 hours). Total drug serum concentrations remained within the safe ranges during the whole treatment course (22.9-927.4 ng mL(-1)). In the case presented, lumbar PVB with bupivacaine in boluses (≤ 137.5 mg · 24 hours(-1)) was an easy to perform, safe, effective method for pain control. Bupivacaine in continuous infusion (≤150 mg · 12 hours(-1)) had an acceptable risk-benefits ratio, but was ineffective.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772751PMC
http://dx.doi.org/10.2147/OTT.S43057DOI Listing

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