Does the blood glucose control have an effect on the success of the painful diabetic neuropathy treatment?

  • Olivera Jovanikic Military Medical Academy, *Neurosurgery Clinic,
  • Gordana Andjelić Military Medical Academy, Institute of Medical Research
  • Milan Lepić Military Medical Academy, Neurosurgery Clinic
  • Dušica Mirković Military Medical Academy, Sector for Pharmacy
  • Bojan Jovanović Military Medical Academy, Clinic for Neurology
  • Toplica Lepić Military Medical Academy, Clinic for Neurology
  • Tamara Dragović Military Medical Academy, Clinic for Endocrinology
Keywords: diabetic neuropathies;, blood glucose;, blood chemical analysis;, surveys and questionnaires;, anesthetics, local;, nerve block;, pain measurement;, treatment outcome

Abstract


Background/Aim. Diabetic neuropathy (DN) is the basic complication of diabetes, associated with impared gluco­regulation, metabolic distrurbances, microvascular vessel damage and increased cardiovascular risk. We monitored the impact of glucoregulation on the efficacy of painful dia­betic neuropathy (PDN) treatment, when all pharmaceutical treatment options were exhausted. Methods. Patients (n = 53, both gender, average age 68.3 ± 12.6) with PDN resis­tant to the pharmacotherapy were treated with the ultra­sound-guided local anesthetic (0.5% procaine hydrochlo­ride, 1% lidocaine, 0.25% levobupivacaine) blocks. Neu­ropathy was confirmed in accordance with the applicable European Federation of Neurological Societies (EFNS) criteria. Glycosylated hemoglobin (HbA1C) and blood glu­cose levels were monitored before and after therapy and one month after the treatment. Neuropathic pain was con­firmed by Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) or Douleur neuropathique (DN4) or pain DE­TECT scales. The pain intensity was assessed by Visual analog scale, Neuropathic pain symptom and Neuropathic pain symptom inventory (VAS, NPS and NPSI, respec­tively) scales before and after therapy and one month after the treatment. The efficacy of the therapy was assessed as: excellent result (> 50% of pain loss), good result (30%–49% of pain loss and the therapy does not work (< 30% of pain loss). The correlation between glucoregulation and the out­come was examined. Results. Because the values of glyce­nia and HbA1c were not different among patients treated with different local anesthetics, they were presented to­gether. All patients had elevated blood glucose and HbA1C levels before (8.23 ± 2.77 mmol/L and 8.53% ± 2.48% re­spectively), after (8.43 ± 2.461 mmol/L and 8.85% ± 2.87%, respectively) and one month after the treatment (8.49 ± 2.22 mmol/L and 8.51% ± 2.09%, respectively). The loss of the pain was not result of the decrease in blood glucose and HbA1C blood levels. VAS, NPS, NPSI values were the following before the therapy: 81.53 ± 11.62 mm; 62.00 ± 13.04; 53.40 ± 17.63, respectively; after the therapy: 29.00 ± 9.23 mm; 13.79 ± 6.65; 11.83 ± 7.93, respectively; and one month later: 26.15 ± 8.41 mm; 12.68 ± 6.03; 9.81 ± 7.64, respectively]. There was no correlation between glucoregulation and excellent outcome. Conclusion. Even though the disturbance of glucose control is the key factor for the progression of PDN, it is not significant for the out­come of the pain treatment. New investigations are re­quired.

Author Biography

Olivera Jovanikic, Military Medical Academy, *Neurosurgery Clinic,

Neurosurgery Clinic

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Published
2020/12/02
Section
Original Paper