Radikülopati ve Pleksopatilerde Nöropatik Ağrının Medikal Tedavisi

Yazarlar

Çağatay Küçükbingöz
https://orcid.org/0000-0002-2527-3510
Barış Arslan

Özet

Nöropatik ağrı, sinir sistemindeki lezyon veya disfonksiyon sonucu oluşan, nosiseptif ağrıdan farklı mekanizmaya sahip ve tedavisi güç kronik bir durumdur. Uluslararası kılavuzlarda trisiklik antidepresanlar (özellikle amitriptilin), serotonin-norepinefrin geri alım inhibitörleri (duloksetin, venlafaksin) ve gabapentinoidler (gabapentin, pregabalin) birinci basamak medikal tedavi olarak önerilmektedir. Pregabalin, kalsiyum kanallarına afinitesi ve protein bağımsız emilimi nedeniyle gabapentine göre daha yüksek analjezik potense sahiptir. Tramadol ikinci basamak; güçlü opioidler, kannabinoidler ve antiepileptikler ise yan etki ile bağımlılık riskleri sebebiyle üçüncü veya dördüncü basamakta yer alır. Odaklanmış ağrılarda topikal lidokain ve kapsaisin tercih edilirken, dirençli vakalarda etkinlik ve yan etki dengesi gözetilerek kombinasyon tedavileri uygulanabilir. İlaçların 3-8 haftalık deneme süreleri bulunmakta, doz ayarlamaları kardiyak riskler ve böbrek/karaciğer yetmezlikleri dikkate alınarak bireyselleştirilmektedir. Tedavinin etkinliği hastanın komorbiditelerine, psikolojik durumuna ve uyku bozukluğu gibi semptomlara göre şekillenmektedir.

Neuropathic pain is a chronic condition caused by a primary lesion or dysfunction in the nervous system, possessing a different mechanism than nociceptive pain, which complicates its treatment. International guidelines recommend tricyclic antidepressants (especially amitriptyline), serotonin-norepinephrine reuptake inhibitors (duloxetine, venlafaxine), and gabapentinoids (gabapentin, pregabalin) as first-line medical treatments. Due to higher affinity for calcium channels and protein-independent absorption, pregabalin exhibits higher analgesic potency compared to gabapentin. Tramadol is suggested as second-line, whereas strong opioids, cannabinoids, and antiepileptics are categorized as third or fourth-line options due to potential side effects and addiction risks. Topical lidocaine and capsaicin are preferred for localized pain, and combination therapies can be utilized in resistant cases to balance efficacy and tolerability profiles. These medications require a trial period of 3 to 8 weeks, and dosage adjustments must be individualized by considering cardiac risks, renal impairment, and hepatic failure. The success of the treatment depends heavily on evaluating the patient's comorbidities, psychological status, and associated symptoms like sleep disturbances.

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7 Mart 2022

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