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Pregabalina na Dor Neuropática - Academia Nacional de Medicina

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<strong>Pregabali<strong>na</strong></strong> – Novo Avanço no<br />

Tratamento da <strong>Dor</strong> Neuropática<br />

Luiz Fer<strong>na</strong>ndo <strong>de</strong> Oliveira<br />

Recentes Avanços<br />

<strong>Aca<strong>de</strong>mia</strong> Nacio<strong>na</strong>l <strong>de</strong> Medici<strong>na</strong> - 2009


DOR NEUROPÁTICA<br />

<strong>Dor</strong> por lesão do sistema nervoso<br />

periférico ou central<br />

Consequente a alterações geradas diretamente pela<br />

lesão ou pelo processo <strong>de</strong> reparação<br />

De curso crônico, progressiva, caracterizada<br />

por alterações da sensibilida<strong>de</strong> (anestesia,<br />

hiperalgesia, alodinia), gran<strong>de</strong> sofrimento e<br />

progressiva incapacida<strong>de</strong> funcio<strong>na</strong>l


DOR NEUROPÁTICA<br />

<strong>Dor</strong> por lesão do sistema nervoso<br />

periférico ou central<br />

Consequente a alterações geradas pela lesão<br />

ou pelo processo <strong>de</strong> reparação<br />

Curso crônico, progressivo, com alterações da<br />

sensibilida<strong>de</strong> (anestesia dolorosa, hiperalgesia,<br />

alodinia), alterações emocio<strong>na</strong>is e progressiva<br />

incapacida<strong>de</strong> funcio<strong>na</strong>l


<strong>Dor</strong> Neuropática<br />

Normalmente <strong>de</strong> curso crônico, progressiva,<br />

caracterizada por alterações da sensibilida<strong>de</strong>,<br />

(hiperalgesia, alodinia), gran<strong>de</strong> sofrimento e<br />

progressiva incapacida<strong>de</strong> funcio<strong>na</strong>l<br />

Po<strong>de</strong> ocorrer como causa única do quadro <strong>de</strong><br />

dor crônica ou como coadjuvante em outros<br />

tipos <strong>de</strong> dor crônica, como no câncer


CARACTERÍSTICAS<br />

1.<strong>Dor</strong> em queimação ou fulgurante<br />

2.<strong>Dor</strong> evocada pelo tato (alodinia)<br />

3.<strong>Dor</strong> espontânea (em crise)<br />

4.Evidência <strong>de</strong> <strong>de</strong>ficit sensitivo<br />

(anestesia dolorosa)<br />

5.Alterações tróficas locais<br />

Todas essas características, ou ape<strong>na</strong>s algumas <strong>de</strong>las,<br />

po<strong>de</strong>m estar presentes


Características<br />

• Crônica<br />

• Hiperalgesia e/ou<br />

Alodinia<br />

• <strong>Dor</strong> em Queimação e/ou<br />

Fulgurante (em<br />

choque)<br />

• Distrofia Simpática<br />

• Incapacida<strong>de</strong> Física<br />

• Alterações Emocio<strong>na</strong>is


DOR NEUROPÁTICA<br />

DOR NEUROPÁTICA PRIMÁRIA<br />

Neuralgia Pós-Herpética<br />

Neuropatia Diabética<br />

Neuralgia do Trigêmeo<br />

S. Pós-Laminectomia<br />

Lesão Medular (Paraplégico)<br />

S. <strong>Dor</strong> Complexa Regio<strong>na</strong>l (DSR)<br />

Membro Fantasma / <strong>Dor</strong> no Coto<br />

<strong>Dor</strong> Central (Pós AVC)<br />

DOR COM COMPONENTE NEUROPÁTICO (2 ario<br />

Câncer<br />

Pós-operatória crônica<br />

ario )


DOR NEUROPÁTICA - Tratamento<br />

Um gran<strong>de</strong> <strong>de</strong>safio<br />

1. Farmacológico<br />

• Anti<strong>de</strong>pressivos<br />

Tricíclicos - Amitriptili<strong>na</strong><br />

INSC(duais) - Duloxeti<strong>na</strong><br />

• Anticonvulsivantes<br />

Carbamazepi<strong>na</strong> - Gabapenti<strong>na</strong><br />

Topiramato<br />

2. Fisioterápico<br />

3. Psicoterápico<br />

4. Bloqueios<br />

5. Cirúrgico (Neuroestimulação)<br />

Insatisfatório !


Porque Anticonvulsivantes <strong>na</strong> <strong>Dor</strong><br />

Neuropática ?<br />

Na dor neuropática há alterações <strong>na</strong> gênese, propagação<br />

e/ou transmissão do impulso nervoso, comuns a<br />

mecanismos da epilepsia<br />

• Ca<strong>na</strong>lopatia com instabilida<strong>de</strong> do potencial <strong>de</strong><br />

membra<strong>na</strong> e aparecimento <strong>de</strong> ativida<strong>de</strong> ectópica<br />

• Envolvimento <strong>de</strong> circuitos reverberantes<br />

• Deaferentação(inibitória)<br />

• Facilitação e sensibilização <strong>de</strong> circuitos excitatórios<br />

• Aparecimento e consolidação <strong>de</strong> si<strong>na</strong>pses anômalas<br />

• Aumento da sensibilida<strong>de</strong> axo<strong>na</strong>l à NA e Glu


<strong>Pregabali<strong>na</strong></strong> – Um novo anticonvulsivante bloqueador<br />

dos ca<strong>na</strong>is N <strong>de</strong> Ca ++ mais potente que a Gabapenti<strong>na</strong><br />

A afinida<strong>de</strong> da pregabali<strong>na</strong> pelo sítio <strong>de</strong> ligação no ca<strong>na</strong>l<br />

(sub-unida<strong>de</strong> unida<strong>de</strong> α2δ) é 6 x maior que a da gabapenti<strong>na</strong><br />

Modula (inibe) os ca<strong>na</strong>is <strong>de</strong> cálcio tipo N nos termi<strong>na</strong>is pré-<br />

sinápticos. Reduz liberação do neurotransmissor excitatório,<br />

especialmente quando esses termi<strong>na</strong>is estão hiperexcitados.<br />

Limita transmissão <strong>de</strong> impulsos <strong>de</strong> alta frequência<br />

<strong>Pregabali<strong>na</strong></strong><br />

Ca<strong>na</strong>l <strong>de</strong> cálcio N<br />

Gabapenti<strong>na</strong>


<strong>Pregabali<strong>na</strong></strong>(Lyrica®) - Indicações<br />

Introduzido em 2005(USA) e no Brasil em agosto/2009<br />

• Neuropatia Pós-Herpética (NPH)<br />

• Neuropatia Diabética<br />

• Fibromialgia<br />

• Outras formas <strong>de</strong> dor neuropática<br />

Em investigação ou sem evidências<br />

Aprovado<br />

FDA<br />

Efeitos Adversos<br />

Sonolência – Tonteira – Náusea – Ataxia


Características Químicas e<br />

Farmacológicas<br />

Its exact mechanism of action is unknown, but its therapeutic action on<br />

neuropathic pain is thought to involve voltage-gated N-type calcium ion<br />

channels. It is thought to bind to the α2δ subunit (1 and 2) [2] of the voltage<strong>de</strong>pen<strong>de</strong>nt<br />

calcium channel in the central nervous system.


Meta-análise análise : Cochrane Database of Systematic Reviews (2009)<br />

7000 pacientes – 19 estudos – 4 a 14 sema<strong>na</strong>s<br />

Efficacy outcomes with different doses of pregabalin in postherpetic neuralgia<br />

Number of<br />

Percent with outcome<br />

Outcome - daily dose Studies Participants Pregabalin Placebo<br />

Relative benefit<br />

(95% CI)<br />

NNT<br />

(95% CI)<br />

At least 30% pain relief<br />

150 mg 1 180 39 17 2.3 (1.4 to 3.8) 4.6 (2.9 to 11)<br />

300 mg 2 369 49 24 2.1 (1.5 to 2.7) 4.0 (2.9 to 6.5)<br />

300 mg (≥ 8 weeks) 1 191 41 17 2.4 (1.4 to 3.9) 4.2 (2.8 to 8.9)<br />

600 mg 3 537 62 24 2.5 (2.0 to 3.2) 2.7 (2.2 to 3.4)<br />

600 mg (≥ 8 weeks) 2 356 58 21 2.8 (2.0 to 3.8) 2.7 (2.2 to 3.7)<br />

At least 50% pain relief<br />

150 mg 3 527 25 11 2.3 (1.6 to 3.4 6.9 (4.8 to 13)<br />

300 mg 4 713 32 13 2.5 (1.9 to 3.4) 5.1 (3.9 to 7.4)<br />

300 mg (≥ 8 weeks) 3 535 30 11 2.7 (1.9 to 4.0) 5.3 (3.9 to 8.1)<br />

600 mg 4 732 41 15 2.7 (2.1 to 3.5) 3.9 (3.1 to 5.1)<br />

600 mg (≥ 8 weeks) 3 551 39 14 2.8 (2.0 to 3.9) 4.0 (3.1 to 5.5)<br />

PGIC much or very much<br />

improved<br />

150 mg *PGIC- Impressão<br />

2 342 27 15 1.8 (1.2 to 2.8) 8.4 (4.9 to 30)<br />

clínica do paciente<br />

300 mg 2 348 32 15 2.2 (1.4 to 3.3) 5.8 (3.9 to 12)<br />

600 mg 1 183 37 16 2.3 (1.3 to 3.9) 4.9 (3.0 to 12)<br />

Lack of efficacy /discontinuation NNTp(95% CI)<br />

150 mg 3 527 8 13 0.6 (0.3 to 1.0) not calculated<br />

300 mg 4 713 4 11 0.4 (0.2 to 0.7) 15 (9 to 34)<br />

300 mg (≥ 8 weeks) 3 535 6 13 0.4 (0.2 to 0.7) 13 (7.9 to 35)<br />

600 mg 4 732 3 11 0.3 (0.1 to 0.5) 13 (9 to 24)<br />

600 mg (≥ 8 weeks) 3 551 3 13 0.3 (0.1 to 0.6) 11 (7.4 to 22)<br />

Moore R Andrew, Straube Sebastian, Wiffen Philip J, Derry Shee<strong>na</strong>, McQuay Henry J<br />

Cochrane Database of Systematic Reviews, Issue 3, 2009


Meta-análise análise : Cochrane Database of Systematic Reviews (2009)<br />

7000 pacientes – 19 estudos – 4 a 14 sema<strong>na</strong>s<br />

Efficacy outcomes with different doses of pregabalin in painful diabetic neuropathy<br />

Number of<br />

Percent with outcome<br />

Outcome - daily dose Studies Participants Pregabalin Placebo<br />

Relative benefit<br />

(95% CI)<br />

NNT<br />

(95% CI)<br />

At least 30% pain relief<br />

150 mg no data<br />

300 mg 2 482 59 45 1.3 (1.1 to 1.6) 6.8 (4.3 to 17)<br />

300 mg (≥ 8 weeks) 1 304 58 52 1.1 (0.9 to 1.4) not calculated<br />

600 mg 3 819 63 43 1.5 (1.3 to 1.7) 5.1 (3.8 to 7.8)<br />

600 mg (≥ 8 weeks) 2 641 62 48 1.3 (1.1 to 1.5) 6.8 (4.4 to 15)<br />

At least 50% pain relief<br />

150 mg 2 359 27 23 1.1 (0.8 to 1.6) not calculated<br />

150 mg (≥ 8 weeks) 1 195 34 30 1.1 (0.8 to 1.7) not calculated<br />

300 mg 4 823 40 26 1.5 (1.2 to 1.8) 7.5 (5.1 to 14)<br />

300 mg (≥ 8 weeks) 3 645 38 29 1.3 (1.1 to 1.6) 11 (6.1 to 54)<br />

600 mg 6 1360 45 25 1.7 (1.5 to 2.0) 5.0 (4.0 to 6.6)<br />

600 mg (≥ 8 weeks) 4 1005 46 30 1.5 (1.3 to 1.8) 6.3 (4.6 to 10)<br />

PGIC much or very much improved<br />

150 mg 1 195 45 34 1.4 (0.96 to 2.0) not calculated<br />

300 mg 2 359 48 30 1.6 (1.2 to 2.1) 5.6 (3.6 to 13)<br />

300 mg (≥ 8 weeks) 1 195 42 33 1.3 (0.9 to 1.8) not calculated<br />

600 mg 4 875 56 33 1.8 (1.5 to 2.1) 4.2 (3.3 to 5.8)<br />

600 mg (≥ 8 weeks) 3 702 54 36 1.5 (1.3 to 1.8) 5.4 (3.9 to 9.2)<br />

Lack of efficacy/discontinuation NNTp (95% CI)<br />

150 mg 2 359 4 7 0.7 (0.3 to 1.5) not calculated<br />

150 mg (≥ 8 weeks) 1 195 8 11 0.7 (0.3 to 1.7) not calculated<br />

300 mg 2 341 3 8 0.4 (0.2 to 1.0) not calculated<br />

600 mg 4 869 4 11 0.3 (0.2 to 0.5) 14 (9 to 31)<br />

600 mg (≥ 8 weeks) 3 702 4 14 0.3 (0.2 to 0.5) 10 (6.9 to 20<br />

Moore R Andrew, Straube Sebastian, Wiffen Philip J, Derry Shee<strong>na</strong>, McQuay Henry J<br />

Cochrane Database of Systematic Reviews, Issue 3, 2009


<strong>Pregabali<strong>na</strong></strong> (Lyrica®) <strong>na</strong> <strong>Dor</strong> Neuropática<br />

Experiência Pessoal (Prelimi<strong>na</strong>r)<br />

TIPO<br />

NPH<br />

DOSE N % Alívio≥50%<br />

150 mg 6 17<br />

300 mg 5 40<br />

450 mg 3 66<br />

N. diabética 150 mg 5 20<br />

300 mg 4 50<br />

450 mg 2 50<br />

SDCR<br />

150 mg 2 0<br />

300 mg 2 50<br />

450 mg 1 100


<strong>Pregabali<strong>na</strong></strong> (Lyrica®) <strong>na</strong> <strong>Dor</strong> Neuropática<br />

Experiência Pessoal (Prelimi<strong>na</strong>r)<br />

EFEITO<br />

Efeitos Adversos<br />

Dose<br />

% Pacientes<br />

Sonolência 150 10<br />

300 25<br />

450 30<br />

Tonteira 150 20<br />

300 33<br />

450 40<br />

Descontinuação 150 10<br />

300 20<br />

450 20


Meta-análise análise : Cochrane Database of Systematic Reviews (2009)<br />

7000 pacientes – 19 estudos – 4 a 14 sema<strong>na</strong>s<br />

Efficacy outcomes with different doses of pregabalin in fibromyalgia (classic trial <strong>de</strong>sign only)<br />

Percent with outcome<br />

Number of<br />

Relative benefit<br />

NNT<br />

Outcome - daily dose<br />

Participants<br />

Pregabalin<br />

Placebo Studies<br />

(95% CI)<br />

(95% CI)<br />

At least 30% pain relief<br />

150 mg 1 263 31 27 1.1 (0.8 to 1.7) not calculated<br />

300 mg 4 1374 39 28 1.4 (1.2 to 1.6) 9.2 (6.3 to 17)<br />

450 mg 4 1376 43 28 1.5 (1.3 to 1.8) 6.6 (5.0 to 9.8)<br />

600 mg 3 1122 39 28 1.4 (1.2 to 1.6) 9.1 (6.1 to 18)<br />

At least 50% pain relief<br />

150 mg 1 263 13 13 1.0 (0.5 to 1.9) not calculated<br />

300 mg 4 1374 21 14 1.5 (1.2 to 1.9) 14 (9.0 to 33)<br />

450 mg 4 1376 25 14 1.7 (1.4 to 2.1) 9.8 (7.0 to 16)<br />

600 mg 3 1122 24 15 1.6 (1.3 to 2.1) 11 (7.1 to 21)<br />

PGIC much or very much improved<br />

150 mg 1 263 32 27 1.2 (0.8 to 1.8) not calculated<br />

300 mg 4 1374 36 28 1.5 (1.2 to 1.9) 11 (7.3 to 26)<br />

450 mg 4 1376 42 28 1.5 (1.3 to 1.8) 6.8 (5.1 to 10)<br />

600 mg 3 1122 41 28 1.5 (1.2 to 1.7) 7.7 (5.4 to 13)<br />

PGIC very much improved<br />

150 mg no data<br />

300 mg 4 1352 17 11 1.7 (1.2 to 2.9) 16 (9.9 to 37)<br />

450 mg 4 1354 19 11 1.8 (1.4 to 2.4) 11 (7.9 to 20)<br />

600 mg 3 1095 12 7 1.7 (1.1 to 2.4) 21 (12 to 83)<br />

Lack of efficacy discontinuation NNTp (95% CI)<br />

150 mg 1 263 9 14 0.7 (0.3 to 1.3) not calculated<br />

300 mg 4 1374 4 10 0.4 (0.3 to 0.7) 18 (12 to 34)<br />

450 mg 4 1376 3 10 0.3 (0.2 to 0.5) 15 (11 to 25)<br />

600 mg 3 1122 2 9 0.3 (0.2 to 0.5) 15 (11 to 26)<br />

Moore R Andrew, Straube Sebastian, Wiffen Philip J, Derry Shee<strong>na</strong>, McQuay Henry J<br />

Cochrane Database of Systematic Reviews, Issue 3, 2009


Meta-análise análise : Cochrane Database of Systematic Reviews (2009)<br />

7000 pacientes – 19 estudos – 4 a 14 sema<strong>na</strong>s<br />

Participants experiencing at least one adverse event or serious adverse event<br />

Percent with outcome<br />

Outcome - daily dose<br />

Number of<br />

Studies<br />

Participants Pregabalin<br />

Placebo<br />

Relative risk<br />

(95% CI)<br />

NNH<br />

(95% CI)<br />

At least one adverse event<br />

150 mg 2 449 77 71 1.2 (0.97 to 1.4) not calculated<br />

300 mg 8 2190 82 67 1.2 (1.17 to 1.29) 6.6 (5.4 to 8.7)<br />

450 mg 4 1379 90 74 1.2 (1.15 to 1.27) 6.3 (5.1 to 8.5)<br />

600 mg 9 2540 83 67 1.3 (1.25 to 1.37) 6.1 (5.1 to 7.7)<br />

At least one serious<br />

adverse event<br />

150 mg 3 542 4.1 4.0 1.0 (0.5 to 2.3) not calculated<br />

300 mg 8 1566 3.6 2.9 1.2 (0.7 to 2.1) not calculated<br />

450 mg 2 740 2.7 1.6 1.7 (0.6 to 4.5) not calculated<br />

600 mg 9 2101 3.7 3.2 1.2 (0.7 to 1.8) not calculated<br />

Moore R Andrew, Straube Sebastian, Wiffen Philip J, Derry Shee<strong>na</strong>, McQuay Henry J<br />

Cochrane Database of Systematic Reviews, Issue 3, 2009


<strong>Pregabali<strong>na</strong></strong><br />

RESUMO<br />

– Evidências <strong>de</strong>monstram sua eficácia <strong>na</strong> dor<br />

neuropática, especialmente <strong>na</strong> NPH e <strong>na</strong> N.<br />

Diabética<br />

– Evidências <strong>de</strong> eficácia também <strong>na</strong> dor da<br />

Fibromialgia<br />

– Bem tolerada<br />

– Baixa incidência <strong>de</strong> efeitos adversos que<br />

levem à <strong>de</strong>scontinuação


Obrigado

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