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JORGE GUERRERO
     Residente 1er año
MedicinaFalimiaryComunitaria
    FarmacologíaClínica
Focus on both the short-term and
longterm impact of COPD on our patients.
EPIDEMIOLOGY




                                      14.78% (2005-2008)


ClinGastroenterolHepatol. 2011 Jun;9(6):524-530.e1; quiz e60. doi: 10.1016/j.cgh.2011.03.020. Epub 2011 Mar 25
DEFINITION CHRONIC OBSTRUCTIVE
PULMONARY DISEASE




    Preventable
  PERSISTENT
   Treatable




                   Chronic
                       Response not Reversible
DEFINITION CHRONIC OBSTRUCTIVE
PULMONARY DISEASE
   This definition does not use the terms
    chronicbronchitis and emphysema and excludes
    asthma (reversible airflow limitation).
Chronic bronchitis, defined as the presence
of cough and sputum production for at least
3 months in each of 2 consecutive years, is
not necessarily associated with airflow
limitation.
Emphysema, defined as destruction
of the alveoli.
SYNTOMS OF COPD
CARDINAL SYNTOMS
WHAT CAUSE COPD ?
   TABACCO SMOKERS
WHAT CAUSE COPD ?
     INDOOR AIR POLLUTION




Biomass fuel used for cooking and heating in poorly vented
dwellings, a risk factor that particularly affects
WHAT CAUSE COPD ?
   OCCUPATIONAL DUST AND CHEMICALS
WHAT CAUSE COPD ?
     OUTDOOR AIR POLLUTION




Total burden of inhaled particles
DIAGNOSIS OF COPD
DIAGNOSIS OF COPD
+    SPIROMETRY (Air flow limitation)
Simple test to measure the amount of air a person
  can breathe out, and the amount of time taken to
  do so.
     FVC (Forced Vital Capacity): maximum volume of air that
      can be exhaled during a forced maneuver.
     FEV1 (Forced Expired Volume in one second): volume
      expired in the first second of maximal expiration after a maximal
      inspiration. This is a measure of how quickly the lungs can be
      emptied.
     FEV1/FVC: FEV1 expressed as a proportion of the FVC, gives a
      clinically useful index of airflow limitation.
WHY DO SPIROMETRY FOR COPD?

 Spirometry is needed to make a clinical
  diagnosis of COPD.
 A normal value for spirometry effectively
  excludes the diagnosis of clinically relevant
  COPD.
 Together with the presence of symptoms,
  spirometry helps gauge COPD severity and
  can be a guide to specific treatment steps.
ASSESMENT OF COPD



• Symptoms (impact on patient’s health status)
• Degree of airflow limitation
(using spirometry)
• Risk of exacerbations
• Comorbidities
ASSESS SYMTOMS

CAT             COPD Assessment Test


        Modified British Medical Research
mMRC     Council breathlessness scale
       measures of health status91 and predicts future mortality risk




CCQ       Clinical COPD Questionnaire
                measure clinical control self administered
ASSESMENT OF COPD




• Symptoms (impact on patient’s health status)
• Degree of airflow limitation
• Risk of exacerbations
• Comorbidities
DEGREE OF AIR FLOW LIMITATION
ASSESMENT OF COPD




• Symptoms (impact on patient’s health status)
• Degree of airflow limitation
• Risk of exacerbations
• Comorbidities
ASSESSMENT OF RISK OF
             EXACERBATIONS
   CONCEPT.
     Acute event.
     Worsening of the patient’s respiratory symptoms.
     leads to a change in medication.


        The best predictor of having frequent
                   exacerbations
                         =
                Previous Exacerbations
ASSESMENT OF COPD




• Symptoms (impact on patient’s health status)
• Degree of airflow limitation
• Risk of exacerbations
• Comorbidities
ASSESSMENT OF COMORBIDITIES
ASSESMENT OF COPD




• Symptoms (impact on patient’s health status)
• Degree of airflow limitation
• Risk of exacerbations
• Comorbidities
COMBINED COPD ASSESMENT




 • Symptoms (impact on patient’s health status)
 • Degree of airflow limitation
 • Risk of exacerbations
 • Comorbidities
COMBINED COPD ASSESMENT




When assessing risk, choose the highest risk according to GOLD
grade or exacerbation history. (One or more hospitalizations for
     COPD exacerbations should be considered high risk.
 Patient Group A – Low Risk, Less Symptoms
Typically GOLD 1 or GOLD 2 (Mild or Moderate
  airflow limitation) and/or 0-1 exacerbation per year
  and mMRC grade 0-1 or CAT score < 10

 Patient Group B – Low Risk, More Symptoms
Typically GOLD 1 or GOLD 2 (Mild or Moderate
  airflow limitation) and/or 0-1 exacerbation per year
  and mMRC grade ≥ 2 or CAT score ≥ 10
 Patient Group C – High Risk, Less Symptoms
Typically GOLD 3 or GOLD 4 (Severe or Very Severe
  airflow limitation) and/or ≥ 2 exacerbations per year
  and mMRC grade 0-1 or CAT score < 10

 Patient Group D – High Risk, More Symptoms
Typically GOLD 3 or GOLD 4 (Severe or Very Severe
  airflow limitation) and/or ≥ 2 exacerbations per year
  and mMRC grade ≥ 2 or CAT score ≥ 10
   Example: Imagine a patient with a CAT score of 18,
    FEV1 of 55% of predicted, and a history of 3
    exacerbations within the last 12 months.
   Example: Imagine a patient with a CAT score of 18,
    FEV1 of 55% of predicted, and a history of 3
    exacerbations within the last 12 months.
TO BE CONTINUED…
ABANDONO DEL TABAQUISMO

   Mayor capacidad de intervencion en la historia
    natural del EPOC.
        Vareniclina
EJERCICIO CARDIOVASCULAR
TRATAMIENTO
        FARMACOLOGICO
Reducir  los sintomas.
Reduce la frecuenciayseveridad
 de lasexacerbaciones.
Controla la toleranciapara el inicio
 del ejercicio.
TRATAMIENTO
         FARMACOLOGICO


 TerapiaIndividualizada.
 Disponibilidad
               del medicamento.
 Costo del medicamento
 Respuestapor parte del paciente
TRATAMIENTO FARMACOLOGICO
BRONCODILATADORES

   Fundamental para el CONTROL de SÍNTOMAS

 Se prefiereporvíaInhalada
 La escogencia entre: beta-2-agonists, anticolinergicos,
  teofilinaoterapiacombinada…’
 Los de largaacción, producen mayor tiempo, libre de
  síntomas.
 Combinacion de broncodilatadoresde
  clasefarmacológicadiferentedisminuye el riesgo de
  efectossecundarios.
TRATAMIENTO FARMACOLOGICO
CORTICOIDES INHALADOS

 Pacientes con FEV1<60%.
 Tratamiento regular: Disminuye los
  síntomas.
 Relacionados con aumentoIncidencia de
  Neumonía.
 NO usar en monoterapia.
TRATAMIENTO FARMACOLOGICO


CORTICOIDES ORALES

Nousar tratamiento a largo plazo
con corticosteroide oral.
TRATAMIENTO FARMACOLOGICO
METILXANTINAS (Bloqueo R Adenosina)

 Menos  efectivas y toleradas que los
  broncodilatadores de larga acción.
 La adición de Teofilina con Salmeterol,
  aumento en el VEF1 yalivio de la disnea.
 Bajasdosis de Teofilinadisminuye los
  síntomas, mas no la funciónpulmonar.
TRATAMIENTO FARMACOLOGICO
INHIBIDORES 4-P-DIESTERASA (AMPc)
 Reduce lasexacerbaciones en sinergismo
  con los
  corticoidesoralesobroncodilatadores de
  largaacción.
TRATAMIENTO FARMACOLOGICO
AGENTES MUCOLÍTICOS
 Pacientes con esputo viscoso, se
  benefician, sin embargo los beneficios son
  leves.
TRATAMIENTO FARMACOLOGICO
AGENTES ANTITUSIVOS
   Example: Imagine a patient with a CAT score of 18,
    FEV1 of 55% of predicted, and a history of 3
    exacerbations within the last 12 months.
TRATAMIENTO FARMACOLOGICO
TRATAMIENTO FARMACOLOGICO
OTROS TRATAMIENTOS
   USO DE VACUNAS
OTROS TRATAMIENTOS



  PaO2menor (55 mmHg) or SaO288%,
  con o sin hipercapniaconfirmada dos
  veces en un periodo de 3 semanas.

  PaO2entre (55 mmHg)y (60 mmHg), o
  SaO2of 88%, con evidencia de HTP,
  edema perifericosugestivo de ICC,
  opolicitemia(hematocrito> 55%).
Oxigeno Terapia (88 – 92%)


  B2 agonista de Acción corta

     Corticoide Oral (30-40mg
     c/dia por 10 - 14 dias)

       Inicio de Antibioticos?

          Dx diferenciales y
          necesidad de Hx?
Gold 2013 farmacologia clinica
Gold 2013 farmacologia clinica

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Gold 2013 farmacologia clinica

  • 1. JORGE GUERRERO Residente 1er año MedicinaFalimiaryComunitaria FarmacologíaClínica
  • 2. Focus on both the short-term and longterm impact of COPD on our patients.
  • 3. EPIDEMIOLOGY 14.78% (2005-2008) ClinGastroenterolHepatol. 2011 Jun;9(6):524-530.e1; quiz e60. doi: 10.1016/j.cgh.2011.03.020. Epub 2011 Mar 25
  • 4. DEFINITION CHRONIC OBSTRUCTIVE PULMONARY DISEASE  Preventable PERSISTENT  Treatable Chronic Response not Reversible
  • 5. DEFINITION CHRONIC OBSTRUCTIVE PULMONARY DISEASE  This definition does not use the terms chronicbronchitis and emphysema and excludes asthma (reversible airflow limitation). Chronic bronchitis, defined as the presence of cough and sputum production for at least 3 months in each of 2 consecutive years, is not necessarily associated with airflow limitation. Emphysema, defined as destruction of the alveoli.
  • 8. WHAT CAUSE COPD ?  TABACCO SMOKERS
  • 9. WHAT CAUSE COPD ?  INDOOR AIR POLLUTION Biomass fuel used for cooking and heating in poorly vented dwellings, a risk factor that particularly affects
  • 10. WHAT CAUSE COPD ?  OCCUPATIONAL DUST AND CHEMICALS
  • 11. WHAT CAUSE COPD ?  OUTDOOR AIR POLLUTION Total burden of inhaled particles
  • 13.
  • 14. DIAGNOSIS OF COPD + SPIROMETRY (Air flow limitation) Simple test to measure the amount of air a person can breathe out, and the amount of time taken to do so.  FVC (Forced Vital Capacity): maximum volume of air that can be exhaled during a forced maneuver.  FEV1 (Forced Expired Volume in one second): volume expired in the first second of maximal expiration after a maximal inspiration. This is a measure of how quickly the lungs can be emptied.  FEV1/FVC: FEV1 expressed as a proportion of the FVC, gives a clinically useful index of airflow limitation.
  • 15. WHY DO SPIROMETRY FOR COPD?  Spirometry is needed to make a clinical diagnosis of COPD.  A normal value for spirometry effectively excludes the diagnosis of clinically relevant COPD.  Together with the presence of symptoms, spirometry helps gauge COPD severity and can be a guide to specific treatment steps.
  • 16.
  • 17. ASSESMENT OF COPD • Symptoms (impact on patient’s health status) • Degree of airflow limitation (using spirometry) • Risk of exacerbations • Comorbidities
  • 18. ASSESS SYMTOMS CAT COPD Assessment Test Modified British Medical Research mMRC Council breathlessness scale measures of health status91 and predicts future mortality risk CCQ Clinical COPD Questionnaire measure clinical control self administered
  • 19.
  • 20. ASSESMENT OF COPD • Symptoms (impact on patient’s health status) • Degree of airflow limitation • Risk of exacerbations • Comorbidities
  • 21. DEGREE OF AIR FLOW LIMITATION
  • 22. ASSESMENT OF COPD • Symptoms (impact on patient’s health status) • Degree of airflow limitation • Risk of exacerbations • Comorbidities
  • 23. ASSESSMENT OF RISK OF EXACERBATIONS  CONCEPT.  Acute event.  Worsening of the patient’s respiratory symptoms.  leads to a change in medication. The best predictor of having frequent exacerbations = Previous Exacerbations
  • 24. ASSESMENT OF COPD • Symptoms (impact on patient’s health status) • Degree of airflow limitation • Risk of exacerbations • Comorbidities
  • 26. ASSESMENT OF COPD • Symptoms (impact on patient’s health status) • Degree of airflow limitation • Risk of exacerbations • Comorbidities
  • 27. COMBINED COPD ASSESMENT • Symptoms (impact on patient’s health status) • Degree of airflow limitation • Risk of exacerbations • Comorbidities
  • 28. COMBINED COPD ASSESMENT When assessing risk, choose the highest risk according to GOLD grade or exacerbation history. (One or more hospitalizations for COPD exacerbations should be considered high risk.
  • 29.  Patient Group A – Low Risk, Less Symptoms Typically GOLD 1 or GOLD 2 (Mild or Moderate airflow limitation) and/or 0-1 exacerbation per year and mMRC grade 0-1 or CAT score < 10  Patient Group B – Low Risk, More Symptoms Typically GOLD 1 or GOLD 2 (Mild or Moderate airflow limitation) and/or 0-1 exacerbation per year and mMRC grade ≥ 2 or CAT score ≥ 10
  • 30.  Patient Group C – High Risk, Less Symptoms Typically GOLD 3 or GOLD 4 (Severe or Very Severe airflow limitation) and/or ≥ 2 exacerbations per year and mMRC grade 0-1 or CAT score < 10  Patient Group D – High Risk, More Symptoms Typically GOLD 3 or GOLD 4 (Severe or Very Severe airflow limitation) and/or ≥ 2 exacerbations per year and mMRC grade ≥ 2 or CAT score ≥ 10
  • 31. Example: Imagine a patient with a CAT score of 18, FEV1 of 55% of predicted, and a history of 3 exacerbations within the last 12 months.
  • 32. Example: Imagine a patient with a CAT score of 18, FEV1 of 55% of predicted, and a history of 3 exacerbations within the last 12 months.
  • 33.
  • 35.
  • 36. ABANDONO DEL TABAQUISMO  Mayor capacidad de intervencion en la historia natural del EPOC. Vareniclina
  • 37.
  • 39. TRATAMIENTO FARMACOLOGICO Reducir los sintomas. Reduce la frecuenciayseveridad de lasexacerbaciones. Controla la toleranciapara el inicio del ejercicio.
  • 40. TRATAMIENTO FARMACOLOGICO  TerapiaIndividualizada.  Disponibilidad del medicamento.  Costo del medicamento  Respuestapor parte del paciente
  • 41. TRATAMIENTO FARMACOLOGICO BRONCODILATADORES  Fundamental para el CONTROL de SÍNTOMAS  Se prefiereporvíaInhalada  La escogencia entre: beta-2-agonists, anticolinergicos, teofilinaoterapiacombinada…’  Los de largaacción, producen mayor tiempo, libre de síntomas.  Combinacion de broncodilatadoresde clasefarmacológicadiferentedisminuye el riesgo de efectossecundarios.
  • 42. TRATAMIENTO FARMACOLOGICO CORTICOIDES INHALADOS  Pacientes con FEV1<60%.  Tratamiento regular: Disminuye los síntomas.  Relacionados con aumentoIncidencia de Neumonía.  NO usar en monoterapia.
  • 43. TRATAMIENTO FARMACOLOGICO CORTICOIDES ORALES Nousar tratamiento a largo plazo con corticosteroide oral.
  • 44. TRATAMIENTO FARMACOLOGICO METILXANTINAS (Bloqueo R Adenosina)  Menos efectivas y toleradas que los broncodilatadores de larga acción.  La adición de Teofilina con Salmeterol, aumento en el VEF1 yalivio de la disnea.  Bajasdosis de Teofilinadisminuye los síntomas, mas no la funciónpulmonar.
  • 45. TRATAMIENTO FARMACOLOGICO INHIBIDORES 4-P-DIESTERASA (AMPc)  Reduce lasexacerbaciones en sinergismo con los corticoidesoralesobroncodilatadores de largaacción.
  • 46. TRATAMIENTO FARMACOLOGICO AGENTES MUCOLÍTICOS  Pacientes con esputo viscoso, se benefician, sin embargo los beneficios son leves.
  • 48. Example: Imagine a patient with a CAT score of 18, FEV1 of 55% of predicted, and a history of 3 exacerbations within the last 12 months.
  • 51. OTROS TRATAMIENTOS  USO DE VACUNAS
  • 52. OTROS TRATAMIENTOS PaO2menor (55 mmHg) or SaO288%, con o sin hipercapniaconfirmada dos veces en un periodo de 3 semanas. PaO2entre (55 mmHg)y (60 mmHg), o SaO2of 88%, con evidencia de HTP, edema perifericosugestivo de ICC, opolicitemia(hematocrito> 55%).
  • 53.
  • 54. Oxigeno Terapia (88 – 92%) B2 agonista de Acción corta Corticoide Oral (30-40mg c/dia por 10 - 14 dias) Inicio de Antibioticos? Dx diferenciales y necesidad de Hx?

Notas del editor

  1. On current knowledge, a cut point of 0-1 CCQ could be considered for Patient Groups A and C; a CCQ ≥1 for Patient Groups B and D.