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Prof. M.C.Bansal
       MBBS,MS,MICOG,FICOG
           Professor OBGY
       Ex-Principal & Controller
  Jhalawar Medical College & Hospital
Mahatma Gandhi Medical College, Jaipur.
Asthma is chronic inflammatory disease of airway
characterized by episodic, reversible, bronchial constriction
due to hyperresponsiveness of tracheobronchial tree to a
multiple stimuli.
Clinically characterized by
       paroxysms of dyspnea,
       cough
       wheezing
Manifested by
- obstruction of airflow
    - damage to airway epithelium
    - constriction of bronchioles
Asthma and pregnancy
It is the most common chronic condition in pregnancy
The prevalence of asthma in the general population is
4-5%. In pregnancy, the prevalence ranges from 1-4%.
Chromosome 5, 6, 11, 12, 14, 16 & 20
15 methyl PGF2 and methylergometrine should be
avoided if possible
Progesterone & estrogen: bronchodilators
Progesterone also suppresses immunity, so in that
sense it is protective or helpful
Pathogenesis & Pathophysiology
 Chronic inflammatory disorder of the airways with recurrent
   exacerbations

Interaction among the residents and infiltrating inflammation cells
  in the airway surface epithelium, inflamatory mediators and
   cytokines
Allergens


               Mast cell



  histamine                leukotrienes
               cytokines

                   bronchospam
bronchospam
                    Mucus production


  Vascular
  permeabili
  ty                Muscle thickening

                   Muscle constriction
Deposition of collagen
         &
Epithelial thickening
Stimuli of Asthma
   Major categories of stimuli of asthma

1) Allegerns- depends on IgE response
        frequently seasonal , observed in childrens & adults
        Non seasonal form are allergy to feathers, animals danders,
          dust mites, molds.
2) Pharmacologic stimuli  like asprin, coloring agents such as
   tartrazine, ß-adrenergic antagonists, sulfiting agents , ACE
   inhibitors
3) Environmental and air pollution
    It includes ozone, NO2, Sulfur dioxide.
4) Occupational factors
    high molecular weight compounds – immuniological mechanism
      wood    , vegetable dust, pharmaceutical agents, biological agents,
       animals and insect dust
    low molecular weight compound – release bronchoconstrictor
       substances
      it   includes metals salts like chromes, nickel, industrial and
        chemical plastics,
5) Infections
respiratory stmuli that evoke acute
   exacerbation of asthma
In young children common is syncytial
 virus and Parainfluenza virus
In older children and adults rhino virus
   and influenza virus
6) Exercise
 exercise is very common precipitants of episodes of
     asthma .
7) Emotional stress
 Psychological factors can version asthma
8) others: some food additives like metabisulphite,
  tartrazine.
9) Hormonal       premenstrual worsening of asthma due to fall in
    progesterone, hypo and hyperthyroididsm can both worsen
    asthma
10) Gastroesopahgeal reflux
Warning Signs of an Asthma
                  Episode
  Examination Findings
 History findings in pregnant and nonpregnant patients
    may include the following:
• Cough
• Shortness of breath
• Chest tightness
• Noisy breathing
• Nocturnal awakenings
• Recurrent episodes of symptom complex
• Exacerbations possibly provoked by nonspecific stimuli
• Personal or family history of other atopic disease (eg, hay
  fever, eczema)
General physical examination findings may include the
      following:
      Tachypnea
      Retraction (sternomastoid, abdominal, pectoralis muscles)
      Agitation, usually a sign of hypoxia or respiratory distress
      Pulsus paradoxicus (>20 mm Hg)


.
Pulmonary findings are as follows:
  Diffuse wheezes - Long, high-pitched sounds on expiration
  and, occasionally, on inspiration)
  Diffuse rhonchi - Short, high- or low-pitched squeaks or
  gurgles on inspiration and/or expiration
  Bronchovesicular sounds
  Expiratory phase of respiration equal to or more prominent
  than inspiratory phase
Signs of fatigue and near-respiratory arrest are as
  follows:
  Alteration in the level of consciousness, such as
  lethargy, which is a sign of respiratory acidosis and
  fatigue
  Abdominal breathing
  Inability to speak in complete sentences
Signs of complicated asthma are as follows:
   Equality of breath sounds: Check for equality of breath sounds
   (pneumonia, mucous plugs, barotrauma). The amount of wheezing
   does not always correlate with the severity of the attack. A silent
   chest in someone in distress is more worrisome.
   Jugular venous distension from increased intrathoracic pressure
   (from a coexistent pneumothorax)
   Hypotension and tachycardia (think tension pneumothorax)
   Fever, a sign of upper or lower respiratory infections
Outcomes and complications of asthma in
              pregnancy
Preeclampsia
Pregnancy-induced hypertension
Uterine hemorrhage
Preterm labor
Premature birth
Congenital anomalies
Fetal growth restriction
Low birth weightNeonatal hypoglycemia, seizures, tachypnea,
and neonatal intensive care unit (ICU) admission
Fetal surveillance during pregnancy
primary affect on the fetus from asthma, or any other
pulmonary disease, is chronic hypoxia.
 The impact of hypoxia can manifest in several ways, including
growth restriction or more significantly, fetal death.
Shortly after a woman with asthma becomes pregnant, she
should have an early ultrasound to confirm her pregnancy
dating.
Women should be instructed to monitor fetal activity during
the course of the pregnancy.
A third-trimester ultrasound can be considered in a woman
with well-controlled asthma who has appropriate growth in
the fundal height.
If the growth is not appropriate or the woman has an acute
exacerbation, fetal testing should be started.
Testing may include umbilical artery Doppler flow velocity
studies, nonstress testing (NST) or biophysical profiles (BPP).
The frequency of such testing would depend on the severity of
the patient’s asthma or the degree of growth restriction .
Other differential diagnosis of asthma are:

 Upper airways obstruction laryngeal edema

 Acute left ventricular failure

 Carciniod tumors

 Recurrent pulmonary emboli

 Endobronchial disease  foreign body aspiration, neoplasm & bronchial
                              stenosis

  Eosinophilc pneumonias
Airway obstruction
Amniotic fluid embolism
Acute congestive heart failure (CHF), secondary to
peripartum cardiomyopathy
Physiologic dyspnea of pregnancy
Measures of Assessment
           and Monitoring

Two aspects:
– Initial assessment and diagnosis of asthma
– Periodic assessment and monitoring
Initial Assessment and Diagnosis of
 Asthma
Determine that:
    Patient has history or presence of episodic symptoms of airflow
     obstruction
    Airflow obstruction is at least partially reversible
    Alternative diagnoses are excluded
Does patient have history or presence of episodic Symptoms of
 airflow obstruction?
   Wheeze, shortness of breath, chest tightness, or cough

    Asthma symptoms vary throughout the day

    Absence of symptoms at the time of the examination does not
     exclude the diagnosis of asthma
Is airflow obstruction at least partially reversible?
 Use spirometry to establish airflow obstruction:

    – FEV1 < 80% predicted;

    – FEV1/FVC <65% or below the lower limit of normal
   Use spirometry to establish reversibility:
    – FEV1 increases >12% and at least 200 mL after using a short-
      acting inhaled beta2-agonist
Are alternative diagnoses excluded?
 Vocal cord dysfunction, vascular rings, foreign bodies, other
  pulmonary diseases
Additional Tests
  Reasons for Additional Tests                                                           The
  Tests
Patient has symptoms but spirometry is             – Assess diurnal variation of peak flow
 normal or near normal                                over 1 to 2 weeks
                                                     – Refer to a specialist for bronchoprovocation
                                                      with methacholine histamine, or exercise;
                                                      negative test may help rule out asthma
Suspect infection, large airway lesions, heart
                                                     – Chest x-ray
  disease, or obstruction by foreign object
Suspect coexisting chronic obstructive pulmonary
                                                      – Additional pulmonary function studies
 disease, restrictive defect, or central airway
 obstruction                                          – Diffusing capacity test
Suspect other factors contribute to asthma           – Allergy tests—skin or in vitro
  (These are not diagnostic tests for asthma.)        – Nasal examination
                                                      – Gastroesophageal reflux assessment
Classification of Asthma Severity: Clinical
         Features Before Treatment
               Days With           Nights With          PEF or               PEF
               Symptoms            Symptoms             FEV1             Variability
Step 4          Continuous            Frequent           60%               >30%
Severe
Persistent
Step 3             Daily              5/month        >60%-<80%             >30%
Moderate
Persistent
Step 2           3-6/week             3-4/month          80%              20-30%
Mild
Persistent
Step 1            2/week                          2/month            80%
    <20%
Mild
Intermittent
Footnote: The patient’s step is determined by the most severe feature.
1. Mild Intermittent Asthma
  •Symptoms less than twice a week
  •Symptoms at night less than twice a month
  • No symptoms between episode
2. Mild Persistent
   • Weekly, but not daily symptoms
   • Episodes that may affect activity and sleep
   • Symptoms at night more than twice a month
3. Moderate Persistent
   • Daily symptoms requiring bronchodialator inhaler use
   • Episodes that affect activity and sleep
   • Symptoms at night more than once a week


4. Severe Persistent
   • Continuous symptoms
   • Episodes that are frequent
   • Symptoms at night all the time
   • Activities are limited because of symptoms
   • Symptoms occur while on maximal therapy
New strategy of asthma management are as below
                            GINA - 2006
Characteristic      Controlled             Partly controlled    Uncontrolled
Day time symptoms    None(twice or less/       More then
                           week)              twice/week
Limitations of              None                  Any
activities                                                         Three or more
                                                                 features of partly
Nocturnal                   None                  Any            controlled asthma
symptoms/awakeni                                                present in any week
ng

Need for             None(twice or less/       More than
reliever/rescue            week)              twice/week
treatment

Lungs function             normal          <80% predicted or
(PEF or FEV1                                personal best (if
                                                known

exacerbation                none           One or more /year     One in any week
step 1                 Step 2                  Step 3                 Step 4                 Step 5




                    Asthma education and environmental control
As need rapid acting
β2 agonist                                    As needed rapid acting β2 agonist
                       Select one              Select one             Add one or more        Add one or both



                       Low dose ICS            Low dose ICS +         Medium or high-dose    Oral glucocortico-
                                               LABA                   ICS + LABA             steroids (lowest dose)


Controller option      Leukotriene modifier    Medium or high dose    Leukotriene modifier   Anti IgE treatment
                                               ICS

                                               Low dose ICS +         Sustained release
                                               leukotriene modifier   theophylline


                                               Low dose ICS +
                                               sustained release
                                               theophylline
DRUGS USED IN ASTHMA


 Bronchodilators                                Anti-inflammatory

                                                              Agents
                                                       Corticosteroids
Beta agonists   Muscarinic    Methyxanthines
                antagonists                                      Slow
                                          Release                Anti-inflammatory
                                          inhibitors             Drugs
Bronchodilators
(a) Beta agonists
    • ß2 selective agonists e.g. albuterol given by inhalation via
      aerosol
    • stimulation of adenylyl cyclase - increases cAMP in bronchial
      smooth muscle - increases bronchodilation
    • extensively used and very effective in asthmatics
    • Salbutamol--- 2-4mg oral, 0.5mg im /sc, 100-200mcg/puff
    • Terbutaline----.25mg sc/inhalation,5mg oral.
    • Long acting---- salmeterol/formoterol---(9-12 hrs)-
      25mcg/puff, 2 puffs B D.
(b) Muscarinic antagonists
       e.g. Ipratropium
Use:
    • Ipratropium is available as pressurized aerosol
    • not as useful as ß2 agonists in majority of asthmatics
    • useful in chronic obstructive pulmonary disease
(c) Methyxanthines
      e.g. theophylline .100-300mg tds
     major therapeutic preparation = aminophylline slow iv
    250-500mg
Use:
•administered as theophylline salt orally
•diminishing use now because of more effective inhaled
bronchodilators
• used in patients who donít respond to anti- inflammatory

  agents or ß2 agonists
Anti-inflammatory Agents
(a) Mast cell stabilisers---
    e.g. Cromolym Na
         prophylactic drugs used as aerosol to inhibit antigen
            and exercise induced asthma
         no effect on smooth muscle tone or bronchospasm

Use:
• inhaled cromolyn prevents allergen or exercise-induced
  asthma
• 1mg/puff,2puff qid
• Nedocromil---4mg/2puff bd.
(b) Corticosteroids
       e.g. lipid soluble corticosteroids
          (beclomethazone, 100,200,250,mcg Budesonide 200-400mcg bd-qid
triamcinolone used in aerosols)
 Use:
 • used in asthma that is non-responsive to bronchodilator therapy
 • high dose for several weeks followed by low dose, then given alternate days
  C) leukotriene antagonist: --monteleukast 10 mg od zafirleukast—20 mg bd.
                                   Md001921.jpg

 d)Anti IgEm(Omalizumab) : s/c inj 2 to 4 weeks
 e)Immunotherapy
When Having a Severe Asthma
Episode
 Go to the emergency room right away
 Signs of a severe episode
 Rescue or inhaler medicine doesn’t help within 15
  minutes
 Person’s lips or fingernails are blue
 Person has trouble walking or talking due to
  shortness of breath
Immediate management:
Oxygen therapy by tight fitting facemask (60%).
Nebulised salbutamol 2.5 +/- 0.5mg ipratropium
Start glucocorticoid therapy - prednisolone 30-60mg p.o. or
 hydrocortisone 200mg i.v.
Urgent chest X-ray to exclude pneumothorax
Urgent blood gas
Reassess in 15 min or if life-threatening features appear
Consider i.v. aminophylline if life-threatening features or fails to
  improve after 15-30 minutes
 ventilation needed if PEFR
  continues to fall despite medical therapy, patient becoming drowsy
 /confused/exhausted or deteriorating blood gases
Late management:
   Step down initially by converting from nebulised to usual
  inhaled device (eg MDI) checking that their technique is
  adequate.

   Patient is discharged only when PEFR normalized (80-90%
    of their best) without dipping. They should also be
   discharged on high-dose inhaled glucocorticoid, which
   should continue, until they are reviewed in clinic.

   The latter is important in preventing early relapse.
LABOUR & DELIVERY
Asthma exacerbations are rare in labor and delivery
due to the increase in serum cortisol
Asthma medications should not be discontinued through labor
and delivery.
Prostaglandin E2 is safe for cervical ripening, as is oxytocin.
The agent 15-methyl prostaglandin F2-alpha should be avoided
because it may cause severe bronchospasm.
methylergonovine may cause dyspnea, asthma is not an absolute
contraindication, and therefore it can be used when appropriate
in the management of postpartum hemorrhage.
Fentanyl is preferred to morphine and meperidine, which can
release histamine.
Epidural anesthesia is usually advised because it decreases
oxygen consumption and minute ventilation. Epidural
anesthesia also decreases the possibility of requiring general
anesthesia if an emergency cesarean becomes indicated during
labor
Postpartum period
  During the postpartum period, women should initially
  continue the same asthma medications they required during
  pregnancy.
  Close peak flow monitoring is indicated, particularly in those
  with poorly controlled or moderate-to-severe asthma.
Thank you all…

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Bronchial asthama and pregnancys

  • 1. Prof. M.C.Bansal MBBS,MS,MICOG,FICOG Professor OBGY Ex-Principal & Controller Jhalawar Medical College & Hospital Mahatma Gandhi Medical College, Jaipur.
  • 2. Asthma is chronic inflammatory disease of airway characterized by episodic, reversible, bronchial constriction due to hyperresponsiveness of tracheobronchial tree to a multiple stimuli. Clinically characterized by paroxysms of dyspnea, cough wheezing
  • 3. Manifested by - obstruction of airflow - damage to airway epithelium - constriction of bronchioles
  • 4. Asthma and pregnancy It is the most common chronic condition in pregnancy The prevalence of asthma in the general population is 4-5%. In pregnancy, the prevalence ranges from 1-4%. Chromosome 5, 6, 11, 12, 14, 16 & 20 15 methyl PGF2 and methylergometrine should be avoided if possible Progesterone & estrogen: bronchodilators Progesterone also suppresses immunity, so in that sense it is protective or helpful
  • 5. Pathogenesis & Pathophysiology  Chronic inflammatory disorder of the airways with recurrent exacerbations Interaction among the residents and infiltrating inflammation cells in the airway surface epithelium, inflamatory mediators and cytokines
  • 6. Allergens Mast cell histamine leukotrienes cytokines bronchospam bronchospam Mucus production Vascular permeabili ty Muscle thickening Muscle constriction Deposition of collagen & Epithelial thickening
  • 7.
  • 8. Stimuli of Asthma Major categories of stimuli of asthma 1) Allegerns- depends on IgE response  frequently seasonal , observed in childrens & adults  Non seasonal form are allergy to feathers, animals danders, dust mites, molds. 2) Pharmacologic stimuli  like asprin, coloring agents such as tartrazine, ß-adrenergic antagonists, sulfiting agents , ACE inhibitors
  • 9. 3) Environmental and air pollution It includes ozone, NO2, Sulfur dioxide. 4) Occupational factors  high molecular weight compounds – immuniological mechanism wood , vegetable dust, pharmaceutical agents, biological agents, animals and insect dust  low molecular weight compound – release bronchoconstrictor substances it includes metals salts like chromes, nickel, industrial and chemical plastics,
  • 10. 5) Infections respiratory stmuli that evoke acute exacerbation of asthma In young children common is syncytial virus and Parainfluenza virus In older children and adults rhino virus and influenza virus
  • 11. 6) Exercise exercise is very common precipitants of episodes of asthma . 7) Emotional stress Psychological factors can version asthma 8) others: some food additives like metabisulphite, tartrazine. 9) Hormonal premenstrual worsening of asthma due to fall in progesterone, hypo and hyperthyroididsm can both worsen asthma 10) Gastroesopahgeal reflux
  • 12. Warning Signs of an Asthma Episode Examination Findings History findings in pregnant and nonpregnant patients may include the following: • Cough • Shortness of breath • Chest tightness • Noisy breathing • Nocturnal awakenings • Recurrent episodes of symptom complex • Exacerbations possibly provoked by nonspecific stimuli • Personal or family history of other atopic disease (eg, hay fever, eczema)
  • 13. General physical examination findings may include the following: Tachypnea Retraction (sternomastoid, abdominal, pectoralis muscles) Agitation, usually a sign of hypoxia or respiratory distress Pulsus paradoxicus (>20 mm Hg) .
  • 14. Pulmonary findings are as follows: Diffuse wheezes - Long, high-pitched sounds on expiration and, occasionally, on inspiration) Diffuse rhonchi - Short, high- or low-pitched squeaks or gurgles on inspiration and/or expiration Bronchovesicular sounds Expiratory phase of respiration equal to or more prominent than inspiratory phase
  • 15. Signs of fatigue and near-respiratory arrest are as follows: Alteration in the level of consciousness, such as lethargy, which is a sign of respiratory acidosis and fatigue Abdominal breathing Inability to speak in complete sentences
  • 16. Signs of complicated asthma are as follows: Equality of breath sounds: Check for equality of breath sounds (pneumonia, mucous plugs, barotrauma). The amount of wheezing does not always correlate with the severity of the attack. A silent chest in someone in distress is more worrisome. Jugular venous distension from increased intrathoracic pressure (from a coexistent pneumothorax) Hypotension and tachycardia (think tension pneumothorax) Fever, a sign of upper or lower respiratory infections
  • 17. Outcomes and complications of asthma in pregnancy Preeclampsia Pregnancy-induced hypertension Uterine hemorrhage Preterm labor Premature birth Congenital anomalies Fetal growth restriction Low birth weightNeonatal hypoglycemia, seizures, tachypnea, and neonatal intensive care unit (ICU) admission
  • 18. Fetal surveillance during pregnancy primary affect on the fetus from asthma, or any other pulmonary disease, is chronic hypoxia. The impact of hypoxia can manifest in several ways, including growth restriction or more significantly, fetal death. Shortly after a woman with asthma becomes pregnant, she should have an early ultrasound to confirm her pregnancy dating. Women should be instructed to monitor fetal activity during the course of the pregnancy. A third-trimester ultrasound can be considered in a woman with well-controlled asthma who has appropriate growth in the fundal height.
  • 19. If the growth is not appropriate or the woman has an acute exacerbation, fetal testing should be started. Testing may include umbilical artery Doppler flow velocity studies, nonstress testing (NST) or biophysical profiles (BPP). The frequency of such testing would depend on the severity of the patient’s asthma or the degree of growth restriction .
  • 20. Other differential diagnosis of asthma are: Upper airways obstruction laryngeal edema Acute left ventricular failure Carciniod tumors Recurrent pulmonary emboli Endobronchial disease  foreign body aspiration, neoplasm & bronchial stenosis Eosinophilc pneumonias
  • 21. Airway obstruction Amniotic fluid embolism Acute congestive heart failure (CHF), secondary to peripartum cardiomyopathy Physiologic dyspnea of pregnancy
  • 22. Measures of Assessment and Monitoring Two aspects: – Initial assessment and diagnosis of asthma – Periodic assessment and monitoring
  • 23. Initial Assessment and Diagnosis of Asthma Determine that:  Patient has history or presence of episodic symptoms of airflow obstruction  Airflow obstruction is at least partially reversible  Alternative diagnoses are excluded Does patient have history or presence of episodic Symptoms of airflow obstruction?  Wheeze, shortness of breath, chest tightness, or cough  Asthma symptoms vary throughout the day  Absence of symptoms at the time of the examination does not exclude the diagnosis of asthma
  • 24. Is airflow obstruction at least partially reversible?  Use spirometry to establish airflow obstruction: – FEV1 < 80% predicted; – FEV1/FVC <65% or below the lower limit of normal  Use spirometry to establish reversibility: – FEV1 increases >12% and at least 200 mL after using a short- acting inhaled beta2-agonist Are alternative diagnoses excluded?  Vocal cord dysfunction, vascular rings, foreign bodies, other pulmonary diseases
  • 25. Additional Tests Reasons for Additional Tests The Tests Patient has symptoms but spirometry is – Assess diurnal variation of peak flow normal or near normal over 1 to 2 weeks – Refer to a specialist for bronchoprovocation with methacholine histamine, or exercise; negative test may help rule out asthma Suspect infection, large airway lesions, heart – Chest x-ray disease, or obstruction by foreign object Suspect coexisting chronic obstructive pulmonary – Additional pulmonary function studies disease, restrictive defect, or central airway obstruction – Diffusing capacity test Suspect other factors contribute to asthma – Allergy tests—skin or in vitro (These are not diagnostic tests for asthma.) – Nasal examination – Gastroesophageal reflux assessment
  • 26. Classification of Asthma Severity: Clinical Features Before Treatment Days With Nights With PEF or PEF Symptoms Symptoms FEV1 Variability Step 4 Continuous Frequent 60% >30% Severe Persistent Step 3 Daily 5/month >60%-<80% >30% Moderate Persistent Step 2 3-6/week 3-4/month 80% 20-30% Mild Persistent Step 1 2/week 2/month 80% <20% Mild Intermittent Footnote: The patient’s step is determined by the most severe feature.
  • 27. 1. Mild Intermittent Asthma •Symptoms less than twice a week •Symptoms at night less than twice a month • No symptoms between episode 2. Mild Persistent • Weekly, but not daily symptoms • Episodes that may affect activity and sleep • Symptoms at night more than twice a month
  • 28. 3. Moderate Persistent • Daily symptoms requiring bronchodialator inhaler use • Episodes that affect activity and sleep • Symptoms at night more than once a week 4. Severe Persistent • Continuous symptoms • Episodes that are frequent • Symptoms at night all the time • Activities are limited because of symptoms • Symptoms occur while on maximal therapy
  • 29. New strategy of asthma management are as below GINA - 2006 Characteristic Controlled Partly controlled Uncontrolled Day time symptoms None(twice or less/ More then week) twice/week Limitations of None Any activities Three or more features of partly Nocturnal None Any controlled asthma symptoms/awakeni present in any week ng Need for None(twice or less/ More than reliever/rescue week) twice/week treatment Lungs function normal <80% predicted or (PEF or FEV1 personal best (if known exacerbation none One or more /year One in any week
  • 30. step 1 Step 2 Step 3 Step 4 Step 5 Asthma education and environmental control As need rapid acting β2 agonist As needed rapid acting β2 agonist Select one Select one Add one or more Add one or both Low dose ICS Low dose ICS + Medium or high-dose Oral glucocortico- LABA ICS + LABA steroids (lowest dose) Controller option Leukotriene modifier Medium or high dose Leukotriene modifier Anti IgE treatment ICS Low dose ICS + Sustained release leukotriene modifier theophylline Low dose ICS + sustained release theophylline
  • 31. DRUGS USED IN ASTHMA Bronchodilators Anti-inflammatory Agents Corticosteroids Beta agonists Muscarinic Methyxanthines antagonists Slow Release Anti-inflammatory inhibitors Drugs
  • 32. Bronchodilators (a) Beta agonists • ß2 selective agonists e.g. albuterol given by inhalation via aerosol • stimulation of adenylyl cyclase - increases cAMP in bronchial smooth muscle - increases bronchodilation • extensively used and very effective in asthmatics • Salbutamol--- 2-4mg oral, 0.5mg im /sc, 100-200mcg/puff • Terbutaline----.25mg sc/inhalation,5mg oral. • Long acting---- salmeterol/formoterol---(9-12 hrs)- 25mcg/puff, 2 puffs B D.
  • 33. (b) Muscarinic antagonists e.g. Ipratropium Use: • Ipratropium is available as pressurized aerosol • not as useful as ß2 agonists in majority of asthmatics • useful in chronic obstructive pulmonary disease
  • 34. (c) Methyxanthines e.g. theophylline .100-300mg tds  major therapeutic preparation = aminophylline slow iv 250-500mg Use: •administered as theophylline salt orally •diminishing use now because of more effective inhaled bronchodilators • used in patients who donít respond to anti- inflammatory agents or ß2 agonists
  • 35. Anti-inflammatory Agents (a) Mast cell stabilisers--- e.g. Cromolym Na  prophylactic drugs used as aerosol to inhibit antigen and exercise induced asthma  no effect on smooth muscle tone or bronchospasm Use: • inhaled cromolyn prevents allergen or exercise-induced asthma • 1mg/puff,2puff qid • Nedocromil---4mg/2puff bd.
  • 36. (b) Corticosteroids e.g. lipid soluble corticosteroids (beclomethazone, 100,200,250,mcg Budesonide 200-400mcg bd-qid triamcinolone used in aerosols) Use: • used in asthma that is non-responsive to bronchodilator therapy • high dose for several weeks followed by low dose, then given alternate days C) leukotriene antagonist: --monteleukast 10 mg od zafirleukast—20 mg bd. Md001921.jpg d)Anti IgEm(Omalizumab) : s/c inj 2 to 4 weeks e)Immunotherapy
  • 37. When Having a Severe Asthma Episode  Go to the emergency room right away  Signs of a severe episode  Rescue or inhaler medicine doesn’t help within 15 minutes  Person’s lips or fingernails are blue  Person has trouble walking or talking due to shortness of breath
  • 38. Immediate management: Oxygen therapy by tight fitting facemask (60%). Nebulised salbutamol 2.5 +/- 0.5mg ipratropium Start glucocorticoid therapy - prednisolone 30-60mg p.o. or hydrocortisone 200mg i.v. Urgent chest X-ray to exclude pneumothorax Urgent blood gas Reassess in 15 min or if life-threatening features appear Consider i.v. aminophylline if life-threatening features or fails to improve after 15-30 minutes  ventilation needed if PEFR continues to fall despite medical therapy, patient becoming drowsy /confused/exhausted or deteriorating blood gases
  • 39. Late management:  Step down initially by converting from nebulised to usual inhaled device (eg MDI) checking that their technique is adequate.  Patient is discharged only when PEFR normalized (80-90% of their best) without dipping. They should also be discharged on high-dose inhaled glucocorticoid, which should continue, until they are reviewed in clinic.  The latter is important in preventing early relapse.
  • 40. LABOUR & DELIVERY Asthma exacerbations are rare in labor and delivery due to the increase in serum cortisol Asthma medications should not be discontinued through labor and delivery. Prostaglandin E2 is safe for cervical ripening, as is oxytocin. The agent 15-methyl prostaglandin F2-alpha should be avoided because it may cause severe bronchospasm. methylergonovine may cause dyspnea, asthma is not an absolute contraindication, and therefore it can be used when appropriate in the management of postpartum hemorrhage.
  • 41. Fentanyl is preferred to morphine and meperidine, which can release histamine. Epidural anesthesia is usually advised because it decreases oxygen consumption and minute ventilation. Epidural anesthesia also decreases the possibility of requiring general anesthesia if an emergency cesarean becomes indicated during labor
  • 42. Postpartum period During the postpartum period, women should initially continue the same asthma medications they required during pregnancy. Close peak flow monitoring is indicated, particularly in those with poorly controlled or moderate-to-severe asthma.

Editor's Notes

  1. Clinically characterized by paroxysms of dysnea, cough and wheezing
  2. Interaction among the residents and infiltrating inflammation cells in the airway surface epithelium inflamatory mediators and cytokines
  3. Vascular Mucus production
  4. 3) Environmental and air pollution
  5. 5) infections
  6. 6) Exercise rtrazine
  7. Types of asthma
  8. growth in the fundal height.
  9. Eosinophilc pneumonias
  10. 1
  11. New strategy of asthma management are below