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Asthma

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05/19/2024

Asthma
• Asthma is the commonest chronic medical illness
• Affecting up to 7% of women of childbearing age
• It is often undiagnosed and when recognized, may be
undertreated.

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Clinical features
• Symptoms
 cough
Breathlessness
Wheezy breathing
Chest tightness

Symptoms are commonly worse at night and in the early morning.

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Clinical features
• Triggers factors are:
Pollen
Animal dander
Dust
Exercise
Cold
Emotion
Upper respiratory tract infections

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Signs
• Signs are often absent unless seen during an acute attack.
Increased respiratory rate
Inability to complete sentences
Wheeze
Use of accessory muscles
Tachycardia

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Pathogenesis

• Reversible bronchoconstriction is caused by the following:

Smooth muscle spasm in the airway walls

Inflammation with swelling and excessive production of mucus

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Diagnosis

•A hallmark of asthma is variability and reversibility of the


bronchoconstriction.

• The degree of bronchoconstriction is measured with PEFR or more


preferably spirometry to measure FEV1 and forced vital capacity(FVC).

• A typical feature is morning ‘dipping; in the peak flow.a > 20% diurnal
variation in PEFR for 3 or more days a week during 2 week PEFR diary is
diagnostic.
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Other diagnostic features

• Greater than 15% improvement in FEV1 following inhalation of beta-


sympathomimetic bronchodilator.

• A greater than 15% fall in FEV 1 following 6 minutes of exercise

• Fractional concentration of expired nitric oxide is raised in


allergic/eosinophilia asthma.

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Effect of pregnancy on asthma
• Asthma may improve, deteriorate or remain unchanged during
pregnancy.
• Women with only mild disease are unlikely to experience problems
• Severe asthma are at a greater risk of deterioration, particularly late in
pregnancy.

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Effect of pregnancy on asthma

• Acute asthma in labour is unlikely because of increased endogenous


steroids at this time.

• Deterioration in disease control is commonly caused by reduction or


even complete cerssation of medications due to fear about its safety.

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Effect of asthma on pregnancy

• There are no adverse effects on pregnancy outcome.

• Poorly controlled asthma, associated with chronic or intermittent


maternal hypoxiaemia, may adversely effect the fetus.

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Effect of asthma on pregnancy
• Some associations exit between maternal asthma and the followings;
Pregnancy induced hypertension/ pre-eclampsia
Preterm birth and preterm labour
Low birth weight infants
Fetal growth restrictions(FGR)
Neonatal morbidity, for example:
o Transient tachypnoea of newborn
o Neonatal hypoglycemia
o Neonatal seizures
o Admission to the neonatal intensive care unit

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Management
• Women should be advised that their asthma is unlikely to adversely
affect their pregnancy.
• Emphasis in the management of asthma is the prevention, rather than
treatment.
• Complete control is defined as the absence of daytime symptoms,
night time awakening due to asthma, need for rescue medication,
exercebations and limitations on activity including exercise, and
normal FFEV1 or PEFR > 80% predicted.

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Management
• Mild intermittent asthma is managed with inhaled short-acting
“reliever” (β2-agonist) medication as required ( step 1).
• If usage of a ‘reliever’ (β2-agonist) inhaler exceeds three times per
week, regular inhaled anti-inflammatory medication with a steroid
‘preventer’ (e.g. beclomethasone) inhaler [400 µg/day] should be
commenced (step 2).
• The next step in therapy is either the addition of a long-acting
‘reliever’ β2-agonist (LABA) e.g. salmeterol, or an increase in the
dose of inhaled steroid (800 µg/ day) (step 3)

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Management
• Further steps involve a trial of additional therapies e.g. leukotriene
receptor antagonist (see later), slow-release oral theophylline or oral
β2-agonist. Alternatively, the dose of inhaled steroid can be increased
to 2000 µg/day (step 4).
• If these measures fail to achieve adequate control, then continuous or
frequent use of oral steroids becomes necessary. The lowest dose
providing adequate control should be used, if necessary with steroid
sparing agents (step 5).

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Management
• Educate women with asthma
– Women should be advised to stop smoking.
– Explanation and reassurance regarding the importance and safety of regular
medication in pregnancy is essential to ensure compliance.
– Women with asthma should be encouraged to avoid known trigger factors.
– Home peak flow monitoring and written personalized self-management plans
should be encouraged.
– Use of a large volume spacer may improve drug delivery and is recommended
with high doses of inhaled steroid.
– Women should be counselled about indications for an increase in inhaled
steroid dosage and if appropriate given an ‘emergency’ supply of oral steroids.

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Management

• The treatment of asthma in pregnancy is essentially no different from


the treatment of asthma in non-pregnant women. All the drugs in
widespread use to treat asthma, including systemic steroids, are safe in
pregnancy and during lactation

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Medication
β2-Agonists

• β2-Agonists from the systemic circulation cross the placenta rapidly,


but very little of a given inhaled dose reaches the lungs and only a
minute fraction of this reaches the systemic circulation.

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Medication

• Studies show no difference in perinatal mortality, congenital


malformations, birthweight, Apgar scores or delivery complications
when pregnant women with asthma treated with inhaled β2-agonists
are compared with women with asthma not using β2-agonists and non-
asthmatic controls

• LABA e.g. salmeterol (Serevent®), are also safe in pregnancy.

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Corticosteroids
• Use of both inhaled and oral steroids is safe in pregnancy.
• Fluticasone propionate (Flixotide®) is a longer acting inhaled
corticosteroid that may be used for those requiring high doses of
inhaled steroids.
• Combination inhalers of corticosteroids plus LABA, for example,
budesonide/ formoterol (Symbicort®) and fluticasone/salmeterol
(Seretide®), are widely available and may aid compliance.

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Corticosteroids

• Prednisolone is metabolized by the placenta, and very little (10%)


active drug reaches the fetus.

• There is no evidence of an increased risk of miscarriage, stillbirth,


other congenital malformations or neonatal death attributable to
maternal steroid therapy.

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Corticosteroids

• Long-term, high-dose steroids may increase the risk of preterm rupture


of the membranes.

• Oral steroids will increase the risk of infection, gestational diabetes


and cause deterioration in blood glucose control in women with
established diabetes in pregnancy. Blood glucose should be checked
regularly.

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Corticosteroids

• The development of hyperglycaemia is not an indication to


discontinue or decrease the dose of oral steroids.

• Oral steroids for medical disorders in the mother should not be


withheld because of pregnancy.

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Leukotriene receptor antagonists

• These agents (e.g. montelukast and zafirlukast) block the effects of


cysteinyl leukotrienes in the airways.

• Studies do not suggest any increased risk of congenital malformations


or other adverse outcomes with their use in pregnancy.

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Acute severe asthma

• Acute severe attacks of asthma are dangerous and should be


vigorously managed in hospital.

• The treatment is no different from the emergency management of


acute severe asthma in the non-pregnant patient.

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Acute severe asthma

• The features of acute severe asthma are:

– PEFR 33%–50% best/predicted


– Respiratory rate >25/min
– Heart rate >110/min
– Inability to complete sentences in one breath

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Management
• – High flow oxygen.
• – β2-agonists (e.g. salbutamol 5 mg) administered via a nebulizer
driven by oxygen.
• β2-agonists can be administered by repeated activations of a metered
dose inhaler via an appropriate large-volume spacer.
• Repeated doses or continuous nebulization (salbutamol 5–10 mg/h)
may be indicated for those with a poor response.

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Management
• – Nebulized ipratropium bromide (0.5 mg 4–6 hourly) should be
added for severe or poorly responding asthma.
• – Corticosteroids (intravenous [i.v.] [hydrocortisone 100 mg] and/or
oral [40– 50 mg prednisolone for at least 5 days]).
• – IV rehydration is often appropriate.
• – Chest x-ray (CXR) should be performed if there is any clinical
suspicion of pneumonia or pneumothorax, or if the woman fails to
improve.

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Life-threatening clinical features:

• – PEFR 4.6 kPa

• – Silent chest, cyanosis, feeble respiratory effort

• – Bradycardia, arrythmia, hypotension

• – Exhaustion, confusion, coma

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Management

• Management of life-threatening or acute severe asthma that fails to


respond should involve consultation with the critical care team and
consideration should be given to
• – i.v. β2-agonists
• – i.v. magnesium sulphate 1.2–2 g infusion over 20 minutes.

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Intrapartum management

• Asthma attacks in labour are exceedingly rare because of endogenous


steroid production.

• Women receiving oral steroids (prednisolone >5 mg/day for >3 weeks
prior to delivery) should receive parenteral hydrocortisone (50–100
mg three or four times/day) to cover the stress of labour, and until oral
medication is restarted.

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Intrapartum management

• Prostaglandin E2, used to induce labour, to ripen the cervix, and


prostaglandin E1 (misoprostol) for termination of pregnancy or for
treatment or prevention of postpartum haemorrhage, are bronchodilators
and are safe to use.

• The use of prostaglandin F2α to treat life-threatening postpartum


haemorrhage may be unavoidable, but it can cause bronchospasm and
should be used with caution in women with asthma.
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Intrapartum management

• All forms of pain relief in labour, including epidural analgesia and


Entonox can be used safely by women with asthma, although in the
unlikely event of an acute severe asthmatic attack, opiates for pain relief
should only be used with extreme caution. Regional, rather than general
anaesthesia, is preferable because of the decreased risk of chest infection
and atelectasis.

• Ergometrine has been reported to cause bronchospasm.


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Conclusion

• Pregnancy itself does not usually influence the severity of asthma. ]

• For the majority of women, asthma has no adverse effect on


pregnancy outcome, and women should be reassured accordingly.

• Poorly controlled severe asthma presents more of a risk to the


pregnancy than the medication used to prevent or treat it. This small
risk is minimized with good control.
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Conclusion

• Education and reassurance, ideally prior to pregnancy, concerning the safety of


asthma medications during pregnancy are integral parts of management.

• Decreasing or stopping inhaled anti-inflammatory therapy during pregnancy is


a frequent cause of potentially dangerous deterioration in disease control.

• Inhaled, oral and i.v. steroids and inhaled, nebulized and i.v. β2-agonists are
safe to use in pregnancy and while breastfeeding.

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Conclusion

• Treatment of asthma in pregnancy differs little from the management


in the non-pregnant patient. Effective control of the disease process
and its accompanying symptoms is a priority.

• An increase in the dose or frequency of inhaled steroids should be the


first step if symptoms are not optimally controlled on the current dose
of inhaled steroids and the inhaler technique is good.

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