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BY
DR.HAFSA
 Pulmonary diseases are one of the major indirect
causes of maternal death.
 Significant physiological changes occur in
pregnancy to meet metabolic needs of both
mother and fetus.
 Hormonal changes in pregnancy affect the URT &
upper airway mucosa, producing hyperemia,
mucosal edema, hypersecretion & increased
mucosal friability.
 Estrogen is responsible for producing tissue
edema, capillary congestion & hyperplasia of
mucous glands.
 The enlarging uterus & the hormonal effects
produce anatomical changes to the thoracic cage.
 The AP/PA & transverse diameter of the thorax
increases.
 Diaphragm function remains normal.
 Anatomical changes to the thorax produce a
decrease in FRC, which is reduced 10-20% by
term.
 The RV can decrease slightly during pregnancy.
 The increased circumference of the thoracic cage
allows VC to remain unchanged & TLC decreases
only minimally by term.
 Hormonal changes do not significantly affect
airway function
 Pregnancy does not change lung compliance.
 The MV increases significantly, beginning in the
first trimester & reaching 20-40% above baseline
at term.
 Alveolar ventilation increases by 50-70%.
 The increase in ventilation occurs because of
increased metabolic CO2 production.
 The VT increases by 30-35%.
 The respiratory rate remains relatively constant.
 Physiological hyperventilation results in
respiratory alkalosis with compensatory renal
excretion of bicarbonate.
 The arterial CO2 pressure reaches a plasma level
of 28-32 mmHg & bicarbonate is ↓ to 18-21
mmol/L, maintaining arterial pH in the range of
7.40-7.47.
 Mild hypoxemia might occur when the patient is
in supine position.
 Oxygen consumption ↑ at the beginning of the
trimester & ↑ by 20-33% by term because of
fetal demands & maternal metabolic processes.
Physiologic dyspnea.
 The increase in minute ventilation that accompanies
pregnancy is often perceived as shortness of breath.
 Shortness of breath at rest or with mild exertion is so
common that it is often referred to as physiologic
dyspnea.
Pathologic dyspnea
 Increased respiratory rate greater than 20 breaths
per minute, arterial PCO2 less than 30 or greater than
35, hypoxemia or abnormal measures on forced
expiratory spirometry, or cardiac echocardiography
 Abrupt or paroxysmal episodes of dyspnea suggest
an abnormal condition
 Dyspnea of pregnancy
 Allergic rhinitis
 Bronchial asthma
 Tuberculosis
 Pneumonia
 Influenza
 Anemia
 Interstitial lung disease
 Pleural diseases
 Pulmonary thromboembolism
 Amniotic fluid embolism
 Pneumothorax
 Gestational trophoblastic disease
 Peripartum cardiomyopathy
 Drugs e.g., tocolytics
 It is one of the most common conditions
complicating the pregnancy.
 Pregnancy is a heterogeneous immune state
affecting the course of the asthma, during which
the latter may worsen or improve or remain
stable with equal distribution.
 Prevalence of bronchial asthma in pregnancy is
about 8%-12%
 Bronchial asthma is safe during pregnancy if
controlled.
 PIH
 Pre eclampia
 Intrauterine growth retardation (IUGR)
 low birth weight
 premature birth
 increased elective caesarian delivery
 Exacerbations during first trimester are
associated with increased risk of congenital
malformations
 Diagnosis of bronchial asthma during pregnancy
is similar to that done in non pregnant state,
which includes
 History
 Clinical examination
 pulmonary function tests(PFT).
 Management of bronchial asthma during
pregnancy is almost similar to non
pregnant.
 Patient education
 avoidance of triggers
 Goals of bronchial asthma management
include decreasing the use of short acting
beta-2 agonists (SABA), preventing the
exacerbations and maintaining near normal
lung function
 Long acting beta-2 agonists(LABA) are used
in step up therapy only if asthma is not
controlled by medium or low dose inhaled
corticosteroids (ICS).
 Systemic corticosteroids are associated with
more adverse effects than inhaled and should be
used only in moderate and severe bronchial
asthma.
 Use of systemic corticosteroids in early
pregnancy is associated with cleft lip, cleft
palate, preeclampsia and gestational diabetes.
 Treatment of acute severe asthma in pregnancy
is almost similar to non pregnant counterparts.
 Initially the patients should be treated with
inhaled albuterol or salbutamol 2.5mg for every
20 min followed by systemic corticosteroids.
 Inhaled ipratropium bromide can be added to
this regimen.
 They are monitored for every 30-60 minutes.
Treating maternal hypoxia and continuous fetal
monitoring are more important
 Risk factors for tuberculosis (TB) in
pregnancy include positive family
history or past history of TB,
residence in area of high prevalence
of TB.
 Treatment of TB in pregnancy is
similar to that administered to non
pregnant women.
 Streptomycin is contraindicated
because of
and vestibular defects in fetus.
 Breast feeding is not
contraindicated in women taking
anti-TB treatment
 Pneumonia is one of the important causes of
indirect maternal mortality
 Most common organisms being
Streptococcus pneumoniae, Haemophilus
influenza, Mycoplasma pneumonia.
 Clinical presentation is similar to that of non-
pregnant woman but risk of respiratory
failure and empyema is increased
 Patient presents with dyspnea. Respiratory
rate is not increased
 Patients with suspected pneumonia should
get a chest radiograph with abdominal
shield.
 Other investigations are sputum microscopy,
sputum culture and serologic tests.
 Quinolones and tetracyclines should be
avoided in pregnancy
 It is most common viral infection in pregnancy
 resulting in increased morbidity and mortality.
 Risk of hospitalization for an acute
cardiopulmonary illness is three to four times
more likely in third trimester
 Influenza(H1N1) should be suspected in patients
not responding to routine antibiotics and in
pneumonia or respiratory failure.
 Increased risk of preterm delivery or a low-birth
weight infant, severe pneumonia, maternal
deaths have been observed
 It includes prevention and supportive care.
 Antipyretics should be used for the treatment of
fever as these not only reduces fetal tachycardia,
but are also been associated to be a protective
agent against congenital abnormalities.
 Dehydration should be avoided.
 The use of antiviral medications in pregnancy is
controversial.
 Neuraminidase inhibitors(zanamivir, oseltamivir)
are also used in the treatment.
Respiratory disorders in pregnancy

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Respiratory disorders in pregnancy

  • 2.  Pulmonary diseases are one of the major indirect causes of maternal death.  Significant physiological changes occur in pregnancy to meet metabolic needs of both mother and fetus.
  • 3.  Hormonal changes in pregnancy affect the URT & upper airway mucosa, producing hyperemia, mucosal edema, hypersecretion & increased mucosal friability.  Estrogen is responsible for producing tissue edema, capillary congestion & hyperplasia of mucous glands.  The enlarging uterus & the hormonal effects produce anatomical changes to the thoracic cage.  The AP/PA & transverse diameter of the thorax increases.  Diaphragm function remains normal.
  • 4.  Anatomical changes to the thorax produce a decrease in FRC, which is reduced 10-20% by term.  The RV can decrease slightly during pregnancy.  The increased circumference of the thoracic cage allows VC to remain unchanged & TLC decreases only minimally by term.  Hormonal changes do not significantly affect airway function  Pregnancy does not change lung compliance.
  • 5.  The MV increases significantly, beginning in the first trimester & reaching 20-40% above baseline at term.  Alveolar ventilation increases by 50-70%.  The increase in ventilation occurs because of increased metabolic CO2 production.  The VT increases by 30-35%.  The respiratory rate remains relatively constant.
  • 6.  Physiological hyperventilation results in respiratory alkalosis with compensatory renal excretion of bicarbonate.  The arterial CO2 pressure reaches a plasma level of 28-32 mmHg & bicarbonate is ↓ to 18-21 mmol/L, maintaining arterial pH in the range of 7.40-7.47.  Mild hypoxemia might occur when the patient is in supine position.  Oxygen consumption ↑ at the beginning of the trimester & ↑ by 20-33% by term because of fetal demands & maternal metabolic processes.
  • 7. Physiologic dyspnea.  The increase in minute ventilation that accompanies pregnancy is often perceived as shortness of breath.  Shortness of breath at rest or with mild exertion is so common that it is often referred to as physiologic dyspnea. Pathologic dyspnea  Increased respiratory rate greater than 20 breaths per minute, arterial PCO2 less than 30 or greater than 35, hypoxemia or abnormal measures on forced expiratory spirometry, or cardiac echocardiography  Abrupt or paroxysmal episodes of dyspnea suggest an abnormal condition
  • 8.  Dyspnea of pregnancy  Allergic rhinitis  Bronchial asthma  Tuberculosis  Pneumonia  Influenza  Anemia  Interstitial lung disease  Pleural diseases  Pulmonary thromboembolism  Amniotic fluid embolism  Pneumothorax  Gestational trophoblastic disease  Peripartum cardiomyopathy  Drugs e.g., tocolytics
  • 9.  It is one of the most common conditions complicating the pregnancy.  Pregnancy is a heterogeneous immune state affecting the course of the asthma, during which the latter may worsen or improve or remain stable with equal distribution.  Prevalence of bronchial asthma in pregnancy is about 8%-12%  Bronchial asthma is safe during pregnancy if controlled.
  • 10.  PIH  Pre eclampia  Intrauterine growth retardation (IUGR)  low birth weight  premature birth  increased elective caesarian delivery  Exacerbations during first trimester are associated with increased risk of congenital malformations
  • 11.  Diagnosis of bronchial asthma during pregnancy is similar to that done in non pregnant state, which includes  History  Clinical examination  pulmonary function tests(PFT).
  • 12.  Management of bronchial asthma during pregnancy is almost similar to non pregnant.  Patient education  avoidance of triggers  Goals of bronchial asthma management include decreasing the use of short acting beta-2 agonists (SABA), preventing the exacerbations and maintaining near normal lung function  Long acting beta-2 agonists(LABA) are used in step up therapy only if asthma is not controlled by medium or low dose inhaled corticosteroids (ICS).
  • 13.  Systemic corticosteroids are associated with more adverse effects than inhaled and should be used only in moderate and severe bronchial asthma.  Use of systemic corticosteroids in early pregnancy is associated with cleft lip, cleft palate, preeclampsia and gestational diabetes.
  • 14.  Treatment of acute severe asthma in pregnancy is almost similar to non pregnant counterparts.  Initially the patients should be treated with inhaled albuterol or salbutamol 2.5mg for every 20 min followed by systemic corticosteroids.  Inhaled ipratropium bromide can be added to this regimen.  They are monitored for every 30-60 minutes. Treating maternal hypoxia and continuous fetal monitoring are more important
  • 15.  Risk factors for tuberculosis (TB) in pregnancy include positive family history or past history of TB, residence in area of high prevalence of TB.  Treatment of TB in pregnancy is similar to that administered to non pregnant women.  Streptomycin is contraindicated because of and vestibular defects in fetus.  Breast feeding is not contraindicated in women taking anti-TB treatment
  • 16.  Pneumonia is one of the important causes of indirect maternal mortality  Most common organisms being Streptococcus pneumoniae, Haemophilus influenza, Mycoplasma pneumonia.  Clinical presentation is similar to that of non- pregnant woman but risk of respiratory failure and empyema is increased  Patient presents with dyspnea. Respiratory rate is not increased  Patients with suspected pneumonia should get a chest radiograph with abdominal shield.  Other investigations are sputum microscopy, sputum culture and serologic tests.  Quinolones and tetracyclines should be avoided in pregnancy
  • 17.  It is most common viral infection in pregnancy  resulting in increased morbidity and mortality.  Risk of hospitalization for an acute cardiopulmonary illness is three to four times more likely in third trimester  Influenza(H1N1) should be suspected in patients not responding to routine antibiotics and in pneumonia or respiratory failure.  Increased risk of preterm delivery or a low-birth weight infant, severe pneumonia, maternal deaths have been observed
  • 18.  It includes prevention and supportive care.  Antipyretics should be used for the treatment of fever as these not only reduces fetal tachycardia, but are also been associated to be a protective agent against congenital abnormalities.  Dehydration should be avoided.  The use of antiviral medications in pregnancy is controversial.  Neuraminidase inhibitors(zanamivir, oseltamivir) are also used in the treatment.