Specificity of UPV in patients with Asthma bronchiale/High School (nurse)

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Epidemiology[edit | edit source]

  • 3-6% of the population (1993 - 6.4%) generally a permanent increase !
  • Asthmatic condition – mortality 12% in intubated patients and 1–2% in non-intubated patients.
  • 80% of patients who died with status asthmaticus have bronchial asthma for more than 5 years.
  • The so-called refractory asthma only about 5% of all patients.

Basic characteristics[edit | edit source]

  • Bronchoconstriction.
  • Airway edema
  • Hyperreactivity of DCs to various stimuli.
  • Airway remodeling.
  • An asthma attack is triggered by SMOKING, dust, pollen, dust mites, drugs (THP, beta blockers, ANP,...), cold, physical exertion.

Pathophysiology from the point of view of UPV[edit | edit source]

  • Increased resistance in DC.
  • Air trapping.
  • Hyperinflation.
  • An increase in the negativity of pleural pressures.
  • Increase in functional residual capacity, residual volume and total lung capacity.
  • An increase in the ventilation-perfusion ratio.
  • Increase in dead space and alveolar ventilation (until exhaustion, then decrease).‏‏

Treatment of acute exacerbation[edit | edit source]

  • Higher FiO 2 and high flow oxygen.
  • Inhaled β-mimetic until signs of overdose (aerosol, spacer).
  • Systemic or inhaled steroids (120–180 mg Methylprednisone/24 hours in 3–4 doses after 48 hours → 60–80 mg until the patient's condition improves).
  • Aminophylins in infusion.
  • Mucolytics.
  • ATB only in case of infection.

Non-standard methods of bronchodilation[edit | edit source]

  • Ketamine 10-40 ucg/kg/min ?
  • Magnesium up to 10 g/24 hours.
  • NO.
  • Helium (the earlier and in more seriously ill patients, the greater the benefit)‏.

UPV in Asthmatics[edit | edit source]

  • UPV complicated and risky.

Indication[edit | edit source]

  • Impairment of consciousness.
  • Respiratory rate above 40 D/min.
  • Rising/falling pulsus paradoxus.
= Heart rate whose waves are smaller during inhalation than during exhalation systolic pressure decreases during inspiration. As a result of the increase in the volume of blood in the chest during inspiration, this difference is to a certain extent physiological.
  • PDrop in pO 2 below 7.5 kPa.
  • Rise of pCO 2 above 7 kPa → acidosis.
  • Persistent lactic acidosis.
  • Barotrauma.
  • Silent chest despite patient's inspiratory efforts.
  • Inability to communicate, muscle fatigue, exhaustion.

Use of ventilation mode[edit | edit source]

The goal of UPV is ventilation and oxygenation support and prevention of extreme pH changes and severe hypoxia.

  • The basis is controlled hypoventilation and permissive hypercapnia.
  • Volume-controlled ventilation with constant inspiratory flow is more suitable.
  • Respiratory rate less than 10 D/min. with a 1:3 to 1:4 ratio of inspira to expiria.
  • Low PEEP 2–4 cmH 2 O → distance therapy (keeping the lung open).
  • The patient is semi-sitting.
  • If there are no complications, the time for UPV in a critical condition is 3-5 days.
  • Extubation when bronchospasm resolves, decreased secretion production, good muscle strength.

Complications of UPV[edit | edit source]

  • Hypotension.
  • PNO.
  • Arrhythmia.
  • ETI dislocation.
  • Pneumonia.
  • Circulation failure.
  • KBleeding into the GIT.
  • Pulmonary embolization.
  • Pneumomediastinum.
  • Subcutaneous emphysema.

Asthma bronchiale in children[edit | edit source]

  • More heterogeneous character and time course different from adults.
  • 10% of children.

A predisposed individual.

  • Repeatedly in contact with adverse environmental influences (polluted air, smoking, unhealthy lifestyle and nutrition, etc.) → contact with the so-called trigger (allergen, exertion, smoke, viral infection, etc.) → airway obstruction (contraction of the smooth muscles in the bronchi, mucosal swelling and increased mucus secretion) with symptoms of expiratory dyspnea and cough.
  • The most common cause of exacerbation in childhood is viral infections.

Causes of asthma problems in children[edit | edit source]

  • The etiology varies in different periods.
  • Respiratory viruses:
  • Infants/toddlers - temperatures are often present → very good prognosis even with recurrences; usually disappear by school age.
  • the exception is especially human rhinoviruses, which damage the mucous membrane of the bronchi and thus can contribute to the later development of persistent asthma.
  • Allergies.
  • Atopic predisposition → worse prognosis, often progression to persistent asthma.
  • The later obstructive bronchitis manifests itself in childhood, the more likely the allergic etiology and progression to persistent asthma.
  • Other.
  • Physical stress, stress, cigarette smoke, etc. → less often in children, schoolchildren/adolescents.
  • Around the age of 3, 3 basic groups of children are symptomatically intertwined:
  • The so-called transient wheezers → children who "grow out" of the problem on their own.
  • Non-atopic wheezers → děti s poškozenými dýchacími cestami v důsNon-atopic wheezers → children with damaged airways due to infection, this defect is reversible in case of non-allergenic terrain.
  • Real asthmatics.

Investigation[edit | edit source]

  • Medical history - family history, especially atopy, smoking, pets,...
  • Laboratory height – inflammatory markers, …
  • Immunological examination including total IgE and ECP, possibly. specific IgE.
  • Spirometry (approx. from 3-4 years).
  • Whole-body body plethysmography → an airtight chamber allowing pressure and volume changes that take place inside to be measured (also possible in non-cooperative children).

Asthma predictive index[edit | edit source]

  • Major criteria – asthma in the parents, atopic eczema in the child, sensitivity to airborne allergens.
  • Small criteria – wheezing outside the cold season, eosinophils in the blood count >4%, food sensitivity
→ presence of one major or 2 minor criteria → probability of asthma.

Therapy[edit | edit source]

Acute bronchial obstruction[edit | edit source]

  • The 1st choice is short-acting inhaled bronchodilators → β 2 -mimetic (salbutamol), anticholinergic (ipratropium bromide) newly questionable meaning.
  • In the case of insufficient effect or severe p.os course; and corticosteroids.
  • Hospitalization if the clinical condition does not improve after 3 repeated inhalations of bronchodilators.

Long-term treatment[edit | edit source]

  • Indicated if the frequency or severity of exacerbations significantly impairs quality of life and asthma is not under control (control criteria same as for adults).
  • 1st choice of inhaled corticosteroids (treatment effectiveness is evaluated after at least 3 months),
→ after control is achieved, the dose is reduced to the lowest level,
→ if there is insufficient control,
→ → necessary control of correct use, compliance with measures → if in order,
→ increase the dose of inhaled corticosteroids (ICS) or add a leukotriene receptor antagonist (montelukast = Singulair).
  • Long-acting β 2 mimetics (=LABA) – they are not recommended in monotherapy, in combination only if ICS alone are not enough.
  • Measures to eliminate causative agents.

Inhaler attachments[edit | edit source]

  • Significant simplification of inhalation, coordination of inhalation and squeezing is eliminated.
  • Wash the spacer and let it dry, do not wipe!!!! → formation of static electricity trapping particles.
  • 1 injection from the dispenser = 5-10x calm inhalation and exhalation without removing the dispenser and spacer.

Determining the fullness of the aerosol dispenser[edit | edit source]

  • Immerse the dispenser in the water and determine the fullness of the dispenser according to the drop towards the bottom (see picture).
File:Bombicky.jpg
Aerosol dispenser

Adverse effects of ICS[edit | edit source]

  • LOCAL:
  • Common: oropharyngeal candidiasis, throat, tongue, pharynx, esophagus irritation, cough.
  • More rarely: early and delayed hypersensitivity reactions in the face, lips, eyes, pharynx, redness, rash, urticaria, eczema, swelling, angioedema, bronchospasm.
  • SYSTEMS:
  • To varying extents with all ICS, they are dose-dependent, but long-term negative effects on children's development have not been proven.
  • Adrenal effects - cortisol synthesis.
  • Induction of osteoporosis, slowing of growth rate.
  • Psychological changes.
  • At high doses, deterioration of healing, atrophy of the skin.
  • Disorders of glucose tolerance.
  • Increased incidence of glaucoma and cataracts.

Links[edit | edit source]

Source of information[edit | edit source]

  • VOJTÍŠEK, Petr. Bronchial asthma in children and adults [lecture for subject Modul UPV, specialization Intensive care nurse - postgraduate study, Higher vocational school medical school Secondary and higher medical school Ústí nad Labem]. Ústí nad Labem. 18.12. 2011. 
  • DOSTÁL, Pavel, et al. Fundamentals of artificial pulmonary ventilation. 2. edition. prague : Maxdorf, 2005. ISBN 80-7345-059-3.