Resp R-W Flashcards

1
Q

What is Respiratory distress syndrome?

A

Respiratory compromise in neonate due to surfactant deficiency

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2
Q

What is the background of Respiratory distress syndrome?

A

50% of infants born 28-32 weeks. Most common <28weeks.

Surfactant deficiency -> high alveolar surface tension -> alveolar collapse -> right to left intraplaural shunting. Deficiency may be:

· Primary: immaturity, hypoxia intrapartum, acidosis, hypothetmia, hypotension

· Secondary: MAS, intrapartum asphyxia, CpulmonaryLD, infections

Respiratory compromise made worse in immature infants due to soft thoracic cage -> ribs and sternum cave in when trying to generate high ithroacic pressure -> seesaw breathing.

Pathology:

· Macroscopic: lung is airless and ruddy – liver looking

· Microscopic: diffuse alectasis of distal air pacesw tih distension of airways and perilymphatic areas.

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3
Q

What is the history and exam findings of Respiratory distress syndrome?

A

Respiratory distress signs: tachypnea, tachycardia, recession, grunting, nasal flaring, seesay breathing, cyanosis, there may be aopnea and hypothermia.

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4
Q

What are the investigations for Respiratory distress syndrome?

A

ABG: respiratory acidosis (alectasis) metabolic acidosis (lactate generation fue to hypoxia) and low O2 (R -> L shunting)

CXR: bilateral diffuse ground glass appearance

Echo: ?PDA

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5
Q

What is the management of Respiratory distress syndrome?

A

Prevention: identify at risk infants, ACT to estimate fetal lung maturity (leptin:sphigomyelin ratio, phosphatydilglycerol presence), prophylactic antenatal steroids in at risk infants to increase surfactant production.

Treatment: Surfactant administration via ETT to be given prophylactically at delivery, correction of hypoglycaemia, hypothermia and electrolyte issues. Prophylactic antibiotics.

Ventilation: CPAP via nasal cannula or conventional. HFOV may have to be used.

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6
Q

What are the complications and prognosis of Respiratory distress syndrome?

A

Acute: PTX, ICH, periventricular leucomalacia, PDA, pulmonary haemorrage, NEC or FG perforation

Chronic: CLD, ROP, neurological impairment

Improving with prenatal steroids and surfactant therapy. Used to be poor (60%M)

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7
Q

What is Transient Tachypnoea of the newborn?

A

Acute, self limiting tachypnea in the absence of another cause (ie. met acidosis, RDS or infection)

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8
Q

What is the background of Transient Tachypnoea of the newborn?

A

Most common cause of respiratory distress in infants. <1% of neonates have this. Occurs in term neonates.

Secondary to impairment in resorption of lung fluid, leading to low pulmonary compliance and decreased tidal volume with increased dead space.

Associated with elective C section, precipitate deliveries, and maternal asthma.

Pathophysiology: In uter lung epithelium secretes CL- and fluid, does not reabsorb Na. Post delivery switch to Na reabsorption due to NA/A production/ Changes in O2 tension. With short delivery or lack of stages (C section) Na+ resorption does not occur -> fluid remains.

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9
Q

What is the history and exam findings of Transient Tachypnoea of the newborn?

A

Occurs within first 1-3h following normal delivery. Most resolve in 72h.

Early onset tachypnea in neonate, may have signs of respiratory distress

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10
Q

What are the investigations for Transient Tachypnoea of the newborn?

A

CXR: Perihilar streaking (distended veins and lymph) patchy infiltrates and fluid, flat diaphragm.

ABG: low pO2

Blod culture: exclude infections or pneumonia

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11
Q

What is the management of Transient Tachypnoea of the newborn?

A

Exclude other causes (RDS, infection by GBS, MAS, pulmonary haemorrage, cerebral yperventilation.

Ventrilatory support may be required, CPAP

IV fluids, NBM until RR <60, to decrease aspiration. Prophylactic antibiotic unless infection excluded.

Diuretics do not improve outome.

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12
Q

What are the complications and prognosis of Transient Tachypnoea of the newborn?

A

None with good tx.

Excellent, self limiting, ?wheezing in childhood. .

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13
Q

What is URT infection?

A

A number of different conditions affecting the upper respiratory tract (coryza, otitis, pharyingitis, tonsillitis)

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14
Q

What is the background of URT infection?

A

Very common with two peaks – starting nursery (2-3) and school (4-5)

· Viruses cause >90% URTI

· Coryza: rhinovirus, coronavirus, RSV

· Pharyngitis: adeno, entero, rhino, GAS

· Tonsillitis: EBV, GAS

· Otitis: flu, paraflu, entero, adeno, Strep pneu, HI, Moraxella

· Non immunized: diphtheria,

Asociated with immunodeficiency if recurrent

Pathology: inflammation of URT with agent leading to production of serous discharge and swelling of mucosal lining.

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15
Q

What is the history and exam findings of URT infection?

A

General: ethargy, poor feeding

Coryza: sneezing, sore throat, fever

Pharyngitis/tonsillitis: cough, pain swallowing, fever, sore abdomen (mesenteric adenitis_

Mono: Prolonged lethargy, malaise, sore throat

Otitis: ear pain, conductive hearing loss.

General: pyrexia, tachycardia, lymphadenopathy (cervical)

Coryza: nasal dischars

Pharyngitis: pharynx, tonsillar fauces and soft palate inflamed.

Tonsillitis: red, swollen tonsils with or without white exudates. Follicular with white exudates EBV, GAS,

Otitis media: red tympanic membrane and conductive hearing loss.

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16
Q

What are the investigations for URT infection?

A

Throat swab: for culture and PCR, GAS. Test diphtheria in non immunized.

Blood: ASOT, monospot.

17
Q

What is the management of URT infection?

A

Symptomatic pyrexia: Control fever and prevent dehydration. Do no use aspiring (Reye syndrome). Reducing fever does not prevent febrile seizures.

Active treatment: oral antibiotics (penicillin, erythromycin) if GAS found, to prevent rheumatic fever.

Surgical: tonsillectomy if recurrent tonsillitis.

18
Q

What are the complications and prognosis of URT infection?

A

Recurrent tonsillitis, peritonsillar abscess (quinsy), post streptococcal immunological response (PSGN, rhF)

Excellent – usually lasts at most 2 weeks.

19
Q

What is Whooping cough (pertussis)?

A

RT infection characterized by cough followed by whoop due to sudden massive inspiratory effort.

20
Q

What is the background of Whooping cough (pertussis)?

A

Boracella pertussis bacterium, incubation of 7-10d and contagious three weeks from cough onset. Preterm infants or those with systemic abnormalities are at higher risk of complications.

594/y in England and wales. Peak age 3, very dangerous if child <6m.

21
Q

What is the history and exam findings of Whooping cough (pertussis)?

A

Three stages:

  1. Catharral stage: 1-2weeks, indistinguishable from common URTI with nasal congestion, cough, sneeze etc.
  2. Paroxysmal stage: 1-6 weeks, consisting of paroxysms coughing with whoop, with vomiting, dyspnea, seizures. <6m no whoop but aopnea instead.
  3. Convalescent stage: weks to months, chronic cough.

Older children: no specific stages.Symptoms in these patients feature continouous coughing, suffocation and strangulation feelings.

22
Q

What are the investigations for Whooping cough (pertussis)?

A

High WCC, lymphocytosis, CRP/ESR.

Immunohistochemistriy DIF testing of nasal swabs.

23
Q

What is the management of Whooping cough (pertussis)?

A

Immunisation is key

Prophylaxis: avoid contact, erythromycin to siblings of affected.

Respiratory isolation of affected for 5d after stargint Abx, or until 3wk post coughing onset.

Admit if M6m, vomiting with dehydration, respiratory distress, aopnea associated with peroxysms.

NOtifiable disease CDCC

24
Q

What are the complications and prognosis of Whooping cough (pertussis)?

A

Peroxysmal cough – may cause petechiae and conjunctival haemorrages. Dehydration and weight loss.

3% seizures. If encephalopathy occurs, 1/3 die, 1/3 remain impaired, 1/3 recover.

Secondary infections: otitis media, bronchiectasis, pneumonia

6-8wk, prolonged illness may occur (100 day cough). Significant mortality in <6m.

25
Q

What is viral induced wheeze?

A
  • An acute viral infection of the lower respiratory tract

* The most common serious respiratory infection of infancy

26
Q

What are the clinical features of viral induced wheeze?

A

Intermittent episodes

• Very common, especially in < 5 years

27
Q

What investigations do you use for viral induced wheeze?

A

clinical diagnosis in < 5 years

28
Q

What is the management of viral induced wheeze?

A

o Salbutamol trial → continue if effective
▪ If child has cough and becoming wheezy and short of breath, can give
4-6 puffs of inhaler with spacer (maximum of 4 hourly)
▪ If symptoms worsening, give 6-10 puffs every 4 hours and arrange to
see GP
▪ If symptoms of respiratory distress, call 999 and give 10 more puffs whilst awaiting ambulance

o Monitoring

29
Q

What is sinusitis?

A

• Symptomatic inflammation of the mucosal lining of the nasal cavity and paranasal
sinuses
• Infection of the paranasal sinuses may occur with viral URTIs
• Occasionally you might get a secondary bacterial infection
• The frontal sinuses are rarely affected because they do not develop until late
childhood

30
Q

When do you refer to hospital with sinusitis?

A

• Refer to hospital if there are symptoms and signs of:
o Severe systemic infection
o Intraorbital or periorbital problems (e.g. periorbital cellulitis, displaced
eyeball, double vision)
o Intracranial complications (e.g. features of meningitis)

31
Q

How do you manage sinusitis if there are symptoms under 10 days?

A

o Do NOT offer an antibiotic
o ADVISE
▪ Acute sinusitis is usually caused by a virus and takes 2-3 weeks to
resolve
• It can be complicated by bacterial infection (2% risk)
▪ Symptoms, such as fever, can be managed using paracetamol or
ibuprofen
▪ Some people may find some relief using nasal saline or nasal
decongestants
▪ Medical advise should be sought if symptoms worsen rapidly, if
they do not improve in 3 weeks or become systemically unwell

32
Q

How do you manage sinusitis if there are symptoms over 10 days?

A

o Consider high-dose nasal corticosteroid for 14 days for adults and children > 12 years old (e.g. mometasone)
▪ May improve symptoms but unlikely to affect duration of illness
▪ Could cause systemic side-effects

o Consider NO antibiotic prescription or back-up prescription
▪ Antibiotics are unlikely to change the course of the illness
▪ The back-up prescription should be used if symptoms get
considerably worse of it is still has not improved by 7 days
▪ 1st line: phenoxymethylpenicillin
• NOTE: clarithromycin if penicillin allergy
▪ 2nd line: co-amoxiclav

o Advise patients to seek medical advice if they develop complications or
their symptoms don’t improve/worsen
▪ Consider alternative diagnoses such as dental infection

o ADVICE: NHS Choices information on Sinusitis