Chest Medicine



Chest Medicine






The ageing lung

Most of the functional impairment of the lungs that is seen in older people is due to disease, often smoking-related. Intrinsic ageing leads only to mild functional deterioration. The respiratory system has a capacity well in excess of that required for normal activity, so intrinsic ageing:



  • Does not lead to symptoms in the non-smoker without respiratory disease


  • In those with respiratory disease (eg emphysema) will cause progressively worsening symptoms with age even if the disease itself remains stable


  • In acute disease, eg pneumonia, may cause earlier decompensation or a more severe presentation


Specific respiratory changes

Seen in healthy older people are similar to those seen in mild chronic obstructive pulmonary disease, and include:



  • Decreased elastic recoil causing small airways to collapse at low lung volumes and increased residual volume


  • Increased chest wall stiffness, due to:



    • Degenerative change in intercostal, intervertebral and costovertebral joints


    • Osteoporosis and kyphoscoliosis


    • Weaker respiratory muscles that may have lower endurance


  • Reduced gas exchange and increased ventilation-perfusion (V/Q) mismatch, due to collapse of peripheral airways while perfusion remains intact


  • Impaired chemoreceptor function, leading to lessened ventilatory response to decreased P a O 2 or increased P a CO 2


  • Impaired microbial defence mechanisms. Less effective mucociliary clearance and less sensitive cough reflex


Observed consequences of these changes

These include:



  • Increased susceptibility to infection (underventilation of and inability to clear sputum from dependent lung zones)


  • Lower maximum minute ventilation (weaker musculature acting against a stiffer chest)


  • An approximately linear fall in PaO2 with age (70.3% /year). Since alveolar oxygen tension remains stable, the alveolar-arterial (A-a) oxygen gradient rises


  • Reduced exercise capacity. However, oxygen consumption and cardiac output decline in proportion to lung function, so the lungs are rarely the limiting factor in exercise performance



Breathlessness in older people is often multifactorial



  • Chronic breathlessness in an individual may be the result of, eg, decreased fitness, obesity, an inefficient gait (osteoarthritis or stroke), kyphosis, previous lung damage (eg apical fibrosis due to tuberculosis (TB)) and intrinsic ageing. In this example, note that only one of the factors is specific to the lung


  • In the acutely breathless patient, pathologies commonly coexist, eg infection, fast AF, and heart failure. The classic treatment triad of digoxin, furosemide, and amoxicillin is not a sign of diagnostic indecision but is often entirely appropriate treatment



Respiratory infections

Cough with or without sputum, shortness of breath, fever or chest pain is a very common presentation in older patients. It is very important to try to distinguish which part of the airway is primarily affected because this implies completely different pathogens, prognoses, and treatment strategies. Try to avoid aggregating all such patients together using the imprecise term ‘chest infection’.


Upper respiratory tract infections

These are caused by viruses, eg rhinovirus, respiratory syncytial virus, influenza, and parainfluenza. Symptoms include nasal discharge and congestion, fever, and sore throat. These may extend to the lower tract and then include cough, wheeze, sputum production, or worsening of existing cardiopulmonary disease.

With increasing age:



  • Upper respiratory tract infection becomes less frequent, but more severe


  • The risk of complications increases. These include:



    • Lower tract infection such as bronchitis or pneumonia, which may be bacterial or viral


    • Bronchospasm


    • Extrapulmonary manifestations such as falls, immobility, and delirium


  • Postinfection weakness, fatigue, and anorexia is more severe and prolonged, maybe lasting several weeks


  • Frequency of hospital admission and death increases substantially


Acute bronchitis

Occurs with inflammation of the bronchial tree with little or no involvement of lung parenchyma (which is pneumonia). Is commoner in those with chronic airways disease (see image ‘Asthma and COPD: assessment’, p.342).

Compared with pneumonia, bronchitis:



  • Has fewer systemic features and a better prognosis


  • Has no chest symptoms and signs, eg pleuritic pain or crepitations, but may have prominent cough and wheeze


  • CXR not routinely indicated


  • Can be managed less aggressively, with more reliance on supportive treatment and bronchodilators than antibiotics. Often viral in origin, if an antibacterial is thought appropriate, give amoxicillin to cover Streptococcus pneumoniae (erythromycin or clarithromycin if penicillin sensitive)




Influenza

This is the most serious viral respiratory tract infection, and is often a severe, systemic illness with pulmonary bacterial superinfection (Staphylococcus aureus, Haemophilus influenzae, Strep. pneumoniae). It occurs most commonly in December-February. Antigenic shifts result in periodic pandemics (large-scale epidemics).

Presentation is similar in young and old, ie rapid onset of fever (rigors, chills), myalgia, headache, and fatigue with variable degrees of prostration. Compared with less threatening viruses such as rhinovirus:



  • Nausea, vomiting, diarrhoea, high fever, rigors and ocular symptoms (eg photophobia) are more common


  • Rhinorrhoea is less common

Less common serious complications include myocarditis and meningoencephalitis. Mild meningism is common, and if combined with other sinister features (eg altered conscious level) is an indication for CSF sampling.

Diagnosis is usually based on combining clinical assessment with epidemiological data, particularly current influenza incidence. Some other viruses can cause an identical clinical syndrome, and serological test results are not immediately available. Thus an initial assessment cannot produce an absolutely confident microbiological diagnosis. The syndrome may therefore most precisely be labelled ‘influenza-like illness’.

Positive virological diagnosis in the context of increased community incidence or a care home outbreak is helpful by prompting vigorous attempts to reduce transmission of infection.






Further reading

NICE. Amantadine, oseltamivir and zanamivir for the treatment of influenza (2009). Online: image www.nice.org.uk/ta168.



Pneumonia


Pneumonia



  • This is a syndrome of acute respiratory infection with shadowing on CXR


  • May be primarily lobar, bronchial or mixed pattern


  • Symptoms may be mild and are often non-organ specific eg fever, malaise


  • Common presenting scenarios include cough (often unproductive), delirium, reduced conscious level, lethargy, anorexia, falls, immobility and dizziness. Rarely patients can present with shock, coma and adult respiratory distress syndrome (ARDS)


  • Chest pain, dyspnoea and high fever are less common than in younger people. Signs may be minimal:



  • Tests often guide management



    • Chest radiograph often reveals minimal infective infiltrate. Associated problems can include malignancy, effusion, or heart failure


    • Blood cultures should be sent, but sputum culture is rarely useful unless TB is suspected


    • White cell count may be raised, normal, or even depressed


    • CRP is often normal early in the illness. A very high CRP suggests pneumococcal disease or severe sepsis of any cause


    • U,C + E guide fluid management. Renal impairment is a sign of poor prognosis


    • Arterial blood gas (ABG) sampling is not usually necessary, unless oxygen saturations are <90% ; oximetry is much better tolerated and usually sufficient to guide oxygen therapy


  • Organisms (see Table 11.1)



    • Often no causative organism is identified


    • Pneumococcus is a common pathogen in all settings, including hospital


    • Viral pneumonia, especially influenza, is under-recognized, and is the second most common cause of community-acquired pneumonia


    • Legionella and Mycoplasma pneumonias are uncommon. Mycoplasma is much more frequent during epidemics, occurring every 3 years or so


    • Unusual organisms are more common in frail patients, in higher dependency environments and in those who have recently received courses of antibiotics. These organisms include Gram negatives (which colonize the oropharynx) and anaerobes (a result of aspiration of gut contents). MRSA pneumonia and septicaemia is an increasing problem and may be contracted in the community, ie not just a hospital problem









Table 11.1 Pneumonia pathogens in various care settings; in approximate order of frequency



































Community-acquired


Care home


Hospital


Strep. pneumoniae (> 30% of cases)


Strep. pneumoniae (> 30% of cases)


Gram-negative aerobic bacilli, eg Klebsiella, Pseudomonas aeruginosa


Viral, eg influenza, parainfluenza, respiratory syncytial virus


Viral, eg influenza, parainfluenza, respiratory syncytial virus


Anaerobes, eg Bacteroides, Clostridium. Especially in those at risk of aspiration, eg immobility, swallowing difficulty, prolonged recumbency or impaired conscious level


Haemophilus influenzae


Gram-negative aerobic bacilli, eg Klebsiella, P. aeruginosa


Staph. aureus


Gram-negative aerobic bacilli, eg Klebsiella, P. aeruginosa


H. influenzae


Strep. pneumoniae and H. influenzae. NB These may be the most common pathogens—in non-acute settings, eg rehabilitation wards—in the well, less frail patient


Legionella pneumophila. Mycoplasma pneumoniae if epidemic


Anaerobes eg Bacteroides, Clostridium. Especially in those at risk of aspiration, eg immobility, swallowing difficulty, prolonged recumbency or impaired conscious level


Viral, eg influenza, parainfluenza, respiratory syncytial virus


Other, eg TB


Other, eg TB



Following influenza, think of secondary bacterial infection, especially with Strep. pneumoniae (most common), H. influenzae or Staph. aureus


Following influenza, think of secondary bacterial infection, especially with Strep. pneumoniae (most common), H. influenzae or Staph. aureus





Pneumonia: treatment

Treatment is much more than antimicrobials alone:



  • Assess and optimize fluid volume status; give oral, s/c, or iv fluid as appropriate. Concurrent heart failure is common, but volume depletion more so


  • If there is subjective dyspnoea or moderate/severe hypoxaemia, then supplement oxygen, titrating the inspired oxygen concentration upwards to achieve arterial oxygen saturations > 90% (see image ‘Oxygen therapy’, p.348). For lesser degrees of hypoxaemia, it is not necessary to subject patients to claustrophobic, uncomfortable oxygen masks: simply monitoring saturations may be sufficient



    • Exercise caution in COPD: observe the patient closely, both clinically and with serial ABG sampling


    • Avoid the use of nasal specs acutely: if ventilatory drive is poor, inspired oxygen concentrations are very uncontrolled


  • Encourage mobility. If immobile, sit upright in bed, and sit out in a chair


  • Request physiotherapy if there is a poor cough, or lobar/lung collapse


  • Use saline nebulizers to loosen secretions which are difficult to expectorate and bronchodilator nebulizers when wheeze suggests associated bronchoconstriction


  • Minimize risk of thromboembolism unless contraindicated through prophylactic heparin, early mobilization, and compression stockings


  • Assess pressure sore risk and act accordingly (see image ‘Pressure sores’, p.502)


  • If dyspnoea, anxiety or pain is very distressing, consider opiates. Side effects include respiratory depression, sedation and delirium, so begin with small doses and assess effect


  • Anticipate possible deterioration, and judge in advance the appropriate levels of intervention. Would renal dialysis, ventilation and/or cardiopulmonary resuscitation be effective and appropriate? (See image ‘Diagnosing dying and estimating when treatment is without hope’, p.666)


  • Keep the family informed. Where possible, enlist their help, eg in encouraging eating and drinking




Antimicrobials

Refer to local guidelines, reflecting pathogen sensitivities, and drug costs.


Community or care home settings



  • Amoxicillin orally is usually effective (vs. Strep. pneumoniae and H. influenzae). Erythromycin or clarithromycin if penicillin-allergic


  • Add clarithromycin (or erythromycin which has more gastric side effects) if there are features of atypical pneumonia, there is a Mycoplasma epidemic, or the patient may have had influenza


  • Co-amoxiclav orally has added activity against some Gram-negatives and Staph. aureus, and may be more effective in the frail patient or where aspiration is likely


  • Ciprofloxacin alone should be used rarely—it has Gram negative activity, but is less effective against Strep. pneumoniae, an important pathogen in most settings. If an antimicrobial is sought that will cover both chest and urinary sepsis, a better choice may be co-amoxiclav or trimethoprim


  • iv antibiotics are only necessary if the patient is very unwell (CURB-65 score of 3 or above) or unable to swallow. Co-administration of cefuroxime and erythromycin is a good choice in the unwell patient, treating all likely pathogens effectively. If you suspect MRSA pneumonia, add vancomycin. Convert to oral therapy and change broad to narrower spectrum drugs when the patient’s condition improves and/or culture results are known to minimize complications, eg CDAD (see imageClostridium difficile-associated diarrhoea’, p.614). Often, only 48hr or less of broad spectrum, iv therapy is needed


Hospital-acquired infection

This presents a difficult dilemma. Hospitalized patients, especially those who are more frail and have spent longer in hospital, are prone to Gramnegative and anaerobic pulmonary infections. However, they are also susceptible to the adverse effects (especially diarrhoea) of broad spectrum antimicrobials.

A hierarchical approach is sensible, considering likely pathogens and illness severity;



  • In the less frail patient who remains well, begin amoxicillin alone, co-amoxiclav or a combination of amoxicillin and ciprofloxacin (all po). Broaden the spectrum only if the patient deteriorates or culture results suggest that the likely pathogen is insensitive


  • If a patient is at high risk of Gram-negative infection (frail, dependency, prolonged stay, invasive procedures, aspiration risk), begin with iv cefuroxime (or equivalent). Narrow the antimicrobial spectrum when the patient’s condition improves and/or a pathogen is identified


  • If the patient has received multiple courses of treatment, seek microbiology advice


  • In all cases take blood cultures, and monitor the patient carefully



Further reading

British Thoracic Society guidelines online: image www.brit.thoracic.org.uk.






Vaccinating against pneumonia and influenza


Vaccine delivery



  • Both vaccines should be offered simultaneously in October or early November to all aged > 65 years, especially:



    • The frail


    • Care home residents


    • The immunosuppressed


    • Those with comorbidity, eg heart failure, COPD


  • Reliable delivery of these vaccinations depends upon effective information management systems in general practice, and substantial efforts by patients, carers, district nurses, and GP nurses


  • A common reason to have missed immunization is to have been a long-term inpatient (eg undergoing rehabilitation) during the autumn immunization period. Hospitals should ensure that these inpatients are immunized


  • Vaccinating healthcare workers, especially those working in long-term care settings, reduces the spread of infection and therefore death due to influenza among patients


Pneumococcal vaccine



  • Pneumovax® II, a multivalent pneumococcal polysaccharide vaccine, is effective against 65% of serotypes


  • Immunity remains for at least five years, perhaps for life


  • Bacteraemia is reduced by at least 50%. The effect on incidence of pneumonia itself is less clear


Influenza vaccine



  • The trivalent vaccine is prepared from currently prevalent serotypes


  • Immunity develops in <2 weeks, and it is therefore useful during epidemics


  • Immunity remains for up to 8 months


  • The risk of pneumonia, hospitalization, or death due to influenza is reduced by over half


Postexposure antiviral prophylaxis



  • Pharmacological prophylaxis of influenza is currently recommended when an unimmunized, high-risk group adult (eg care home resident) has had close contact with a person with influenza-like illness during a period when flu is prevalent (NICE 2008)


  • Treatment with neuraminidase inhibitors must be initiated within 24hr (for oseltamivir) or 24hr (for zanamivir) (see image ‘Upper respiratory tract infections’, p.314)


  • Consider why immunization was not performed. Is it too late to administer this year (this contact may not have ‘flu, but the next one might)? If not, then optimize the chances of immunization next year



Pulmonary fibrosis

This common problem is much underdiagnosed in older people due to a combination of under-investigation and overlap of clinical signs with common pathologies such as heart failure.

Consider when breathlessness coexists with profuse fine chest crepitations, with or without clubbing. On CXR, there may be bilateral pulmonary shadowing consistent with pulmonary oedema, but with little supporting evidence (eg normal heart size, absent Kerley B lines).


Causes



  • Idiopathic. The most common type in older people, known as usual interstitial pneumonia


  • Connective tissue disease, eg rheumatoid arthritis (most common), systemic lupus erythematosus, sarcoidosis. Lung involvement is sometimes the first manifestation of the multisystem disease


  • Drugs, eg amiodarone, nitrofurantoin rarely


  • Occupational exposure, eg asbestos, silica


  • If localized, consider TB, bronchiectasis, and radiotherapy


Tests



  • The diagnosis is usually confirmed by high-resolution CT scanning, which can also help distinguish subgroups likely to respond to immunosuppressive treatment


  • Respiratory function tests may be useful (a restrictive picture with decreased transfer factor is usual) but typically adds little in the frail older person


  • Refer to a respiratory physician to confirm diagnosis and guidance on management


Prognosis

This is very variable—about a third are clinically stable, a third improve and a third deteriorate at rates that vary greatly between individuals. Some can live with pulmonary fibrosis for years without significant functional impairment.

Jul 22, 2016 | Posted by in GERIATRICS | Comments Off on Chest Medicine

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