The authors would like to acknowledge David A. Miller for his contributions that remain unchanged from the first edition.
Acute respiratory distress syndrome, 518.5
Cardiogenic pulmonary edema, 514
Congestive heart failure, 428.0
Idiopathic pulmonary fibrosis, 515
Pneumonia, 486
Pulmonary edema, 514
Restrictive (inflammatory) lung diseases, 518.89
Sarcoidosis, 135
Tuberculosis, 011.90
PNEUMONIA
I. Definition of pneumonia
A. Acute febrile inflammatory disorder of the lung(s), associated with cough and exertional dyspnea
B. Infiltrate is present on chest x-ray; the appearance of the infiltrate may lag behind the appearance of symptoms by 24 to 48 hours, justifying a repeat chest x-ray at that time.
C. Leukocytosis may be present.
III. Classification of pneumonia
A. “Typical” pneumonias manifest with “classic” findings.
1. Fever
2. Chills
3. Leukocytosis
4. Cough
5. Sputum production
B. “Atypical” pneumonias vary in their presentation.
1. Fever may be high.
2. Leukocytosis
a. May be absent
b. May be associated with a “left shift” in the differential white blood cell count to include a high number of “band” forms
3. Cough is often dry.
D. Occurrence information may assist in defining the type of pneumonia present.
1. Time of year
2. Known epidemic disease
3. Presence of comorbid conditions
E. Community-acquired pneumonias are those acquired within the community setting.
F. Nosocomial pneumonias result from exposure to infection during a stay in a health care facility.
1. Hospital
2. Nursing home
3. Rehabilitation facility
G. Pneumonias are often categorized by risk factors present that predispose the patient to pneumonia.
1. Aspiration pneumonias (related to altered mental status)
2. Obstructive lesions of the airway
a. Tumor
b. Retained bronchopulmonary secretions
3. Inhalation injury–related pneumonia
a. Hypersensitivity pneumonia
b. Near-drowning
IV. Evaluation for possible pneumonia
A. Historical information
B. Physical examination
1. Tachypnea
2. Tachycardia
3. Fever
4. Discomfort
5. Rales (or “crackles”) on auscultation over the affected area(s)
C. Chest x-ray, in a search for new pulmonary infiltrates
D. Laboratory studies
1. CBC, including differential WBC count
2. Blood cultures
3. Gram’s stain and culture of sputum
4. Arterial blood gases and/or pulse oximetry
V. Treatment
A. Antimicrobial therapy with cultures pending (see Chapter 31 for specific treatment guidelines).
B. Antimicrobial therapy should be revised as culture information becomes available and as improvement occurs. In general, the narrowest spectrum antimicrobial to which known organisms are expected to respond should be used.
C. Simultaneous treatment of coexisting illnesses is needed.
1. Chronic obstructive pulmonary disease
2. Congestive heart failure
3. Diabetes
4. Dehydration
D. Not all patients, especially young adults, need hospitalization for pneumonia.
1. The decision to hospitalize a patient with pneumonia should be guided by the following:
a. The possibility of rapidly progressive disease
b. Overall status of the patient (coexisting problems)
c. The patient’s ability to reliably self-administer medication for this illness
2. If in doubt, it is reasonable to observe the patient in hospital during initial therapy and to reassess early response to treatment.
VI. Prevention of pneumonia
A. Vaccination against influenza: Fluvax
1. Repeated annually
2. Some revaccinate within a season in the following circumstances:
If the patient
a. Is immunocompromised
b. Has severe underlying chronic obstructive pulmonary disease or heart disease
B. Vaccination against S. pneumoniae: Pneumovax
1. Repeated every 7 to 10 years or as recommended by the Centers for Disease Control and Prevention
2. Covers only the 23 most virulent strains of S. pneumoniae
TUBERCULOSIS (TB)
I. Etiology: Mycobacterium tuberculosis
II. Incidence
A. The rates of new infection by M. tuberculosis are increasing, especially among the homeless and among those living in crowded conditions in larger metropolitan areas.
B. Alarmingly, the incidence of multidrug-resistant TB (defined as resistant to isoniazid and to rifampin) also appears to be rising, especially along the East and West Coasts of the U.S.
C. This rise has coincided with increased numbers of patients with HIV and AIDS.
IV. Treatment
A. Patient isolation during initial evaluation and treatment, according to Occupational Safety and Health Administration (OSHA) standards, is mandatory.
B. Suspected disease, or smear-positive disease, pending the return of sputum cultures
1. Four-drug therapy
b. Rifampin/rifampicin, 600 mg PO each day (or 10 mg/kg daily; maximum, 600 mg/dose)
c. Ethambutol (Myambutol), 5-25 mg/kg PO each day (maximum, 2.5 g/dose), preceded by screening of color vision. Note: Ethambutol may cause red/green color blindness as an adverse effect, as well as changes in visual acuity.
d. Pyrazinamide, 15-30 mg/kg in three divided doses daily (maximum, 2 g/dose)
2. Revision of therapy when drug sensitivities are known, usually to INH with rifampin
3. Therapy is continued usually for 6 to 9 months (6 months for most patients, 9 months for HIV-positive patients). Intermittent directly observed therapy (DOT) may follow one of three regimens:
a. INH + rifampin + pyrazinamide + ethambutol for 2 months, followed by INH + rifampin 2 to 3 times weekly for an additional 4 months, especially if susceptibility to INH/rifampin is noted
b. INH + rifampin + pyrazinamide + ethambutol daily for 2 weeks, followed by the same agents 2 times weekly for 6 weeks, then INH + rifampin 2 times weekly for 4 months, if susceptibility to INH/rifampin is noted
c. Thrice-weekly dosing of INH + rifampin + pyrazinamide + ethambutol for 6 months
4. For nonadherent patients, DOT may be initiated at 3 times per week, usually after 2 weeks of observed therapy, often in hospital.
C. Prophylaxis
1. Consider for the following patients:
a. Asymptomatic, with a positive PPD and a normal chest x-ray
b. Exposed to active TB who have a negative PPD
c. Undergoing immunosuppressive therapy for other reasons
d. Who have HIV infection
2. Treatment
a. INH, 300 mg PO daily, although controversy exists as to whether 6 months or up to 1 year of therapy should be given
b. Pyridoxine, 50 mg PO daily, may be also chosen during INH therapy.
ACUTE RESPIRATORY DISTRESS SYNDROME (ARDS)/ACUTE LUNG INJURY
I. Etiologies: any of the numerous causes of acute systemic inflammation
A. Bacteremia or other severe systemic infections