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Pneumonia in Immunocompromised Patients

by Sanjay Sethi, MD

Pneumonia in immunocompromised patients is often caused by unusual pathogens but may also be caused by the same pathogens as those that cause community-acquired pneumonia (see Community-Acquired Pneumonia and see Overview of Pneumonia). Symptoms and signs depend on the pathogen and on the conditions compromising the immune system. Diagnosis is based on blood cultures and bronchoscopic sampling of respiratory secretions, sometimes with quantitative cultures. Treatment depends on the immune system defect and the pathogen.

The potential pathogens in patients with compromised immune system defenses are legion. Likely pathogens depend on the type of defect in immune system defenses (see Table: Pneumonia in Immunocompromised Patients). However, respiratory symptoms and changes on chest x-rays in immunocompromised patients may be due to various processes other than infection, such as pulmonary hemorrhage, pulmonary edema, radiation injury, pulmonary toxicity due to cytotoxic drugs, and tumor infiltrates.

Pneumonia in Immunocompromised Patients

Hmmune System Defect

Disorders Or Therapy Associated With Defect*

Likely Pathogens

Defective PMNs


Acute leukemia, aplastic anemia, cancer chemotherapy

Gram-negative bacteria, Staphylococcus aureus, Aspergillus sp, Candida sp

Defective chemotaxis

Diabetes mellitus

S. aureus, gram-negative aerobes

Defective intracellular killing

Chronic granulomatous disease

S. aureus

Defective alternative pathway

Sickle cell disease

Streptococcus pneumoniae, Haemophilus influenzae

C5 deficiency

Congenital disorder

S. pneumoniae, S. aureus, gram-negative bacteria

Cell-mediated immunity

T-cell deficiency or dysfunction

Hodgkin lymphoma, cancer chemotherapy, corticosteroid therapy

Mycobacteria, viruses (eg, herpes simplex virus, cytomegalovirus), Strongyloides sp, opportunistic fungi (eg, Aspergillus, Mucor, Cryptococcus spp), Nocardia sp, Toxoplasma sp


Pneumocystis jirovecii, Toxoplasma sp, cytomegalovirus, herpes simplex virus, opportunistic fungi (eg, Aspergillus, Mucor, Cryptococcus spp), mycobacteria

Humoral immunodeficiency

B-cell deficiency or dysfunction

Multiple myeloma, agammaglobulinemia

S. pneumoniae, H. influenzae, Neisseria meningitidis

Selective deficiency: IgA, IgG, IgM

S. pneumoniae, H. influenzae


P. jirovecii, cytomegalovirus, S. pneumoniae, H. influenzae

*Examples. Many disorders cause multiple defects.

PMN = polymorphonuclear leukocytes.

Symptoms and Signs

Symptoms and signs may be the same as those that occur with community-acquired pneumonia (see Community-Acquired Pneumonia : Symptoms and Signs) or hospital-acquired pneumonia (see Hospital-Acquired Pneumonia : Symptoms and Signs) in immunocompetent patients. Symptoms may include malaise, chills, fever, rigor, cough, dyspnea, and chest pain. However, immunocompromised patients may have no fever or respiratory signs and are less likely to have purulent sputum if they are neutropenic. In some patients, the only sign is fever.

Pearls & Pitfalls

  • Have a high index of suspicion for pneumonia in immunocompromised patients because symptoms can be atypical.or muted.


  • Chest x-ray

  • Assessment of oxygenation

  • Induction or bronchoscopy to obtain sputum

  • Blood cultures

  • Pathogens predicted based on symptoms, x-ray changes, and type of immunodeficiency

Chest x-ray and assessment of oxygenation (usually by pulse oximetry) is done in immunocompromised patients with respiratory symptoms, signs, or fever. If an infiltrate or hypoxemia is present, diagnostic studies should be done. Chest x-ray may be normal in Pneumocystis jirovecii pneumonia, but hypoxia is usually present.

Sputum testing and blood cultures are done. Sputum testing should include Gram stain, mycobacterial and fungal stains and cultures, and sometimes testing for viruses (eg, PCR for cytomegalovirus in a transplant patient or in a patient with AIDS). If signs, symptoms, or risk factors for Aspergillus infection are present (see Aspergillosis : Pathophysiology), serum galactomannan assay should be done.

Optimally, a firm diagnosis is made with induced sputum, bronchoscopy, or both, especially in patients with mild pneumonia, severe defects in immune function, or failure to respond to broad-spectrum antibiotics.

Likely pathogens can often be predicted based on symptoms, x-ray changes, and the type of immunodeficiency. In patients with acute symptoms, the differential diagnosis includes bacterial infection, hemorrhage, pulmonary edema, a leukocyte agglutinin reaction to transfusion of blood products, and pulmonary emboli. M An indolent time course is more suggestive of a fungal or mycobacterial infection, an opportunistic viral infection, P. jirovecii pneumonia, tumor, a cytotoxic drug reaction, or radiation injury.

X-rays showing localized consolidation usually indicate an infection involving bacteria, mycobacteria, fungi, or Nocardia sp. A diffuse interstitial pattern is more likely to represent a viral infection, P. jirovecii pneumonia, drug or radiation injury, or pulmonary edema. Diffuse nodular lesions suggest mycobacteria, Nocardia sp, fungi, or tumor. Cavitary disease suggests mycobacteria, Nocardia sp, fungi, or bacteria, particularly S. aureus.

In organ or bone marrow transplantation recipients with bilateral interstitial pneumonia, the usual cause is cytomegalovirus, or the disease is idiopathic. A pleural-based consolidation is usually aspergillosis. In patients with AIDS, bilateral pneumonia is usually P. jirovecii pneumonia. About 30% of patients with HIV infection have P. jirovecii pneumonia as the initial AIDS-defining diagnosis, and > 80% of AIDS patients have this infection at some time if prophylaxis is not given (see Prevention of opportunistic infections). Patients with HIV infection become vulnerable to P. jirovecii pneumonia when the CD4+ helper cell count is < 200/μL (see Pneumocystis jirovecii Pneumonia).


  • Broad-spectrum antimicrobial therapy

The antimicrobial therapy depends on the immune system defect and the risk factors for specific pathogens. Consultation with an infectious diseases specialist is usually indicated. In patients with neutropenia, empiric treatment depends on the immune system defect, x-ray findings, and severity of illness. Generally, broad-spectrum antibiotics that are effective against gram-negative bacilli, Staphylococcus aureus, and anaerobes are needed, as for hospital-acquired pneumonia (see Hospital-Acquired Pneumonia : Treatment). If patients with conditions other than HIV infection do not improve with 5 days of antibiotic therapy, antifungal therapy is frequently added empirically.

Therapies to enhance immune system function (see Pneumonia in Immunocompromised Patients : Prevention) are an important adjunct for the treatment of pneumonia in immunocompromised patients.


Therapies to enhance immune system function are indicated for the prevention of pneumonia in immunocompromised patients. For example, patients with chemotherapy-induced neutropenia should receive granulocyte-colony stimulating factor (G-CSF, or filgrastim), and patients with hypogammaglobulinemia due to an inherited or acquired disease (eg, multiple myeloma, leukemia) should receive IV immune globulin.

Patients with HIV and CD4+ helper cell count < 200/μL should receive daily prophylactic therapy with trimethoprim/sulfamethoxazole or other appropriate therapy.

Vaccination is also important in these patients. For example, patients at risk of pneumonia with encapsulated bacteria (eg, hypogammaglobulinemia, asplenia) should receive vaccinations again pneumococcus and H. influenzae.

Key Points

  • Consider typical as well as unusual pathogens in immunocompromised patients who have pneumonia.

  • If patients have hypoxemia or an abnormal chest x-ray, do further testing, including sputum testing, ideally with induced or bronchgoscopically obtained sample.

  • Begin with broad-spectrum antimicrobial therapy.

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