Pneumonia in Immunocompromised Patients

Pneumonia in Immunocompromised Patients

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Pneumonia in the immunocompromised host is a complex infection and inflammation of the lower respiratory tract, complicated by widespread multi-drug antibiotic resistance, and aided by medical advances such as improvements in diagnostic measures and immunosuppressive agents. Though overall patient survival has increased, pneumonia is both the most common invasive infection in immunocompromised patients and continues to carry a high mortality and morbidity rate. [1, 2, 3, 4, 5]

The major immunocompromised host groups are those with:

HIV/AIDS

Solid organ and hematopoietic cell transplants

Malignancy on chemotherapy or radiation therapy

Primary immunodeficiencies and autoimmune diseases

Acquired immunodeficiencies: asplenia, long-term steroid use

Complications

Pneumonia in immunocompromised is often complicated by superinfection, drug toxicity, empyema, sepsis, pneumothorax, and acute respiratory distress syndrome (ARDS).

The number of potential pulmonary pathogens is increasing as a result of new immunosuppressive therapies, the emergence of multi-drug­-resistant organisms, and improved diagnostic modalities.

There are four major groups of pathogens responsible for pneumonia in immunocompromised patients. Depending on the underlying immune defect, the likelihood of each of these etiologies for infection is varied.

Bacterial: Tuberculosis (TB) and non-­TB mycobacteria, mainly Mycobacterium avium complex (MAC)

Fungal: Pneumocystis jirovecii, Aspergillus fumigatus, Candida, Cryptococcus neoformans, Mucormycosis species, and other fungi including Coccidioides immitis and Histoplasma capsulatum.

Viruses: ­Cytomegalovirus (CMV), community-acquired respiratory infections including influenza, and herpes simplex virus (HSV) and varicella zoster virus (VZV)

Parasites: ­Strongyloides, Toxoplasmosis

Patients with human immunodeficiency virus (HIV) are at risk for a number of pulmonary infections. Pneumocystis jirovecii (formerly Pneumocystis carinii) remains the most common opportunistic infection in this group, while the incidence of mycobacterial infections has decreased significantly. [6]

HIV causes dysfunction of cell-mediated and humoral immunity. CD4 T cells principally help other cells achieve their effector function. Low CD4 counts, which correlate with the degree of immunosuppression, cause a disruption of B-cell differentiation. Impaired B-cell functions, particularly memory cells, are correlated with increased risk of infection. [7]

Despite the advances in the development of highly active antiretroviral therapy (HAART), pulmonary disease remains an important cause of mortality and morbidity in persons with HIV/AIDS. [8, 9, 10]

HIV is considered to be the greatest risk factor for TB. [11] Patients with HIV are more likely not only to contract TB, but progress from latent to active TB. [12] In addition, they have a higher mortality risk from TB. 

The clinical manifestations of TB in persons with HIV depend on the degree of immunosuppression. In severely immunocompromised individuals, the typical presentation of TB becomes less frequent. Instead of upper lobe cavitary disease, some of these patients present with lower lobe primary pneumonias, nonspecific patterns, or even no chest radiograph findings. [13]

Tuberculin skin test (TST) is more likely to be negative in persons with HIV. Typically, interferon-gamma release assays (IGRAs) are the gold standard for identification of TB-infected individuals; however, in HIV patients, the sensitivity of IGRAs is diminished. In studies, IGRAs perform similarly to the TST. Since both methods have a modest predictive value and suboptimal sensitivity, the choice of test should be based on country guidelines and resource considerations. [14]

Recent studies have shown that the timing of HAART and tuberculosis therapy is important in those concurrently infected. Withholding HAART until the third week of anti-tuberculosis therapy likely reduced TB mortality. [15]

The most common bacterial causes of community-acquired pneumonia (CAP) in patients with HIV are the same as those in the general population [16] , the top three being Streptococcus pneumoniae, Haemophilus influenzae, and Staphylococcus aureus. [17, 18, 19]

However, the risks of contracting Streptococcus pneumonia are increased 10,000-fold in a patient with HIV. [20]  Protease inhibitor (PI)­ containing ART regimens show great effect in lowering this risk. [21]

In a nosocomial setting, Pseudomonas aeruginosa, Staphylococcus aureus, Klebsiella pneumoniae, and Enterobacter species are common.

Fungal pneumonias are divided into opportunistic (i.e. PCP, Candida, Aspergillus, Mucor species) and endemic (Histoplasma capsulatum, Coccidioides immitis, Cryptococcus neoformans).

 

Opportunistic: Pneumocystis jirovecii pneumonia (PJP)

Pneumocystis jirovecii infection remains the most common opportunistic infection among patients with HIV.

It becomes a concern in individuals when CD4 count drops below 200, which is when prophylaxis with Trimethoprim-sulfamethoxazole (TMP-SMX) is recommended. When the A-a gradient is >35 or a room air arterial blood gas pO2< 70, adjuvant corticosteroids are recommended.

Transmission and infectivity of P. jirovecii is incompletely understood, in most cases attributed to reactivation of latently colonized patients. [22]

Opportunistic: Aspergillus

Invasive aspergillus pneumonia is one of the four aspergillosis syndromes that primarily affects immunosuppressed individuals.

In solid organ and hematopoietic transplant patients, there is a bimodal distribution of incidence with peaks during 1. prolonged neutropenia before engraftment and 2. in later stages with corticosteroid therapy in treatment of graft-versus-host disease.

Patients with leukemia and lymphoma have a higher incidence of invasive aspergillosis which is associated with a higher mortality rate. [23]

Invasive aspergillosis is also being increasingly observed in patients with severe COPD who remain on long-term corticosteroid therapy. [24]

There are no reliable biomarkers for detection of fungal cell wall constituents or other specific measures, thus, the recommendation continues to be close monitoring of clinical signs and symptoms for prevention and prophylaxis of opportunistic fungal pneumonias. [25]

Endemic: Cryptococcus neoformans

Cryptococcal pneumonia is more severe in patients with HIV. Patients with pulmonary disease frequently progress to disseminated disease.​ [26]

Most cases are the result of the reactivation of a latent infection.

Endemic: Histoplasma capsulatum

For the immunocompetent host, histoplasmosis is frequently asymptomatic or self-­limited. In the setting of HIV/AIDS, this infection is much more common and frequently progresses to disseminated disease.

This infection is endemic to certain areas of the United States, particularly in states bordering the Ohio River valley and the lower Mississippi River.

Spores of the mold phase are inhaled and cause a localized or patchy bronchopneumonia. CD4 lymphocytes normally activate macrophages to control the infection. [27]

Endemic: Coccidioides immitis

Coccidioides immitis is an organism endemic to large parts of the southwestern United States.

Spores are inhaled and then ingested by pulmonary macrophages. Impaired cell­-mediated immunity in persons with HIV accounts for an increased risk of infection in these patients. [28]  

Viruses

Varicella ­zoster virus

Visceral dissemination of primary varicella, especially pneumonitis, has been reported in persons with HIV. [29]

Parasites

Strongyloides stercoralis

Strongyloides is an human intestinal nematode which can reproduce and persist in the body indefinitely, and affects millions of people worldwide. In immunocompromised individuals, this autoinfective cycle can be amplified into a hyperinfection syndrome. Increased parasite burden migrates rom the gastrointestinal tract, where it causes GI bleeding, into a systemic process. Filariform larvae have been found in the respiratory system, where they cause respiratory distress and sepsis secondary to pneumonia, and the neurological system causing meningitis.

Though the two conditions most often shown to trigger hyperinfection are glucocorticoid treatment and human T-lymphotropic virus type 1 infection, it is also associated with HIV/AIDS and hematologic malignancy. Anthelmintic agents such as ivermectin have been used successfully in both treatment as well as primary and secondary prevention in patients with risk factors. [30]

 

Malignancy, especially hematologic malignancy, is a large risk factor for developing pneumonia. The pathogenicity and severity of disease is related to the degree and duration of neutropenia. Most infectious etiologies are polymicrobial including gram-positive and gram-negative organisms from the upper respiratory tract. However, in about 10-25% of patients, an infectious focus is not identified in sputum, with the only evidence of infection being a positive blood culture. [31]

Patients with profound, prolonged neutropenia are more susceptible to invasive fungal pathogens such as aspergillus species, and the agents of mucormycosis. 

Viruses are also involved, primarily VZV. Respiratory viruses such as influenza, respiratory syncytial virus (RSV), Adenovirus, and Metapneumovirus are increasingly documented in neutropenic patients.

Mortality in patients with febrile neutropenia is 30-50%. [32, 33]

The American Society of Clinical Oncology (ASCO) recommend prophylaxis (eg, with trimethoprim-sulfamethoxazole) for patients receiving chemotherapy regimens associated with >3.5% risk for Pneumocystis jirovecii pneumonia. [34, 35]

 

Solid-organ and bone-marrow transplant patients have a heightened risk of pulmonary infection as well. The specific organ, timeframe since transplant, and use of immunosuppressive medications are all important in predicting these complications.

CMV pneumonitis is common in solid organ transplant, particularly lung, recipients. The risk is higher if the donor is seropositive and the recipient seronegative. Interestingly, the opposite is seen in hematological stem cell transplant (HCT) patients, where there is a higher risk for CMV pneumonitis among seropositive recipients transplanted with seronegative stem cells.

Nocardia species are another notable cause of pulmonary infection in organ transplant patients requiring long-term immunosuppression.

Reactivation of viruses causing pneumonia is a large concern in HCT patients, even in autologous transplants. Human herpesvirus 6 (HHV-6) reactivation is most common (seen in up to 60% of patients), followed by EBV (up to 30%). [36, 37, 38]

HHV-6 infection is especially important in that it has been shown to be a predictor of subsequent CMV infection. [39]

Solid organ and HCT recipient are at risk also of hyperinfection with Strongyloides stercoralis, which may be accompanied by gram-negative bacterial sepsis and pneumonia.

Infections in persons with autoimmune conditions can result from the effects of immunosuppressive therapies as well as their underlying condition.

In systemic lupus erythematosus (SLE), distinguishing infection from an autoimmune flare is important. Treatment with steroids in the setting of infection could be deleterious. 

Complement deficiencies and elevated Fc gamma III and granulocyte-macrophage colony-stimulating factor (GM-CSF) levels may contribute to increased susceptibility to infection in patients with SLE. [40]  

Low complement, the use of more than 20 mg prednisone daily, and the use of cyclophosphamide in patients with SLE were important risk factors in multivariate analyses. [41]

Consideration of initiating prophylaxis for Pneumocystic jiroveci in SLE patients exceeding 20 mg of prednisone a day or with usage of cyclophosphamide has been proposed. [42]

The large majority of infectious complications are due to bacterial pathogens. Viral infections (CMV, VZV) are also common.

In connective tissue diseases, the primary condition and the use of immunosuppressive medications place patients at increased risk. One meta-analysis showed that 29% of patients developed a serious infection, and 24% died from this infection—most reported as bacteremia or pneumonia. [43]

Persons with primary immunodeficiencies are susceptible to pulmonary infections, the spectrum of which is largely determined by their underlying immune dysfunction: humoral, cellular, or combined deficiencies.

Humoral immunity deficiencies impact the ability to create functional antibodies. Characteristic infections are bacterial-based, recurrent, upper and lower respiratory tract infections. Common pathogens include the encapsulated bacteria Streptococcus pneumoniae, Haemophilus influenzae type b, and Neisseria meningitidis, as well as Giardia, Cryptosporidia, and Campylobacter.

Cellular deficiencies affect T-cell development and function. Dysfunction of T cells invariably has an impact on B-cell activity; therefore, most of these conditions manifest as combined deficiencies. Infections are common from viruses (RSV, HSV, VZV, CMV, EBV, influenza), mycobacteria, and fungi (Candida, Cryptococcus, and Pneumocystis).

Patients taking steroids long-term are at higher risk for pulmonary infections. [44]

Steroids alter phagocytic function of alveolar macrophages, delay the mobilization of immune cells, and affect antigen presentation. 

The dose and duration of use are predictive of increased risk of pneumonia. Low-dose and short-term use carry minimal additional risk of pneumonia, while dosages more than 10 mg/d or cumulatively 700 mg of prednisone increase patients’ risk of pulmonary infection. [45]

Asplenic patients are at particularly high risk for acquiring infections from encapsulated organisms. [20] They also have a higher rate of infection from pneumonias overall. [46]

In asplenic patients, the overall incidence of invasive pneumococcal disease is 500 cases per 100,000 per year. [20]

The underlying cause of immunosuppression is a crucial aspect of the history.

Nonspecific findings may include the following:

Fever

Exertional dyspnea, followed by dyspnea at rest with progression of disease

Cough, most often nonproductive in patients with HIV/AIDS

Pleuritic chest pain

Anorexia and weight loss

Abdominal pain

Pulmonary findings may be nonspecific in immunocompromised patients.

Findings at physical examination may include the following:

Fever

Tachypnea

Tachycardia or bradycardia

Rales or rhonchi

Decreased breath sounds

Dullness to percussion

Egophony

The differential diagnosis for pneumonia in immunocompromised patients includes the noninfectious causes of pulmonary disease:

Radiation induced injury

Drug induced pulmonary disease

Idiopathic pneumonia syndrome

Engraftment syndrome

Primary connective tissue/collagen disease

Transfusion related acute lung injury (TRALI)

ARDS secondary to extra pulmonary processes

Laboratory studies that should be obtained include a complete blood count (CBC) with differential, basic metabolic panel, arterial blood gas (ABG), lactate dehydrogenase (LDH) level, erythrocyte sedimentation rate (ESR), and C reactive protein (CRP).

If tuberculosis is suspected, sputum culture, sputum Gram stain, acid-fast bacillus (AFB) smear, and AFB culture should be collected while patients are in isolation. 

Two sets of blood cultures, despite their low yield and infrequent impact on care, are considered standard of care. [47, 48]  They are especially important in immunosuppressed individuals as they may at times be the only objective finding of infection.

Recently, procalcitonin (PCT) level has been shown to be a reliable biomarker with good sensitivity and specificity for bacterial causes of pneumonia or other infection. As it is triggered by bacterial endotoxin, procalcitonin levels can be a useful adjuvant to distinguish bacterial etiologies of infection from viral, fungal, or autoimmune causes. Trending of PCT level is also established to be useful for initiating and guiding antibiotic therapy. [49, 50, 51]

Other routine laboratory studies may be clinically indicated, such as viral nasal swabs, urine antigen testing (Legionella pneumophila, Histoplasma capsulatum, Streptococcus pneumoniae), PCR studies (CMV, HHV6), serum antigen testing (cryptococcus, galactomannan), and other assays such as serum 1,3 beta-D-Glucan. [52]

Chest radiography is usually the initial imaging modality.

The timing, progression, and distribution of findings are helpful in identifying correlations.

The most typical findings on chest radiography include infiltrates with consolidation, peribronchovascular lesions, and nodular space-occupying lesions. 

Other findings include atelectasis, cavitation, pleural effusions, lymphadenopathy, and cardiomegaly.

Some findings are correlated with certain etiologies of pulmonary infection; however, the pattern of radiographic findings is often unreliable in immunocompromised patients given the decreased inflammatory response.

For instance, as many as 14% of chest radiographic findings are normal in AIDS patients with pulmonary TB. [53]

Chest computed tomography (CT) can often detect abnormalities that may or may not be well visualized on chest radiography, and thus are useful in identifying small or early consolidations, characterizing extent and heterogenicity of disease, facilitating earlier diagnoses, and directing therapeutic management. [54]

CT is especially effective at defining extent of disease, including when multiple patterns of injury are occurring simultaneously.

The other major benefit of CT imaging is its utility in therapeutic procedures, including lung biopsy and tissue excision.

Lung sampling may be performed by bronchoscopy, transbronchial biopsy (TBB), or video-assisted thoracic surgery (VATS).

Bronchoscopy, the least invasive of these three sampling modalities, allows collection of diagnostic samples by bronchoalveolar lavage (BAL), fibrobronchial aspirate (FBAS), and protected specimen brush (PSB). This technique is high-yield for diagnosis of pneumonias, especially in conjunction with clinical and non-invasive methods. BAL has been specifically shown to be a highly sensitive and moderately specific test to diagnose of Pneumocystic jirovecii in HIV patients. [55]

The role of BAL in diagnosing pulmonary infections also established in non-HIV immunocompromised patients. [56, 57] Some sources suggest transbronchial biopsy in conjunction with BAL in non-HIV immunocompromised patients to detect other processes such as drug-induced lung injury or bronchiolitis obliterans.

TBB is established in diagnosis of diffuse parenchymal lung disease including interstitial fibrosis, but has shown promise in identifying fungal or viral pneumonia and inflammatory reactions. [58, 59]

Prehospital care should be initiated as soon as possible, and includes:

Establishment of intravenous access

Vital sign monitoring including oxygen saturation and cardiac monitoring

Emergency department care encompasses the same measures as prehospital care above, but also includes:

Empiric antimicrobial therapy based on most likely pathogens

In the case of PCP pneumonia, recommendations are for adjuvant corticosteroid therapy when a room air arterial blood gas pO2 is < 70, or if the A-a gradient is >35. In a recent double-blinded RCT in HIV-infected infants, early administration of prednisolone at 48 hours after clinical diagnosis of PJP significantly reduced mortality in hospital and 6 months after discharge. [60] New research suggests that the current guidelines of a 21-day therapy can safely be reduced to 14 days in 60% of moderate-to-severe HIV-PCP and 90% of moderate cases. [61]

Consultation with the following consultants may be considered:

Pulmonologist and/or critical care specialist

Infectious disease specialist

Immunologist in cases of known or suspected primary immunodeficiency

If outpatient management is possible, arrange for follow-up with a primary care practitioner within 24 hours.

Pharmacologic therapy consists mainly of empiric antibiotics awaiting results of diagnostic studies.

Taking into consideration each patient’s characteristics and risk factors, a narrow differential diagnosis can be established and help tailor therapy to the most likely organism and prevent overuse of anti-microbe therapy.

A meta-analysis by Wang et al indicated that in HIV-infected patients with P jiroveci pneumonia, early adjunctive corticosteroid treatment may lead to a 0.55 times reduced risk of mortality compared with patients who do not receive the adjunctive therapy. [62]

Optimization of treatment of the underlying immunocompromise is a first approach to prevention of pneumonia in immunocompromised individuals. This includes HAART, chemo and radiation therapy, and other measures depending on the type of immunocompromise.

However, despite optimal therapy, prevention of opportunistic and endemic pulmonary infections can be difficult.

Vaccination against pneumococcal and influenza, as well as prophylaxis against bacteria, viruses, and fungi, are other methods of prevention.

In rheumatologic disorders in which corticosteroids and/or immunomodulators such as TNF-inhibitors play a role in symptom control, the optimization of the level of immunosuppression is as important as prophylaxis against microbial infection.

 

Overview

How is pneumonia characterized in immunocompromised patients?

Which immunocompromised host groups are at highest risk for pneumonia?

What are the possible complications of pneumonia in immunocompromised patients?

What causes pneumonia in immunocompromised patients?

What causes pneumonia in patients with HIV infection?

What is the clinical presentation of TB in patients with HIV infection?

How is TB diagnosed and treated in patients with HIV infection?

What causes bacterial pneumonia in patients with HIV infection?

What are the types of fungal pneumonia in patients with HIV infection?

How does Pneumocystis jirovecii pneumonia (PJP) develop in patients with HIV infection?

Which immunocompromised patients have the highest incidence of aspergillus pneumonia?

What causes cryptococcal pneumonia in immunocompromised patients?

What causes histoplasmosis pneumonia in immunocompromised patients?

What causes coccidioides immitis pneumonia in immunocompromised patients?

Which viruses cause pneumonia in immunocompromised patients?

How do strongyloides cause pneumonia in immunocompromised patients?

What are the risk factors for pneumonia in immunocompromised cancer patients?

What are the risk factors for pneumonia in immunocompromised transplant patients?

What are the risk factors for pneumonia in immunocompromised patients with autoimmune conditions?

What are the risk factors for pneumonia in patients with primary immunodeficiencies?

What is the increased risk for pneumonia in immunocompromised patients on long-term steroid therapy?

What is the incidence of pneumonia in immunocompromised asplenic patients?

Which clinical history findings are characteristic of pneumonia in immunocompromised patients?

Which physical findings are characteristic of pneumonia in immunocompromised patients?

Which conditions are included in the differential diagnoses of pneumonia in immunocompromised patients?

What is the role of lab tests in the workup of pneumonia in immunocompromised patients?

What is the role of chest radiography in the workup of pneumonia in immunocompromised patients?

What is the role of chest CT scanning in the workup of pneumonia in immunocompromised patients?

What is the role of lung sampling in the workup of pneumonia in immunocompromised patients?

What is included in prehospital care for immunocompromised patients with pneumonia?

What is the initial ED treatment of suspected pneumonia in immunocompromised patients?

Which diagnostic tests are performed in the ED when pneumonia is suspected in immunocompromised patients?

How is pneumonia in immunocompromised patients treated?

Which specialist consultations are beneficial to immunocompromised patients with pneumonia?

What is the role of medications in the treatment of pneumonia in immunocompromised patients?

How is pneumonia prevented in immunocompromised patients?

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Julie B Zhao, MD Physician, Department of Emergency Medicine, NewYork-Presbyterian-Weill Cornell Medical Center

Disclosure: Nothing to disclose.

Richard D Shin, MD Director of Simulation, Department of Emergency Medicine, New York-Presbyterian Queens; Clinical Assistant Professor of Emergency Medicine in Medicine, Weill Cornell Medical College; Emergency Physician, Envision Physician Services

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Paul Blackburn, DO, FACOEP, FACEP Attending Physician, Department of Emergency Medicine, Maricopa Medical Center

Paul Blackburn, DO, FACOEP, FACEP is a member of the following medical societies: American College of Emergency Physicians, Arizona Medical Association, American College of Osteopathic Emergency Physicians, American Medical Association

Disclosure: Nothing to disclose.

Barry E Brenner, MD, PhD, FACEP Professor of Emergency Medicine, Professor of Internal Medicine, Program Director for Emergency Medicine, Sanz Laniado Medical Center, Netanya, Israel

Barry E Brenner, MD, PhD, FACEP is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Chest Physicians, American College of Emergency Physicians, American College of Physicians, American Heart Association, American Thoracic Society, New York Academy of Medicine, New York Academy of Sciences, Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Christopher I Doty, MD, FAAEM, FACEP Associate Professor of Emergency Medicine, Residency Program Director, Vice-Chair for Education, Department of Emergency Medicine, University of Kentucky-Chandler Medical Center

Christopher I Doty, MD, FAAEM, FACEP is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, Council of Emergency Medicine Residency Directors, Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Dana A Stearns, MD Assistant Director of Undergraduate Education, Department of Emergency Medicine, Massachusetts General Hospital; Associate Director, Undergraduate Clerkship in Surgery, Massachusetts General Hospital/Harvard Medical School; Assistant Professor of Surgery, Harvard Medical School

Dana A Stearns, MD is a member of the following medical societies: American College of Emergency Physicians

Disclosure: Nothing to disclose.

Michael H Augenbraun, MD, FACP Professor of Medicine and Preventive Medicine and Community Health, Director of 3rd Year Medical Clerkship, State University of New York Downstate College of Medicine; Hospital Epidemiologist and Director, Department of Epidemiology, University Hospital of Brooklyn; Medical Director of Sexually Transmitted Diseases Clinic, Director of Lumbar Puncture Clinic, Kings County Hospital Center

Michael H Augenbraun, MD, FACP is a member of the following medical societies: American College of Physicians, Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Marie Abdallah, MD Primary Care and Infectious Diseases Physician, Kings County Hospital

Marie Abdallah, MD is a member of the following medical societies: American College of Physicians

Disclosure: Nothing to disclose.

David J Wallace, MD, MPH Critical Care Medicine Fellow, University of Pittsburgh Medical Center

David J Wallace, MD, MPH is a member of the following medical societies: Alpha Omega Alpha, American College of Emergency Physicians, and Society of Critical Care Medicine

Disclosure: Nothing to disclose.

Pneumonia in Immunocompromised Patients

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