Stenotrophomonas maltophilia Infection in a Patient with Acute Exacerbation of Chronic Obstructive Pulmonary Disease (COPD): A Colonizer or True Infection?

Background

Stenotrophomonas maltophilia is an aerobic, motile, nonfermentative, non-sporulating, gram-negative bacillus that is a multi-drug resistant organism associated with infections such as bacteremia, pneumonia, urinary infection, endocarditis, meningitis, and peritonitis as a nosocomial infection, particularly in immunocompromised patients. It has also been reported in patients with acute exacerbation of COPD with known history of endotracheal intubation or mechanical ventilation [1–8]. Stenotrophomonas maltophilia is believed to be a colonizer in patients with chronic lung diseases, such as cystic fibrosis. We present a case of Stenotrophomonas maltophilia infection in a patient with acute exacerbation of COPD without history of frequent hospitalization or prior intubation.

Case Report

INVESTIGATIONS:

A chest x-ray showed no infiltrate, pleural effusion, or vascular congestion. Arterial blood gas showed pH 7.36, bicarbonate 27.4 meq/L, pCO2 49 mmHg, and pO2 87 mmHg while on bi-level positive airway pressure. BNP was 2598 pg/ml, troponin was elevated at 0.09 ng/ml, and EKG was without ST-T wave changes. A chest CT showed secretions in the lower-lobe bronchi and small scattered clustered nodules consistent with bronchitis/mild bronchopneumonia, without evidence of pulmonary embolism or bronchiectasis. A sputum sample was collected on day 2 of admission. White blood cells were elevated at 22 200/μL. Liver transaminases were within normal limits.

DIFFERENTIAL DIAGNOSIS:

Based on the history and examination, the initial diagnosis was acute hypoxemic hypercapnic respiratory failure secondary to COPD exacerbation and new-onset congestive heart failure exacerbation based on clinical findings. A diagnosis of community-acquired pneumonia was also considered. Given her elevated troponin at admission, an echocardiogram was performed, showing ejection fraction of 35% and marked hypokinesis of the middle cavity through the apex of the left ventricle circumferentially. However, catheterization showed a normal right dominant coronary artery and normal left main bifurcated into the normal left anterior descending and circumflex arteries.

TREATMENT:

The patient was diuresed with intravenous furosemide for new-onset heart failure. She was also administered azithromycin 500 mg daily for 5 days, albuterol and ipratropium nebulization, formoterol fumarate, and budesonide for a presumed COPD exacerbation. At day 5, the result of the sputum culture showed Stenotrophomonas maltophilia, and she was started on trimethoprim/sulfamethoxazole for 10 days. A decision was made to treat this as a true infection because she was not improving on the empiric antibiotics and continued to have persistent mucus stasis. She improved after the initiation of trimethoprim/sulfamethoxazole for Stenotrophomonas maltophilia. She was also started on carvedilol and lisinopril for stress-induced cardiomyopathy, but developed hypotension and acute kidney injury, leading to subsequent discontinuation of these medications.

OUTCOME AND FOLLOW-UP:

Her respiratory symptoms improved after initiation of trimethoprim/sulfamethoxazole, but she developed acute kidney injury in the setting of treatment with trimethoprim/sulfamethoxazole, lisinopril, and reduced oral intake. She also developed hypotension from treatment with carvedilol and reduced oral intake. With discontinuation of lisinopril, carvedilol, and fluid repletion, her acute kidney injury resolved, and blood pressure stabilized. She was then discharged to short-term rehabilitation.

Discussion

Although COPD exacerbations are often triggered by respiratory viral infections, bacterial infections may also contribute to or trigger these events [9]. Stenotrophomonas maltophilia has been described more recently as a nosocomial infection, particularly in immunocompromised people, with comorbidities, and those with chronic diseases, and patients with bacteremia have a high mortality rate [3,10–12]. It has been isolated in nosocomial sources such as mechanical ventilators, central venous catheters, and other medical devices in the hospital setting [13]. It has also been reported as a community-acquired infection among immunocompetent patients in a systematic review by Falagas et al. in 2009 [14]. It has also been found in patients with acute exacerbation of COPD and bronchiectasis or requiring intubation and mechanical ventilation. Other factors that could increase the risk of COPD patients to these multidrug-resistant organisms include frequent hospitalization, long-term corticosteroid use, prior antibiotic use, and nutritional impairment [15,16]. Many of these reported cases were admitted to the intensive care unit.

However, for many clinicians there is still the question of whether Stenotrophomonas maltophilia is a colonizer or a true infection. Isolation of this organism in patients with severe COPD or signs and symptoms of infection, including pneumonia, should not be ignored [17–19].

Our severe COPD patient did not have frequent hospitalizations, prior invasive mechanical ventilation, or antibiotic use, but was found to have a sputum culture positive for Stenotrophomonas maltophilia. A decision was made to treat this infection because the patient was not improving on the empiric antibiotics and continued to have persistent mucus stasis. Her condition improved after the initiation of trimethoprim/sulfamethoxazole for Stenotrophomonas maltophilia.

Stenotrophomonas maltophilia identification is frequently delayed awaiting growth of sputum culture and is not typically covered for in empiric antibiotic regimens for acute exacerbation of COPD, which may lead to higher mortality rates among these patients [20]. It has been recommended that a sputum culture be obtained from patients with frequent exacerbations, severe airflow limitations, and/or acute exacerbations requiring mechanical ventilation. Early sputum culture identification is very helpful in effective management of Stenotrophomonas maltophilia, as strains are frequently resistant, and given the limited treatment options available for this infection [13,21]. Resistance is thought to be due to slow bacterial growth and a high rate of mutation [7]. However, trimethoprim/sulfamethoxazole still remains the drug of choice and is typically very effective in treating this infection [1]. Alternatives for treatment include ciprofloxacin, ceftazidime, ceftriaxone, and ticarcillin/clavulanate if co-trimoxazole cannot be taken [14,22].

Conclusions

Although Stenotrophomonas maltophilia was previously thought to be a colonizer, it can be a true infection in immunocompromised patients or those with chronic diseases such as severe COPD. Therefore, early identification with sputum culture and prompt treatment of Stenotrophomonas maltophilia infection is important for a favorable outcome.