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Infectious Diseases > MEDICAL TOPICS
Stenotrophomonas Maltophilia
Article Last Updated: Jul 28, 2008
AUTHOR AND EDITOR INFORMATION
Section 1 of 10
Author: Burke A Cunha, MD, Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital
Burke A Cunha is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, and Infectious Diseases Society of America
Editors: Charles S Levy, MD, Associate Professor, Department of Medicine, Section of Infectious Disease, George Washington University School of Medicine; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Ronald A Greenfield, MD, Professor, Department of Internal Medicine, Section of Infectious Diseases, University of Oklahoma College of Medicine; Eleftherios Mylonakis, MD, Clinical and Research Fellow, Department of Internal Medicine, Division of Infectious Diseases, Massachusetts General Hospital; Michael Stuart Bronze, MD, Professor, Stewart G Wolf Chair in Internal Medicine, Department of Medicine, University of Oklahoma Health Science Center
Author and Editor Disclosure
Synonyms and related keywords:
Stenotrophomonas maltophilia, S maltophilia, Stenotrophomonas maltophilia infection, S maltophilia infection, Stenotrophomonas maltophilia pneumonia, S maltophilia pneumonia, Pseudomonas maltophilia infection, P maltophilia
Background
Stenotrophomonas (Pseudomonas) maltophilia is an aerobic gram-negative bacillus that is found in various aquatic environments. It is an uncommon pathogen in humans. S maltophilia is an organism of low virulence and frequently colonizes fluids used in the hospital setting (eg, irrigation solutions, intravenous fluids) and patient secretions (eg, respiratory secretions, urine, wound exudates). S maltophilia usually must bypass normal host defenses to cause human infection. For example, if an irrigation solution becomes colonized with this organism, irrigating an open wound can cause colonization or infection of the wound. S maltophilia is usually incapable of causing disease in healthy hosts without the assistance of invasive medical devices that bypass normal host defenses.
Pathophysiology
S maltophilia has few pathogenic mechanisms and, for this reason, predominantly results in colonization rather than infection. If infection does occur, invasive medical devices are usually the vehicles through which the organism bypasses normal host defenses. Otherwise, the pathophysiology of this nonfermentative aerobic gram-negative bacillus does not differ from other nonfermentative aerobic organisms.
Frequency
United States
S maltophilia is a noninvasive organism that has low virulence. It frequently colonizes body fluids but rarely causes infection (eg, intravenous line infections).
International
S maltophilia frequently colonizes the respiratory tract in patients with cystic fibrosis.
Mortality/Morbidity
Mortality and morbidity relate to the inoculum of S maltophilia that is able to bypass normal host defense mechanisms. - If an intravenous infusion contains large numbers of S maltophilia, then direct injection into the bloodstream may result in the signs and symptoms associated with gram-negative bacteremia.
- Similarly, in the urinary tract, if urological irrigation fluids that contain large numbers of S maltophilia are used during an invasive urological procedure, eg, cystoscopy, then gram-negative bacteremia may occur with its attendant mortality and morbidity, which depend on host factors.
History
- Because S maltophilia infections are extremely uncommon, no specific patient history suggests its presence other than contact with other colonized individuals.
- Obtaining a history of the use of irrigant solutions that could potentially contain S maltophilia is important in an epidemiological setting rather than in a clinical setting.
Physical
Signs and symptoms of S maltophilia infections are related to the organ system involved and are indistinguishable from infections with other pathogens.
Causes
- S maltophilia is a nonfermentative aerobic gram-negative bacillus formerly classified in the genus Pseudomonas. Unlike Pseudomonas aeruginosa, S maltophilia is an organism of low virulence with limited ability to cause infection in humans.
- S maltophilia is a water organism, and it survives and multiplies in aqueous environments, particularly respiratory secretions, urine, intravenous fluids, and irrigant solutions.
- S maltophilia may persist in an aquatic environment for extended periods.
- Sources of S maltophilia colonization include the following:
- Personnel
- Hands
- Antiseptic soaps
- Hand lotion
- Respiratory equipment and/or fluids
- Ultrasonic nebulizers
- Inhalation medications
- Respirator tubing condensate
- Intravenous lines and/or fluids
- Intravenous solutions
- Central venous catheters
- Pressure monitoring devices - Pressure transducer fluids
- Urine and/or fluids
- Indwelling Foley catheters
- Urometers
- Irrigation solutions
Other Problems to be Considered
The main clinical problem presented by S maltophilia is failing to recognize its significance in the clinical context. The recovery of S maltophilia from respiratory secretions or from the urine of catheterized patients should be regarded as colonization until proven otherwise. S maltophilia is a common cause of catheter-associated bacteruria in hospitalized patients. S maltophilia commonly colonizes the urine and is potentially pathogenic only in those with impaired host defenses, ie, patients with diabetes, systemic lupus erythematosus (SLE), cirrhosis, multiple myeloma, and those on steroids. S maltophilia recovered from blood cultures may have come from contaminated intravenous fluids or from a distant infected source, eg, secondary bacteremia from the urinary tract in a patient who recently underwent instrumentation during a genitourinary (GU) procedure. S maltophilia recovered from a wound with a clear or a serosanguineous discharge is of no clinical significance. If recovered from a purulent wound, S maltophilia may be the cause of the patient's wound infection. The most common cause of confusion regarding S maltophilia is assuming that its recovery from body fluids implies a pathogenic role. S maltophilia is a rare cause of nosocomial pneumonia in patients who are ventilated and presumed to have nosocomial pneumonia because of fever, pulmonary infiltrates, and leukocytosis.40 The recovery of S maltophilia from respiratory secretions almost always represents colonization rather than infection, and its presence should not be addressed therapeutically. Table 1. Hospital-Acquired S maltophilia Infections Infection
| Predisposing Factor
| Catheter-associated bacteriuria
| Indwelling urinary catheters
| Intravenous line infections
| Central intravenous catheters
| Urosepsis
| Urinary tract instrumentation
| Primary bacteremia
| Arterial monitoring devices
| Pseudobacteremia
| Contamination of blood during collection/processing of blood cultures
|
Lab Studies
Culture of the organism from body fluids and proper identification from the microbiology laboratory confirms the presence of S maltophilia. Usually, the presence of S maltophilia represents colonization. A potential pathogenic role must be evaluated by an infectious disease specialist. The mere recovery of a potential pathogen from any body fluid does not indicate a pathogenic role for the organism.
Histologic Findings
The histology of S maltophilia in the rare situations when it causes infection is indistinguishable from the histology of infections caused by other aerobic gram-negative bacilli.
Medical Care
- Colonization of body fluids in hospitalized patients should be minimized if possible. Foley catheters should be used only as long as necessary and should be avoided if at all possible in immunocompromised hosts predisposed to urinary tract infections, eg, patients with diabetes, SLE, or multiple myeloma.
- Colonization of respiratory secretions in intubated patients in ICUs is the rule and is difficult to prevent.
- Patient-to-patient spread of organisms may be minimized or prevented by effective infection-control measures.
Consultations
A consultation with an infectious disease specialist is essential for differentiating colonization from infection in patients with S maltophilia isolated from various body fluids.
Because S maltophilia is predominantly a colonizer, antimicrobial treatment is unnecessary and may be potentially harmful. As a general principle, colonization should not be treated with antimicrobial therapy. S maltophilia, as a non–aeruginosa pseudomonad, is usually resistant to aminoglycosides, antipseudomonal penicillins, and antipseudomonal third-generation cephalosporins. S maltophilia is consistently susceptible to trimethoprim-sulfamethoxazole (TMP-SMX). If TMP-SMX cannot be used, the organism is usually sensitive to meropenem, minocycline, respiratory quinolones, or colistin/polymyxin B.
Drug Category: Antibiotics
Therapy must be comprehensive and cover all likely pathogens in the context of the clinical setting.
| Drug Name | Sulfamethoxazole/trimethoprim (Bactrim, Bactrim DS, Septra, Septra DS) |
| Description | Inhibits bacterial growth by inhibiting synthesis of dihydrofolic acid. Antibacterial activity includes common urinary tract pathogens, except P aeruginosa. |
| Adult Dose | 160 mg TMP 800 mg SMX PO q12h for 10-14 d |
| Pediatric Dose | <2 months: Do not administer >2 months: 15-20 mg/kg/d (based on TMP) PO tid/qid for 14 d |
| Contraindications | Documented hypersensitivity; megaloblastic anemia resulting from a folate deficiency |
| Interactions | May increase PT when used with warfarin (perform coagulation tests and adjust dose accordingly); coadministration with dapsone may increase blood levels of both drugs; coadministration of diuretics increases incidence of thrombocytopenia purpura in elderly individuals; phenytoin levels may increase with coadministration; may potentiate effects of methotrexate in patients with bone marrow depression; hypoglycemic response to sulfonylureas may increase with coadministration; may increase levels of zidovudine |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Discontinue at first appearance of skin rash or sign of adverse reaction; obtain CBC counts frequently; discontinue therapy if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; prolonged IV infusions or high doses may cause bone marrow depression (if signs occur, administer 5-15 mg/d leucovorin); caution in patients with a folate deficiency (eg, those with chronic alcoholism, elderly individuals, those receiving anticonvulsant therapy, those with a malabsorption syndrome); hemolysis may occur in patients who are G-6-PD deficient; patients with AIDS may not tolerate or respond; caution in patients with renal or hepatic impairment (perform urinalyses and renal function tests during therapy); administer fluids to prevent crystalluria and stone formation |
| Drug Name | Cefepime (Maxipime) |
| Description | Fourth-generation cephalosporin with good gram-negative coverage, similar to ceftazidime, but better gram-positive coverage. |
| Adult Dose | 2 g IV q12h |
| Pediatric Dose | 50 mg/kg IV q8h |
| Contraindications | Documented hypersensitivity |
| Interactions | Probenecid at a high dose decreases clearance |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Adjust dose in patients with severe renal insufficiency |
| Drug Name | Minocycline (Dynacin, Minocin) |
| Description | Treats infections caused by susceptible gram-negative and gram-positive organisms, in addition to infections caused by susceptible Chlamydia, Rickettsia, and Mycoplasma. |
| Adult Dose | 100 mg PO bid for 5-7 d |
| Pediatric Dose | <8 years: Not recommended >8 years: 4 mg/kg PO initially, followed with 2 mg/kg q12h |
| Contraindications | Documented hypersensitivity; severe hepatic dysfunction |
| Interactions | Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy; tetracyclines can increase hypoprothrombinemic effects of anticoagulants |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
|
| Precautions | Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (last one-half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines; hepatitis or lupuslike syndromes may occur |
| Drug Name | Tigecycline (Tygacil) |
| Description | A glycylcycline antibiotic that is structurally similar to tetracycline antibiotics. Inhibits bacterial protein translation by binding to 30S ribosomal subunit, and blocks entry of amino-acyl tRNA molecules in ribosome A site. Indicated for complicated skin and skin structure infections caused by E coli, E faecalis (vancomycin-susceptible isolates only), S aureus (methicillin-susceptible and -resistant isolates), S agalactiae, S anginosus group (includes S anginosus, S intermedius, and S constellatus), S pyogenes, and B fragilis. |
| Adult Dose | Infuse each dose over 30-60 min 100 mg IV once, then 50 mg IV q12h Severe hepatic impairment (ie, Child Pugh class C): 100 mg IV once, then 25 mg IV q12h |
| Pediatric Dose | <18 years: Not established >18 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Coadministration decreases warfarin clearance and increases warfarin Cmax and AUC (monitor aPTT and INR); coadministration of antibiotics with oral contraceptives may decrease contraceptive effect |
| Pregnancy | D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
|
| Precautions | Caution in severe hepatic impairment (reduce dose); may adversely effect tooth development; may permit clostridia overgrowth, resulting in antibiotic-associated colitis; may have adverse effects similar to tetracyclines (eg, photosensitivity, pseudotumor cerebri, pancreatitis, antianabolic action) |
| Drug Name | Meropenem (Merrem IV) |
| Description | Bactericidal broad-spectrum carbapenem antibiotic that inhibits cell-wall synthesis. Effective against most gram-positive and gram-negative bacteria. Has slightly increased activity against gram-negative bacteria and slightly decreased activity against staphylococci and streptococci compared with imipenem.
|
| Adult Dose | 1 g IV q8h |
| Pediatric Dose | 40 mg/kg IV q8h |
| Contraindications | Documented hypersensitivity |
| Interactions | Probenecid may inhibit renal excretion of meropenem, increasing meropenem levels |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
|
| Precautions | Dosage adjustments (adult adjustments) CrCl (mL/min) 50-10: 0.5-1 g q12h CrCl <10: 0.5 g/d HD: As for CrCl <10, with an extra 0.5 g after HD Pseudomembranous colitis and thrombocytopenia may occur, requiring immediate discontinuation of medication |
Deterrence/Prevention
- Because S maltophilia is a common nosocomial colonizer in patients and medical fluids, the recovery of S maltophilia should be considered nonpathogenic unless proven otherwise.
- If S maltophilia is recovered from several patients in the same area, sections of an ICU or ward can become the focus of further spread within the hospital setting.
- Effective infection control measures can minimize or limit the spread of this and other organisms in the ICU.
- Appropriate isolation procedures, rather than antimicrobial therapy, should be used to control the spread of S maltophilia.
- Medical personnel, including medical students, housekeeping staff, attending physicians, nursing personnel, and respiratory therapists, are potential carriers of the organism from patient to patient.
Medical/Legal Pitfalls
- Clinicians often make the mistake of treating S maltophilia colonization with antibiotics. Except when the pathogenic role of S maltophilia is clear (ie, intravenous line sepsis secondary to contaminating infusions, colonization related to intravenous monitoring devices, urological instrumentation resulting in colonization), the mere presence of S maltophilia should not prompt treatment because it usually implies colonization rather than infection.
- The most common clinical pitfall with S maltophilia colonization is to treat it when the organism is recovered from urine. S maltophilia bacteriuria ordinarily should not be treated. In a patient with an indwelling Foley catheter, S maltophilia may be accompanied by pyuria, which represents colonization rather than infection unless recent antecedent urological instrumentation has been performed.
- The most common clinical error with S maltophilia colonization involves treating patients on respirators in ICUs because S maltophilia was recovered from their respiratory secretions.
- Because S maltophilia has not been reported to cause pneumonia except in rare cases involving cystic fibrosis or bronchiectasis, colonization should not be treated in patients who are ventilated, even if they have fever, pulmonary infiltrates, and leukocytosis.
- The needless and inappropriate treatment of S maltophilia with antibiotics may predispose patients to adverse drug effects, eg, drug fever or drug rash secondary to the sulfisoxazole component of TMP-SMX.
- The treatment of S maltophilia colonization may also predispose patients to fungal colonization or infection because of the selective pressures on the microbial milieu in the ICU.
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Stenotrophomonas Maltophilia excerpt Article Last Updated: Jul 28, 2008
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