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1.
Clin Infect Dis ; 71(7): e178-e185, 2020 10 23.
Article in English | MEDLINE | ID: mdl-31872853

ABSTRACT

BACKGROUND: In July 2018, the Arkansas Department of Health (ADH) was notified by hospital A of 3 patients with bloodstream infections (BSIs) with a rapidly growing nontuberculous Mycobacterium (NTM) species; on 5 September 2018, 6 additional BSIs were reported. All were among oncology patients at clinic A. We investigated to identify sources and to prevent further infections. METHODS: ADH performed an onsite investigation at clinic A on 7 September 2018 and reviewed patient charts, obtained environmental samples, and cultured isolates. The isolates were sequenced (whole genome, 16S, rpoB) by the Centers for Disease Control and Prevention to determine species identity and relatedness. RESULTS: By 31 December 2018, 52 of 151 (34%) oncology patients with chemotherapy ports accessed at clinic A during 22 March-12 September 2018 had NTM BSIs. Infected patients received significantly more saline flushes than uninfected patients (P < .001) during the risk period. NTM grew from 6 unused saline flushes compounded by clinic A. The identified species was novel and designated Mycobacterium FVL 201832. Isolates from patients and saline flushes were highly related by whole-genome sequencing, indicating a common source. Clinic A changed to prefilled saline flushes on 12 September as recommended. CONCLUSIONS: Mycobacterium FVL 201832 caused BSIs in oncology clinic patients. Laboratory data allowed investigators to rapidly link infections to contaminated saline flushes; cooperation between multiple institutions resulted in timely outbreak resolution. New state policies being considered because of this outbreak include adding extrapulmonary NTM to ADH's reportable disease list and providing more oversight to outpatient oncology clinics.


Subject(s)
Mycobacterium Infections, Nontuberculous , Neoplasms , Sepsis , Arkansas , Humans , Mycobacterium Infections, Nontuberculous/epidemiology , Neoplasms/complications , Nontuberculous Mycobacteria , Outpatients
2.
Clin Infect Dis ; 71(6): 1367-1376, 2020 09 12.
Article in English | MEDLINE | ID: mdl-31802125

ABSTRACT

BACKGROUND: Invasive fungal diseases (IFDs) remain important causes of morbidity and mortality. The consensus definitions of the Infectious Diseases Group of the European Organization for Research and Treatment of Cancer and the Mycoses Study Group have been of immense value to researchers who conduct clinical trials of antifungals, assess diagnostic tests, and undertake epidemiologic studies. However, their utility has not extended beyond patients with cancer or recipients of stem cell or solid organ transplants. With newer diagnostic techniques available, it was clear that an update of these definitions was essential. METHODS: To achieve this, 10 working groups looked closely at imaging, laboratory diagnosis, and special populations at risk of IFD. A final version of the manuscript was agreed upon after the groups' findings were presented at a scientific symposium and after a 3-month period for public comment. There were several rounds of discussion before a final version of the manuscript was approved. RESULTS: There is no change in the classifications of "proven," "probable," and "possible" IFD, although the definition of "probable" has been expanded and the scope of the category "possible" has been diminished. The category of proven IFD can apply to any patient, regardless of whether the patient is immunocompromised. The probable and possible categories are proposed for immunocompromised patients only, except for endemic mycoses. CONCLUSIONS: These updated definitions of IFDs should prove applicable in clinical, diagnostic, and epidemiologic research of a broader range of patients at high-risk.


Subject(s)
Invasive Fungal Infections , Mycoses , Neoplasms , Antifungal Agents/therapeutic use , Consensus , Humans , Immunocompromised Host , Invasive Fungal Infections/diagnosis , Invasive Fungal Infections/drug therapy , Mycoses/diagnosis , Mycoses/drug therapy , Mycoses/epidemiology , Neoplasms/drug therapy
3.
South Med J ; 112(7): 401-405, 2019 07.
Article in English | MEDLINE | ID: mdl-31282971

ABSTRACT

OBJECTIVES: Intravenous balanced crystalloid fluid therapy may improve mortality and other outcomes in critically ill adult patients, but data are conflicting. We conducted a meta-analysis and literature review to evaluate the impact of intravenous balanced crystalloid, as compared with normal saline, fluid therapy on outcomes in critically ill adult patients. METHODS: We searched PubMed, Scopus, MEDLINE, and the Cochrane Register of Clinical Trials for relevant studies. Randomized controlled trials comparing the effects of balanced intravenous crystalloids with normal saline on intensive care unit (ICU) or hospital mortality were included. Pooled risk ratios (RRs) were calculated using a fixed effects model. Heterogeneity was calculated using the I2 statistic. The risk of bias was assessed using the Cochrane tool. RESULTS: Seven randomized controlled trials with 20,171 patients (10,179 participants received balanced crystalloids and 9992 participants received normal saline) were included. For hospital mortality, the pooled RR (95% confidence interval [CI]) was 0.92 (0.85-1.00). For ICU mortality, the pooled RR (95% CI) was 0.91 (0.82-1.00). For major adverse kidney events at 30 days, pooled RR (95% CI) was 0.95 (0.88-1.01). For stage ≥2 acute kidney injury, the pooled RR (95% CI) was 0.94 (0.86-1.02). For receipt of new renal replacement therapy, the pooled RR (95% CI) was 0.91 (0.77-1.07). None of these findings reached statistical significance. CONCLUSIONS: Intravenous balanced crystalloid use, compared with normal saline, does not result in a statistically significant reduction in hospital or ICU mortality, major adverse kidney events at 30 days, stage ≥2 acute kidney injury, or receipt of new renal replacement therapy in critically ill adult patients.


Subject(s)
Critical Illness/mortality , Critical Illness/therapy , Crystalloid Solutions/therapeutic use , Fluid Therapy/methods , Adult , Hospital Mortality , Humans
4.
Clin Infect Dis ; 64(11): 1622-1625, 2017 Jun 01.
Article in English | MEDLINE | ID: mdl-28329282

ABSTRACT

A patient with asplenia and multiple red blood cell transfusions acquired babesiosis infection with Babesia divergens-like/MO-1 organisms and not Babesia microti, the common United States species. He had no known tick exposure. This is believed to be the first transfusion-transmitted case and the fifth documented case of B. divergens-like/MO-1 infection.


Subject(s)
Babesiosis/transmission , Blood Transfusion , Aged, 80 and over , Arkansas , Babesia/isolation & purification , Babesiosis/drug therapy , Babesiosis/parasitology , Clindamycin/administration & dosage , Clindamycin/therapeutic use , Doxycycline/administration & dosage , Doxycycline/therapeutic use , Fatal Outcome , Humans , Male , Platelet Transfusion , Quinine/administration & dosage , Quinine/therapeutic use , United States
5.
Trans Am Clin Climatol Assoc ; 125: 188-202; discussion 202-3, 2014.
Article in English | MEDLINE | ID: mdl-25125734

ABSTRACT

One of the endemic fungi, Blastomyces dermatitidis, can cause epidemics of infection with multiple persons involved in a point source outbreak but more commonly causes sporadic cases of infection within the areas of endemicity. Blastomycosis can present as an acute pneumonia which is often misdiagnosed as acute pneumococcal pneumonia or the infection may present as a chronic pneumonia along with weight loss, night sweats, hemoptysis, and a lung mass suggesting tuberculosis or carcinoma of the lung. Extrapulmonary infection with B. dermatitidis is protean with many different manifestations. Most commonly, skin or subcutaneous lesions are found with either a verrucous or warty appearance or in an ulcerative form. Cases have been misidentified as keratoacanthoma, pyoderma gangrenosum, carcinoma, or as Weber-Christian panniculitis if there are nodular subcutaneous lesions. Essentially any site or organ can have lesions of disseminated blastomycosis. In our series, cases of laryngeal carcinoma, adrenal insufficiency, thyroid nodules, granulomatous hypercalcemia, abnormal mammograms thought to represent breast carcinoma, otitis media with cranial extension, immune thrombocytopenic purpura, and hemolytic anemia of unknown cause have been misdiagnosed and blastomycosis subsequently identified as the cause. This infection causes manifestations which mimic many other more commonly diagnosed conditions and must always be considered by clinicians practicing in the endemic region.


Subject(s)
Blastomycosis/diagnosis , Endemic Diseases , Antifungal Agents/therapeutic use , Blastomycosis/drug therapy , Blastomycosis/epidemiology , Blastomycosis/microbiology , Diagnosis, Differential , Diagnostic Errors/prevention & control , Humans , Male , Middle Aged , Predictive Value of Tests , Remission Induction , Treatment Outcome
6.
WMJ ; 120(2): 142-144, 2021 Jul.
Article in English | MEDLINE | ID: mdl-34255955

ABSTRACT

Renal cell cancer is the third most common urological malignancy following prostate and bladder malignancies. Cardiac metastases to the right side of the heart without inferior vena cava (IVC) involvement are exceedingly rare, with only a handful of cases described in the literature. Metastasis to the head and neck region is also rare, occurring in an estimated 1% of cases. Here we present a case of a patient with recurrent syncopal events secondary to renal cell carcinoma without IVC involvement, with metastases both to the right ventricle and cervical lymph nodes. To our knowledge, this is the first case that presents with both of these rare findings together and that highlights cancer screening in patients with high risk factors and new exam findings in patients with syncopal events having negative initial workup.


Subject(s)
Carcinoma, Renal Cell , Kidney Neoplasms , Lymphadenopathy , Humans , Male , Vena Cava, Inferior/diagnostic imaging
7.
Clin Infect Dis ; 50(6): 797-804, 2010 Mar 15.
Article in English | MEDLINE | ID: mdl-20166817

ABSTRACT

BACKGROUND: Central nervous system (CNS) involvement with Blastomyces dermatitidis is an uncommon and potentially fatal complication of blastomycosis. METHODS: We retrospectively reviewed 22 patients with CNS blastomycosis at our institutions from 1990 through 2008 (13 proven, 5 probable, and 4 possible cases). RESULTS: Magnetic resonance imaging was used in most patients, alone or in addition to computed tomography. CNS blastomycosis manifested as epidural abscess (1 of 22), meningitis (7 of 22), intracranial mass lesions (10 of 22), and concomitant intracranial mass lesions and meningitis (4 of 22). All patients received amphotericin B deoxycholate or a lipid formulation of amphotericin B as part of their treatment regimens. Most patients received amphotericin B followed by a prolonged course of oral azole therapy (voriconazole, fluconazole, or itraconazole). Four (18%) of 22 patients died during follow-up. CONCLUSIONS: On the basis of these data, we recommend initial treatment with a lipid formulation of amphotericin B followed by a prolonged course of oral azole therapy, preferably voriconazole.


Subject(s)
Antifungal Agents/therapeutic use , Blastomyces/isolation & purification , Blastomycosis/diagnosis , Blastomycosis/drug therapy , Central Nervous System Fungal Infections/diagnosis , Central Nervous System Fungal Infections/drug therapy , Adolescent , Adult , Blastomycosis/mortality , Central Nervous System Fungal Infections/mortality , Female , Head/diagnostic imaging , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Radiography , Retrospective Studies , Tomography , Treatment Outcome , Young Adult
8.
J Ark Med Soc ; 106(8): 186-8, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20218039

ABSTRACT

Lyme disease is the most common tick-borne disease in the northern hemisphere. Since it was first described more than 30 years ago, Lyme disease has generated a great deal of controversy. Lyme disease is not endemic in Arkansas, and testing for Borrelia burgdorferi can lead to clinical confusion, unnecessary treatment and excess cost. This article will present a brief review of Lyme disease, with an emphasis on what is known regarding Lyme disease in Arkansas.


Subject(s)
Borrelia burgdorferi , Ixodes/microbiology , Lyme Disease/diagnosis , Lyme Disease/epidemiology , Animals , Arkansas/epidemiology , Humans , Lyme Disease/physiopathology
9.
Open Forum Infect Dis ; 6(10): ofz413, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31660371

ABSTRACT

We present a young pregnant woman who developed ulceroglandular tularaemia following a bite wound from a kitten. She grew Francisella tularensis from the ulcer. While awaiting bacterial culture results and serology for Bartonella, she was treated with azithromycin, with resolution of fever and axillary tenderness. Treatment recommendations for tularemia are either gentamicin or doxycycline, both of which can be perilous to the fetus. A Centers for Disease Control and Prevention report on the macrolide susceptibility of North American isolates of this organism has been underappreciated. The unanticipated result from this patient may give another potential option for treatment of tularemia in pregnancy.

10.
Clin Infect Dis ; 46(12): 1801-12, 2008 Jun 15.
Article in English | MEDLINE | ID: mdl-18462107

ABSTRACT

Evidence-based guidelines for the management of patients with blastomycosis were prepared by an Expert Panel of the Infectious Diseases Society of America. These updated guidelines replace the previous management guidelines published in the April 2000 issue of Clinical Infectious Diseases. The guidelines are intended for use by health care providers who care for patients who have blastomycosis. Since 2000, several new antifungal agents have become available, and blastomycosis has been noted more frequently among immunosuppressed patients. New information, based on publications between 2000 and 2006, is incorporated in this guideline document, and recommendations for treating children with blastomycosis have been noted.


Subject(s)
Antifungal Agents , Blastomycosis , Humans , Antifungal Agents/therapeutic use , Blastomycosis/diagnosis , Blastomycosis/drug therapy , United States
11.
Clin Infect Dis ; 44(6): 777-84, 2007 Mar 15.
Article in English | MEDLINE | ID: mdl-17304447

ABSTRACT

BACKGROUND: Conflicting data exist on the role of antimicrobial therapy for the treatment of uncomplicated community-onset methicillin-resistant Staphylococcus aureus (MRSA) skin and soft-tissue infections (SSTIs). METHODS: We performed a retrospective cohort study of 492 adult patients with 531 independent episodes of community-onset MRSA SSTIs, which consisted of abscesses, furuncles/carbuncles, and cellulitis, at 2 tertiary care medical centers. The purpose of the study was to determine the impact of active antimicrobial therapy (i.e., the use of an agent to which the organism is susceptible) and other potential risk factors on the outcome for patients with uncomplicated community-onset MRSA SSTIs. Treatment failure was the primary outcome of interest and was defined as worsening signs of infection associated with microbiological and/or therapeutic indicators of an unsuccessful outcome. Bivariate analyses and logistic regression analyses were preformed to determine predictors of treatment failure. RESULTS: An incision and drainage procedure was performed for the majority of patients. Treatment failure occurred in 45 (8%) of 531 episodes of community-onset MRSA SSTI. Therapy was successful for 296 (95%) of 312 patients who received an active antibiotic, compared with 190 (87%) of 219 of those who did not (P=.001 in bivariate analysis). Use of an inactive antimicrobial agent was an independent predictor of treatment failure on logistic regression analysis (adjusted odds ratio, 2.80; 95% confidence interval, 1.26-6.22; P=.01). CONCLUSIONS: Our findings suggest that certain patients with SSTIs that are likely caused by MRSA would benefit from treatment with an antimicrobial agent with activity against this organism.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Community-Acquired Infections/drug therapy , Methicillin Resistance , Soft Tissue Infections/drug therapy , Staphylococcal Skin Infections/drug therapy , Adult , Aged , Cohort Studies , Community-Acquired Infections/diagnosis , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Follow-Up Studies , Humans , Logistic Models , Male , Microbial Sensitivity Tests , Middle Aged , Probability , Retrospective Studies , Risk Assessment , Severity of Illness Index , Soft Tissue Infections/diagnosis , Staphylococcal Infections/diagnosis , Staphylococcal Infections/drug therapy , Staphylococcal Skin Infections/diagnosis , Staphylococcus aureus/drug effects , Statistics, Nonparametric , Treatment Outcome
13.
J Crit Care ; 42: 282-288, 2017 12.
Article in English | MEDLINE | ID: mdl-28810207

ABSTRACT

PURPOSE: Medical patients whose care needs exceed what is feasible on a general ward, but who do not clearly require critical care, may be admitted to an intermediate care unit (IMCU). Some IMCU patients deteriorate and require medical intensive care unit (MICU) admission. In 2012, staff in the Johns Hopkins IMCU expressed concern that patient acuity and the threshold for MICU admission were too high. Further, shared triage decision-making between residents and supervising physicians did not consistently occur. METHODS: To improve our triage process, we used a 4Es quality improvement framework (engage, educate, execute, evaluate) to (1) educate residents and fellows regarding principles of triage and (2) facilitate real-time communication between MICU residents conducting triage and supervising physicians. RESULTS: Among patients transferred from the IMCU to the MICU during baseline (n=83;July-December 2012) and intervention phases (n=94;July-December 2013), unadjusted mortality decreased from 34% to 21% (p=0.06). After adjusting for severity of illness, admitting diagnosis, and bed availability, the odds of death were lower during the intervention vs. baseline phase (OR 0.33; 95%CI 0.11-0.98). CONCLUSIONS: Using a structured quality improvement process targeting triage education and increased resident/supervisor communication, we demonstrated reduced mortality among patients transferred from the IMCU to the MICU.


Subject(s)
Critical Illness/mortality , Patient Transfer , Quality Improvement , Triage/standards , APACHE , Adult , Aged , Baltimore , Critical Care , Critical Illness/therapy , Female , Hospital Mortality , Hospitals, University , Humans , Intensive Care Units/standards , Male , Middle Aged , Simplified Acute Physiology Score
14.
Am J Crit Care ; 26(1): e1-e10, 2017 01.
Article in English | MEDLINE | ID: mdl-27965236

ABSTRACT

BACKGROUND: An important, but not well characterized, population receiving intermediate care is that of medical patients admitted directly from the emergency department. OBJECTIVE: To characterize emergency medical patients and their outcomes when admitted to an intermediate care unit with clearly defined admission guidelines. METHODS: Demographic data, admitting diagnoses, illness severity, comorbid conditions, lengths of stay, and hospital mortality were characterized for all emergency medical patients admitted directly to an intermediate care unit from July through December 2012. RESULTS: A total of 317 unique patients were admitted (mean age, 54 [SD, 16] years). Most patients were admitted with respiratory (26.5%) or cardiac (17.0%) syndromes. The mean (SD) Acute Physiology and Chronic Health Evaluation score version II, Simplified Acute Physiology Score version II, and Charlson Comorbidity Index were 15.6 (6.5), 20.7 (11.8), and 2.7 (2.3), respectively. Severity of illness and length of stay were significantly different for patients who required intensive care within 24 hours of admission (n = 16) or later (n = 25), patients who continued with inter mediate care for more than 24 hours (n = 247), and patients who were downgraded or discharged in less than 24 hours (n = 29). Overall hospital mortality was 4.4% (14 deaths). CONCLUSIONS: Emergency medical patients with moderate severity of illness and comorbidity can be admitted to an intermediate level of care with relatively infrequent transfer to intensive care and relatively low mortality.


Subject(s)
Intermediate Care Facilities/standards , Length of Stay , Patient Admission/standards , Practice Guidelines as Topic , Severity of Illness Index , APACHE , Adult , Aged , Comorbidity , Critical Care , Emergency Service, Hospital , Female , Hospital Mortality , Humans , Male , Middle Aged , Patient Discharge , Treatment Outcome
16.
Clin Infect Dis ; 40(10): 1429-34, 2005 May 15.
Article in English | MEDLINE | ID: mdl-15844065

ABSTRACT

BACKGROUND: Few data exist on the efficacy of the long-acting tetracyclines doxycycline and minocycline against methicillin-resistant Staphylococcus aureus (MRSA) infection. METHODS: The medical records of 24 patients with serious tetracycline-susceptible MRSA infections who were treated with doxycycline or minocycline were reviewed. A review of the literature on the use of these antibiotics for treatment of both methicillin-susceptible and methicillin-resistant S. aureus infection was also performed. RESULTS: Complicated skin and skin-structure infections were most common (67%). Clinical cure was achieved in 20 (83%) of 24 patients in our case series. Both drugs were well-tolerated. The review of the literature on a total of 85 patients with S. aureus infection revealed similar results. CONCLUSIONS: Long-acting tetracyclines may be a reasonable treatment alternative for patients with certain types of MRSA infection.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Methicillin Resistance , Staphylococcal Infections/drug therapy , Staphylococcal Infections/microbiology , Staphylococcus aureus/drug effects , Tetracyclines/therapeutic use , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/administration & dosage , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Staphylococcus aureus/physiology , Tetracyclines/administration & dosage
17.
Clin Infect Dis ; 36(10): 1221-8, 2003 May 15.
Article in English | MEDLINE | ID: mdl-12746765

ABSTRACT

A randomized, blinded, multicenter trial was conducted to compare fluconazole (800 mg per day) plus placebo with fluconazole plus amphotericin B (AmB) deoxycholate (0.7 mg/kg per day, with the placebo/AmB component given only for the first 5-6 days) as therapy for candidemia due to species other than Candida krusei in adults without neutropenia. A total of 219 patients met criteria for a modified intent-to-treat analysis. The groups were similar except that those who were treated with fluconazole plus placebo had a higher mean (+/- standard error) Acute Physiology and Chronic Health Evaluation II score (16.8+/-0.6 vs. 15.0+/-0.7; P=.039). Success rates on study day 30 by Kaplan-Meier time-to-failure analysis were 57% for fluconazole plus placebo and 69% for fluconazole plus AmB (P=.08). Overall success rates were 56% (60 of 107 patients) and 69% (77 of 112 patients; P=.043), respectively; the bloodstream infection failed to clear in 17% and 6% of subjects, respectively (P=.02). In nonneutropenic subjects, the combination of fluconazole plus AmB was not antagonistic compared with fluconazole alone, and the combination trended toward improved success and more-rapid clearance from the bloodstream.


Subject(s)
Amphotericin B/therapeutic use , Antifungal Agents/therapeutic use , Candidiasis/drug therapy , Fluconazole/therapeutic use , Fungemia/drug therapy , Adult , Amphotericin B/adverse effects , Antifungal Agents/adverse effects , Candida/drug effects , Candidiasis/physiopathology , Catheterization , Double-Blind Method , Drug Therapy, Combination , Female , Fluconazole/adverse effects , Fungemia/physiopathology , Humans , Male , Middle Aged , Neutropenia/etiology , Treatment Outcome
18.
Pediatr Infect Dis J ; 23(2): 110-4, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14872174

ABSTRACT

BACKGROUND: Bloodstream infections with Pseudomonas aeruginosa have been well-described in neonatal intensive care units (NICU) and have resulted in the temporary closure of some nurseries to new admissions. Nosocomial transmission of these infections has been verified by fingerprint analysis of the isolates. We utilized molecular fingerprinting to identify the source of bloodstream infections in an NICU and used this information to apply infection control measures that allowed the nursery to stay open and continue to accept referrals. METHODS: In June 1998 three premature infants transferred to our hospital (Hospital A) from Hospitals B and C had bloodstream infections with P. aeruginosa. Subsequently one additional neonate transferred from Hospital B was colonized with P. aeruginosa. Random amplification of polymorphic deoxyribonucleic acid (RAPD) was performed on the four isolates. All transfers from Hospital B were cultured, and surveillance programs were instituted in Hospitals A and B. Targeted infection control measures for all transfers were implemented. RESULTS: The four isolates were the same clone by RAPD. Investigation of the environment in Hospital A did not identify any source of the organism. Surveillance cultures on 49 neonates at Hospital A revealed only one patient colonized at an endotracheal tube. This patient was also a transfer from Hospital B. Results from Hospital B identified 4 of 40 (10%) neonates colonized. All isolates were clones identical with the bloodstream isolates from the neonates with bloodstream infections. Infection control measures for all babies transferred from Hospital B resulted in no new cases of P. aeruginosa bacteremia during the next 5 years. CONCLUSIONS: The use of molecular fingerprinting of isolates of P. aeruginosa allowed for a prompt and directed infection control plan to be implemented in Hospitals A and B. It also allowed the NICU in Hospital A to continue to accept referrals from other hospitals and to implement a targeted infection control plan for patients transferred from Hospital B.


Subject(s)
Bacteremia/diagnosis , Cross Infection/diagnosis , DNA Fingerprinting , Health Facility Closure , Infection Control/methods , Intensive Care Units, Neonatal , Pseudomonas Infections/diagnosis , Pseudomonas aeruginosa/isolation & purification , Bacteremia/mortality , Bacteremia/prevention & control , Blood-Borne Pathogens/isolation & purification , Cross Infection/prevention & control , Decision Making , Female , Humans , Infant, Low Birth Weight , Infant, Newborn , Male , Polymerase Chain Reaction , Pseudomonas Infections/mortality , Pseudomonas Infections/prevention & control , Pseudomonas aeruginosa/genetics , Risk Assessment , Sensitivity and Specificity , Survival Rate , United States
19.
Infect Dis Clin North Am ; 17(1): 21-40, vii, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12751259

ABSTRACT

Blastomycosis is an endemic mycoses in the central United States caused by a dimorphic fungus, Blastomyces dermatitidis, that exists in nature in mycelial phase and converts to yeast phase at body temperature. The organism may produce epidemics of infection following a point source of infection or sporadic endemic infection. Blastomycosis can be a subclinical illness with subsequent protection against progressive infection afforded by cellular immune mechanisms, but it may present with progressive disease with either pulmonary or extrapulmonary disease or both. Itraconazole has been shown to be the drug of choice for both infections, except in cases of life-threatening infection when amphotericin B should be used.


Subject(s)
Blastomycosis , Blastomyces/pathogenicity , Blastomycosis/diagnosis , Blastomycosis/drug therapy , Blastomycosis/epidemiology , Blastomycosis/pathology , Bone Diseases/microbiology , Bone Diseases/pathology , Clinical Protocols , Female Urogenital Diseases/microbiology , Female Urogenital Diseases/pathology , Humans , Lung Diseases, Fungal/epidemiology , Lung Diseases, Fungal/therapy , Male Urogenital Diseases , Onygenales/classification , Onygenales/genetics , Onygenales/pathogenicity , Skin Diseases/microbiology , Skin Diseases/pathology
20.
Open Forum Infect Dis ; 1(2): ofu050, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25734122

ABSTRACT

BACKGROUND: In the era of cost-consciousness regarding healthcare , provision of medical services in an outpatient setting has become increasingly attractive. We report an influenza outbreak in an ambulatory stem cell transplant center in 2013 that highlights unique identification and infection control challenges in this setting. METHODS: Nasopharyngeal swabs were performed on patients with suspected influenza-like illnesses (ILI), defined by subjective fever or measured temperature of ≥37.7°C (≥100°F) with cough or sore throat during July 25, 2013 through August 7, 2013. In addition, testing was triggered by an elevated C-reactive protein (CRP). Specimens were analyzed by using eSensor Respiratory Viral Panel. Clinical and epidemiologic information was collected in real time, and frequencies were calculated on demographics, baseline clinical parameters, treatment methods, comorbidities, and symptoms of affected persons. RESULTS: Thirty-one patients had influenza A (H3N2) infection during July 25, 2013 through August 7, 2013. Only 7 patients (23%) met the Centers for Disease Control and Prevention and Council of State and Territorial Epidemiologists ILI case definition. Twenty-five patients (81%) had received ≥1 transplant, with 13 (42%) having occurred within 1 year before the outbreak. Twenty-five patients (81%) had received B-cell active chemotherapy <60 days before influenza diagnosis, 6 (19%) were neutropenic, and 25 (81%) lymphopenic. Among clinical and laboratory markers analyzed, abnormal CRP was the most sensitive screening tool for influenza. Twelve (39%) patients were hospitalized (median stay, 10 days; range, 2-20). No deaths occurred. CONCLUSIONS: Immunocompromised hosts with influenza have atypical presentations. Existing surveillance case definitions might be insufficient to reliably identify influenza outbreaks in such patients.

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