Jose Montero
University of South Florida
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Jose Montero.
American Journal of Infection Control | 2013
Sally Alrabaa; Phuong Thuy Nguyen; Roger Sanderson; Aliyah Baluch; Ramon L. Sandin; Danashree Kelker; Chaitanya Karlapalem; Peggy Thompson; Kay Sams; Stacy Martin; Jose Montero; John N. Greene
Klebsiella producing carbapenemase is an emerging pathogen. We report transmission of this organism by contaminated endoscopic instruments. Quick identification of source, staff education, contact precautions, and emphasis on hand and environmental hygiene led to case control and prevention of outbreak.
Open Forum Infectious Diseases | 2015
Nicholas W. Carris; Joe Pardo; Jose Montero; Kristy M. Shaeer
Doxycycline remains on intermittent shortage. Evidence supports the substitution of minocycline in skin and soft-tissue infections and carefully selected cases of pneumonia. Minocycline may be carefully considered in Lyme disease prophylaxis and Rickettsial disease in the complete absence of doxycycline.
Transplantation | 2015
Nina Singh; Costi D. Sifri; Fernanda P. Silveira; Rachel Miller; Kevin S. Gregg; Shirish Huprikar; Erika D. Lease; Andrea Zimmer; J. Stephen Dummer; W Cedric; C. Koval; David B. Banach; Miloni Shroff; Jade Le; Darin Ostrander; Robin K. Avery; Albert Eid; Raymund R. Razonable; Jose Montero; Emily A. Blumberg; Ahlaam Alynbiawi; Michele I. Morris; Henry B. Randall; George Alangaden; Jeffrey M. Tessier; Marilyn M. Wagener; Hsin-Yun Sun
Background The outcomes and optimal management of cirrhotic patients who develop cryptococcosis before transplantation are not fully known. Methods We conducted a multicenter study involving consecutive patients with cirrhosis and cryptococcosis between January 2000 and March 2014. Data collected were generated as standard of care. Results In all, 112 patients were followed until death or up to 9 years. Disseminated disease and fungemia were present in 76.8% (86/112) and 90-day mortality was 57.1% (64/112). Of the 39 patients listed for transplant, 20.5% (8) underwent liver transplantation, including 2 with active but unrecognized disease before transplantation. Median duration of pretransplant antifungal therapy and posttransplant therapy was 43 days (interquartile range, 8-130 days) and 272 days (interquartile range, 180-630 days), respectively. Transplantation was associated with lower mortality (P = 0.002). None of the transplant recipients developed disease progression during the median follow-up of 3.5 years with a survival rate of 87.5%. Conclusions Cryptococcosis in patients with cirrhosis has grave prognosis. Our findings suggest that transplantation after recent cryptococcal disease may not be a categorical exclusion and may be cautiously undertaken in liver transplant candidates who are otherwise deemed clinically stable.
Infection | 2016
Jose Montero; Sally Alrabaa; Todd S. Wills
A 30-year-old man with history of neonatal hydrocephalus requiring ventriculoperitoneal shunt placement presented with Mycobacterium abscessus shunt infection despite no shunt manipulation over 10xa0years prior to presentation. Cure was not achieved until complete removal of all CNS shunt foreign body was performed despite initial adequate antimicrobial therapy.
Transplant Infectious Disease | 2017
Sally Alrabaa; Ripal Jariwala; Kristen Zeitler; Jose Montero
Clostridium difficile infection (CDI) is a major infectious disease focus for which fecal microbiota transplantation (FMT) has been used with success in various patient populations.
Journal of The International Association of Physicians in Aids Care (jiapac) | 2011
Tri Pham; Sally Alrabaa; Charurut Somboonwit; Le Hung; Jose Montero
Background: Approaches to treatment-experienced HIV-infected patients with persistent low-level viremia are limited by current commercial resistance genotyping assays when the viral load (VL) is <500 copies/mL. The best intervention to achieve virologic suppression in this population is unclear. Methods: This is a case control retrospective chart review study of 149 HIV-infected patients with a VL of 50 to 1000 copies/mL. Patients were in either regimen unchanged group or intervention group (intensification of regimen or switch without guidance from resistance testing). End point was VL < 100 copies/mL. Results: At 6 months post change, 30.8% of patients with intervention versus 36.6% with no intervention achieved a complete virologic suppression. There were no statistically significant differences between these 2 groups (P = .254). The majority of patients without regimen change eventually progressed to complete virologic failure. Conclusion: Patients with persistent low levels of viremia are likely to progress to have virologic failure. This supports the adoption of a more proactive approach to treatment and more sensitive technique to identify drug resistance.
Cancer Control | 1998
Petros E. Tsambiras; Jose Montero; John N. Greene; Ramon L. Sandin
Beta-Hemolytic streptococcal infections can be categorized into Lancefield groups A to H and K to V. Groups A, B, C, D, and G are most often involved in human disease. Group A (Streptococcus pyogenes), one of the most common causes of pharyngitis, produces a variety of skin and soft-tissue infections including cellulitis, erysipelas, and necrotizing fasciitis. Group B (S. agalactiae) has been associated with a history of breast cancer and with sepsis and meningitis in neonates and peripartum fever in women. Group D includes the nonenterococci (ie, S. bovis) that are associated with gastrointestinal neoplasms and the enterococci (ie, Enterococcus faecalis, E. faecium) that are associated with urinary tract infections and polymicrobial intra-abdominal infections. Less commonly, beta-hemolytic streptococcal infections are caused by Lancefield groups C and G.
Infectious Diseases in Clinical Practice | 2018
Cristina García; Erika S. Abel; Kellee L. Oller; Charurut Somboonwit; Jose Montero
CASE REPORTA 50-year-old man with medical history of hepatitis C (with a low viral load treated a decade prior) initially presented to an outside provider with a progressive rash, digit swelling, and joint pain and was evaluated for oligoarticular synovitis. Joints affected included the right knee,
Archive | 2017
Charurut Somboonwit; Jose Montero; John T. Sinnott; Paul Shapshak
The central nervous system (CNS) can act as a compartment in which HIV can replicate independently from plasma. HIV infection of the brain and the ongoing immune response leads to neurocognitive impairment. Therefore, besides optimally suppressing HIV viral load in the plasma, it is essential to reach adequate concentrations of antiretrovirals (ARVs) in the CNS to prevent and improve neurocognitive impairments. ARVs have limitations in their ability to enter the brain due the blood-brain barrier (BBB) and different efficient efflux mechanisms. Moreover, ARVs exposed to the CNS show variability and distinctiveness of their characteristics including molecular weight, lipophilicity, protein binding, and on their capacity as substrates for efflux transporters.
Archive | 2017
Kelly Kynaston; Minh Ho; Robert Castro; Jose Montero
Neurologic opportunistic infections in individuals with human immunodeficiency virus remain significant causes of morbidity and mortality despite the availability of highly active antiretroviral therapy. These pathogens are generally ubiquitous or are very commonly acquired by humans but reactivate during periods of profound immunosuppression. Diagnosis can be very challenging, relying on a combination of recognition of clinical syndromes, radiographic findings, and cerebrospinal fluid analysis. Newer molecular tests provide means for diagnosis at times when culture-based diagnosis is limited. With experience, guidance in treating these infections has been published focusing on therapies and immune reconstitution utilizing antiretroviral therapy. Prevention of these neurologic infections relies mostly on restoring or preserving cell-mediated immunity but can be enhanced in a few by avoidance of primary infection, treatment, or suppression of infection and at times screening for early detection and treatment.