P0689 A RETROSPECTIVE STUDY COMPARING CEFOPERAZONE/SULBACTAM WITH PIPERACILLIN/TAZOBACTAM AS EMPIRICAL THERAPY FOR FEBRILE NEUTROPENIA IN ADULTS WITH HEMATOLOGICAL DISORDERS

2009 ◽  
Vol 20 ◽  
pp. S225
Author(s):  
Berivan Bitik ◽  
Sehnaz Alp ◽  
Nursel Calik Basaran ◽  
Murat Akova ◽  
Omrum Uzun ◽  
...  
2017 ◽  
Vol 6 (10) ◽  
pp. 92 ◽  
Author(s):  
Emmanuel Andrès ◽  
Rachel Mourot-Cottet ◽  
Frédéric Maloisel ◽  
Olivier Keller ◽  
Thomas Vogel ◽  
...  

2017 ◽  
Vol 46 ◽  
pp. e13-e14 ◽  
Author(s):  
Emmanuel Andrès ◽  
Rachel Mourot-Cottet ◽  
Frédéric Maloisel ◽  
Thomas Vogel ◽  
Martine Tebacher ◽  
...  

2015 ◽  
Vol 10 (3) ◽  
pp. 357-365 ◽  
Author(s):  
Elio Castagnola ◽  
Ilaria Caviglia ◽  
Luisa Pescetto ◽  
Francesca Bagnasco ◽  
Riccardo Haupt ◽  
...  

Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 4379-4379 ◽  
Author(s):  
Radovan Vrhovac ◽  
Zinaida Peric ◽  
Matko Kalac ◽  
Alen Ostojic ◽  
Visnja Kovacevic ◽  
...  

Abstract Background: Infections remain a major cause of morbidity and mortality in patients with lymphoma treated with autologous hematopoietic stem cell transplantation. Knowledge of local microbiological epidemiology and patients’ risk factors are essential for optimal management of these infections. Aims: to determine incidence of febrile neutropenia (FN) in patients with lymphoma treated with autologous peripheral blood stem cell transplantation (PBSCT) and to investigate correlations of a number of variables available on the day of FN onset with the severity of infection. Patients and Methods: 102 consecutive patients (median age 44, range 19–68 yrs, 58M/44F) with relapsed or refractory Non-Hodgkin’s Lymphoma (NHL, n=78) and Hodgkin’s Disease (HD, n=24) treated with PBSCT in a single center have been evaluated for infectious complications following transplantation. Results: Febrile neutropenia occurred in 67 (65.7%) patients at a mean of 6 days after transplantation (range 1–9, SD 1.71). Microbiological work-up was done and empirical antibiotic therapy with piperacillin-tazobactam was initiated in all but 15 patients who received a carbapenem. Empirical therapy was modified in 31 (46.3%) patients. Vancomycin was added in 22 patients (32.8%), a sistemic antifungal in 4 (6.0%) and both in 6 (9.0%) patients. Three patiens died as a consequence of sepsis (TRM=2.9%). Twenty two patients (32.8%) had proven bacteremias while 27 (40.3%) had other microbiologically documented infections (MDIs). Gram+ microorganisms were responsible for the majority of all documented infections (63.6% of bacteremias and 54.5% of other MDIs). Correlations of a number of variables available at time of FN onset with the duration of febrile episode have been investigated. Patients with higher CRP levels at FN onset and those with earlier onset of fever following PBSCT had significantly longer (p=0.047 and p=0.0066, respectively) duration of fever. Other variables, including age, No. of previous lines of therapy, No. of stem cells reinfused, ANC and monocyte counts as well as peak temperature values at day of fever onset did not show statistically significant correlations with duration of fever. All patients with diabetes developed FN and, although not reaching statistical significance (p=0.09), its duration was longer in comparison to other patients. Conclusions: Infections are serious but manageable complications of PBSCT. Gram+ microorganisms remain the major cause of documented infections. Early empirical antimicrobial therapy, tailored according to local microbiological epidemiology is essential for their optimal treatment.


2020 ◽  
Vol 38 (15_suppl) ◽  
pp. e23573-e23573
Author(s):  
Neha Pancholy ◽  
Vonn Walter ◽  
Joseph J. Drabick ◽  
Edward J Fox ◽  
Nicholas George Zaorsky ◽  
...  

e23573 Background: Surgery still remains the mainstay of treatment with curative intent for high grade extremity soft tissue non rhabdomyosarcoma sarcomas (HG ESTS). Adjuvant/neoadjuvant Chemotherapy (CT) is still debatable, but most experts agree about its role in HG-ESTS in combination with radiation (R). Interdigitated CT+R is an attractive method of delivering these modalities of treatment in short time prior to surgery, however safety of using growth factor (GF) while administering CT+R in HG ESTS is largely unknown. We conducted a retrospective study of the toxicities associated with GF administration in this setting at a single institution. Methods: Electronic medical records at one institution were reviewed to identify patients having a diagnosis of extremity STS between October 2017- January 2020. Demographics, details of tumor characteristics, and treatment details were noted. Details of Interdigitated (ID)CRT were noted; the intended CT regimen was doxorubicin/ifosphamide/mesna (MAI) at 100% of the intended dosing. Data regarding the toxicities associated with GF administration were also evaluated in these patients; specifically, the development of febrile neutropenia, thrombocytopenia and pulmonary toxicity were evaluated. Patients who presented with metastatic disease were excluded from this analysis. Results: 22 patients were identified. Median age was 63 years. Of these, 9 patients (40%) were smokers. At diagnosis, 6 patients (27%) had metastatic disease. The most common site of primary disease was the thigh (50%). The most common histology was undifferentiated pleomorphic sarcoma (59%). CT monotherapy was administered in 3 patients. RT was administered in 14 patients, out of whom interdigitated CRT was administered in 10 patients. 60% of patients who initiated were able to receive 3 cycles of ID-CRT prior to Surgery. GF was administered in 14 patients who received regimens including CT. Of patients receiving ID-CRT who received GF, 60% completed ID-CRT without delays. No delays occurred due to thrombocytopenia. Febrile neutropenia occured in 22% of patients who received GF. Only 1 patient who received GF suffered prolonged thrombocytopenia. No patients who received GF were noted to have pulmonary toxicity. Conclusions: For adults with HG ESTS, GF administration with ID-CRT does not appear to cause any additional delay in treatment due to prolonged thrombocytopenia or lung toxicity. Inclusion of GF administration in further prospective trials of ID-CRT appears feasible.


2016 ◽  
Vol 22 (7) ◽  
pp. 466-471 ◽  
Author(s):  
Hideo Koh ◽  
Mizuki Aimoto ◽  
Takako Katayama ◽  
Masamichi Hashiba ◽  
Ayumi Sato ◽  
...  

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