scholarly journals Innovative Technologies for Advancement of WHO Risk Group 4 Pathogens Research

Author(s):  
James Logue ◽  
Jeffrey Solomon ◽  
Brian F. Niemeyer ◽  
Kambez H. Benam ◽  
Aaron E. Lin ◽  
...  
2020 ◽  
Vol 19 (1) ◽  
pp. 85-103
Author(s):  
James Logue ◽  
Ian Crozier ◽  
Peter B Jahrling ◽  
Jens H Kuhn

2021 ◽  
Author(s):  
Fabienne Lesueur ◽  
Douglas F. Easton ◽  
Anne-Laure Renault ◽  
Sean V. Tavtigian ◽  
Jonine L. Bernstein ◽  
...  

Author(s):  
Wei-Ti Su ◽  
Shao-Chun Wu ◽  
Chun-Ying Huang ◽  
Sheng-En Chou ◽  
Ching-Hua Tsai ◽  
...  

Background: Malnutrition is frequently underdiagnosed in geriatric patients and is considered to be a contributing factor for worse outcomes during hospitalization. In addition, elderly patients who undergo trauma are often malnourished at the time of incurring fractures. The geriatric nutritional risk index (GNRI), calculated based on the serum albumin level and the ratio of present body weight to ideal body weight, was proposed for the assessment of the nutritional status of elderly patients with various illnesses. This study aimed to investigate whether the GNRI has a prognostic value that links the nutritional status and mortality outcomes of elderly patients who have previously undergone trauma with femoral fractures. Methods: From January 1, 2009 to December 31, 2019, a total of 678 elderly patients with femoral fractures were categorized into four nutritional risk groups: a major-risk group (GNRI < 82; group 1, n = 127), moderate-risk group (GNRI 82–92; group 2, n = 179), low-risk group (GNRI 92–98; group 3, n = 123), and no-risk group (GNRI > 98; group 4, n = 249). To minimize the confounding effects of sex, age, preexisting comorbidities, and injury severity of patients on outcome measurements, propensity score-matched patient cohorts were created to assess the impact of patients being in different nutritional risk groups on the in-hospital mortality outcomes against the no-risk group. Results: The patients in groups 1–3 were significantly older and presented a significantly lower body mass index and lower serum albumin levels than those in group 4. Compared with patients in group 4 (3.6%), a significantly higher mortality rate was found in the patients in group 1 (17.3%, p < 0.001), but not in those in group 2 (6.7%) or group 3 (2.4%). The study of propensity score-matched patient cohorts provided similar results; group 1 patients had significantly higher odds of mortality than group 4 patients (odds ratio, 6.3; 95% confidence interval, 1.34–29.37; p = 0.009), but there were no significant differences in mortality risks among patients in groups 2 and 3 compared with those in group 4. Conclusions: This preliminary study suggested that the GNRI may be used as a screening tool to identify patients with malnutrition at a high risk of mortality among elderly patients with femoral fractures. A prospective study is needed to validate the suggestion.


1997 ◽  
Vol 2 (4) ◽  
pp. 26-35 ◽  
Author(s):  
G. Abraham ◽  
P. Hooper ◽  
M. Williamson ◽  
J. Muschialli ◽  
D. Martin ◽  
...  

The safe experimental handling of animals infected with a new Risk Category 4 virus posed significant biosafety challenges. Novel approaches for restraining, handling and inoculating horses, cats and large fruit-eating bats with equine morbillivirus were developed. Equipment was designed to allow staff working in encapsulating suits access to all parts of a large animal room capable of accommodating seven horses individually. Procedures were developed for the safe handling, anesthesia and euthanasia of experimental animals and for the disposal of infected horse carcasses. Comprehensive staff training for this demanding work included safety consciousness, teamwork and training in first aid and emergency procedures.


1998 ◽  
Vol 3 (1) ◽  
pp. 7-7

JABSA regrets omitting the name of one of the authors of the article entitled, “Handling of Large Experimental Animals Infected with a Risk Group 4 Virus” which was published in Volume 2, Number 4, 1997. The authors are affiliated with the Australian Animal Health Laboratory in Geelong, Victoria, Australia. The full list of authors is: G. Abraham P. Hooper M. Williamson J. Muschialli D. Martin I. Duff S. Edwards


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 1124-1124
Author(s):  
Suman L. Sood ◽  
Cathy Stabler ◽  
Angela E. Hawley ◽  
Kenneth E. Guire ◽  
Susan Blackburn ◽  
...  

Abstract Introduction Within the first weeks of ICU admission, 10-30% of medical/surgical patients develop venous thromboembolism (VTE), and up to 60% of trauma patients. VTE has significant morbidity including longer mechanical ventilation, ICU and hospital stay. The Caprini VTE risk assessment model (Ann Surg, 2010; 251[2]:344-50) is based on clinical factors such as age and comorbidities. Previous data from our lab has demonstrated the role of soluble P-selectin (sPsel), D-dimer, CRP, von Willebrand factor activity (VWF), and ADAMTS13 in the diagnosis of DVT. The aim of this study is to determine levels of biomarkers and clinical characteristics in relation to Caprini risk level in patients both with and without DVT upon admission to the ICU. Methods We performed a prospective cohort study at the University of Michigan with patients from the surgical, neurological, trauma and medical ICUs. Inclusion criteria: age > 18 and at risk for DVT (i.e. not on therapeutic anticoagulation) when admitted to the ICU. At baseline, clinical information including demographics and comorbidities, Wells’ and APACHE score was collected, blood was drawn for biomarkers and upper and lower extremity duplex ultrasound (DVU) was performed. Blood samples and DVU were repeated every 7 days. Subjects were recruited within 24 hrs of ICU admission and stratified into low/moderate (Group 1), high (Group 2), and highest (Group 3) risk groups according to the Caprini model; Group 4 were DVT positive on screening ultrasound. Patients were followed until DVT positivity, floor transfer, or 35 days. All patients received VTE prophylaxis and had imaging performed as clinically indicated. ELISAs were performed for sPsel, D-dimer, CRP, and VWF activity, and slightly modified FRETS-VWF73 assay for ADAMTS-13 activity. ANOVA and t-test were used to compare continuous, and Chi-square categorical, variables between the groups. Spearman correlation coefficients were performed to assess the relationship between Caprini score and other variables. Results From 12/08-10/12, 145 subjects were recruited. The age range was 20-88 years. DVT positive patients on screening ultrasound were significantly older, more likely to be male, and have a personal history of VTE. There was no difference in BMI or family history of VTE. DVT positive subjects (Group 4) had a significantly higher baseline mean D-dimer, sPsel, day 1 Wells’ and APACHE score compared to the lowest risk group (Group 1), and a significantly lower ADAMTS13 level (see Table). Baseline D-dimer, Wells’ and APACHE scores rose with increasing Caprini risk group and were also significantly higher in Group 4 vs. Groups 2 and 3. There was a trend towards increasing baseline sPsel and declining ADAMTS13 level with increasing Caprini score. Increasing baseline CRP and VWF was also significantly correlated with increasing Caprini score. Eight patients (6.2%) developed a new DVT within the 35 day observation period (average day 10); 6/8 (75%) were in the highest risk group (Group 3). There was a trend towards higher baseline D-dimer, CRP, Wells’ and APACHE score in subjects who developed DVT vs. stayed negative. In patients who developed DVT, these markers did not significantly increase over time with serial sampling. There was a significantly higher BMI (mean, SE) 35.9 ± 3.3 vs. 29.4 ± 0.6 kg/m2, p<0.01, in those who turned positive vs. stayed negative. Conclusions Patients with DVT on presentation to the ICU have higher levels of biomarkers and more severe clinical characteristics including higher Wells’ and APACHE scores, than patients without DVT, with variations related to Caprini risk. For the 6.2% of patients who were initially negative and went on to develop DVT, there was a tendency to increased biomarker levels and more severe clinical characteristics at baseline but not on serial testing. Disclosures: No relevant conflicts of interest to declare.


Author(s):  
P. Bagavandoss ◽  
JoAnne S. Richards ◽  
A. Rees Midgley

During follicular development in the mammalian ovary, several functional changes occur in the granulosa cells in response to steroid hormones and gonadotropins (1,2). In particular, marked changes in the content of membrane-associated receptors for the gonadotropins have been observed (1).We report here scanning electron microscope observations of morphological changes that occur on the granulosa cell surface in response to the administration of estradiol, human follicle stimulating hormone (hFSH), and human chorionic gonadotropin (hCG).Immature female rats that were hypophysectcmized on day 24 of age were treated in the following manner. Group 1: control groups were injected once a day with 0.1 ml phosphate buffered saline (PBS) for 3 days; group 2: estradiol (1.5 mg/0.2 ml propylene glycol) once a day for 3 days; group 3: estradiol for 3 days followed by 2 days of hFSH (1 μg/0.1 ml) twice daily, group 4: same as in group 3; group 5: same as in group 3 with a final injection of hCG (5 IU/0.1 ml) on the fifth day.


Author(s):  
E.J. Prendiville ◽  
S. Laliberté Verdon ◽  
K. E. Gould ◽  
K. Ramberg ◽  
R. J. Connolly ◽  
...  

Endothelial cell (EC) seeding is postulated as a mechanism of improving patency in small caliber vascular grafts. However the majority of seeded EC are lost within 24 hours of restoration of blood flow in previous canine studies . We postulate that the cells have insufficient time to fully develop their attachment to the graft surface prior to exposure to hemodynamic stress. We allowed EC to incubate on fibronectin-coated ePTFE grafts for four different time periods after seeding and measured EC retention after perfusion in a canine ex vivo shunt circuit.Autologous canine EC, were enzymatically harvested, grown to confluence, and labeled with 30 μCi 111 Indium-oxine/80 cm 2 flask. Four groups of 5 cm x 4 mm ID ePTFE vascular prostheses were coated with 1.5 μg/cm.2 human fibronectin, and seeded with 1.5 x 105 EC/ cm.2. After seeding grafts in Group 1 were incubated in complete growth medium for 90 minutes, Group 2 were incubated for 24 hours, Group 3 for 72 hours and Group 4 for 6 days. Grafts were then placed in the canine ex vivo circuit, constructed between femoral artery and vein, and subjected to blood flow of 75 ml per minute for 6 hours. Continuous counting of γ-activity was made possible by placing the seeded graft inside the γ-counter detection crystal for the duration of perfusion. EC retention data after 30 minutes, 2 hours and 6 hours of flow are shown in the table.


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