18 results on '"Michael Spiro"'
Search Results
2. Understanding recruitment to a perioperative randomised controlled trial: protocol for a mixed-methods substudy nested within a feasibility trial of octreotide infusion during liver transplantation
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Duncan Wagstaff, S Ramani Moonesinghe, Jez Fabes, Michael Spiro, Edgar Brodkin, Ee-Neng Loh, and Vivienne Hannon
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Medicine - Abstract
Introduction Recruitment to perioperative randomised controlled trials is known to be challenging. Qualitative methods offer insight into barriers and enablers to participation. This is a substudy within a feasibility randomised controlled trial of octreotide infusion during liver transplantation at two National Health Service hospitals, which will evaluate patient and staff experiences of trial processes. By sharing formative understanding from these methods with the trials team we aim to improve staff–patient interactions and hence recruitment rates.Methods and analysis This prospective mixed-methods study will comprise two workstreams. First, after consent to the randomised controlled trial is sought, all patients will be invited to complete a questionnaire to explore their perceptions of the information given to them and motivating factors that influenced their decision to consent or not. Questionnaires will be analysed using descriptive statistics and framework analysis.If the recruitment:approach ratio drops below a predetermined ratio or if there are any specific recruitment concerns from the trials team, a second workstream involving mixed-methods fieldwork will be implemented. This will involve audiorecording of recruitment consultations and a follow-up semistructured interview to explore patients’ perception of their decision-making regarding recruitment. Semistructured interviews will also be conducted with the recruitment team to establish their views about the trial, barriers to recruitment and ways to overcome them. Recruitment consultations will be analysed using Q-QAT methodology and interviews will be analysed using framework analysis. Findings from both workstreams will be formatively fed back to the trials team to enable iterative improvement to recruitment processes.Ethics and dissemination Approval has been granted by Greater Manchester West Research Ethics Committee (ref 20/NW/0071), the Health Research Authority and the local Research and Development offices. A manuscript detailing the summative findings will be submitted to peer-reviewed journals.Trial registration number NCT04941911.
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- 2022
- Full Text
- View/download PDF
3. Protocol for a prospective double-blind, randomised, placebo-controlled feasibility trial of octreotide infusion during liver transplantation
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Gareth Ambler, Norman R Williams, Brian R Davidson, Jeremy Fabes, Bina Shah, and Michael Spiro
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Medicine - Abstract
Introduction Liver transplantation is a complex operation that can provide significant improvements in quality of life and survival to the recipients. However, serious complications are common and include major haemorrhage, hypotension and renal failure. Blood transfusion and the development of acute kidney injury lead to both short-term and long-term poor patient outcomes, including an increased risk of death, graft failure, length of stay and reduced quality of life. Octreotide may reduce the incidence of renal dysfunction, perioperative haemorrhage and enhance intraoperative blood pressure. However, octreotide does have risks, including resistant bradycardia, hyperglycaemia and hypoglycaemia and QT prolongation. Hence, a randomised controlled trial of octreotide during liver transplantation is needed to determine the cost-efficacy and safety of its use; this study represents a feasibility study prior to this trial.Methods and analysis We describe a multicentre, double-blind, randomised, placebo-controlled feasibility study of continuous infusion of octreotide during liver transplantation surgery. We will recruit 30 adult patients at two liver transplant centres. A blinded infusion during surgery will be administered in a 2:1 ratio of octreotide:placebo. The primary outcomes will determine the feasibility of this study design. These include the recruitment ratio, correct administration of blinded study intervention, adverse event rates, patient and clinician enrolment refusal and completion of data collection. Secondary outcome measures of efficacy and safety will help shape future trials by assessing potential primary outcome measures and monitoring safety end points. No formal statistical tests are planned. This manuscript represents study protocol number 1.3, dated 2 June 2021.Ethics and dissemination This study has received Research Ethics Committee approval. The main study outcomes will be submitted to an open-access journal.Trial sponsor The Joint Research Office, University College London, UK.Neither the sponsor nor the funder have any role in study design, collection, management, analysis and interpretation of data, writing of the study report or the decision to submit the report for publication.Trial registration The study is registered with ClinicalTrials.gov (NCT04941911) with recruitment due to start in August 2021 with anticipated completion in July 2022.Clinical trials unit Surgical and Interventional Group, Division of Surgery & Interventional Science, University College London.
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- 2021
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- View/download PDF
4. Fatal primary dengue-induced Haemophagocytic Lymphohistiocytosis (HLH) in a returning traveller from India treated with anakinra for the first time
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Tanmay Kanitkar, Charlotte Richardson, Antonia Scobie, Amy Ireson, Animesh Singh, Michael Jacobs, Jim Buckley, and Michael Spiro
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Dengue ,Haemophagocytic lymphohistiocytosis ,Anakinra ,Severe dengue ,Returning traveller ,Infectious and parasitic diseases ,RC109-216 - Abstract
Background: Dengue fever is an arthropod-borne flavivirus infection that is highly prevalent in the tropics. A proportion of clinical cases develop severe dengue, defined by life-threatening complications including haemorrhage, capillary leak and multi-organ failure. Recently there has been increasing recognition that some cases of severe dengue may be a consequence of HLH. To our knowledge, this is the first report of treatment with Anakinra for dengue-induced HLH. Case report: We report a case of Dengue fever triggering HLH in an eighteen-year-old female returning traveller from India, diagnosed with systemic lupus erythematosus (SLE) two months prior to presentation. The patient initially presented to a district general hospital emergency department (ED) with a three-day history of flu-like symptoms, fever, erythematous rash, widespread joint pain, nausea and chills. Acute Dengue virus infection was confirmed with serum polymerase chain reaction (PCR) testing. On day two, she was admitted to intensive care for multi-organ support necessitated by refractory hypotension, oligo-anuric severe acute kidney injury (AKI), acute liver failure with lactataemia and type one respiratory failure.The possibility of Dengue-induced HLH was considered early with multiple criteria for diagnosis met including hyperferritinaemia, pancytopenia, lipaemia and a marked transaminitis. HLH-directed therapy was commenced with intravenous immunoglobulins (IVIG), intravenous methylprednisolone (IVMP) and Anakinra. Subsequent bone marrow biopsy analysis demonstrated clear evidence of HLH, in the context of a persistent and marked Dengue viraemia. We observed resolution of HLH markers as well as reducing requirements for multi-organ support after initiation of Anakinra therapy.During her recovery, the patient unexpectedly developed focal neurology; intracranial imaging demonstrated widespread, discreet parenchymal lesions thought to be haemorrhagic in nature, which were deemed too severe an insult to recover from. On day 19, the difficult decision of withdrawing care after deep discussion with the family was reached, soon after which the patient passed away. A post-mortem examination was not arranged.
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- 2020
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5. Numerical analysis of thermal enhanced oil recovery methods
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Youtsos, Michael Spiro
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620 ,Enhanced oil recovery ,Thermal oil recovery - Published
- 2014
6. Does machine perfusion improve immediate and short-term outcomes by enhancing graft function and recipient recovery after liver transplantation? - A systematic review of the literature, meta-analysis and expert panel recommendations
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Alejandro, Ramírez-Del Val, James, Guarrera, Robert J, Porte, Markus, Selzner, Michael, Spiro, Dimitri Aristotle, Raptis, Peter J, Friend, and David, Nasralla
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Perfusion ,Transplantation ,Liver ,Graft Survival ,Humans ,Organ Preservation ,Liver Transplantation - Abstract
BACKGROUND: Recent evidence supports the use of machine perfusion technologies (MP) for marginal liver grafts. Their effect on enhanced recovery, however, remains uncertain. OBJECTIVES: To identify areas in which MP might contribute to an ERAS program and to provide expert panel recommendations. DATA SOURCES: Ovid MEDLINE, Embase, Scopus, Google Scholar, and Cochrane Central. METHODS: Systematic review and meta-analysis following PRISMA guidelines and recommendations using the GRADE approach. CRD42021237713 RESULTS: Both hypothermic (HMP) and normothermic (NMP) machine perfusion demonstrated significant benefits in preventing post-reperfusion syndrome (PRS) (HMP OR 0.33, 0.15-0.75 CI; NMP OR 0.51, 0.29-0.90 CI) and early allograft dysfunction (EAD) (HMP OR 0.51, 0.35-0.75 CI; NMP OR 0.66, 0.45-0.97 CI), while shortening LOS (HMP MD -3.9; NMP MD -12.41). Only NMP showed a significant decrease in the length of ICU stay (L-ICU) (MD -7.07, -8.76; -5.38 CI), while only HMP diminishes the likelihood of major complications. Normothermic regional perfusion (NRP) reduces EAD (OR 0.52, 0.38-0.70 CI) and primary non-function (PNF) (OR 0.51, 0.27-0.98 CI) without effect on L-ICU and LOS. CONCLUSIONS: The use of HMP decreases PRS and EAD, specifically for marginal grafts. This is supported by a shorter LOS and a lower rate of major post-operative complications. (QOE; moderate | Recommendation; Strong). NMP reduces the incidence of PRS and EAD with associated shortening in L-ICU for both DBD and DCD grafts. (QOE; moderate | Recommendation; High) This technology also shortens the length of hospital stay (QOE; low | Recommendation; Strong) NRP decreases the likelihood of EAD (QOE; moderate) and the risk of PNF (QOE; low) when compared to both DBD and SRR-DCD grafts preserved in SCS. (Recommendation; Strong) This article is protected by copyright. All rights reserved.
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- 2022
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7. The role of T-tubes and abdominal drains on short-term outcomes in liver transplantation – A systematic review of the literature and expert panel recommendations
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Marit, Kalisvaart, Jeroen, de Jonge, Peter, Abt, Susan, Orloff, Paolo, Muiesan, Sander, Florman, Michael, Spiro, Dimitri Aristotle, Raptis, Bijan, Eghtesad, and Surgery
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Transplantation - Abstract
This systematic review and expert panel recommendation aims to answer the question regarding the routine use of T-tubes or abdominal drains to better manage complications and thereby improve outcomes after liver transplantation.Systematic review following PRISMA guidelines and recommendations using the GRADE approach derived from an international expert panel to assess the potential risks and benefits of T-tubes and intra-abdominal drainage in liver transplantation (CRD42021243036).Of the 2996 screened records, 33 studies were included in the systematic review, of which 29 (6 RCT) assessed the use of T-tubes and 4 regarding surgical drains. Although some studies reported less strictures when using a T-tube, there was a trend towards more biliary complications with T-tubes, mainly related to biliary leakage. Due to the small number of studies, there was a paucity of evidence on the effect of abdominal drains with no clear benefit for or against the use of drainage. However, one study investigating the open vs. closed circuit drains found a significantly higher incidence of intra-abdominal infections when open-circuit drains were used.Due to the potential risk of biliary leakage and infections, the routine intraoperative insertion of T-tubes is not recommended (Level of Evidence moderate - very low; grade of recommendation strong). However, a T-tube can be considered in cases at risk for biliary stenosis. Due to the scant evidence on abdominal drainage, no change in clinical practice in individual centers is recommended. (Level of Evidence very low; weak recommendation). This article is protected by copyright. All rights reserved.
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- 2022
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8. Protocol for a prospective double-blind, randomised, placebo-controlled feasibility trial of octreotide infusion during liver transplantation
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Norman R. Williams, Michael Spiro, Bina Shah, Gareth Ambler, Brian R. Davidson, Jeremy Fabes, and Daniel Martin
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Adult ,medicine.medical_specialty ,medicine.medical_treatment ,Octreotide ,Liver transplantation ,Placebo ,hepatobiliary disease ,law.invention ,Anaesthesia ,Double-Blind Method ,Randomized controlled trial ,law ,medicine ,Humans ,Multicenter Studies as Topic ,Prospective Studies ,adult anaesthesia ,Adverse effect ,adult intensive & critical care ,Randomized Controlled Trials as Topic ,SARS-CoV-2 ,business.industry ,Hepatobiliary disease ,COVID-19 ,General Medicine ,Perioperative ,hepatobiliary surgery ,Liver Transplantation ,Treatment Outcome ,Clinical trials unit ,transplant surgery ,hepatology ,Emergency medicine ,Quality of Life ,Feasibility Studies ,Medicine ,business ,medicine.drug - Abstract
IntroductionLiver transplantation is a complex operation that can provide significant improvements in quality of life and survival to the recipients. However, serious complications are common and include major haemorrhage, hypotension and renal failure. Blood transfusion and the development of acute kidney injury lead to both short-term and long-term poor patient outcomes, including an increased risk of death, graft failure, length of stay and reduced quality of life. Octreotide may reduce the incidence of renal dysfunction, perioperative haemorrhage and enhance intraoperative blood pressure. However, octreotide does have risks, including resistant bradycardia, hyperglycaemia and hypoglycaemia and QT prolongation. Hence, a randomised controlled trial of octreotide during liver transplantation is needed to determine the cost-efficacy and safety of its use; this study represents a feasibility study prior to this trial.Methods and analysisWe describe a multicentre, double-blind, randomised, placebo-controlled feasibility study of continuous infusion of octreotide during liver transplantation surgery. We will recruit 30 adult patients at two liver transplant centres. A blinded infusion during surgery will be administered in a 2:1 ratio of octreotide:placebo. The primary outcomes will determine the feasibility of this study design. These include the recruitment ratio, correct administration of blinded study intervention, adverse event rates, patient and clinician enrolment refusal and completion of data collection. Secondary outcome measures of efficacy and safety will help shape future trials by assessing potential primary outcome measures and monitoring safety end points. No formal statistical tests are planned. This manuscript represents study protocol number 1.3, dated 2 June 2021.Ethics and disseminationThis study has received Research Ethics Committee approval. The main study outcomes will be submitted to an open-access journal.Trial sponsorThe Joint Research Office, University College London, UK.Neither the sponsor nor the funder have any role in study design, collection, management, analysis and interpretation of data, writing of the study report or the decision to submit the report for publication.Trial registrationThe study is registered with ClinicalTrials.gov (NCT04941911) with recruitment due to start in August 2021 with anticipated completion in July 2022.Clinical trials unitSurgical and Interventional Group, Division of Surgery & Interventional Science, University College London.
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- 2021
9. Thromboelastography demonstrates progressive hypercoagulability in COVID-19 patients admitted to ICU with respiratory failure
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Kunal Joshi, Michael Spiro, Clare Melikian, and Jeremy Fabes
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medicine.medical_specialty ,2019-20 coronavirus outbreak ,medicine.diagnostic_test ,Coronavirus disease 2019 (COVID-19) ,business.industry ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Disease ,Critical Care and Intensive Care Medicine ,Critical Care Nursing ,Fibrinogen ,Thromboelastography ,Respiratory failure ,Internal medicine ,medicine ,business ,Brief Communications ,medicine.drug - Abstract
Thromboembolic complications are associated with COVID-19 owing to the hypercoagulable nature of the disease. Although patients with COVID-19 often have higher levels of fibrinogen and D-dimers, hypercoagulability has been attributed to various other factors too. In this prospective observational study conducted between April 2020 and June 2020, we compared coagulation parameters using thromboelastography in COVID-19 patients to non-COVID-19 patients admitted to ICU with respiratory failure. This study demonstrated a significant difference between the cohorts in functional fibrinogen (CFF) progressively from third day of ICU admission whilst there was no difference in the Clauss fibrinogen levels. COVID-19 patients also demonstarted supranormal R time indicating hypocoagulability. These mixed coagulation changes suggest targeting fibrinogen or platelets may prevent thromboembolic complications in COVID-19.
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- 2021
10. Fatal primary dengue-induced Haemophagocytic Lymphohistiocytosis (HLH) in a returning traveller from India treated with anakinra for the first time
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Charlotte Richardson, Antonia Scobie, Animesh Singh, Michael Spiro, Tanmay Kanitkar, Amy Ireson, Jim Buckley, and Michael Jacobs
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Pediatrics ,medicine.medical_specialty ,Anakinra ,business.industry ,Returning traveller ,Acute kidney injury ,Context (language use) ,General Medicine ,Dengue virus ,medicine.disease_cause ,medicine.disease ,Pancytopenia ,Dengue fever ,lcsh:Infectious and parasitic diseases ,Dengue ,Haemophagocytic lymphohistiocytosis ,Intensive care ,Medicine ,Chills ,lcsh:RC109-216 ,medicine.symptom ,business ,medicine.drug ,Severe dengue - Abstract
Background Dengue fever is an arthropod-borne flavivirus infection that is highly prevalent in the tropics. A proportion of clinical cases develop severe dengue, defined by life-threatening complications including haemorrhage, capillary leak and multi-organ failure. Recently there has been increasing recognition that some cases of severe dengue may be a consequence of HLH. To our knowledge, this is the first report of treatment with Anakinra for dengue-induced HLH. Case report We report a case of Dengue fever triggering HLH in an eighteen-year-old female returning traveller from India, diagnosed with systemic lupus erythematosus (SLE) two months prior to presentation. The patient initially presented to a district general hospital emergency department (ED) with a three-day history of flu-like symptoms, fever, erythematous rash, widespread joint pain, nausea and chills. Acute Dengue virus infection was confirmed with serum polymerase chain reaction (PCR) testing. On day two, she was admitted to intensive care for multi-organ support necessitated by refractory hypotension, oligo-anuric severe acute kidney injury (AKI), acute liver failure with lactataemia and type one respiratory failure. The possibility of Dengue-induced HLH was considered early with multiple criteria for diagnosis met including hyperferritinaemia, pancytopenia, lipaemia and a marked transaminitis. HLH-directed therapy was commenced with intravenous immunoglobulins (IVIG), intravenous methylprednisolone (IVMP) and Anakinra. Subsequent bone marrow biopsy analysis demonstrated clear evidence of HLH, in the context of a persistent and marked Dengue viraemia. We observed resolution of HLH markers as well as reducing requirements for multi-organ support after initiation of Anakinra therapy. During her recovery, the patient unexpectedly developed focal neurology; intracranial imaging demonstrated widespread, discreet parenchymal lesions thought to be haemorrhagic in nature, which were deemed too severe an insult to recover from. On day 19, the difficult decision of withdrawing care after deep discussion with the family was reached, soon after which the patient passed away. A post-mortem examination was not arranged.
- Published
- 2020
11. COVID-19 and Pneumothorax: A Multicentre Retrospective Case Series
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Simon E. Brill, Avinash Aujayeb, James Melhorn, Judith Babar, Nicholas Lane, James Murray, Anthony W. Martinelli, Ian Smith, Alexander J.K. Wilkinson, Razeen Mahroof, Kevin Conroy, Aldrin Adeni, AJ Shah, Lewis Standing, Stefan J. Marciniak, Matthew Matson, Sarah Trenfield, Karl Jackson, Nairi Tchrakian, Iftikhar Nadeem, Stephane Ledot, Sujal R. Desai, Oliver Collas, Anthony J. Rostron, William Ricketts, Stephanie Uys, Anant Patel, Nick Woznitza, Joseph Newman, Margaret M. Huang, Beenish Iqbal, Kai Lee, Revati Naran, Helen E. Davies, S.S. Hare, Tejas Ingle, Maria Kokosi, Michael Spiro, Sarah Bigham, Martinelli, Anthony W [0000-0002-7285-7498], Jackson, Karl [0000-0002-6464-7474], Lane, Nicholas D [0000-0002-9954-6366], Rostron, Anthony J [0000-0002-9336-1723], Woznitza, Nick [0000-0001-9598-189X], Ledot, Stephane [0000-0001-9261-3186], Ricketts, William [0000-0002-0475-0744], Aujayeb, Avinash [0000-0002-0859-5550], Marciniak, Stefan J [0000-0001-8472-7183], and Apollo - University of Cambridge Repository
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Pulmonary and Respiratory Medicine ,Adult ,Male ,medicine.medical_specialty ,medicine.medical_treatment ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Extracorporeal Membrane Oxygenation ,Sex Factors ,Extracorporeal membrane oxygenation ,Medicine ,Humans ,030212 general & internal medicine ,Pneumomediastinum ,Survival rate ,Mediastinal Emphysema ,Aged ,Retrospective Studies ,Aged, 80 and over ,business.industry ,SARS-CoV-2 ,Incidence (epidemiology) ,Medical record ,Incidence ,Age Factors ,COVID-19 ,Pneumothorax ,Retrospective cohort study ,Middle Aged ,medicine.disease ,Prognosis ,Respiration, Artificial ,United Kingdom ,Surgery ,Hospitalization ,Survival Rate ,030228 respiratory system ,Female ,Original Article ,business ,Complication - Abstract
Introduction Pneumothorax and pneumomediastinum have both been noted to complicate cases of COVID-19 requiring hospital admission. We report the largest case series yet described of patients with both these pathologies that includes non-ventilated patients. Methods Cases were collected retrospectively from UK hospitals with inclusion criteria limited to a diagnosis of COVID-19 and the presence of either pneumothorax or pneumomediastinum. Patients included in the study presented between March and June 2020. Details obtained from the medical record included demographics, radiology, laboratory investigations, clinical management and survival. Results Seventy-one patients from 16 centres were included in the study, of whom 60 patients had pneumothoraces (six also with pneumomediastinum), whilst 11 patients had pneumomediastinum alone. Two of these patients had two distinct episodes of pneumothorax, occurring bilaterally in sequential fashion, bringing the total number of pneumothoraces included to 62. Clinical scenarios included patients who had presented to hospital with pneumothorax, patients who had developed pneumothorax or pneumomediastinum during their inpatient admission with COVID-19 and patients who developed their complication whilst intubated and ventilated, either with or without concurrent extracorporeal membrane oxygenation. Survival at 28 days was not significantly different following pneumothorax (63.1%±6.5%) or isolated pneumomediastinum (53.0%±18.7%; p=0.854). The incidence of pneumothorax was higher in males. The 28-day survival was not different between the sexes (males 62.5%±7.7% versus females 68.4%±10.7%; p=0.619). Patients above the age of 70 had a significantly lower 28-day survival than younger individuals (≥70 years 41.7%±13.5% survival versus, Roughly 1% of patients admitted with COVID-19 develop pneumothorax. This can occur without pre-existing lung disease or mechanical ventilation. Two thirds of patients survive, but age >70 years and acidosis are associated with poor prognosis.
- Published
- 2020
12. Implementation of a Virtual Interprofessional ICU Learning Collaborative: Successes, Challenges, and Initial Reactions From the Structured Team-Based Optimal Patient-Centered Care for Virus COVID-19 Collaborators
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Simon Zec, MD, Nika Zorko Garbajs, MD, Yue Dong, MD, Ognjen Gajic, MD, Christina Kordik, MA, Lori Harmon, RRT, MBA, CPHQ, Marija Bogojevic, MD, Romil Singh, MD, Yuqiang Sun, MD, Vikas Bansal, MD, Linh Vu, MD, Kelly Cawcutt, MD, John M. Litell, DO, Sarah Redmond, PhD, Eleanor Fitzpatrick, RN, Kirstin J. Kooda, PharmD, Michelle Biehl, MD, Neha S. Dangayach, MD, Viren Kaul, MD, June M. Chae, MD, Aaron Leppin, MD, Mathew Siuba, MD, Rahul Kashyap, MBBS, Allan J. Walkey, MD, Alexander S. Niven, MD, on behalf of the Structured Team-based Optimal Patient-Centered Care for Virus COVID-19 (STOP-VIRUS) Collaborative, Anthony Martinez, MD, Dean Meadows, MD, Helen Stinnett, BA, RRT, Michael Allison, MD, Olubukola Adeyemi, PharmD, Terry Herbert, BSN, RN, Gerald L. Weinhouse, MD, Namrata Patil, MD, MPH, Gaspar Hacobian, PharmD, BCPS, Kamen Rangelov, MD, Jillian Parker, RRT, Michael P. Smith, PharmD, BCCCP, Rachel Smith, RN, MSN, MBA, CCRN, Eliza Deery, MD, Andrea Harper, MS, Emily Davis, RN, CCRN, Grace M. Arteaga, MD, FAAP, FCCM, Jennifer L. Fleegel, RN, CCRN, Julie M. Duncan, RN, Kevin K. Graner, RPh, Tammy J. Schultz, RRT, LRT, Abhishek Giri, MBBS, Ashley Gill, RRT, Catherine L. Mielke, MS, APRN, CNS, Devang Sanghavi, MD, MHA, Jonathan K. Clark, RRT, Julie Shimp, RN, Lisa Marshall, MSN, RN, Michael Spiros, MSN, RN, Nirmaljot Kaur, MD, Sean P. Kiley, MD, Siva Naga Yarrarapu, MBBS, Teresa Keister, RN, Gage Stroope, LRT, CRT, Jackie Stark, PharmD, BCPS, Jessica Poehler, RN, Juan Pablo, Domecq Garces, MD, Nitesh Kumar Jain, MD, MBBS, Syed Anjum Khan, MD, Thoyaja Koritala, MD, Abigail La Nou, MD, FACEP, Christina Hall, MS, RN, Cindy Christensen, MSN, RN, FNP-BC, Kirsten Holbrook, RRT, Sara Toufar, PharmD, RPh, Sarah Normand, PharmD, RPh, Amy Spitzner, RN, CCRN, Carissa Quinn, APRN, CNS, DNP, Christina Xia, PharmD, BCCCP, Holly D. Behrns, LRT, RRT, Erin Barreto, PharmD, RPh, Jennifer Elmer, APRN, CNS, DNP, Sarah Chalmers, MD, PCCM, Macy Cooper, RN, Aaron Harthan, PharmD, BCPPS, Edmundo A. Martinez, MD, Jennifer A. Bandy, RN, BSN, John Sanford, RRT-ACCS, RRT-NPS, Jackie A. Guiliani, BSRT, RRT-NPS, Megan Kupferschmid, MSN, RN, P-CCRN, Anand Pariyadath, MD, Brandy Vitielliss, BSN, RN, Daniel Temas, MD, Smith F. Heavner, MS, RN, PCCN, Amanda Frary, MSN, RN, Murtaza Akhter, MD, Rania Rahman, MD, Mary Mulrow, RN, MN, CCRP, Tracy Cooper, RN, John M. Litell, DO, FACEP, June Mee Chae, MD, Kelly Cawcutt, MD, MS, FACP, FIDSA, Kirstin J. Kooda, PharmD, RPh, Neha S. Dangayach, MD, MSCR, Matthew Siuba, DO, Aaron B. Holley, MD, Alexander A. Kon, MD, MS, Amita Avadhani, PhD, DNP, CNE, DCC, ACNP-BC, NP-C, CCRN, FAANP, FCCM, Amy L. Dzierba, PharmD, FCCP, BCCCP, FCCM, Andre C. Kalil, MD, MPH, FACP, Ashley D. DePriest, MS, RDN, CNSC, Bradley Peters, PharmD, RPh, BCSP, BCCCP, Brenda T. Pun, DNP, RN, FCCM, Courtney E. Bennett, DO, Eric Kriner, BS, RRT, Erin S. DeMartino, MD, Erin Strong, BSN, RN, CCRN, Giora Netzer, MD, Greg S. Martin, MD, MSc, FCCM, Jerry J. Zimmerman, MD, PhD, FCCM, Julia Taylor, MD, MA, HEC-C, Karen A. Korzick, MD, MA, FCCP, FACP, FCCM, Katherine Fischkoff, MD, MPA, FACS, Lewis J. Kaplan, MD, FACS, FCCM, Marlies Ostermann, MD, PhD, Mary Susan Gaeta, MD, FACP, Mary Faith Marshall, HEC-C, PhD, Nahreen Ahmed, MD, MPH, Paul Alan Nyquist, MD, MPH, Pooja A. Nawathe, MD, FAAP, CHSE-A, CHSOS, FCCM, Preeti R. John, MD, MPH, FACS, CPE, HEC-C, and Uzma Syed, DO, FIDSA
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Medical emergencies. Critical care. Intensive care. First aid ,RC86-88.9 - Abstract
IMPORTANCE:. Initial Society of Critical Care Medicine Discovery Viral Infection and Respiratory illness Universal Study (VIRUS) Registry analysis suggested that improvements in critical care processes offered the greatest modifiable opportunity to improve critically ill COVID-19 patient outcomes. OBJECTIVES:. The Structured Team-based Optimal Patient-Centered Care for Virus COVID-19 ICU Collaborative was created to identify and speed implementation of best evidence based COVID-19 practices. DESIGN, SETTING, AND PARTICIPANTS:. This 6-month project included volunteer interprofessional teams from VIRUS Registry sites, who received online training on the Checklist for Early Recognition and Treatment of Acute Illness and iNjury approach, a structured and systematic method for delivering evidence based critical care. Collaborators participated in weekly 1-hour videoconference sessions on high impact topics, monthly quality improvement (QI) coaching sessions, and received extensive additional resources for asynchronous learning. MAIN OUTCOMES AND MEASURES:. Outcomes included learner engagement, satisfaction, and number of QI projects initiated by participating teams. RESULTS:. Eleven of 13 initial sites participated in the Collaborative from March 2, 2021, to September 29, 2021. A total of 67 learners participated in the Collaborative, including 23 nurses, 22 physicians, 10 pharmacists, nine respiratory therapists, and three nonclinicians. Site attendance among the 11 sites in the 25 videoconference sessions ranged between 82% and 100%, with three sites providing at least one team member for 100% of sessions. The majority reported that topics matched their scope of practice (69%) and would highly recommend the program to colleagues (77%). A total of nine QI projects were initiated across three clinical domains and focused on improving adherence to established critical care practice bundles, reducing nosocomial complications, and strengthening patient- and family-centered care in the ICU. Major factors impacting successful Collaborative engagement included an engaged interprofessional team; an established culture of engagement; opportunities to benchmark performance and accelerate institutional innovation, networking, and acclaim; and ready access to data that could be leveraged for QI purposes. CONCLUSIONS AND RELEVANCE:. Use of a virtual platform to establish a learning collaborative to accelerate the identification, dissemination, and implementation of critical care best practices for COVID-19 is feasible. Our experience offers important lessons for future collaborative efforts focused on improving ICU processes of care.
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- 2023
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13. Conga Drummer's Guidebook
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Michael Spiro
- Published
- 1970
14. Language of the Masters: Etudes and Transcription of 10 Master Latin Percussionists
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Michael Spiro
- Published
- 1970
15. Electrochemistry, Past and Present
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JOHN T. STOCK, MARY VIRGINIA ORNA, John T. Stock, Melvyn C. Usselman, Frank A. J. L. James, Stella V. F. Butler, Keith J. Laidler, R. Heyrovska, Michael Spiro, Mary D. Archer, Alfred W. von Smolinski, Carl E. Moore, Bruno Jaselskis, Roger G. Bates, B. E. Conway, W. A. E. McBryde, Manuel M. Baizer, J
16. Neutrino physics and astrophysics
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Daniel Vignaud, Michael Spiro, Lantz, Simone, Physique Corpusculaire et Cosmologie - Collège de France (PCC), and Collège de France (CdF (institution))-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)
- Subjects
Nuclear and High Energy Physics ,Particle physics ,[PHYS.HEXP] Physics [physics]/High Energy Physics - Experiment [hep-ex] ,Physics::Instrumentation and Detectors ,Astrophysics::High Energy Astrophysical Phenomena ,Solar neutrino ,General Physics and Astronomy ,Astrophysics ,01 natural sciences ,7. Clean energy ,Nuclear physics ,0103 physical sciences ,[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex] ,Astrophysics::Solar and Stellar Astrophysics ,Neutrino oscillation ,010306 general physics ,010303 astronomy & astrophysics ,Physics ,010308 nuclear & particles physics ,High Energy Physics::Phenomenology ,General Chemistry ,Solar neutrino problem ,Cosmic neutrino background ,Neutrino detector ,13. Climate action ,Measurements of neutrino speed ,High Energy Physics::Experiment ,Neutrino astronomy ,Neutrino - Abstract
Les neutrinos jouent un role cle, a la fois en physique des particules et en astrophysique. Les sources de neutrinos sont multiples dans l'Univers et ceux-ci sont produits en abondance. Sur Terre, les principales sources sont les accelerateurs ou les reacteurs nucleaires. Cette revue se focalise sur la recherche actuelle de la masse des neutrinos, principalement via la recherche du phenomene appele « oscillations des neutrinos », dans l'etude des neutrinos solaires, des neutrinos « atmospheriques » et des neutrinos issus des accelerateurs ou des reacteurs.
- Published
- 1999
17. Mechanism of ‘in situ’ gold crystallisation
- Author
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Michael Spiro
- Subjects
In situ ,Materials science ,Metallurgy ,humanities ,law.invention ,Inorganic Chemistry ,Electroless plating ,Materials Science(all) ,law ,Gold particles ,Metallic materials ,General Materials Science ,Crystallization ,Deposition (law) - Abstract
Electroless plating is suggested as a mechanism for the deposition of the small gold particles found on the surface of the Parker Gold Piece.
- Full Text
- View/download PDF
18. Electrochemistry, Past and Present
- Author
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JOHN T. STOCK, MARY VIRGINIA ORNA, Melvyn C. Usselman, Frank A. J. L. James, Stella V. F. Butler, Keith J. Laidler, R. Heyrovska, Michael Spiro, Mary D. Archer, Alfred W. von Smolinski, Carl E. Moore, Bruno Jaselskis, Roger G. Bates, B. E. Conway, W. A. E. McBryde, Manuel M. Baizer, James M. Bobbitt, M. J. Allen, H. Gunasingham, Alfred von Smolinski, K. L. Cheng, J. D. R. Thomas, Brenda R. Shaw, Petr Zuman, Michael Heyrovský, Ladislav Novotný, Ivan Smoler, Janet Osteryoung, Carolyn Wechter, L. B. Rogers, Galen W. Ewing, H. A. Laitinen, Truman S. Light, William R. Heineman, William B. Jensen, Lisa Mae Robinson, James J. Leddy, P. R. Roberge, Robert V. V. Nicholls, Silvia Tejada, Sankar Das Gupta, Bernard Fleet, J. A. McGeough, M. B. Barker, JOHN T. STOCK, MARY VIRGINIA ORNA, Melvyn C. Usselman, Frank A. J. L. James, Stella V. F. Butler, Keith J. Laidler, R. Heyrovska, Michael Spiro, Mary D. Archer, Alfred W. von Smolinski, Carl E. Moore, Bruno Jaselskis, Roger G. Bates, B. E. Conway, W. A. E. McBryde, Manuel M. Baizer, James M. Bobbitt, M. J. Allen, H. Gunasingham, Alfred von Smolinski, K. L. Cheng, J. D. R. Thomas, Brenda R. Shaw, Petr Zuman, Michael Heyrovský, Ladislav Novotný, Ivan Smoler, Janet Osteryoung, Carolyn Wechter, L. B. Rogers, Galen W. Ewing, H. A. Laitinen, Truman S. Light, William R. Heineman, William B. Jensen, Lisa Mae Robinson, James J. Leddy, P. R. Roberge, Robert V. V. Nicholls, Silvia Tejada, Sankar Das Gupta, Bernard Fleet, J. A. McGeough, and M. B. Barker
- Subjects
- Electrochemistry--Congresses, Electrochemistry--History--Congresses
- Published
- 1989
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