11 research outputs found
Interns are from Venus, consultants are from Mars: differential perception among clinicians
- Publication venue
- Australasian Medical Publishing Company
- Publication date
- 01/12/2003
- Field of study
OBJECTIVE: To test for the presence of sex-based differences in perception (the notion that men and women "think" differently, and that differences in perception are biologically based) among healthcare professionals. DESIGN: Prospective survey. SETTING AND PARTICIPANTS: 90 medical personnel at a tertiary care hospital in Newcastle, NSW. INTERVENTION: Healthcare professionals were shown two pictures that could be interpreted as depicting either a young or an old person, and a word that could be seen as geometric shapes. MAIN OUTCOME MEASURES: The effects of sex, age, seniority, and specialisation in relation to the first impression of the image, the ability to change one\u27s perception, and the speed of perception. RESULTS: Contrary to popular opinion, male physicians were more likely to perceive the older figures, and just as likely as women to be able to change their perception. Surgeons and junior staff were more likely to see, as well as being faster to form, an impression requiring abstract thought, and were more able to change their perceptions. CONCLUSIONS: Traditional sex stereotypes do not apply to medical personnel, but other age-based stereotypes, and professional rivalries (medical versus surgical) may have some empiric basis
Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries.
- Author
- Ab Majid MA
- Ab Rahman AS
- Ab Rahman R
- Abayasinghe C
- Abbott T
- Abdullah NH
- Abdur-Rahman L
- Abeloos J
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- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2016
- Field of study
BACKGROUND: As global initiatives increase patient access to surgical treatments, there remains a need to understand the adverse effects of surgery and define appropriate levels of perioperative care. METHODS: We designed a prospective international 7-day cohort study of outcomes following elective adult inpatient surgery in 27 countries. The primary outcome was in-hospital complications. Secondary outcomes were death following a complication (failure to rescue) and death in hospital. Process measures were admission to critical care immediately after surgery or to treat a complication and duration of hospital stay. A single definition of critical care was used for all countries. RESULTS: A total of 474 hospitals in 19 high-, 7 middle- and 1 low-income country were included in the primary analysis. Data included 44 814 patients with a median hospital stay of 4 (range 2-7) days. A total of 7508 patients (16.8%) developed one or more postoperative complication and 207 died (0.5%). The overall mortality among patients who developed complications was 2.8%. Mortality following complications ranged from 2.4% for pulmonary embolism to 43.9% for cardiac arrest. A total of 4360 (9.7%) patients were admitted to a critical care unit as routine immediately after surgery, of whom 2198 (50.4%) developed a complication, with 105 (2.4%) deaths. A total of 1233 patients (16.4%) were admitted to a critical care unit to treat complications, with 119 (9.7%) deaths. Despite lower baseline risk, outcomes were similar in low- and middle-income compared with high-income countries. CONCLUSIONS: Poor patient outcomes are common after inpatient surgery. Global initiatives to increase access to surgical treatments should also address the need for safe perioperative care. STUDY REGISTRATION: ISRCTN5181700
Impact of Organic Food Agritourism on a Small Rural Economy: A Social Accounting Matrix Approach
- Author
- Benjamin Stevens
- C R Weeden
- Carolyn Dimitri
- D B Weaver
- D Ralston
- Datamonitor
- David I Kass
- David W Roland-Holst
- Doug Henwood
- Earl L Grinols
- Erik Thorbecke
- G Shaw
- Gillis
- Graham Pyatt
- Harvey Armstrong
- Implan Minnesota
- Implan Minnesota
- J F Parr
- John L Crompton
- Karen Klonsky
- Lawrence F Katz
- Lazarus
- M Hitchcock
- Mary Ahearn
- Michael J Webber
- Michael Porter
- N G Mcgehee
- Nancy G Creamer
- Norma Nickerson
- Paul Krugman
- Paul R Eberts
- Peter K Eisinger
- Philippe Aghion
- Ramu Govidnasamy
- Robert G Lynch
- Ronald E Miller
- Rudi Kortbech-Olesen
- Sean Swezey
- Steven G Koven
- Susan E Clarke
- Tad Hara
- Thomas Piketty
- Timothy J Tyrrell
- Toshihiko Kawagoe
- W Eadington
- William Knudson
- World Bank
- Yuri Mansury
- Zhenhua Liu
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2006
- Field of study
Covalent Docking Predicts Substrates for Haloalkanoate Dehalogenase Superfamily Phosphatases
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- Akiva E.
- Allen K. N.
- Altschul S. F.
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- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
peer reviewedBACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets. © 2017 Massachusetts Medical Society
Evolocumab and clinical outcomes in patients with cardiovascular disease
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- Zieba B
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- Zilahi Z
- Zrazhevskiy K
- Östergren J
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND Evolocumab is a monoclonal antibody that inhibits proprotein convertase subtilisin-kexin type 9 (PCSK9) and lowers low-density lipoprotein (LDL) cholesterol levels by approximately 60%. Whether it prevents cardiovascular events is uncertain. METHODS We conducted a randomized, double-blind, placebo-controlled trial involving 27,564 patients with atherosclerotic cardiovascular disease and LDL cholesterol levels of 70 mg per deciliter (1.8 mmol per liter) or higher who were receiving statin therapy. Patients were randomly assigned to receive evolocumab (either 140 mg every 2 weeks or 420 mg monthly) or matching placebo as subcutaneous injections. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization. The key secondary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. The median duration of follow-up was 2.2 years. RESULTS At 48 weeks, the least-squares mean percentage reduction in LDL cholesterol levels with evolocumab, as compared with placebo, was 59%, from a median baseline value of 92 mg per deciliter (2.4 mmol per liter) to 30 mg per deciliter (0.78 mmol per liter) (P<0.001). Relative to placebo, evolocumab treatment significantly reduced the risk of the primary end point (1344 patients [9.8%] vs. 1563 patients [11.3%]; hazard ratio, 0.85; 95% confidence interval [CI], 0.79 to 0.92; P<0.001) and the key secondary end point (816 [5.9%] vs. 1013 [7.4%]; hazard ratio, 0.80; 95% CI, 0.73 to 0.88; P<0.001). The results were consistent across key subgroups, including the subgroup of patients in the lowest quartile for baseline LDL cholesterol levels (median, 74 mg per deciliter [1.9 mmol per liter]). There was no significant difference between the study groups with regard to adverse events (including new-onset diabetes and neurocognitive events), with the exception of injection-site reactions, which were more common with evolocumab (2.1% vs. 1.6%). CONCLUSIONS In our trial, inhibition of PCSK9 with evolocumab on a background of statin therapy lowered LDL cholesterol levels to a median of 30 mg per deciliter (0.78 mmol per liter) and reduced the risk of cardiovascular events. These findings show that patients with atherosclerotic cardiovascular disease benefit from lowering of LDL cholesterol levels below current targets
Hunters and gatherers past and present: Perspectives on diversity, teaching, and information transmission
- Author
- Anderson David G.
- Arnold Jeanne A.
- Barnard Alan
- Barnard Alan
- Bicchieri Marco G.
- Biesele Megan
- Biesele Megan
- Biette Lucas M.
- Binford Lewis R.
- Binford Lewis R.
- Blurton-Jones Nicholas
- Boas Franz
- Boyette Adam H.
- Burch Ernest S.
- Chapin Mac
- Child Brenda J.
- Clottes Jean
- Codding Brian F.
- Crittenden Alyssa N.
- Cummings Vicki
- Dahlberg Frances
- Damas David
- Davis L. B.
- Draper Patricia
- Du Plessis Pierre
- Finlayson Bill
- Finlayson Bill
- Friederich Reinhard
- Glassow Michael
- Grier Colin
- Guenther Mathias G.
- Hewlett Barry S.
- Hewlett Barry S.
- Hewlett Bonnie L.
- Hodder I.
- Huffman Terry
- Ikeya Kazunobu
- Ikeya Kazunobu
- Ingold Tim
- Ingold Tim
- Jochim Michael A.
- Johnson Amber
- Kehoe Alice
- Konner Melvin
- Konner Melvin
- Kramer Karen L.
- Krebs J. R.
- Lavi Noa
- Leacock Eleanor
- Lee Richard B.
- Lee Richard B.
- Lee Richard B.
- Lee Richard B.
- Lee Richard B.
- Liebenberg Louis
- Lombard Marlize
- Marshall Lorna
- Minter Tessa
- Mitchell Peter
- Morris Job
- Oetelaar Gerald A.
- Oswalt Wendell H.
- Panter-Brick C.
- Persoon Gerard
- Peterson Nicolas J.
- Pianka Eric R.
- Politis Gustavo
- Price T.
- Puckett R. Fleming
- Radcliffe-Brown A. R.
- Renfrew Colin
- Robert K. Hitchcock
- Sahlins Marshall D.
- Schrire Carmel
- Schweitzer Peter S.
- Sellet Frederic
- Service Elman
- Silberbauer George B.
- Smith Eric Alden
- Sonoda Koji
- Steward Julian H.
- Steward Julian H.
- Takada Akira
- Takada Akira
- Takada Akira
- Tanaka Jiro
- Tanaka Jiro
- Temple Daniel H.
- Tushingham Shannon
- Vaarzon-Morel Petronella
- Whitridge Peter
- Widlok Thomas
- Winterhalder Bruce
- Woodburn James
- Woodburn James
- Yellen John E.
- Publication venue
- 'Informa UK Limited'
- Publication date
- Field of study
Kuluttajabarometri maakunnittain 2000, 2. neljännes
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- McGregor E
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- Metodiev Y
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- Papapanagiotou I
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- Papavasilopoulou T
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- Pnevmatikos I
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- Pozidou I
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- Sfakianakis K
- Sfyras D
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- Sibilio A
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- Suen A
- Sukawi I
- Sulaiman HA
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- Tsimpoukas F
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- Turner A
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- Ugwu I
- Ullah S
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- Ungureanu LL
- Urias E
- Ursache E
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- Utkin I
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- Wan X
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- Wendling PR
- Wessels JD
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- whitehouse A
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- Winterton D
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- Xouplidis K
- Xu G-J
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- Yagnik A
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- Yao S
- Yao Y
- Yap HL
- Yarwood J
- Yassaee A
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- Ye H
- Yegnaram S
- Yeh E
- Yin N
- Yip CP
- Yong J
- Yu HC
- Yu S
- Yu T
- Yu Y
- Yuan D
- Yuan F
- Yuan J
- Yuan J
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- Yuliana A
- Zaimi D
- Zakynthinos S
- Zamudio D
- Zangrillo A
- Zapata DDM
- Zbitnew G
- Zeidan L
- Zeng Q
- Zerman L
- Zettergren J
- Zhang B
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- Zhang H
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- Zhang J
- Zhang K
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- Zhang R
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- Zhang X
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- Zhao B
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- Zhao J
- Zhao J
- Zhao L
- Zhao L
- Zhao S
- Zhao T
- Zhao W
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- Zhong Y
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- Zhou J
- Zhou X-J
- Zhu X
- Zhu X
- Zhu Y
- Zhu Z
- Zhuang X
- Zilis G
- Zin NHM
- Zingerle N
- Zingg U
- Zoerner F
- Zonneveldt H
- Zou X
- Zoulamoglou M
- Zsisku L
- Publication venue
- Tilastokeskus
- Publication date
- 11/07/2000
- Field of study
Suomen virallinen tilasto (SVT