11 research outputs found
Involvement of focal adhesion kinase in cellular invasion of head and neck squamous cell carcinomas via regulation of MMP-2 expression
- Author
- A Forastiere
- A Hamadi
- A Katayama
- A Serrels
- AK Sood
- B Hu
- C Recher
- C Suarez
- C Yan
- CE Turner
- CH Chung
- CR Hauck
- D Ilic
- DA Hsia
- DD Schlaepfer
- DD Schlaepfer
- DJ Sieg
- E Allonca
- EI Deryugina
- EK Han
- GW McLean
- J Folkman
- JA Aguirre Ghiso
- JH Gonzalez-Botas
- JT Parsons
- LH Xu
- LH Xu
- LH Xu
- LL Vindelov
- M C Frame
- M Canel
- M Canel
- M Garzón-Arango
- M Nagata
- M Segarra
- M Xie
- M-D Chiara
- MD Schaller
- MD Schaller
- MJ van Nimwegen
- MJ van Nimwegen
- NN Mon
- NN Mon
- P Roepman
- P Secades
- PJ Ruest
- R Del Toro
- R Sankaranarayanan
- RJ Craven
- RL Klemke
- SK Mitra
- SK Mitra
- SK Mitra
- SL Bellis
- T Miyazaki
- TP Hecker
- TP Hecker
- TT Sein
- V Brunton
- V Gabarra-Niecko
- V Golubovskaya
- V Petit
- VG Brunton
- WG Cance
- Y Sonoda
- Y Sonoda
- Y Zhang
- ZZ Zeng
- Publication venue
- Nature Publishing Group
- Publication date
- 01/01/2008
- Field of study
Focal adhesion kinase (FAK) is considered intimately involved in cancer progression. Our previous research has demonstrated that overexpression of FAK is an early and frequent event in squamous cell carcinomas of the supraglottic larynx, and it is associated with the presence of metastases in cervical lymph nodes. The purpose of this study was to examine the functional role of FAK in the progression of head and neck squamous cell carcinomas (HNSCC). To this end, expression of FAK-related nonkinase (FRNK) or small interfering RNA (siRNA) against FAK was used to disrupt the FAK-induced signal transduction pathways in the HNSCC-derived SCC40 and SCC38 cell lines. Similar phenotypic effects were observed with the two methodological approaches in both cell lines. Decreased cell attachment, motility and invasion were induced by FRNK and FAK siRNA, whereas cell proliferation was not impaired. In addition, increased cell invasion was observed upon FAK overexpression in SCC cells. FRNK expression resulted in a downregulation of MMP-2 and MMP-9 expression. Interestingly, MMP-2 overexpression in FRNK-expressing cells rescued FRNK inhibition of cell invasion. This is the first demonstration of a direct rescue of impaired cell invasion by the re-expression of MMP-2 in a tumour cell type with decreased expression of functional FAK. Collectively, these data reported here support the conclusion that FAK enhances invasion of HNSCC by promoting both increased cell motility and MMP-2 production, thus providing new insights into possible therapeutic intervention strategies
Effects of alirocumab on types of myocardial infarction: insights from the ODYSSEY OUTCOMES trial
- Author
- Abbas J
- Abbate A
- Abdullakutty J
- Abhyanakar AD
- Aboyans V
- Abrantes JAM
- Abu-Fadel M
- Acevedo M
- Adamkova V
- Adhyapak S
- Agarwal H
- Aggarwal R
- Aggarwal RK
- Aguirre A
- Ahmed H
- Ahremark U
- Ahuad Guerrero RA
- Aidar Ayoub JC
- Airaksinen JK
- Aitken D
- Akatova E
- Akhter F
- Ako J
- Akright L
- Akyea-Djamson A
- Al Joundi T
- Al-Windy NYY
- Alan D
- Alcocer Gamba MA
- Alexander JH
- Alexander K
- Alexandru TM
- Alings M
- Alonso Martin JJ
- Alvarisqueta AF
- Alves De Lima AE
- Amarasekera S
- Amarasena N
- Amir O
- Amlani M
- Amosova E
- Amuchastegui M
- Andersen K
- Andersen R
- Anderson J
- Ando K
- Angel Hominal M
- Annam S
- Anscombe R
- Apostolovic SR
- Appel K-F
- Arandjelovic A
- Araneda G
- Arango Benecke JL
- Arbel Y
- Arif I
- Armaganijan L
- Arroyo JAC
- Arstall MA
- Asanin MR
- Atar S
- Athyros V
- Auguadro C
- Ayala CAC
- Aylward PE
- Azizad MM
- Bagai A
- Bagriy A
- Bahit MC
- Bai F
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- Baldari D
- Balinovac J
- Ball E
- Bang LE
- Banuru S
- Barakovic F
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- Barone-Rochette G
- Barr C
- Barrucco R
- Bartels GL
- Bashir R
- Basson MMDV
- Bastos JM
- Bata I
- Batushkin V
- Bayat J
- Bayram Llamas EA
- Bayron C
- Beauloye C
- Bednarski J
- Behrens S
- Belhassane A
- Benedicto A
- Bengus CM
- Benov HO
- Berger R
- Berglund S
- Berk M
- Berland J
- Berli MA
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- Bhagwat A
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- Bhatt DL
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- Birchem J
- Bittner VA
- Blicharski T
- Blok T
- Blumberg EDS
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- Bodanese LC
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- Boecker D
- Bojovski S
- Bokarev I
- Bokern MJJA
- Bonfanti AJC
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- Groenemeijer BE
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- II TC
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- Ilic S
- Ilieva-Pandeva KA
- Ince C
- Iniguez A
- Investigators ODYSSEYOUTCOMES
- Iqbal SMR
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- Ito K
- Ivanov IG
- Ivanova R
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- Iyengar SS
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- Zuniga JDH
- Zurakowski A
- Zuran I
- Zweiker R
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2019
- Field of study
Aims The third Universal Definition of Myocardial Infarction (MI) Task Force classified MIs into five types: Type 1, spontaneous; Type 2, related to oxygen supply/demand imbalance; Type 3, fatal without ascertainment of cardiac biomarkers; Type 4, related to percutaneous coronary intervention; and Type 5, related to coronary artery bypass surgery. Low-density lipoprotein cholesterol (LDL-C) reduction with statins and proprotein convertase subtilisin–kexin Type 9 (PCSK9) inhibitors reduces risk of MI, but less is known about effects on types of MI. ODYSSEY OUTCOMES compared the PCSK9 inhibitor alirocumab with placebo in 18 924 patients with recent acute coronary syndrome (ACS) and elevated LDL-C (≥1.8 mmol/L) despite intensive statin therapy. In a pre-specified analysis, we assessed the effects of alirocumab on types of MI. Methods and results Median follow-up was 2.8 years. Myocardial infarction types were prospectively adjudicated and classified. Of 1860 total MIs, 1223 (65.8%) were adjudicated as Type 1, 386 (20.8%) as Type 2, and 244 (13.1%) as Type 4. Few events were Type 3 (n = 2) or Type 5 (n = 5). Alirocumab reduced first MIs [hazard ratio (HR) 0.85, 95% confidence interval (CI) 0.77–0.95; P = 0.003], with reductions in both Type 1 (HR 0.87, 95% CI 0.77–0.99; P = 0.032) and Type 2 (0.77, 0.61–0.97; P = 0.025), but not Type 4 MI. Conclusion After ACS, alirocumab added to intensive statin therapy favourably impacted on Type 1 and 2 MIs. The data indicate for the first time that a lipid-lowering therapy can attenuate the risk of Type 2 MI. Low-density lipoprotein cholesterol reduction below levels achievable with statins is an effective preventive strategy for both MI types.For complete list of authors see http://dx.doi.org/10.1093/eurheartj/ehz299</p
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- Álvarez ÉMC
- Ávalos Y
- Önal G
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- Čolić M
- Đokić J
- Žerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Effect of alirocumab on mortality after acute coronary syndromes. An analysis of the ODYSSEY OUTCOMES randomized clinical trial
- Author
- Abbas J
- Abbate A
- Abdullakutty J
- Abdullkutty J
- Abhyanakar AD
- Aboyans V
- Abrantes JAM
- Abu-Fadel M
- Acevedo M
- Adamkova V
- Adamo A
- Adhyapak S
- Agarwal H
- Aggarwal R
- Aggarwal RK
- Agnetti V
- Aguirre A
- Ahmed H
- Ahremark U
- Ahuad Guerrero RA
- Aidar Ayoub JC
- Airaksinen JK
- Aitken D
- Akatova E
- Akhter F
- Ako J
- Akright L
- Akyea-Djamson A
- Al Joundi T
- Al-Windy NYY
- Alan D
- Alcocer Gamba MA
- Alexander JH
- Alexander K
- Alexandru TM
- Alexopoulos D
- Alings M
- Alonso Martin JJ
- Alonso Orcajo N
- Alsweiler C
- Alvarisqueta AF
- Alves De Lima AE
- Amarasekera S
- Amarasena N
- Amir O
- Amlani M
- Amosova E
- Amuchastegui M
- Anchante Hernandez HA
- Andersen D
- Andersen K
- Andersen R
- Anderson J
- Ando K
- Angel Hominal M
- Annam S
- Anscombe R
- Apostolovic SR
- Appel K-F
- Arandjelovic A
- Araneda G
- Arbel Y
- Arif I
- Armaganijan L
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- Arroyo JAC
- Arstall MA
- Asanin MR
- Atar S
- Athyros V
- Auguadro C
- Aylward P
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- Aylward PE
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- Waider W
- Waisman GD
- Waites JH
- Wali A
- Walichiewicz PM
- Waltenberger J
- Waltman J
- Wang J
- Wang J
- Wang J
- Wattanakit K
- Wei M
- Weidinger F
- Weil J
- Weintraub H
- Weissbrodt M
- Welka S
- Welker J
- Wells T
- Werner N
- Westbrook M
- Westerhausen D
- Whitaker J
- White HD
- White L
- White M
- Wiersma JJ
- Wilkins G
- Wilkinson P
- Willems FF
- Wilson MD
- Winkelmann B
- Wiseman A
- Witt N
- Wlodarczak A
- Wojewod P
- Wollaert B
- Wong Y-K
- Wongpraparut N
- Wozniak J
- Wright S
- Wu C
- Xavier D
- Xenakis M
- Xu B
- Xu D
- Xu X
- Xu Y
- Yagensky A
- Yakushin S
- Yan AT-K
- Yan BPY
- Yanez M
- Yang E
- Yang X
- Yang X
- Yao Z
- Yazdani S
- Yerra SK
- Yin W-H
- Yong H
- Yoon JH
- Younis L
- Yu Y
- Yuan Z
- Yusoff K
- Yusoff K
- Zahger D
- Zaidman CJ
- Zainea M
- Zaman A
- Zapata G
- Zdravko B
- Zea Nunez CA
- Zeiher AM
- Zeiher AM
- Zhang R
- Zhang W
- Zhang X
- Zhang Z
- Zhao X
- Zheleznyy V
- Zheng Y
- Zheng Z
- Zhou Y
- Zhu C
- Zhu H
- Zhu J
- Zirlik A
- Zizka J
- Zobouyan I
- Zong W
- Zrazhevsky K
- Zurakowski A
- Zuran I
- Zweiker R
- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 04/01/2019
- Field of study
Background: Previous trials of PCSK9 (proprotein convertase subtilisin-kexin type 9) inhibitors demonstrated reductions in major adverse cardiovascular events, but not death. We assessed the effects of alirocumab on death after index acute coronary syndrome. Methods: ODYSSEY OUTCOMES (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab) was a double-blind, randomized comparison of alirocumab or placebo in 18 924 patients who had an ACS 1 to 12 months previously and elevated atherogenic lipoproteins despite intensive statin therapy. Alirocumab dose was blindly titrated to target achieved low-density lipoprotein cholesterol (LDL-C) between 25 and 50 mg/dL. We examined the effects of treatment on all-cause death and its components, cardiovascular and noncardiovascular death, with log-rank testing. Joint semiparametric models tested associations between nonfatal cardiovascular events and cardiovascular or noncardiovascular death. Results: Median follow-up was 2.8 years. Death occurred in 334 (3.5%) and 392 (4.1%) patients, respectively, in the alirocumab and placebo groups (hazard ratio [HR], 0.85; 95% CI, 0.73 to 0.98; P=0.03, nominal P value). This resulted from nonsignificantly fewer cardiovascular (240 [2.5%] vs 271 [2.9%]; HR, 0.88; 95% CI, 0.74 to 1.05; P=0.15) and noncardiovascular (94 [1.0%] vs 121 [1.3%]; HR, 0.77; 95% CI, 0.59 to 1.01; P=0.06) deaths with alirocumab. In a prespecified analysis of 8242 patients eligible for ≥3 years follow-up, alirocumab reduced death (HR, 0.78; 95% CI, 0.65 to 0.94; P=0.01). Patients with nonfatal cardiovascular events were at increased risk for cardiovascular and noncardiovascular deaths (P<0.0001 for the associations). Alirocumab reduced total nonfatal cardiovascular events (P<0.001) and thereby may have attenuated the number of cardiovascular and noncardiovascular deaths. A post hoc analysis found that, compared to patients with lower LDL-C, patients with baseline LDL-C ≥100 mg/dL (2.59 mmol/L) had a greater absolute risk of death and a larger mortality benefit from alirocumab (HR, 0.71; 95% CI, 0.56 to 0.90; Pinteraction=0.007). In the alirocumab group, all-cause death declined wit h achieved LDL-C at 4 months of treatment, to a level of approximately 30 mg/dL (adjusted P=0.017 for linear trend). Conclusions: Alirocumab added to intensive statin therapy has the potential to reduce death after acute coronary syndrome, particularly if treatment is maintained for ≥3 years, if baseline LDL-C is ≥100 mg/dL, or if achieved LDL-C is low. Clinical Trial Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01663402
Olfactory dysfunction revisited: a reappraisal of work-related olfactory dysfunction caused by chemicals
- Author
- A Haehner
- A Hamidovic
- A Muttray
- A Muttray
- A Muttray
- A Muttray
- A Muttray
- A Muttray
- A Sorokowska
- A Sorokowska
- A Welge-Lüssen
- AD Mayer
- AE Mott
- AH Moberly
- Anonymous
- B Palouzier-Paulignan
- B Rydzewski
- B Sandmark
- BS Schwartz
- BS Schwartz
- BW Jafek
- C Edling
- C Herberhold
- C Jia
- CA Duncan-Lewis
- CG Smith
- CL Potts
- CR Spealman
- CR Williams
- CS Rose
- D Mergler
- DC Dorman
- DFG (Deutsche Forschungsgemeinschaft)
- DH Matulionis
- DL Eisenbrandt
- E Iannilli
- E Lenhardt
- Eberhard Nies
- EW Baader
- EW Baader
- F Gobba
- F Kitamura
- F Tisdall
- FR Cassee
- FW Sunderman Jr
- G Bello
- G Cruzan
- G Cruzan
- G Kobal
- G Liu
- G Oberdörster
- GD Burd
- GE Pyatayev
- GM Calvert
- H Hatt
- H Seeber
- H Seeber
- H Shiga
- H Shiga
- H Tjalve
- H Tjalve
- H Tjalve
- HJ Hoffman
- I Croy
- J Amoore
- J Henriksson
- J Herranz Gonzalez-Botas
- J Lewis
- J Noel
- J Tallkvist
- J Zhao
- J Zou
- JE Evans
- JE Schwob
- JH Arts
- JH Lim
- JL Mattsson
- JR Alberts
- JR Bondier
- JW Harding
- K Dżaman
- K McBride
- KH Kilburn
- KJ Thompson
- KW Altman
- L Colin-Barenque
- L Friberg
- L Gao
- L Klimek
- LA Czarnecki
- LA Czarnecki
- LE Hopkins
- LF Hansen
- M Guarneros
- M Hisamitsu
- M Holmström
- M Miyake
- M Witt
- MB Antunes
- MI Greenberg
- MJ Osmond-McLeod
- ML Foster
- ML Miller
- N Viswaprakash
- National Toxicology Program
- National Toxicology Program
- P Cancalon
- P Dalton
- P Dalton
- P Dalton
- P Mascagni
- PH Dalton
- Q Zhang
- R Ahlstrom
- R Lucchini
- RG Adams
- RG Aiyer
- RG Lucchini
- RL Doty
- RL Doty
- RL Doty
- RM Bowler
- RM Bowler
- RM Patel
- S Benvenuti
- S Casjens
- S Fonteyn
- S Gebel
- S Sen
- S Shrestha
- S Watanabe
- SA Quandt
- SA Wardlaw
- Sabine Werner
- SB Mossad
- SF Cheng
- SH Gautam
- SS Winans
- T Green
- T Green
- T Hummel
- T Hummel
- T Hummel
- T Kuner
- TH Alexander
- TJ Sun
- TM Davidson
- U Glück
- VJ Feron
- W Mücke
- WJ Sulkowski
- Y Li
- YF Brunner
- YZ Liu
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Cardiovascular Efficacy and Safety of Bococizumab in High-Risk Patients
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- Abbott Jd
- Abdullah S
- Abib E Jr
- Ables Lr
- Abrantes Ja
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- Albert M
- Alfieri Ad
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- Alpizar-Salazar M
- Altafullah Im
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- Alvarez Ca
- Alvarez Jg
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- Angoulvant D
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- Violante Ortiz R
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- Visser Rp
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- Vodnansky P
- Voehringer Hf
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- Volkova A
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- von Engelhardt Cb
- von Hodenberg Ef
- Vora Kn
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- Voros P
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- Vukotic G
- Wadud K
- Wainstein J
- Wakefield Ph
- Wakeling J
- Walczak M
- Walczewska J
- Walukiewica P
- Wang D
- Wang E
- Wang G
- Wang Y
- Wasserburger B
- Waxler Ar
- Wayne Jd
- Weber D
- Weber K
- Wegner J
- Wei C
- Weigmann I
- Weinstein Dl
- Weiss R
- Welker Ja
- Welty F
- Wenetz Lm
- Wermuth S
- Wesson T
- West Sh
- Westerndorp I
- Wetzel T
- White H.
- Whitlock L
- Whitney Rt
- Wiggers H
- William M
- Williams Dg
- Williams M
- Willis Jg
- Willits Vl
- Winkelmann B
- Witt N
- Wittmann I
- Woehrle J
- Worner Diz F
- Wozniak I
- Wright R. S.
- Wronska D
- Wuerzner G
- Wychota K
- Xu P
- Xue L
- Yakusevich Vv
- Yang P
- Yang X
- Yao Lc
- Yared Z
- Yarows Sa
- Yigit Z
- Yoon J
- Yunis C.
- Zadra R
- Zaidman Cj
- Zamorano Gomez Jl
- Zannad F
- Zarandon Rb
- Zarich Sw
- Zateyshchikov D
- Zavaro Sh
- Zebrack Js
- Zeig S
- Zemek S
- Zemour G
- Zeng X
- Zeno Ml
- Zhang L
- Zhang X
- Zhang Y
- Zhao Y
- Zhou C
- Zhou Y
- Zhu Y
- Zidkova E
- Zieba B
- Zilahi Z
- Zoet-Nugteren Sk
- Zrazhevskiy K
- Zubek V
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Bococizumab is a humanized monoclonal antibody that inhibits proprotein convertase subtilisin- kexin type 9 (PCSK9) and reduces levels of low-density lipoprotein (LDL) cholesterol. We sought to evaluate the efficacy of bococizumab in patients at high cardiovascular risk. METHODS In two parallel, multinational trials with different entry criteria for LDL cholesterol levels, we randomly assigned the 27,438 patients in the combined trials to receive bococizumab (at a dose of 150 mg) subcutaneously every 2 weeks or placebo. The primary end point was nonfatal myocardial infarction, nonfatal stroke, hospitalization for unstable angina requiring urgent revascularization, or cardiovascular death; 93% of the patients were receiving statin therapy at baseline. The trials were stopped early after the sponsor elected to discontinue the development of bococizumab owing in part to the development of high rates of antidrug antibodies, as seen in data from other studies in the program. The median follow-up was 10 months. RESULTS At 14 weeks, patients in the combined trials had a mean change from baseline in LDL cholesterol levels of -56.0% in the bococizumab group and +2.9% in the placebo group, for a between-group difference of -59.0 percentage points (P<0.001) and a median reduction from baseline of 64.2% (P<0.001). In the lower-risk, shorter-duration trial (in which the patients had a baseline LDL cholesterol level of ≥70 mg per deciliter [1.8 mmol per liter] and the median follow-up was 7 months), major cardiovascular events occurred in 173 patients each in the bococizumab group and the placebo group (hazard ratio, 0.99; 95% confidence interval [CI], 0.80 to 1.22; P = 0.94). In the higher-risk, longer-duration trial (in which the patients had a baseline LDL cholesterol level of ≥100 mg per deciliter [2.6 mmol per liter] and the median follow-up was 12 months), major cardiovascular events occurred in 179 and 224 patients, respectively (hazard ratio, 0.79; 95% CI, 0.65 to 0.97; P = 0.02). The hazard ratio for the primary end point in the combined trials was 0.88 (95% CI, 0.76 to 1.02; P = 0.08). Injection-site reactions were more common in the bococizumab group than in the placebo group (10.4% vs. 1.3%, P<0.001). CONCLUSIONS In two randomized trials comparing the PCSK9 inhibitor bococizumab with placebo, bococizumab had no benefit with respect to major adverse cardiovascular events in the trial involving lower-risk patients but did have a significant benefit in the trial involving higher-risk patients
Molecular Genetics of Obesity and Cardiovascular Diseases
- Author
- Al-Kateb H
- Allan CM
- Almasy L
- Anand A
- Arch JR
- Argyropoulos G
- Arya R
- Arya R
- Baghaei F
- Baghaei F
- Baier LJ
- Beattie JH
- Berard AM
- Blake WL
- Boekholdt SM
- Boord JB
- Boord JB
- Borecki IB
- Borecki IB
- Bosse Y
- Bosse Y
- Boucher N
- Boutin P
- Brenn T
- Broeckel U
- Brown S
- Burnett JR
- Callow MJ
- Cao H
- Castensson A
- Castro-Chavez F
- Chagnon Y
- Chagnon YC
- Chagnon YC
- Chagnon YC
- Chagnon YC
- Chen HC
- Chen HC
- Cheng LS
- Choy HA
- Chruscinski AJ
- Ciccarese M
- Coleman DL
- Collins CA
- Comuzzie AG
- Comuzzie AG
- Conde-Knape K
- Coon H
- Cummings DE
- Dionne IJ
- Do MS
- Dracheva S
- Duggirala R
- Duggirala R
- Eden ER
- Ehrenborg E
- Ek J
- Elbein SC
- Engert JC
- Epstein LH
- Eurlings PM
- Faith MS
- Fazio S
- Febbraio M
- Feitosa MF
- Fiegenbaum M
- Fisher RM
- Foger B
- Frank PG
- Fruhbeck G
- Fumeron F
- Funakoshi A
- Gainetdinov RR
- Garenc C
- Garenc C
- Garenc C
- Garenc C
- Gautier T
- Geary N
- Gelernter-Yaniv L
- Gerdes C
- Goldin LR
- Gonzalez-Sanchez JL
- Goudriaan JR
- Grass DS
- Gudayol M
- Gunn TM
- Gurnell M
- Hanson RL
- Harada K
- Hayek T
- Hayek T
- Hegele RA
- Hegele RA
- Hegele RA
- Hegele RA
- Henderson HE
- Hessle L
- Hewitt KN
- Hixson JE
- Hokanson JE
- Hong SH
- Hong Y
- Hotamisligil GS
- Hsu LA
- Huan JN
- Hubacek JA
- Huggins KW
- Hunt SC
- Ibrahimi A
- Imperatore G
- Inui A
- Ishibashi S
- Ishimura-Oka K
- Ishiyama-Shigemoto S
- Iwamoto K
- Jimenez M
- Jones ME
- Jong MC
- Jong MC
- Jong MC
- Kamboh MI
- Kammerer CM
- Kao WH
- Kawano K
- Ke Y
- Kissebah AH
- Klos KL
- Knoblauch H
- Kohn Y
- Kozak LP
- Kuniyoshi A
- Lambert JC
- Lawn RM
- Lee JH
- Lefevre M
- Linton MF
- Lopez-Miranda J
- Ma YQ
- Maeda N
- Mahaney MC
- Martinez-Botas J
- Masucci-Magoulas L
- Matsuoka N
- Matsushima Y
- Maziade M
- Maziade M
- McCarthy MI
- Meirhaeghe A
- Meirhaeghe A
- Meirhaeghe A
- Menzaghi C
- Mitchell BD
- Mitchell BD
- Mori Y
- Mottagui-Tabar S
- Nagle DL
- Namiki M
- Newman DL
- Norman RA
- Ober C
- Ohman M
- Ordovas JM
- Osgood D
- Ozata M
- Pajukanta P
- Pajukanta P
- Pasagian-Macaulay A
- Peacock JM
- Perusse L
- Peterfy M
- Pihlajamaki J
- Planas JV
- Plump AS
- Pravenec M
- Purcell-Huynh DA
- Rainwater DL
- Rainwater DL
- Rainwater DL
- Rajput-Williams J
- Reed DR
- Rice T
- Ristow M
- Robitaille J
- Rohrer DK
- Rohrer DK
- Scholz M
- Schwartz GJ
- Selby JV
- Sellers TA
- Serra C
- Shachter NS
- Shachter NS
- Shaughnessy S
- Shearman AM
- Shimada M
- Shimano H
- Sklar P
- Smith AC
- Soro A
- Speer G
- St-Pierre J
- Stern MP
- Stone S
- Stork O
- Stork O
- Strobel A
- Sun Y
- Susulic VS
- Talmud PJ
- Talmud PJ
- Tan MS
- Tsukiyama-Kohara K
- Ukkola O
- Ukkola O
- van Bockxmeer FM
- van der Kallen CJ
- Varret M
- Vassileva G
- Viitanen L
- Vink T
- Walczak R
- Wang CH
- wards KL
- Watanabe RM
- Weinstock PH
- Westberg L
- Whitfield AJ
- Wilson CJ
- Wittekoek ME
- Wu X
- Xu Y
- Yagyu H
- Yamashita S
- Yuan B
- Zhang SH
- Zhao SP
- Zietz B
- Publication venue
- 'Informa UK Limited'
- Publication date
- Field of study
Risk categorization using New American College of Cardiology/American Heart Association guidelines for cholesterol management and its relation to alirocumab treatment following acute coronary syndromes
- Author
- Abbas J
- Abbate A
- Abdullakutty J
- Abdullkutty J
- Abhyanakar AD
- Aboyans V
- Abrantes JAM
- Abu-Fadel M
- Acevedo M
- Adamkova V
- Adamo A
- Adhyapak S
- Agarwal H
- Aggarwal R
- Aggarwal RK
- Agnetti V
- Aguirre A
- Ahmed H
- Ahremark U
- Ahuad Guerrero RA
- Aidar Ayoub JC
- Airaksinen JK
- Aitken D
- Akatova E
- Akhter F
- Ako J
- Akright L
- Akyea-Djamson A
- Al Joundi T
- Al-Windy NYY
- Alan D
- Alcocer Gamba MA
- Alexander JH
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- Shah AV
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- Sheldon W
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- Silva PGMDB
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- Siu DCW
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- Skorski M
- Skoumas I
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- Soonfuang W
- Soopold U
- Soots M
- Sopena S
- Soran H
- Soroka E
- Sotnikova T
- Sotty M
- Sousa L
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- Sparby JA
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- Spinar J
- Sporn D
- Spriggs D
- Sritara P
- Stambuk K
- Staneta P
- Stanislavchuk M
- Stankovic A
- Starcevic B
- Starmer G
- Stasek J
- Stasiewski A
- Steg PG
- Steg PG
- Steiner S
- Stellbrink C
- Stewart R
- Stojic S
- Stone J
- Storey R
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- Strelnieks A
- Striekwold H
- Stringfellow K
- Strozzi M
- Stryuk R
- Su G
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- Subkovas E
- Sudnik W
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- Suh D
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- Sukonthasarn A
- Suligoj NC
- Sulit DJ
- Sumner A
- Sun Y
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- Sundelin T
- Sundram PS
- Suryapranata H
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- Taguchi S
- Tahk S-J
- Takahashi T
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- Ternouth I
- Terzic I
- Tesloianu DN
- Tespili M
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- Thao H
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- Tomulic V
- Tonnessen G
- Torstensson I
- Toursarkissian N
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- Treasure C
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- Trevelyan J
- Triana MAU
- Tricoci P
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- Trotter C
- Tsai W-C
- Tse H-F
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- Tunon Fernandez J
- Tunon J
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- Tzekova ML
- Ueda Y
- Uehara H
- Ueng K-C
- Ungi I
- Ural E
- Ushakov O
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- Vahula V
- Vakaluyk I
- Valdivielso P
- Valdovinos PCM
- Valdovinos PCM
- Valgimigli M
- Valiris J
- Vallejo GS
- Vallejos JA
- Van Der Wal RMA
- Van Der Zwaan CC
- Van Diepen SFP
- Van Huysduynen-Monraats PSH
- Van Zyl LJ
- Vardas P
- Vardi G
- Vargas Gonzales RJ
- Varleta P
- Vatutin M
- Vedere A
- Vejar M
- Velcheva ES
- Verdel GJE
- Vered Z
- Verrier M
- Vervoort G
- Vico ML
- Vida M
- Videbaek L
- Vidotti MH
- Vidovich M
- Viergever EP
- Viigimaa M
- Vijay N
- Vijayaraghavan R
- Vikman S
- Viktorova I
- Vincendet M
- Violini R
- Vishnevsky AY
- Vizel S
- Vo A
- Voeller H
- Voevoda MI
- Vogel R
- Vohra R
- Vora K
- Voyce S
- Vrolix MCM
- Vulic D
- Vuurmans T
- Wada A
- Waider W
- Waisman GD
- Waites JH
- Wali A
- Walichiewicz PM
- Waltenberger J
- Waltman J
- Wang J
- Wang J
- Wang J
- Wattanakit K
- Wei M
- Weidinger F
- Weil J
- Weintraub H
- Weissbrodt M
- Welka S
- Welker J
- Wells T
- Werner N
- Westbrook M
- Westerhausen D
- Whitaker J
- White HD
- White L
- White M
- Wiersma JJ
- Wilkins G
- Wilkinson P
- Willems FF
- Wilson MD
- Winkelmann B
- Wiseman A
- Witt N
- Wlodarczak A
- Wojewod P
- Wollaert B
- Wong Y-K
- Wongpraparut N
- Wozniak J
- Wright S
- Wu C
- Xavier D
- Xenakis M
- Xu B
- Xu D
- Xu X
- Xu Y
- Yagensky A
- Yakushin S
- Yan AT-K
- Yan BPY
- Yanez M
- Yang E
- Yang X
- Yang X
- Yao Z
- Yazdani S
- Yerra SK
- Yin W-H
- Yong H
- Yoon JH
- Younis L
- Yu Y
- Yuan Z
- Yusoff K
- Yusoff K
- Zahger D
- Zaidman CJ
- Zainea M
- Zaman A
- Zapata G
- Zdravko B
- Zea Nunez CA
- Zeiher AM
- Zeiher AM
- Zhang R
- Zhang W
- Zhang X
- Zhang Z
- Zhao X
- Zheleznyy V
- Zheng Y
- Zheng Z
- Zhou Y
- Zhu C
- Zhu H
- Zhu J
- Zirlik A
- Zizka J
- Zobouyan I
- Zong W
- Zrazhevsky K
- Zurakowski A
- Zuran I
- Zweiker R
- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 01/08/2019
- Field of study
Background: The 2018 US cholesterol management guidelines recommend additional lipid-lowering therapies for secondary prevention in patients with low-density lipoprotein cholesterol ≥70 mg/dL or non−high-density lipoprotein cholesterol ≥100 mg/dL despite maximum tolerated statin therapy. Such patients are considered at very high risk (VHR) based on a history of >1 major atherosclerotic cardiovascular disease (ASCVD) event or a single ASCVD event and multiple high-risk conditions. We investigated the association of US guideline-defined risk categories with the occurrence of ischemic events after acute coronary syndrome and reduction of those events by alirocumab, a PCSK9 (proprotein convertase subtilisin/kexin type 9) inhibitor. Methods: In the ODYSSEY OUTCOMES trial (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab), patients with recent acute coronary syndrome and residual dyslipidemia despite optimal statin therapy were randomly assigned to alirocumab or placebo. The primary trial outcome (major adverse cardiovascular events, ie, coronary heart disease death, nonfatal myocardial infarction, ischemic stroke, or hospitalization for unstable angina) was examined according to American College of Cardiology/American Heart Association risk category. Results: Of 18 924 participants followed for a median of 2.8 years, 11 935 (63.1%) were classified as VHR: 4450 (37.3%) had multiple prior ASCVD events and 7485 (62.7%) had 1 major ASCVD event and multiple high-risk conditions. Major adverse cardiovascular events occurred in 14.4% of placebo-treated patients at VHR versus 5.6% of those not at VHR. In the VHR category, major adverse cardiovascular events occurred in 20.4% with multiple prior ASCVD events versus 10.7% with 1 ASCVD event and multiple high-risk conditions. Alirocumab was associated with consistent relative risk reductions in both risk categories (hazard ratio=0.84 for VHR; hazard ratio=0.86 for not VHR; Pinteraction=0.820) and by stratification within the VHR group (hazard ratio=0.86 for multiple prior ASCVD events; hazard ratio=0.82 for 1 major ASCVD event and multiple high-risk conditions; Pinteraction=0.672). The absolute risk reduction for major adverse cardiovascular events with alirocumab was numerically greater (but not statistically different) in the VHR group versus those not at VHR (2.1% versus 0.8%; Pinteraction=0.095) and among patients at VHR with multiple prior ASCVD events versus a single prior ASCVD event (2.4% versus 1.8%; Pinteraction=0.661). Conclusions: The US guideline criteria identify patients with recent acute coronary syndrome and dyslipidemia who are at VHR for recurrent ischemic events and who may derive a larger absolute benefit from treatment with alirocumab. Clinical Trial Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01663402
Regulation of glucose and lipid metabolism in health and disease
- Author
- A Bartelt
- A Barthel
- A Brooks-Wilson
- A Chorlay
- A Consoli
- A César-Razquin
- A Das
- A Fedoseienko
- A Lass
- A Melnikov
- A Nohturfft
- A Orr
- A Radhakrishnan
- A Radhakrishnan
- A Romanauska
- A Wagschal
- AC Goldberg
- AD Gillon
- AJ Brown
- AJM Santos
- AK Bhattacharyya
- AK Khachadurian
- AK Khachadurian
- AK Madiraju
- AK Rines
- AK Soutar
- AK Soutar
- AL Williams
- AM Cypess
- AP Bailey
- AP Halestrap
- AP Halestrap
- AR Kimmel
- AS Greenberg
- AS Joshi
- AS Rambold
- AT Gatta
- B Hubbard
- B Jones
- B Kadereit
- B Liu
- B Wang
- B Zinker
- BA Hemmings
- Bao-Liang Song
- BB Adhyaru
- BB Chu
- BG Nordestgaard
- BM Castellano
- BR Cartwright
- BT Emmer
- BU Fitzky
- C Barlowe
- C Barlowe
- C Butkinaree
- C Gürkan
- C Meyer
- C Muller
- C Romere
- C Sztalryd
- C Vrins
- C Wallace
- C Wu
- C Wu
- C Xie
- C Xie
- C Xie
- C Xie
- C Zhang
- CA Wassif
- CD Davidson
- CH Vite
- CJ Willer
- CJ Willer
- CK Barlowe
- CK Garcia
- CL Hyde
- CM Anderson
- CM Kazda
- CR Warren
- D Fotiadis
- D Frescas
- D Jansson
- D Klarin
- D Xu
- DA Gordon
- DA Gross
- DA Okar
- DG Hardie
- DJ Kazierad
- DJ Liu
- DM Erion
- DQH Wang
- DW Russell
- DW Zhang
- E Gonzalez
- E Li
- E Mossessova
- E Nisoli
- E Perland
- E Sezgin
- E Usifo
- EA Miller
- EF Rehberg
- EG Yoo
- ET Chouchani
- F Palmieri
- F Veglia
- F Wilfling
- FD Porter
- FD Porter
- FE Dewey
- G Annesi
- G Assmann
- G Di Paolo
- G Haemmerle
- G Haemmerle
- G He
- G Mithieux
- G Qiang
- G Schonfeld
- G Schonfeld
- G Weber
- G Zanetti
- G Zhou
- G Zuliani
- GA Gonzalez
- GA Graf
- GA Wyant
- GC Band
- GD Kolovou
- GT Shubeita
- H Doege
- H Doege
- H Hariri
- H Koepsell
- H Luo
- H Ou
- H Qian
- H Shimano
- H Tanaka
- H Wang
- H Wang
- H Wang
- H Yang
- HG Hers
- HH Hobbs
- HJ Kwon
- HJ Kwon
- HR Fernandez
- HR Waterham
- HV Lin
- I Gouni-Berthold
- I Surakka
- I Tabas
- I Tikhanovich
- IC Gelissen
- IJ Kurland
- IM Heid
- IY Benador
- IY Benador
- J Arias
- J Boren
- J Cho
- J Cho
- J Cohen
- J Dupuis
- J Fischer
- J Flannick
- J Girard
- J Gong
- J Han
- J Li
- J Magré
- J Martinez-Botas
- J Osuga
- J Radziuk
- J Sakai
- J Tao
- J Wei
- J Yu
- JA Olzmann
- JA Porter
- JAM Foody
- JC Chrivia
- JC Cohen
- JC Cohen
- JC Fromme
- JC Ulirsch
- JD Horton
- JD Horton
- JD Horton
- JD Mancias
- JD Mancias
- JE Ayala
- JG Granneman
- JH Exton
- JH Zhang
- JJ Bahl
- JJ Egan
- JL Best
- JL Brodsky
- JL Goldstein
- JL Goldstein
- JL Goldstein
- JL Goldstein
- JL Goldstein
- JL Goldstein
- JM Agati
- JM Lizcano
- JR Wetterau
- JS Kooner
- JS Striffler
- JS Weiss
- JY Altarejos
- JY Lee
- K Ben M’barek
- K Ekberg
- K Kotani
- K Lu
- K Milger
- K Musunuru
- K Nagao
- K Nakagawa
- K Ohashi
- K Ozaki
- K Schwarz
- K Sharabi
- K Tan
- KD Nguyen
- KE Berge
- KJ Roberg
- KM Szymanski
- L Carneiro
- L Chen
- L Ge
- L Ge
- L Liscum
- L Liu
- L Liu
- L Liu
- LA Lange
- LA Solt
- LA Weiss
- LC Bickford
- LF Reeskamp
- LF Soria
- Ligong Chen
- LJ Wang
- LJ Wang
- LL Listenberger
- LN Zhang
- LP Sun
- LP Sun
- LR Brunham
- M Abifadel
- M Arca
- M Bodzioch
- M Foretz
- M Futema
- M Gao
- M Garcia-Calvo
- M Ghosh
- M Harms
- M Hatting
- M Ishigami
- M Lu
- M Matsumoto
- M Mueckler
- M Puntoni
- M Rebsamen
- M Saberi
- M Vazquez-Chantada
- MA Austin
- MA Hediger
- MA Mitsche
- MA Ravier
- MA Welte
- MC Izar
- MC Moore
- MC Petersen
- MC Phillips
- MCS Lee
- MD Svoboda
- MF Hogan
- MJ Betz
- MJM Nowaczyk
- ML Wang
- MM Mihaylova
- MM Schumacher
- MM Schumacher
- MR Johnson
- MR Lang
- MRF Linton
- MS Bosner
- MS Brown
- MS Brown
- MS Brown
- MS Brown
- MS Brown
- MS Brown
- MS Perez-Poyato
- MS Sabatine
- MS Sandhu
- MT Maurano
- MT Vanier
- N Cano
- N Kory
- N Kory
- N Krahmer
- N Kumar
- N Rasouli
- NG Seidah
- NO Davidson
- NS Abul-Husn
- NW DiTullio
- P Anand
- P Bartuzi
- P Bianchi
- P Boström
- P Chakrabarti
- P Costet
- P Durrington
- P Hossain
- P Li
- P Puigserver
- P Roingeard
- P Zanoni
- PD van Poelje
- PJ Espenshade
- PM Lewis
- PR Shepherd
- PS Li
- Q Gu
- R Bartz
- R Dentin
- R Henderson
- R Khoriaty
- R Peng
- R Saxena
- R Schekman
- R Singh
- R Yan
- R Zechner
- R Zimmermann
- RA Rizza
- RA Screaton
- RC Andrews
- RE Temel
- RJ Perry
- RJ Shaw
- RK Hall
- RPS Kwok
- S Cermelli
- S Datta
- S Eliahu
- S Gandotra
- S Gill
- S Herzig
- S Huang
- S Kathiresan
- S Kathiresan
- S Kaushik
- S Kc
- S Lengacher
- S Ozeki
- S Raychaudhuri
- S Rust
- S Wang
- S Wang
- S Xu
- S Yue
- SA Boyadjiev
- SA Boyadjiev
- SB Widenmaier
- SG Pfisterer
- SG Young
- SG Young
- SH Koo
- SH Moon
- SJ Fisher
- SJ Pilkis
- SJ Pilkis
- SM Grundy
- SR Myers
- SY Jiang
- SY Jiang
- T Nagashima
- TA Lagace
- TB Nguyen
- TB Strøm
- TC Walther
- TJ Flynn
- TJ Hoffmann
- TM Teslovich
- TY Chang
- TY Li
- TY Liu
- V Bansal
- V Choudhary
- V Iacobazzi
- V Infantino
- V Malhotra
- V Mugoni
- V Rusu
- V Saini
- VA Lira
- VT Salo
- W Fei
- W Fei
- W Fei
- W Song
- WB Kannel
- WG Jerome
- X Bi
- X Gong
- X Hua
- X Huang
- X Li
- X Lu
- X Lu
- X Lu
- X Sui
- X Xiao
- X Yang
- X Zhang
- XG Zhu
- Xiao-Wei Chen
- Xun Huang
- XW Chen
- Y Guo
- Y Jo
- Y Lange
- Y Lange
- Y Lee
- Y Lee
- Y Liao
- Y Liu
- Y Miyanari
- Y Shimoni
- Y Tian
- Y Wang
- Y Wang
- Y Wang
- Y Wang
- Y Wang
- Y Wang
- Y Xiong
- Y Zhang
- Y Zhang
- Y Zhao
- Yan Wang
- Yiguo Wang
- YJ Wang
- YS Aulchenko
- YY Zhang
- Z Li
- Z Li
- Z Sun
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Mortality after surgery in Europe: a 7 day cohort study
- Author
- Aakeroey K
- Acan I
- Adams D
- Adams T
- Adanic M
- Adolfsson A
- Afonso O
- Afshari A
- Agarwal B
- Agnic I
- Aguado DN
- Ahern R
- Ahonen T
- Aignatoaie M
- Akotia N
- Akouds E
- Al Abdaly A
- Al Subaie N
- Alagarsamy F
- Alameda LE
- Alaspää A
- Albalad DD
- Albaladejo P
- Albante A
- Alberdi F
- Albu C
- Alcaide CM
- Alcantud JF
- Aldecoa C
- Aldecoa C
- Alderson L
- Aleixandre IS
- Aleksic D
- Aleman M
- Alexander D
- Alexander P
- Algarra RR
- Ali ZS
- Aliste P
- Allué RM
- Almeida E
- Almeida IM
- Almeras L
- Alonso AE
- Alonso E
- Alvarez AA
- Alvarez LR
- Amaniti E
- Amatya S
- Ampuero MS
- Anchuelo AH
- Andabaka T
- Andersen JD
- Anderson H
- Andresen B
- Angulo GO
- Anna US
- Anthopoulos G
- Antolinos MA
- Apsokardos A
- Aracil N
- Aranzubia M
- Arawwawala D
- Arcas JJ
- Arevalo J
- Argente GR
- Arif F
- Armaganidis A
- Armaganidis A
- Arnaoutoglou E
- Arnold G
- Arocas B
- Arpino I
- Arroyo MM
- Arteta DA
- Artigas A
- Artigas X
- Arvaniti K
- Arviza LP
- Asensio MA
- Assunção JP
- Aubrun F
- Auer P
- Austine P
- Aversano M
- Awlakpui E
- Axelsson P
- Ayman M
- Baban O
- Bacak Kocman I
- Bacci A
- Baciu M
- Baddeley S
- Bailey K
- Baker A
- Baker J
- Bakosova E
- Balaji P
- Balasa C
- Balciscueta G
- Balenovic I
- Ball C
- Ballington R
- Balust C
- Balust J
- Bandic D
- Baraldi S
- Baranovic S
- Barber R
- Barbes A
- Baricocchi E
- Barižon M
- Baroselli A
- Barr K
- Barrachima BB
- Barrasa H
- Barrios F
- Barrios J
- Barros F
- Barros N
- Barthel F
- Bartolomé MJ
- Bataillard A
- Batchelor N
- Bates D
- Batinica IM
- Battistella M
- Bauer P
- Bauer W
- Bauer ZŠ
- Baumgarten R
- Baxter I
- Bazin M
- Beach M
- Becanne X
- Beck O
- Beckingsale A
- Bekos V
- Belavic M
- Belcher A
- Belciu I
- Belenguer Muncharaz A
- Belhaj A
- Belikova B
- Bellotti F
- Belvert BQ
- Benayoun L
- Bento HC
- Bento L
- Bergamini E
- Berger K
- Berger P
- Bergin A
- Bermejo FJ
- Bernal DG
- Bernat Álvarez MJ
- Berneanu M
- Berntsen S
- Bestle M
- Betancor NO
- Bettelli G
- Bewley J
- Bešlic G
- Bhaskaran S
- Bianchin A
- Bicek V
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- Bierbaum K
- Bigeon JY
- Bignami E
- Bille AB
- Bingold F
- Bis B
- Biston P
- Björne H
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- Blanco IA
- Bland M
- Blauwen Nd
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- Bloos F
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- Blöndal Á
- Bobinac M
- Bodega BM
- Boerma C
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- Bogdan P
- Boksasp OD
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- Bonet A
- Boninsegna D
- Bonnet A
- Bonnet F
- Bonnett A
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- Bonnländer G
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- Borovsak Z
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- Botelho MM
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- Corradetti F
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- Corsini LM
- Cortes JG
- Cortés AF
- Costagliola R
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- Crespo Mdel R
- Crespo P
- Cristina MV
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- Crowley S
- Csomos A
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- Cuarental A
- Cubillos DN
- Cupitt J
- Currie V
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- Czeslick E
- Cíková A
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- De Michele M
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- de Rabago RB
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- De Simone M
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- Debelic D
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- Del Olmo M
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- Dempsey G
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- Derumeaux P
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- Desikan S
- Deutsch PA
- Di Mauro P
- Di Noto A
- Diaconescu C
- Diaz A
- Diaz Boladeras RM
- Diaz DS
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- Dresden C
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- Duque P
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- Duzel V
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- ElMiloudi F
- Elomaa E
- Elson MZ
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- Elósegui I
- Engelen WC
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- Erkens U
- Erler I
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- Esteva GE
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- Fernández LF
- Fernández PT
- Fernández SR
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- García V
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- Saravanmuthu R
- Sardo E
- Sari F
- Sarkar S
- Sartzi M
- Saunders D
- Savelsberg S
- Saña FJ
- Sbai H
- Scarth E
- Scheidemann M
- Schiere S
- Schmutzler M
- Schneider G
- Scholler A
- Scholz L
- Schoorl M
- Schreiner F
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- Schröder S
- Schultz C
- Schwarzkopf K
- Schüttler J
- Seale T
- Secher EL
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- Seisdedos ÁA
- Sekulic A
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- Seppänen H
- Sepúlveda I
- Serena G
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- Serrano LG
- Serrano MG
- Serrano PD
- Sevilla FC
- Sfyras D
- Shahzad A
- Sheshgiri B
- Shinner G
- Siegmueller C
- Sieiro JM
- Sigurbjörnsson FT
- Sigurdardottir EE
- Sigurdsson G
- Sigurdsson GH
- Silva L
- Silvasti P
- Silvestre FP
- Silvius N
- Simeón RG
- Simkova A
- Simon M
- Simon V
- Simonsen M
- Singh N
- Singh R
- Sintes D
- Sipylaite J
- Sjövall S
- Smith A
- Smith A
- Smith N
- Smith R
- Smitz C
- Smoje M
- Snaier C
- Snaith C
- Snell J
- Snelson C
- Soar J
- Sobona V
- Sockalingam S
- Soldatou O
- Sole MJ
- Somaini M
- Soro M
- Soto CL
- Soto RA
- Soto TT
- Soultati I
- Soumpasis I
- Spagnesi L
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- Spanjersberg R
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- Spena C
- Spielvogel C
- Spies C
- Spring A
- Sprunck A
- Spyropoulou E
- Spyropoulou Pagdatoglou K
- Srecko M
- Stafylaraki M
- Stanzani MR
- Stathopoulos A
- Stecher A
- Stegmann N
- Steib A
- Steiner L
- Stelian DS
- Stendell L
- Stepanovs J
- Stephens R
- Stewart H
- Stier M
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- Stivan F
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- Struthers R
- Stuart Smith K
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- Tassinati T
- Taylor A
- Templeton M
- Tena B
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- Theodorou V
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- van der Hoven B
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- van Klei W
- Van Mossevelde V
- van Obbergh L
- Vanlinthout L
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- Varela IP
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- Westbrook A
- Westbrook A
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- Wiegand Löhnert C
- Wiese O
- Wigmore T
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- Yemnga B
- Yepes MJ
- Yeung J
- Ytrebo LM
- Zaballos J
- Zabarte M
- Zacharouli D
- Zacharovska A
- Zadrazilova K
- Zafiridis T
- Zahorec R
- Zahorec R
- Zaldibar E
- Zamora JF
- Zandvliet R
- Zantua K
- Zearo E
- Zeba S
- Ziekenhuis A
- Zittling R
- Zocca E
- Zoltowski MK
- Zompanti V
- Zsisku L
- Zunic F
- Zuzan O
- Álvaro JL
- Ålvarez JT
- Íñigo JA
- Šakic K
- Šaric JP
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2012
- Field of study
Background: Clinical outcomes after major surgery are poorly described at the national level. Evidence of heterogeneity between hospitals and health-care systems suggests potential to improve care for patients but this potential remains unconfirmed. The European Surgical Outcomes Study was an international study designed to assess outcomes after non-cardiac surgery in Europe.Methods: We did this 7 day cohort study between April 4 and April 11, 2011. We collected data describing consecutive patients aged 16 years and older undergoing inpatient non-cardiac surgery in 498 hospitals across 28 European nations. Patients were followed up for a maximum of 60 days. The primary endpoint was in-hospital mortality. Secondary outcome measures were duration of hospital stay and admission to critical care. We used χ² and Fisher’s exact tests to compare categorical variables and the t test or the Mann-Whitney U test to compare continuous variables. Significance was set at p<0·05. We constructed multilevel logistic regression models to adjust for the differences in mortality rates between countries.Findings: We included 46 539 patients, of whom 1855 (4%) died before hospital discharge. 3599 (8%) patients were admitted to critical care after surgery with a median length of stay of 1·2 days (IQR 0·9–3·6). 1358 (73%) patients who died were not admitted to critical care at any stage after surgery. Crude mortality rates varied widely between countries (from 1·2% [95% CI 0·0–3·0] for Iceland to 21·5% [16·9–26·2] for Latvia). After adjustment for confounding variables, important differences remained between countries when compared with the UK, the country with the largest dataset (OR range from 0·44 [95% CI 0·19 1·05; p=0·06] for Finland to 6·92 [2·37–20·27; p=0·0004] for Poland).Interpretation: The mortality rate for patients undergoing inpatient non-cardiac surgery was higher than anticipated. Variations in mortality between countries suggest the need for national and international strategies to improve care for this group of patients.Funding: European Society of Intensive Care Medicine, European Society of Anaesthesiology