60 research outputs found
Albendazole versus Praziquantel in the Treatment of Neurocysticercosis: A Meta-analysis of Comparative Trials
- Author
- A Carpio
- AC White Jr.
- AL Willingham III
- B Miller
- D Moher
- Dimitrios K. Matthaiou
- Eleni S. Adamidi
- Georgios Panos
- H Jung
- HH Garcia
- HH Garcia
- Hélène Carabin
- J Sotelo
- J Sotelo
- J Sotelo
- JH Noble Jr.
- JP Higgins
- KS Khan
- M Cruz
- M Egger
- Matthew E. Falagas
- ML Vazquez
- MT Medina
- MW Hawk
- N Mantel
- OH Del Brutto
- OH Del Brutto
- OM Takayanagui
- OM Takayanagui
- PR Bittencourt
- PR Bittencourt
- R DerSimonian
- R Kraft
- R Rangel
- RK Garg
- T Corona
- WD Dachman
- WX Shandera
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2008
- Field of study
Neurocysticercosis is a parasitic disease caused by the pork tapeworm, Taenia solium, when the larval form of the parasite lodges in the central nervous system. This disease is most commonly found among members of agricultural societies with poor sanitary conditions and economies based on breeding livestock (especially pigs) with low hygiene standards. It is a disease with long history in humans, and the usual therapeutic intervention was surgery until the development of antiparasitic cysticidal agents, the most common being praziquantel and albendazole. T. solium infection can take many different forms in humans, but we concentrated on parenchymal neurocysticercosis with viable cysts. A consensus statement by a panel of experts on the subject supports the use of antiparasitic treatment, but does not indicate either albendazole or praziquantel as the drug of choice for this type of neurocysticercosis, because data from single relevant clinical trials are not conclusive. We conducted a meta-analysis to further evaluate the comparative effectiveness and safety of albendazole and praziquantel for this particular type of neurocysticercosis. The outcomes of our meta-analysis suggest that albendazole is more effective than praziquantel in controlling seizures in affected patients and in leading to the total disappearance of cysts and subsequently cure of patients with neurocysticercosis
Approaches in biotechnological applications of natural polymers
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- Publication venue
- 'American Institute of Mathematical Sciences (AIMS)'
- Publication date
- 01/01/2016
- Field of study
Natural polymers, such as gums and mucilage, are biocompatible, cheap, easily available and non-toxic materials of native origin. These polymers are increasingly preferred over synthetic materials for industrial applications due to their intrinsic properties, as well as they are considered alternative sources of raw materials since they present characteristics of sustainability, biodegradability and biosafety. As definition, gums and mucilages are polysaccharides or complex carbohydrates consisting of one or more monosaccharides or their derivatives linked in bewildering variety of linkages and structures. Natural gums are considered polysaccharides naturally occurring in varieties of plant seeds and exudates, tree or shrub exudates, seaweed extracts, fungi, bacteria, and animal sources. Water-soluble gums, also known as hydrocolloids, are considered exudates and are pathological products; therefore, they do not form a part of cell wall. On the other hand, mucilages are part of cell and physiological products. It is important to highlight that gums represent the largest amounts of polymer materials derived from plants. Gums have enormously large and broad applications in both food and non-food industries, being commonly used as thickening, binding, emulsifying, suspending, stabilizing agents and matrices for drug release in pharmaceutical and cosmetic industries. In the food industry, their gelling properties and the ability to mold edible films and coatings are extensively studied. The use of gums depends on the intrinsic properties that they provide, often at costs below those of synthetic polymers. For upgrading the value of gums, they are being processed into various forms, including the most recent nanomaterials, for various biotechnological applications. Thus, the main natural polymers including galactomannans, cellulose, chitin, agar, carrageenan, alginate, cashew gum, pectin and starch, in addition to the current researches about them are reviewed in this article.. }To the Conselho Nacional de Desenvolvimento Cientfíico e Tecnológico (CNPq) for fellowships (LCBBC and MGCC) and the Coordenação de Aperfeiçoamento de Pessoal de Nvíel Superior (CAPES) (PBSA). This study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit, the Project RECI/BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462) and COMPETE 2020 (POCI-01-0145-FEDER-006684) (JAT)
Consensus guidelines for the use and interpretation of angiogenesis assays
- Author
- A Adini
- A Anisimov
- A Aspelund
- A Bikfalvi
- A Bouchet
- A Caporali
- A Fantin
- A Folch
- A Fraccaroli
- A Grutzkau
- A Haeger
- A Hayer
- A Helisch
- A Hruscha
- A Johns
- A Khademhosseini
- A Laude
- A Moldobaeva
- A Ny
- A Otani
- A Passaniti
- A Poltorak
- A Reade
- A Rossi
- A Sadanandam
- A Sakaue-Sawano
- A Scarpa
- A Scott
- A Stahl
- A Stahl
- A Stahl
- A Vargas
- A Vargas
- A Warth
- A Weiss
- A Weiss
- A Weiss
- A Zumsteg
- AA Hellingman
- AA Keskinov
- AA Nazarov
- AC Aplin
- AC Aplin
- AC Newman
- AC Tufan
- Adrian L. Harris
- AE Birsner
- AF Alghanem
- AF Orozco
- Agnes Noel
- AH Rizvi
- AJ Bastiaansen
- AJ Bastiaansen
- AJ Donato
- Alfred C. Aplin
- AM Cimpean
- AM Cimpean
- AM Ochsenbein
- Amber N. Stratman
- AN Stratman
- AN Stratman
- AN Stratman
- AN Stratman
- AN Stratman
- AN Stratman
- Anca M. Cimpean
- Andreas Bikfalvi
- Andrew C. Dudley
- Andrey Anisimov
- Anna Dimberg
- Anna M. Randi
- Anna-Karin Olsson
- AO Dokun
- AO Dokun
- AO Smith
- AQ Reuwer
- Arjan W. Griffioen
- AS Harney
- AV Gore
- AW Griffioen
- AW Griffioen
- AW Griffioen
- AW Griffioen
- AW Griffioen
- AY Nossent
- B Blouw
- B Garmy-Susini
- B Huang
- B St Croix
- B Uzzan
- Bahar Yetkin-Arik
- Barbara C. Böck
- Bart Ghesquière
- Bertan Cakir
- BH Annex
- BJ Vakoc
- BL Roman
- BM Hogan
- BM Kenyon
- BM Weinstein
- BM Weinstein
- BP Dranka
- Brant M. Weinstein
- Brenda R. Kwak
- C Abe
- C Bais
- C Betz
- C D’Souza-Schorey
- C Gentile
- C Korn
- C Monaco
- C Navarro-Requena
- C Poelma
- C Sarkar
- C Secondini
- C Stockmann
- C Viallard
- CA Bichsel
- CA Fernandez
- CA Staton
- CB Kimmel
- CB Moens
- CD Sarsons
- CF Buchanan
- Christopher C. W. Hughes
- CM Clavel
- CM Clavel
- CM Svensson
- CP Dagg
- CT Farrar
- CT Guy
- Curzio Ruegg
- CV Crosby
- CW Chiu
- D Boulate
- D Butler
- D Chalothorn
- D Fukumura
- D Fukumura
- D Fukumura
- D Gau
- D Hanahan
- D Hanahan
- D Hanahan
- D Huh
- D Kardamakis
- D Ribatti
- D Ribatti
- D Ribatti
- D Ribatti
- D Ribatti
- D Stibal
- D Thomas
- D Verdegem
- DA Berk
- DA Ingram
- DA MacDonald
- Dai Fukumura
- Daniel Castranova
- David O. Bates
- DC Duffy
- DC West
- DG DeNardo
- DH Ausprunk
- DH Ausprunk
- DH Nguyen
- DM Roth
- DO Croci
- DO Traktuev
- Domenico Ribatti
- DP Kodack
- DR Enis
- DR Senger
- DS Dohle
- DS Friedman
- DT Nguyen
- DTT Phan
- DY Stainier
- E Akbari
- E Allen
- E Berthier
- E Boscolo
- E Brown
- E Debefve
- E Morgan
- E Passalidou
- E Paunescu
- E Raymond
- E Rooijen van
- E Stabile
- E Wienholds
- E Zudaire
- EA Kleibeuker
- EA Kuczynski
- EA Pierce
- EB Brown
- ED Perryn
- EI Deryugina
- EI Deryugina
- EJ Huijbers
- EJ Yeo
- EK Sackmann
- Elisabeth Kuczynski
- Elizabeth Allen
- EY Lin
- EY Lin
- EY Lin
- EY Lin
- F Bussolino
- F Denizot
- F Hillen
- F Kuonen
- F Pezzella
- F Pezzella
- F Piffaretti
- F Pisati
- F Soulet
- F Soulet
- F Winkler
- F Yuan
- F Yuan
- Federico Bussolino
- FO Kok
- G Alexandrakis
- G Benton
- G Bergers
- G Bergers
- G Bergers
- G Bergers
- G Cheng
- G Christofori
- G Costa
- G Degenfeld von
- G Gruionu
- G Helmlinger
- G Hendrikx
- G Lorusso
- G Martano
- G Seano
- G Serini
- G Solinas
- G Tang
- GA Truskey
- Gabriel A. Rabinovich
- Gabriele Bergers
- GE Davis
- George Coukos
- George E. Davis
- GH Algire
- GJ Patti
- GK Varshney
- GK Varshney
- GM Birdsey
- GM Whitesides
- GR Martin
- GT Motz
- H Gerhardt
- H Huang
- H Lee
- H Naito
- H Ozaki
- H Xin
- Hellmut G. Augustin
- HF Clark
- HG Augustin-Voss
- HK Kleinman
- HM Jung
- HM Jung
- HM Shapiro
- Hong Xin
- HS Jeong
- HS Jeong
- Hynda K. Kleinmann
- I Ahmet
- I Keklikoglou
- I Kholova
- I Martinez-Corral
- I Masaki
- I Mattsby-Baltzer
- I Moreno-Jimenez
- IF Tannock
- IK Zervantonakis
- IK Zervantonakis
- IL Weissman
- IM Aspalter
- Ingeborg Klaassen
- International Chicken Genome Sequencing C
- IP Torres Filho
- IW Tattersal
- J Borges
- J Chen
- J Folkman
- J Folkman
- J Folkman
- J Folkman
- J Hoarau-Vechot
- J Kalucka
- J Laurent
- J Laurent
- J LeCouter
- J Loegl
- J Muppidi
- J Nissanov
- J Nurro
- J Patel
- J Sandison
- J Torres-Vazquez
- J Waltenberger
- J Wilting
- J Zhang
- J Zhou
- JA Nagy
- JA Villefranc
- JA Villefranc
- JA Yu
- Jan Kitajewski
- JB Wyckoff
- JC Wigle
- JC Yao
- JE Lahteenvuo
- Jeffrey W. Pollard
- JH Gao
- JH Harmey
- JI Lundin
- Jimmy Stalin
- JJ Belch
- JJ Sheu
- JK Patel
- JL Lucitti
- JM Buescher
- JM Herbert
- JM Melero-Martin
- JM Melero-Martin
- JM Melero-Martin
- Joanna Kalucka
- Johannes Waltenberger
- Jonathan W. Song
- Joyce Bischoff
- JP Cooke
- JP Nolan
- JP Sleeman
- JQ Yu
- JR Beijnum van
- JR Beijnum van
- JR Beijnum van
- JR Beijnum van
- JR Beijnum van
- JR Beijnum van
- JR Beijnum van
- JR Neely
- JS Miller
- JS Schechner
- JS Silvestre
- Juan M. Melero-Martin
- Judy R. van Beijnum
- Jussi Nurro
- JW Baish
- JW Baish
- JW Song
- JW Song
- JW Song
- JY Perentes
- K Bock De
- K Hida
- K Inagaki
- K Jung
- K Kawakami
- K Lu
- K Norrby
- K Yaniv
- K Zhi
- K-T Kang
- Kari Alitalo
- KE Bogt van der
- KH Wong
- KJ Gotink
- KM Argraves
- KM Chrobak
- KM Connor
- KM Downs
- KM Downs
- KM Downs
- KM Kwan
- KM Malinda
- KM Malinda
- KM Marien
- KM Shaw
- Koen Marien
- Kristian Pietras
- KS Samkoe
- KS Samkoe
- KT Kang
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- L Dumartin
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- L Gambardella
- L Guedez
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- L Huang
- L Jakobsson
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- L Nebuloni
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- L Schaad
- LA Herzenberg
- Lance L. Munn
- LB Rivera
- LB Rivera
- LC Hamming
- LE Jao
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- LE Smith
- LI Shlush
- LK Chang
- LL Bischel
- LM Ebert
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- Lois E. H. Smith
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- M Baker
- M Bani
- M Bulkowska
- M Chen
- M Chiba
- M Dellian
- M Fujita
- M Garcia-Caballero
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- M Jost
- M Kamei
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- M Mura
- M Nguyen
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- Valentin Djonov
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- YH Hsu
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- YR Cha
- Z Raval
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
The formation of new blood vessels, or angiogenesis, is a complex process that plays important roles in growth and development, tissue and organ regeneration, as well as numerous pathological conditions. Angiogenesis undergoes multiple discrete steps that can be individually evaluated and quantified by a large number of bioassays. These independent assessments hold advantages but also have limitations. This article describes in vivo, ex vivo, and in vitro bioassays that are available for the evaluation of angiogenesis and highlights critical aspects that are relevant for their execution and proper interpretation. As such, this collaborative work is the first edition of consensus guidelines on angiogenesis bioassays to serve for current and future reference
Multi-messenger observations of a binary neutron star merger
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- Observat Toros Transient Robotic
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- Palmerio JT
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- Pan Howard
- Pan Huang-Wei
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- Pan-STARRS
- Pandey SB
- Pandya H
- Paneque D
- Pang B
- Pang PTH
- Pankova DV
- Pankow C
- Pannarale F
- Pant BC
- Panter M
- Paoletti F
- Paoletti F
- Paoli A
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- Parra A
- Parsons RD
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- Passaquieti R
- Passuello D
- Pastorello A
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- Pearlstone BL
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- Peixoto CJ Todero
- Pekeur NW
- Pekowsky L
- Pelayo R
- Pele A
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- Pelletier G
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- Penn S
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- Piccinni OJ
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- Piergiovanni F
- Pierog T
- Pierro V
- Pignata G
- Pike S
- Pilia M
- Pillant G
- Pimenta M
- Pinard L
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- Pinto IM
- Piotrowski LW
- Piran T
- Piran T
- Piranomonte S
- Pirello M
- Piro AL
- Piro L
- Piron F
- Pirronello V
- Pisanu T
- Pita S
- Pitkin M
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- Podesta RC
- Podsiadlowski P
- Poe M
- Poggiani R
- Poh J
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- Pollmann A Obertacke
- Poolakkil S
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- Prokoph H
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- Pulone L
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- Reimer A
- Reimer O
- Reimer O
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- Relethford B
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- Ren Z
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- Renzi V
- Reposeur T
- Resconi E
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- Reyes R De Los
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- Rosell A Carnero
- Rosenberg M
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- Rumyantsev VV
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- Sadler EM
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- Saffe C
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- Sahakian V
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- Sakellariadou M
- Sako M
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- Salamida F
- Salazar H
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- Salvadori I
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- Samtleben DFE
- Sanchez B
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- Sanchez LE
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- Shimomukai R
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- Shoemaker DH
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- Siemens X
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- Slagmolen BJJ
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- Stratta G
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- Strunk A
- Stubbs CW
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- Sullivan GW
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- Summerscales TZ
- Sun L
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- Tyurina NV
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- Ulrich R
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- Publication venue
- 'American Astronomical Society'
- Publication date
- 01/01/2017
- Field of study
On 2017 August 17 a binary neutron star coalescence candidate (later designated GW170817) with merger time 12:41:04 UTC was observed through gravitational waves by the Advanced LIGO and Advanced Virgo detectors. The Fermi Gamma-ray Burst Monitor independently detected a gamma-ray burst (GRB 170817A) with a time delay of ~1.7 s with respect to the merger time. From the gravitational-wave signal, the source was initially localized to a sky region of 31 deg2 at a luminosity distance of 40+8-8 Mpc and with component masses consistent with neutron stars. The component masses were later measured to be in the range 0.86 to 2.26 Mo. An extensive observing campaign was launched across the electromagnetic spectrum leading to the discovery of a bright optical transient (SSS17a, now with the IAU identification of AT 2017gfo) in NGC 4993 (at ~40 Mpc) less than 11 hours after the merger by the One- Meter, Two Hemisphere (1M2H) team using the 1 m Swope Telescope. The optical transient was independently detected by multiple teams within an hour. Subsequent observations targeted the object and its environment. Early ultraviolet observations revealed a blue transient that faded within 48 hours. Optical and infrared observations showed a redward evolution over ~10 days. Following early non-detections, X-ray and radio emission were discovered at the transient’s position ~9 and ~16 days, respectively, after the merger. Both the X-ray and radio emission likely arise from a physical process that is distinct from the one that generates the UV/optical/near-infrared emission. No ultra-high-energy gamma-rays and no neutrino candidates consistent with the source were found in follow-up searches. These observations support the hypothesis that GW170817 was produced by the merger of two neutron stars in NGC4993 followed by a short gamma-ray burst (GRB 170817A) and a kilonova/macronova powered by the radioactive decay of r-process nuclei synthesized in the ejecta
Laparoscopy in management of appendicitis in high-, middle-, and low-income countries: a multicenter, prospective, cohort study.
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- Abantanga F
- Abbas M
- Abbo O
- Abd El Galeel A
- Abd El Hameed OS
- Abd El Hamid N
- Abd El Salam Y
- Abd El Slam M
- Abd El-Salam F
- Abd Elrasoul Y
- Abd-Elrasoul Y
- Abdallah E
- Abdel-Wahab NYE
- AbdelFattah I
- Abdelgelil A
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- Abdelkader M
- Abdelkareem A
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- Abdulgawad M
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
BACKGROUND: Appendicitis is the most common abdominal surgical emergency worldwide. Differences between high- and low-income settings in the availability of laparoscopic appendectomy, alternative management choices, and outcomes are poorly described. The aim was to identify variation in surgical management and outcomes of appendicitis within low-, middle-, and high-Human Development Index (HDI) countries worldwide. METHODS: This is a multicenter, international prospective cohort study. Consecutive sampling of patients undergoing emergency appendectomy over 6 months was conducted. Follow-up lasted 30 days. RESULTS: 4546 patients from 52 countries underwent appendectomy (2499 high-, 1540 middle-, and 507 low-HDI groups). Surgical site infection (SSI) rates were higher in low-HDI (OR 2.57, 95% CI 1.33-4.99, p = 0.005) but not middle-HDI countries (OR 1.38, 95% CI 0.76-2.52, p = 0.291), compared with high-HDI countries after adjustment. A laparoscopic approach was common in high-HDI countries (1693/2499, 67.7%), but infrequent in low-HDI (41/507, 8.1%) and middle-HDI (132/1540, 8.6%) groups. After accounting for case-mix, laparoscopy was still associated with fewer overall complications (OR 0.55, 95% CI 0.42-0.71, p < 0.001) and SSIs (OR 0.22, 95% CI 0.14-0.33, p < 0.001). In propensity-score matched groups within low-/middle-HDI countries, laparoscopy was still associated with fewer overall complications (OR 0.23 95% CI 0.11-0.44) and SSI (OR 0.21 95% CI 0.09-0.45). CONCLUSION: A laparoscopic approach is associated with better outcomes and availability appears to differ by country HDI. Despite the profound clinical, operational, and financial barriers to its widespread introduction, laparoscopy could significantly improve outcomes for patients in low-resource environments. TRIAL REGISTRATION: NCT02179112
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
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- A Agafina
- A Akyea-Djamson
- A Alan
- A Alfieri
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- Zieve F
- Zineldine A.
- Zirlik A
- Zucchetti C
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
Search for strongly interacting massive particles generating trackless jets in proton-proton collisions at s = 13 TeV
- Author
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- Österberg K
- Özçelik Ö
- Široký J
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
A search for dark matter in the form of strongly interacting massive particles (SIMPs) using the CMS detector at the LHC is presented. The SIMPs would be produced in pairs that manifest themselves as pairs of jets without tracks. The energy fraction of jets carried by charged particles is used as a key discriminator to suppress efficiently the large multijet background, and the remaining background is estimated directly from data. The search is performed using proton-proton collision data corresponding to an integrated luminosity of 16.1 fb - 1 , collected with the CMS detector in 2016. No significant excess of events is observed above the expected background. For the simplified dark matter model under consideration, SIMPs with masses up to 100 GeV are excluded and further sensitivity is explored towards higher masses
Evidence for Top Quark Production in Nucleus-Nucleus Collisions
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- Zuolo D
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- Álvarez Fernández A
- Özçelik Ö
- Publication venue
- Publication date
- 01/01/2019
- Field of study
Peer reviewe
Observation of the B-s(0) -> X(3872)phi Decay
- Author
- Aarrestad TK
- Aarup Petersen H
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abercrombie D
- Acharya H
- Acosta D
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- Publication venue
- Publication date
- 01/01/2020
- Field of study
Using a data sample of proton-proton collisions at root s = 13 TeV, corresponding to an integrated luminosity of 140 fb(-1) collected by the CMS experiment in 2016-2018, the B-s(0) -> X(3872)phi decay is observed. Decays into J/psi pi(+)pi(-) and K+K- are used to reconstruct, respectively, the X(3872) and phi. The ratio of the product of branching fractions B[B-s(0) -> X(3872)phi]B[X(3872) -> J/psi pi(+)pi(-)] to the product B[B-s(0) ->psi(2S)phi]B[psi(2S) -> J/psi pi(+)pi(-)] is measured to be [2.21 +/- 0.29(stat) +/- 0.17(syst)]%. The ratio B[B-s(0) -> X(3872)phi]/B[B-0 -> X(3872)K-0] is found to be consistent with one, while the ratio B[B-s(0) -> X(3872)phi]/B[B+-> X(3872)K+] is two times smaller. This suggests a difference in the production dynamics of the X(3872) in B-0 and B(0)s meson decays compared to B+. The reported observation may shed new light on the nature of the X(3872) particle.Peer reviewe
Pooled analysis of WHO Surgical Safety Checklist use and mortality after emergency laparotomy
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- Aaniana K
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- Lopez C
- Lopez M
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- Lorenzon L
- Lossius WJ
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- Lytras D
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- Ma J
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- Macchitella Y
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- Macdonald A
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- Maceviciute K
- Macfarlane A
- Machaca M
- Machain Vega GM
- Machain Vega GM
- Maciejec L
- Madiba T
- Madkor MH
- Madrid Barrientos LA
- Maffioli A
- Maffioli A
- Magdy A
- Magdy B
- Magdy E
- Magdy H
- Magdy M
- Magdy S
- Magee C
- Maghrabi A
- Maghrabi AA
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- Mahanty S
- Maharaj G
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- Mahmoud B
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- Mahmoud MI
- Mahmoud S
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- Maison K
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- Mamdouh E
- Mamdouh R
- Manatakis DK
- Manchego Bautista AC
- Manchego Bautista AC
- Manfreda S
- Mangan C
- Mangan C
- Mangiapane M
- Manipal CE
- Maniscalco A
- Mann T
- Mannu GS
- Mano MJB
- Manrique Sila G
- Manrique Sila GC
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- Mansor EY
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- Marinkovic B
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- Marroquin Rodriguez DE
- Marshall DC
- Martian B-V
- Martin A
- Mas R
- Mason C
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- Mathew SW
- Matos-Puig R
- Mattar O
- Matter SM
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- Mendoza I
- Menegussi J
- Mensah E
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- Mentula P
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- Merlini D
- Merlo MS
- Mesbah N
- Meshref A
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- Metwally MM
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- Mihaljevic AL
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- Minguez Garcia J
- Minguez G
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- Mircea H
- Mirghani D
- Mironescu A
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- Mironescu AS
- Mironescu AS
- Mirza A
- Mirza S
- Mistry A
- Mitrasinovic S
- Mitroudi M
- Mitroudis N
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- Miyarde Leon A
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- Moaty M
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- Modolo MM
- Moe TT
- Mogan YP
- Moghazy ME
- Mohamed A
- Mohamed A
- Mohamed AM
- Mohamed AR
- Mohamed B
- Mohamed F
- Mohamed I
- Mohamed M
- Mohamed MA
- Mohamed MAEH
- Mohamed MM
- Mohamed O
- Mohamed SR
- Mohameden A
- Mohammad A
- Mohammad A
- Mohammed A
- Mohammed A
- Mohammed AR
- Mohammed H
- Mohammed MM
- Mohammed MMH
- Mohammed S
- Mohan H
- Mohan M
- Mohan M
- Mok YT
- Mokhtar A
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- Monteleone M
- Monteleone M
- Montes I
- Montes I
- Montoya Botero JA
- Montrimaite M
- Montrimaite M
- Moodley Y
- Moore R
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- Mora JJV
- Morales C
- Morandi E
- Moreira G
- Moreno SC
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- Morshedy EM
- Morsi A
- Morsi M
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- Morton R
- Mosad A
- Mosalum O
- Mostafa HA
- Mostafa M
- Mostafa M
- Mousa M
- Moussa O
- Moustafa A
- Mouttalib S
- Mowafy B
- Mphatsoe AM
- Mshelbwala P
- Msiska N
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- Muktar U
- Mukuzunga C
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- Munipalle PC
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- Musowoya J
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- Mutlu V
- Muzio E
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- Nanthakumaran S
- Napolitano L
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- Naqvi SA
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- Naranjo Aristizaibal FA
- Narayanan R
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- Nashidengo P
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- Nataraja R
- Natili A
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- Nazir M
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- Ndlovu SR
- Ndwambi P
- Negida A
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- Nepogodiev D
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- Nestorovic M
- Nevieraite V
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- Ngwa TE
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- Njokanma I
- Nnajiuba H
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- Nofal E
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- Noukpozounkou B
- Novak A
- Nowers J
- Nsengimana VJP
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- Nurqistan HD
- Nwabuoku E
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- Palomino Castillo VD
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- Papaskarlatos I-A
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- Pena L
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- Perez Velasquez CI
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- Pertersen Servin GR
- Pesenti G
- Petrikenas S
- Peycelon M
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- Pezas T
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- Pezelj N
- Phillips N
- Picardo A
- Picciariello A
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- Pinkney T
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- Prabhudesai A
- Pranevicius R
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- Preckailaite E
- Primavesi F
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- Pronin S
- Prudhomme T
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- Punja V
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- Qureshi AU
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- Ramarez Cabrera CC
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- Samaraweera DI
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- Sandoval Barrantes AM
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- Sarafilovic H
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- Schivo D
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- Schuetz T
- Schultz JK
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- Scott M
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- Semeda N
- Semiz A
- Sena-Ruiz F
- Senanayake KJ
- Senanayake WSMKJ
- Setiawan J
- Seto DM
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- Sfougaris D
- Sgroi G
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- Shachykava T
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- Shahbaz AR
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- Smedley A
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- Snyder E
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- Sobnach S
- Sodde P
- Soeselo DA
- Sokratous A
- Solaini L
- Solar Garcia L
- Solar Garcia L
- Soldevila-Verdeguer C
- Soley R
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- Soliman A
- Soliman AR
- Soliman N
- Soliman NA
- Soliman S
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- Sollazzo V
- Soltani N
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- Soulou V
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- Sproule L
- Spurr M
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- Srinivasan R
- Sriram A
- Sroor F
- Sruogiene EZ
- Staerkle RF
- Starr N
- Stasinou T
- Steccanella F
- Stefanopoulos A
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- Stewart D
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- Suarez AAB
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- Suleiman SI
- Summerour V
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- Sundstrom SM
- Suresh S
- Sutandi N
- Sutanto EPR
- Sutton P
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- Suyadi A
- Swann J
- Swaroop M
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- Syibrah KZ
- Sykes M
- Szczap A
- Szeto CCL
- Szeto KJ-Y
- Tabiri S
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- Tabiri S
- Tabiri S
- Tabiri S
- Tackie E
- Taddei A
- Tade A
- Tafazal H
- Taha EMS
- Tahboub H
- Taher AA
- Taher M
- Taher MM
- Taieb C
- Taiwo A
- Taiwo O
- Taiwo O
- Talaat M
- Tale F
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- Talukder S
- Talukder S
- Talving P
- Talving P
- Tammam A
- Tan C
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- Tan CY
- Tan JJ
- Tan JK
- Tan KSK
- Tan RCK
- Tan YK
- Tan YW
- Tanase A
- Tanase A
- Tang A
- Tang L
- Tani SI
- Tansoker I
- Tarek A
- Tarek A
- Tarek D
- Targa S
- Tariq S
- Tata MD
- Tatagiba LS
- Tawfik BA
- Tawfik G
- Tawfik G
- Taylor F
- Teasdale E
- Teasdale E
- Teasdale E
- Teasdale E
- Tedeschi U
- Tedjaatmadja C
- Telfah MM
- Tembo T
- Temoche E
- Tennakoon A
- Teo SY
- Ter EZ
- Tessera G
- Teufelberger G
- Tew YY
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- Tewari S
- Th'ng F
- Thabet W
- Thalgaspitiya SPB
- Tham JC
- Thanusan V
- Tharmalingam S
- Theodosopoulos T
- Thollot A
- Thomas E
- Thomas HS
- Thompson B
- Thomson P
- Thorarinsdottir H
- Thorarinsdottir H
- Thorell A
- Thorell A
- Thorsen K
- Thurairaja R
- Tierney G
- Tilston TW
- Timothy OK
- Ting JRS
- To K
- To K
- Todd KO
- Toeema AG
- Tolba H
- Tolg C
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- Tolotra TEC
- Tomas K
- Tori SA
- Toribio Orbegozo PA
- Torrance HD
- Torrance HD
- Torres Cardozo J
- Toto OF
- Tou S
- Townsend D
- Tracy J
- Trompetto M
- Tselos A
- Tshisola SK
- Tugnoli G
- Tugnoli G
- Tun AK
- Tun M
- Tun M
- Turati L
- Turati L
- Turkustani S
- Turner M
- Turpo Espinoza K
- Turpo Espinoza K
- Tutino R
- Tverskis Z
- Tyler R
- Tyler R
- Tze RGE
- Tze RGE
- Tzikos G
- Ubhi HK
- Ubiali P
- Ugalde P
- Ukwenya Y
- Ulusahin M
- Upadhyaya V
- Upchurch E
- Urbanavicius L
- Urbina Rojas NM
- Urbonas T
- Urbonas T
- Urniezius Z
- Urniezius Z
- Usaityte A
- Uscinas L
- Utter M
- Uzabumwana N
- Vaicius A
- Valcarcel-Saldana M
- Valente Laufer LA
- Valioulis I
- Van Der Naald N
- Van Duren B
- Van Niekerk M
- Van Straten S
- Varcada M
- Vargas M
- Varkalys K
- Vartanoglu T
- Vartic M
- Vartic M
- Vasquez G
- Vasquez I
- Veen T
- Velasquez R
- Vella-Baldacchino M
- Venclauskas L
- Vendramin E
- Venskutonis D
- Venskutonis D
- Venskutonis D
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- Venugopal C
- Verbeek A
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- Vergara Mejia AG
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- Vicario E
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- Vida LC
- Vida LC
- Vilcinskas M
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- Vincent J
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- Warwick AM
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- Wold TB
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- Yahaya MT
- Yakubu M
- Yallop L
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- Yaseen TM
- Yau JD
- Yavuz MA
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- Yeang LJ
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- Yeo LS
- Yeung ENW
- Yeung MHA
- Yifieyeh A
- Yildirim R
- Yip C
- Ymeri S
- Yoganathan P
- Yolcu S
- Yong CO
- Yong GL
- Younis A
- Youssef D
- Youssef H
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- Youssif JH
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- Yusufali T
- Zaa'treh R
- Zachariades D-C
- Zadoroznas A
- Zahran D
- Zakaria E
- Zakaria M
- Zakaria Y
- Zaki A
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- Zamarin K
- Zammit S
- Zampitis N
- Zani A
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- Zapata Ponze De Leon M
- Zapata Ponze De Leon M
- Zapata F
- Zarb C
- Zardab A
- Zegarra S
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- Zelada Alvarez II
- Zerihun AB
- Zeta Solis LA
- Zhang Z
- Zheng F
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- Zimmermann EF
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- Publication venue
- Publication date
- 15/10/2018
- Field of study
Background The World Health Organization (WHO) Surgical Safety Checklist has fostered safe practice for 10 years, yet its place in emergency surgery has not been assessed on a global scale. The aim of this study was to evaluate reported checklist use in emergency settings and examine the relationship with perioperative mortality in patients who had emergency laparotomy. Methods In two multinational cohort studies, adults undergoing emergency laparotomy were compared with those having elective gastrointestinal surgery. Relationships between reported checklist use and mortality were determined using multivariable logistic regression and bootstrapped simulation. Results Of 12 296 patients included from 76 countries, 4843 underwent emergency laparotomy. After adjusting for patient and disease factors, checklist use before emergency laparotomy was more common in countries with a high Human Development Index (HDI) (2455 of 2741, 89.6 per cent) compared with that in countries with a middle (753 of 1242, 60.6 per cent; odds ratio (OR) 0.17, 95 per cent c.i. 0.14 to 0.21, P <0001) or low (363 of 860, 422 per cent; OR 008, 007 to 010, P <0.001) HDI. Checklist use was less common in elective surgery than for emergency laparotomy in high-HDI countries (risk difference -94 (95 per cent c.i. -11.9 to -6.9) per cent; P <0001), but the relationship was reversed in low-HDI countries (+121 (+7.0 to +173) per cent; P <0001). In multivariable models, checklist use was associated with a lower 30-day perioperative mortality (OR 0.60, 0.50 to 073; P <0.001). The greatest absolute benefit was seen for emergency surgery in low- and middle-HDI countries. Conclusion Checklist use in emergency laparotomy was associated with a significantly lower perioperative mortality rate. Checklist use in low-HDI countries was half that in high-HDI countries.Peer reviewe
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