90 research outputs found
The magnitude of syphilis: from prevalence to vertical transmission
- Author
- Publication venue
- Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
- Publication date
- 01/01/2017
- Field of study
Introduction: In 2013, the World Health Organization (WHO) reported that 1.9 million pregnant women were infected with syphilis worldwide, of which 66.5% had adverse fetal effects in cases of untreated syphilis. Congenital syphilis contributes significantly to infant mortality, accounting for 305,000 perinatal deaths worldwide annually. Aim: To estimate the prevalence of syphilis in parturients, the incidence of congenital syphilis and the vertical transmission rate. Material and methods: a cross-sectional study with data collected from 2041 parturients who had undergone treatment between 2012 and 2014 in the maternity section of the Pedro Ernesto Hospital of the State University of Rio de Janeiro, in the metropolitan area of Rio de Janeiro. The inclusion criterion was positive VDRL and treponemal test in a hospital environment. Results: the prevalence of syphilis in pregnant women was 4.1% in 2012, 3.1% in 2013 and 5% in 2014, with official reporting of 15.6%, 25.0% and 48.1%, respectively. The incidence of congenital syphilis (CS) was 22/1,000 in live births (LB) in 2012; 17/1,000 LB in 2013 and 44.8/1,000 LB in 2014. CS underreporting during the period was 6.7%. Vertical transmission occurred in 65.8% of infants from infected mothers. It was concluded that, in 34.6% of the CS cases, maternal VDRL titers were = 1/4. Conclusion: Results demonstrate the magnitude of the disease, fragility of the reporting system in the assessment of the actual prevalence, impact on perinatal outcomes, and they are a warning about the real situation of syphilis, which is still underestimated in the State
Modeled O 2 nightglow distributions in the Venusian atmosphere
- Author
- Amanda S. Brecht
- Badger
- Bailey
- Bougher
- Bougher
- Bougher
- Bougher
- Bougher
- Brecht
- Campbell
- Clancy
- Connes
- Cox
- Crisp
- Findlay
- Gagné
- García Muñoz
- Gronoff
- Gérard
- Gérard
- Gérard
- Gérard
- Gérard
- Gérard
- Hoshino
- Hueso
- Kimberly Strong
- Krasnopolsky
- Krasnopolsky
- Lafferty
- Leiss
- Marie-Ève Gagné
- Melo
- Migliorini
- Nair
- Ohtsuki
- Ohtsuki
- Patzold
- Piccioni
- Reed
- Royer
- Schofield
- Shakun
- Slanger
- Slanger
- Slanger
- Smith
- Smith
- Soret
- Stella M. L. Melo
- Stephen W. Bougher
- Tellmann
- Zhang
- Publication venue
- 'American Geophysical Union (AGU)'
- Publication date
- 01/12/2012
- Field of study
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/96410/1/jgre3128.pd
Prediction of Antibacterial Activity from Physicochemical Properties of Antimicrobial Peptides
- Author
- A Giacometti
- A Giacometti
- A Peschel
- A Tossi
- B Lugtenberg
- C Matos
- C Subbalakshmi
- CL Friedrich
- CS Alves
- D Bray
- D Tran
- E Badosa
- E Jawetz
- Eduard Bardají
- FR Blattner
- G Sessa
- G van den Bogaart
- H Leontiadou
- HS Sader
- HW Huang
- J Blazyk
- JE Cronan
- JF Szoka
- KA Brogden
- L Stella
- LD Mayer
- Lídia Feliu
- M Castle
- M Loferer-Krossbacher
- Manuel N. Melo
- Marta Planas
- Miguel A. R. B. Castanho
- MN Melo
- MN Melo
- MR Yeaman
- NC Santos
- R Ferre
- R Ferre
- R Milo
- R Rosen
- Rafael Ferre
- Rizwan Hasan Khan
- S Pistolesi
- S Sundararaj
- SE Blondelle
- SH White
- SW Chiu
- T Kaneshiro
- T Pott
- W Nernst
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Consensus is gathering that antimicrobial peptides that exert their antibacterial action at the membrane level must reach a local concentration threshold to become active. Studies of peptide interaction with model membranes do identify such disruptive thresholds but demonstrations of the possible correlation of these with the in vivo onset of activity have only recently been proposed. In addition, such thresholds observed in model membranes occur at local peptide concentrations close to full membrane coverage. In this work we fully develop an interaction model of antimicrobial peptides with biological membranes; by exploring the consequences of the underlying partition formalism we arrive at a relationship that provides antibacterial activity prediction from two biophysical parameters: the affinity of the peptide to the membrane and the critical bound peptide to lipid ratio. A straightforward and robust method to implement this relationship, with potential application to high-throughput screening approaches, is presented and tested. In addition, disruptive thresholds in model membranes and the onset of antibacterial peptide activity are shown to occur over the same range of locally bound peptide concentrations (10 to 100 mM), which conciliates the two types of observations
The magnitude of syphilis: from prevalence to vertical transmission
- Author
- Alexandre J. B. Trajano
- Araújo MA
- Bianca De Melo Araújo
- Cambricoli F
- Cavalcante MS
- Denise L. M. Monteiro
- Domingues RM
- Domingues RM
- Domingues RM
- Domingues RM
- Flavio Monteiro de Souza
- Klausner JD
- Kuo M
- Kupek E
- Lomotey CJ
- Luciane Rodrigues Pedreira de Cerqueira
- McClure EM
- Miranda AE
- Nascimento MI
- Newman L
- Nonato SM
- Nádia C. P. Rodrigues
- Stella R. Taquette
- Szwarcwald CL
- Taylor MM
- Thomas DD
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Cyclodextrin Complexes of Reduced Bromonoscapine in Guar Gum Microspheres Enhance Colonic Drug Delivery
- Author
- Amidon G. L.
- Anand O.
- Aneja R.
- Banchero M.
- Banerjee A.
- Bharat Baruah
- Case D. A.
- Celik S. E.
- Chatjigakis A. K.
- Chourasia M. K.
- Clayton Yates
- Crociani F.
- Darden T.
- de Melo N. F.
- Dennington R.
- Donald Hamelberg
- Esseku F.
- Fan L. F.
- Forgo P.
- Hoda A.
- Jain A.
- Jitender Madan
- Jorgensen W. L.
- Kirschner K. N.
- Kollman P. A.
- Krishnaiah Y. S.
- Krishnaiah Y. S. R.
- Lamprecht A.
- Madan J.
- Madan J.
- Madan J.
- Michelle D. Reid
- Mosmann T.
- Mulpuri Nagaraju
- Nehal Siddiqui M. D.
- Niv Y.
- Olsson B.
- Pascall B.
- Ritu Aneja
- Ryckaert J. P.
- Soares da Silva L. F.
- Stella V. J.
- Sushma R. Gundala
- Thornton J. R.
- Timothy Turner
- Trott O.
- Ungell A. L.
- Vaidya A.
- Vijay Rangari
- Wang J.
- Yang Z. R.
- Zhou J.
- Zhou J.
- Publication venue
- ScholarWorks @ Georgia State University
- Publication date
- 01/10/2014
- Field of study
Here, we report improved solubility and enhanced colonic delivery of reduced bromonoscapine (Red-Br-Nos), a cyclic ether brominated analogue of noscapine, upon encapsulation of its cyclodextrin (CD) complexes in bioresponsive guar gum microspheres (GGM). Phase−solubility analysis suggested that Red-Br-Nos complexed with β-CD and methyl-β-CD in a 1:1 stoichiometry, with a stability constant (Kc) of 2.29 × 103 M−1 and 4.27 × 103 M−1. Fourier transforms infrared spectroscopy indicated entrance of an O−CH2 or OCH3−C6H4−OCH3 moiety of Red-Br-Nos in the β-CD or methyl-β- CD cavity. Furthermore, the cage complex of Red-Br-Nos with β-CD and methyl-β-CD was validated by several spectral techniques. Rotating frame Overhauser enhancement spectroscopy revealed that the Ha proton of the OCH3−C6H4−OCH3 moiety was closer to the H5 proton of β-CD and the H3 proton of the methyl-β-CD cavity. The solubility of Red-Br-Nos in phosphate buffer saline (PBS, pH ∼ 7.4) was improved by ∼10.7-fold and ∼21.2-fold when mixed with β-CD and methyl-β-CD, respectively. This increase in solubility led to a favorable decline in the IC50 by ∼2-fold and ∼3-fold for Red-Br-Nos−β-CD-GGM and Red-Br-Nos−methyl-β-CD-GGM formulations respectively, compared to free Red-Br-Nos−β-CD and Red-Br-Nos−methyl-β-CD in human colon HT-29 cells. GGM-bearing drug complex formulations were found to be highly cytotoxic to the HT-29 cell line and further effective with simultaneous continuous release of Red-Br-Nos from microspheres. This is the first study to showing the preparation of drug-complex loaded GGMS for colon delivery of Red-Br-Nos that warrants preclinical assessment for the effective management of colon cancer
Evolução do crescimento do cafeeiro (Coffea arabica L.) irrigado e não irrigado em duas intensidades de plantio
- Author
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine
- Author
- A Boing
- A Gaspari
- A Kübler
- A Marudi
- A Matheson
- A Tridente
- A. A. Amelia
- A. Abbas
- A. Adams
- A. Agnoli
- A. Al Khulaifi
- A. Al Khulaifi
- A. Aldawood
- A. AlHussain
- A. Ali
- A. Almenyar
- A. Alrashid
- A. Alsheikhly
- A. Alves
- A. Ankuli
- A. Arbouti
- A. Armaganidis
- A. Artigas
- A. Asimakos
- A. B. Belli
- A. B. Cayci Sivri
- A. Bandyopadhyay
- A. Basu
- A. Bedova
- A. Belli
- A. Ben Souissi
- A. Ben Souissi
- A. Ben Souissi
- A. Ben Souissi
- A. Bond
- A. Borgman
- A. Borowska
- A. Boutin
- A. Boutin
- A. Boyce
- A. Braschi
- A. Budnyuk
- A. C. Rodrigues
- A. Cariou
- A. Casazza
- A. Chakraborty
- A. Cirodde
- A. Crizaldo Toledo
- A. Cudia
- A. Cuoghi
- A. D. Dubrawski
- A. Dardashti
- A. Dean
- A. Dean
- A. Delfosse
- A. Dhaliwal
- A. Dhaliwal
- A. Dobru
- A. Docherty
- A. Doronzio
- A. Douvdevani
- A. Dukoff-Gordon
- A. Durward
- A. E Van den Berg
- A. Eden
- A. Eissa
- A. Enguix-Armada
- A. Escalante
- A. Escalante
- A. Ezzamouri
- A. F. Francke
- A. F. Turgeon
- A. F. Turgeon
- A. F. Van Rootselaar
- A. F. Van Rootselaar
- A. Fayed
- A. Fernandez
- A. Fischer
- A. Fogagnolo
- A. Fuller
- A. Fuller
- A. G. Murchison
- A. G. Proudfoot
- A. Garcia
- A. Garcia-Alcantara
- A. Garcia-De la Torre
- A. Garland
- A. Garland
- A. Gaspari
- A. Ghuysen
- A. Giannini
- A. Gobatto
- A. Goloubev
- A. Grubb
- A. Gruber
- A. Gultekin
- A. H. Zwinderman
- A. Hagiwara
- A. Hana
- A. Hana
- A. Harts
- A. Hejazi
- A. Hernández-Lozano
- A. Hernández-Lozano
- A. Hovingh
- A. Huber
- A. Itani
- A. J. Groeneveld
- A. J. Hoogendijk
- A. K. Kink
- A. K. Kuzovlev
- A. K. Tashima
- A. Kapuagasi
- A. Kar
- A. Kaskovagheorgescu
- A. Kaushal
- A. Khaghani
- A. Kindawi
- A. Kleinsasser
- A. Kodaira
- A. Kutz
- A. Kuzovlev
- A. Körner
- A. L Luciani
- A. L. Lange
- A. Lepape
- A. Lesmes
- A. Lima
- A. Lima
- A. Linder
- A. Loza
- A. López Lago
- A. M. Magnuson
- A. M. Tuip-de Boer
- A. Maaoui
- A. Machado
- A. Mahrous
- A. Malamas
- A. Marinho
- A. Marinho
- A. Marinho
- A. Marinho
- A. Marinho
- A. Marinho
- A. Marinho
- A. Martins
- A. Marudi
- A. Marudi
- A. Matroud
- A. Mebazaa
- A. Mignon
- A. Min
- A. Molokhia
- A. Molokhia
- A. Molokhia
- A. Molokhia
- A. Molokhia
- A. Morelli
- A. Morris
- A. Motos
- A. N. Ahmad
- A. Nadeem
- A. Nau
- A. Neill
- A. Nyman
- A. Núñez
- A. Oglinda
- A. Omar
- A. Omar
- A. Omar
- A. Omar
- A. Orlando
- A. Osipov
- A. Ozcan
- A. O’Loughlin
- A. O’Sullivan
- A. O’Sullivan
- A. O’Sullivan
- A. P. Pagano
- A. P. Torelly
- A. Pagano
- A. Patarchi
- A. Pautova
- A. Pavli
- A. Pesenti
- A. Prekates
- A. Psirides
- A. Puerto-Morlan
- A. Puxty
- A. Pérez-Calatayud
- A. R. Robles Caballero
- A. Radford
- A. Raithatha
- A. Raithatha
- A. Raithatha
- A. Reiter
- A. Rhodes
- A. Rhodes
- A. Rhodes
- A. Riahi
- A. Riahi
- A. Riahi
- A. Riahi
- A. Riviere
- A. Riviere
- A. Riviere
- A. Robles
- A. Rogers
- A. Rousseau
- A. Roze des Ordons
- A. Ruijter
- A. Rutten
- A. S. Alsaawi
- A. S. Stieglitz
- A. Salgueiro
- A. Salgueiro
- A. Salgueiro
- A. Sarmento
- A. Sarmento
- A. Savitsky
- A. Scheirer
- A. Schiavi
- A. Seldon
- A. Sell
- A. Sen
- A. Sergeev
- A. Shabanov
- A. Shafie
- A. Shafquat
- A. Shiraishi
- A. Silva-Pinto
- A. Silva-Pinto
- A. Spassov
- A. Stella
- A. Steuber
- A. Stieglitz
- A. Stilwell
- A. Sánchez-López
- A. Sánchez-López
- A. Taha
- A. Taha
- A. Taskin
- A. Temple
- A. Tinmouth
- A. Tinmouth
- A. Torres
- A. Torres
- A. Torres
- A. Touborg Lassen
- A. Tridente
- A. Tridente
- A. Tridente
- A. Tridente
- A. Trifi
- A. Trifi
- A. Tsimogianni
- A. Turgeon
- A. Turgeon
- A. Vakalos
- A. Vakalos
- A. Vakalos
- A. Vakalos
- A. Van Assche
- A. Van Assche
- A. Varma
- A. Vassi
- A. Vercueil
- A. Vieillard-Baron
- A. Violaki
- A. Violaki
- A. Vuylsteke
- A. W. Waldmann
- A. Wald
- A. Waldmann
- A. Waldmann
- A. Webber
- A. Wheeler
- A. Yalcin
- A. Zepeda-Mendoza
- A. Zerman
- AF Donneau
- AK Güler
- AT Tesnieres
- B Adamik
- B Avard
- B. Al Raiy
- B. AlGhamdi
- B. Alhamadi
- B. Alotaibi
- B. Avard
- B. Avard
- B. Balicco
- B. Basarýk Aydogan
- B. Besen
- B. Bilgili
- B. Bilgili
- B. Borgatta
- B. Bouhemad
- B. C. Civantos
- B. Carr
- B. Civantos
- B. De Cagny
- B. De Cagny
- B. De Cagny
- B. De Cagny
- B. De Laat
- B. Delwarde
- B. Eilers
- B. François
- B. François
- B. Fyntanidou
- B. Fyntanidou
- B. Fyntanidou
- B. Goncalves
- B. Guidet
- B. J. Hunt
- B. Jeribi
- B. Jones
- B. K. Lopansri
- B. Khwannimit
- B. Khwannimit
- B. Köves
- B. Laribi
- B. Laribi
- B. Lord
- B. Loureiro
- B. López Matamala
- B. Miles
- B. Mueller
- B. Mueller
- B. Mueller
- B. Nyamaizi
- B. O. Alotabi
- B. Oliveira
- B. Oliveira
- B. Oliveira
- B. P. Scicluna
- B. Pasquet
- B. Peroni
- B. Saugel
- B. Sauneuf
- B. Shenkman
- B. Sloan
- B. Stessel
- B. Stessel
- B. Söderquist
- B. Tudor
- B. Vidal
- B. Waldum-Grevbo
- B. Wanta
- B. Xavier
- C. A. Volta
- C. Aldecoa
- C. Aldecoa
- C. Arrowsmith
- C. Ashton
- C. Battle
- C. Battle
- C. Battle
- C. Bell
- C. Bor
- C. Bor
- C. Brunborg
- C. Carvalho
- C. Chaddock
- C. Chiurazzi
- C. Choong
- C. Cobilinschi
- C. Cobilinschi
- C. Cobilinschi
- C. Cobilinschi
- C. Cohen
- C. Dalrymple
- C. De Deyne
- C. De Haro
- C. Dinter
- C. Doig
- C. Doree
- C. Downey
- C. Dridi
- C. E. Luyt
- C. Ertmer
- C. Ertmer
- C. F. Fuchs
- C. Feldmann
- C. Fenlon
- C. Fitton
- C. Fleischmann
- C. Fleischmann
- C. G. Ellis
- C. Gemelli
- C. Genbrugge
- C. Gerrard
- C. Glynos
- C. Gogos
- C. Goldfuss
- C. Goossens
- C. Gu
- C. H. Toh
- C. Haas
- C. Haas
- C. Hamilton-Davies
- C. Hawthorne
- C. Heidegger
- C. Hoermann
- C. Hoffmann
- C. Hymers
- C. Ince
- C. Ince
- C. Ince
- C. J. Hodiamont
- C. J. Kirwan
- C. J. Kirwan
- C. J. Voscopoulos
- C. J. Voscopoulos
- C. J. Voscopoulos
- C. J. Voscopoulos
- C. K. Karagiannidis
- C. Karagiannidis
- C. Karagiannidis
- C. Karnjanarachata
- C. Katsenos
- C. Kaymak
- C. Kirwan
- C. Kongkamol
- C. Koutsogiannidis
- C. Krenn
- C. Kruger
- C. L. Sprung
- C. Lee
- C. Lemaire
- C. Leon
- C. Leães
- C. Lister
- C. Lum
- C. Lum
- C. Lynch
- C. Magalhaes
- C. Magalhaes
- C. Marenghi
- C. Martín Parra
- C. Martínez Díaz
- C. Maury
- C. Mazo Torre
- C. McBride
- C. Mcgrath
- C. Mitaka
- C. Oglinda
- C. Ostrowska
- C. P. Lee
- C. Palazzi
- C. Park
- C. Patet
- C. Pelletier
- C. Pereira
- C. Peters
- C. Pichard
- C. Pierrakos
- C. Plourde
- C. Poi
- C. Pretty
- C. Pretty
- C. Pritchett
- C. Reutelingsperger
- C. Rodrigues
- C. Rodríguez Gallego
- C. Routsi
- C. Ryan
- C. S. Bouman
- C. S. Scheer
- C. S. Serra
- C. Sampson
- C. Scarrot
- C. Senver
- C. Sittipunt
- C. Skourtis
- C. Stone
- C. Suthisisang
- C. Svensen
- C. Tordoff
- C. Travierso
- C. Turrini
- C. Ugur Yilmaz
- C. Ulusoy
- C. Valdez
- C. Valencia
- C. Van Walraven
- C. Van Walraven
- C. Volta
- C. Volta
- C. Vrettou
- C. W. Park
- C. W. Park
- C. W. Park
- C. Walsh
- C. Willars
- C. Wissmann
- D Bryden
- D Jakubczyk
- D. A. Fergusson
- D. Adukauskiene
- D. Amin
- D. Ballesteros
- D. Bastoni
- D. Benoit
- D. Berger
- D. Bergmans
- D. Brown
- D. Bryden
- D. Bryden
- D. C. Angus
- D. Castanares-Zapatero
- D. Chroni
- D. Ciprandi
- D. Dawson
- D. De Bels
- D. Diedrich
- D. Dreyfuss
- D. Dreyfuss
- D. Du Cheyron
- D. Enoch
- D. Eschbach
- D. Eversole
- D. Evoy
- D. Fergusson
- D. Fergusson
- D. Fineberg
- D. Forte
- D. Forte
- D. Forte
- D. Freitag
- D. Gavrychenko
- D. Gavrychenko
- D. Gineityte
- D. Gokmen
- D. Griesdale
- D. Griesdale
- D. Griesdale
- D. Griesdale
- D. Heyland
- D. Heyland
- D. Heyland
- D. Huskens
- D. Inverarity
- D. Jacobsen
- D. Jarczak
- D. Kindgen-Milles
- D. Koutete
- D. L. Lucchesi
- D. M. Dalcomune
- D. M. Dalcomune
- D. M. Dalcomune
- D. Macias
- D. Mackle
- D. Mackle
- D. Markopoulou
- D. Memis
- D. Miller
- D. Moisidou
- D. Moisidou
- D. Moisidou
- D. Monkhouse
- D. Mota
- D. O. Thomas-Rüddel
- D. Pandit
- D. Pavlovic
- D. Pilsgaard Henriksen
- D. R. Cranendonk
- D. Reuter
- D. Ricci
- D. Ringaitiene
- D. S. Stavi
- D. Sangaran
- D. Sbiti-Rohr
- D. Silva
- D. Stott
- D. Thevenin
- D. Thomas-Rueddel
- D. Titeca
- D. Titeca
- D. Titeca
- D. Titeca
- D. Tomescu
- D. Tomescu
- D. Tomescu
- D. Tomescu
- D. Tomescu
- D. Tomescu
- D. Valanciene
- D. Wyncoll
- D. Ysebaert
- E Bertellini
- E George
- E Prandi
- E. A Volakli
- E. A. Osawa
- E. A. Volakli
- E. Aguilera
- E. Akin Korhan
- E. Akýn Korhan
- E. Almeida
- E. Antoniadou
- E. Antypa
- E. Arch-Tirado
- E. Arita
- E. B. Dias
- E. Bellazzi
- E. Bertellini
- E. Bertellini
- E. Boezeman
- E. Borg-Seng-Shu
- E. C. Carella
- E. Carlson
- E. Cerrato
- E. Chernevskaya
- E. Chinou
- E. Chochliourou
- E. Chochliourou
- E. Colombaroli
- E. Colombaroli
- E. Colombaroli
- E. D. Arul
- E. Dalampini
- E. Dalampini
- E. Der Kinderen
- E. Derom
- E. Doumaki
- E. Dubief
- E. Fan
- E. Frenoy
- E. G. Gayat
- E. George
- E. George
- E. Ghosh
- E. Giamarellos-Bourboulis
- E. Grins
- E. Gómez-Pesquera
- E. Gómez-Pesquera
- E. Gómez-Sánchez
- E. Gómez-Sánchez
- E. Helme
- E. Helme
- E. Herrera-Ramos
- E. Hoste
- E. Ischaki
- E. Jeong
- E. Joelsson-Alm
- E. K. Kishinevsky
- E. Kaya
- E. Kompanje
- E. Koonthalloor
- E. Kotzapanagiotou
- E. L. V. Costa
- E. Lafuente
- E. Lafuente
- E. Lafuente
- E. Llopart
- E. M. Siqueira
- E. Mancini
- E. Marrinan
- E. McCarron
- E. McCarron
- E. Michael
- E. Moltchanova
- E. Moreira
- E. Mukeria
- E. Mukeria
- E. Nakstad
- E. Nieuwkoop
- E. Nsutebu
- E. Nyberg
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- Field of study
[This corrects the article DOI: 10.1186/s13054-016-1208-6.]
Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries.
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- Zoerner F
- Zonneveldt H
- Zou X
- Zoulamoglou M
- Zsisku L
- 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
New national curricula guidelines that support the use of interprofessional education in Brazilian context : an analysis of key documents
- Author
- Agreli H. L. F.
- Aldaísa Cassanho Forster
- Bardin L.
- Bardin L.
- Becker H. S.
- CAIPE [Centre for the Advancement of Interprofessional Education]
- Caseiro C. C. F.
- Ceccim R. B.
- CIHC [Canadian Interprofessional Health Collaborative]
- Figueiredo N. M. A. D.
- Gergen K. J.
- José Rodrigues Freire Filho
- Lampert J. B.
- Lampert J. B.
- Marcelo Viana Da Costa
- Melo B. D. C.
- Schonwetter D. J.
- Scott Reeves
- Stella R. C. D. R.
- WHO [World Health Organization]
- WHO [World Health Organization]
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2017
- Field of study
The National Curricular Guidelines (NCGs) are important documents for understanding the history of academic health professions education in Brazil. Key policies within the NCGs have helped to re-orient health professions education and have stimulated curricular changes, including active learning methodologies, more integrated teaching-service environments and, more recently, have introduced interprofessional education (IPE) in both undergraduate and postgraduate sectors. This paper presents the findings of a study that examined the NCGs for nursing, dentistry and medicine courses as juridical foundations for adopting strategies that promote IPE across higher education institutions in Brazil. We employed a comparative and exploratory documentary analysis to understand the role of IPE or collaborative practices in NCGs for the three largest professions in Brazil. Following a thematic analysis of these texts, four key themes emerged: faculty development; competencies for teamwork; curricular structure; and learning metrics. Key findings related to each of these themes are presented and discussed in relation to the wider interprofessional literature. The paper goes on to argue that the statements contained in the NCGs about adoption of IPE and collaborative practices will have an important influence in shaping the future of health professions education in Brazil
Multi-messenger observations of a binary neutron star merger
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- Aartsen MG
- Abbott BP
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- Abbott TD
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- Abramo LR
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- Adhikari RX
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- Albuquerque IFM
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- Aresu G
- Argan A
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- Arnaud N
- Array LWA Long Wavelength
- Array MWA Murchison Widefield
- Arrieta M
- Arsene N
- Arteaga-Velzquez JC
- Artola R
- Arun KG
- Asakura Y
- Asaoka Y
- Ascenzi S
- Ashall C
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- Bae S
- Bagherpour H
- Bai X
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- Baker PT
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- Balanutsa PV
- Balasubramanian A
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- Barwick SW
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- Basti A
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- Baum V
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- Beardmore AP
- Beardsley A
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- Bechtol K
- Becker KH
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- Belhorma B
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- Bohm C
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- Bond IA
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- Bonnefoy S
- Bonoli S
- Booler T
- Boom BA
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- Bos F
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- Bose D
- Bose S
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- Botner O
- Bottacini E
- Bottcher M
- Botti AM
- Botticella MT
- Bouffanais Y
- Bourbeau E
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- Brinkmann M
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- Bron S
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- Buitink S
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- Bulger J
- Bulik T
- Bulik T
- Bulla M
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- Buonanno A
- Burgay M
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- Buson S
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- Cabero M
- Cabral J
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- Cadonati L
- Cagnoli G
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- Calloni E
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- Camilo F
- Camp JB
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- Camuccio R
- Cancio A
- Canepa M
- Canfora F
- Canizares P
- Cannella C
- Cannizzaro G
- Cannon KC
- Cano Z
- Cao H
- Cao J
- Cao XL
- Capaccioli M
- Capano CD
- Capasso M
- Capistrn T
- Capocasa E
- Capone A
- Capozzi D
- Cappellaro E
- Caputo R
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- Caraveo P
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- Chamberlin SJ
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- Chatterjee D
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- Chatziioannou K
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- Cordero-Carrion I
- Corley KR
- Cornish N
- Corongiu A
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- Costa E
- Costa-Duarte MV
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- Cotti U
- Cotzomi J
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- Coughlin SB
- Coulon J-P
- Coulter DA
- Countryman ST
- Courvoisier TJ-L
- Coutu S
- Couvares P
- Covas PB
- Covault CE
- Covino S
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- Coward DM
- Coward DM
- Cowart MJ
- Cowen DF
- Cowperthwaite P
- Coyle P
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- Creusot A
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- Di Mauro M
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- Djannati-Atao A
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- Dobie D
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- Doctor Z
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- Egron E
- Ehrens P
- Ehrhardt T
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- Eichmann B
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- Eikenberry SS
- Eisenstein RA
- El Bojaddaini I
- El Khayati N
- El Moursli R Cherkaoui
- Elias-Rosa N
- Elipe G Torralba
- Eller P
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- Elmer E
- Elsasser D
- Emery G
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- Emrich D
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- Escobar CO
- Espadanal J
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- Fauth AC
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- Feicht J
- Feindt U
- Fejer MM
- Feldbusch F
- Felde J
- Felis I
- Fender RP
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- Fenu F
- Fermi GBM
- Fernandes MV
- Fernandez D
- Fernandez E
- Fernandez G Rodriguez
- Fernandez-Galiana A
- Feroci M
- Ferrante I
- Ferrari A
- Ferreira EC
- Ferrigno C
- Ferrini F
- Fiasson A
- Fick B
- Fidecaro F
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- Fioretti V
- Fiori I
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- Firth RE
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- Fitz-Axen M
- Flaminio R
- Flaugher B
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- Forsyth PWF
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- Fosalba P
- Foster K
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- Fox OD
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- Fraija N
- Frail DA
- Franckowiak A
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- Franzen T
- Frasca S
- Frasconi F
- Fraser M
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- Fremling C
- Frey R
- Frey S
- Frey V
- Friedman E
- Frieman JA
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- Fritschel P
- Frohmaier C
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- Frolov VV
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- Fryer CL
- Fryer CL
- Fssling M
- Fu MX
- Fuchs T
- Fujii T
- Fujii YI
- Fujiyoshi T
- Fukazawa Y
- Fulda P
- Funk S
- Funk S
- Furusawa H
- Fuschino F
- Fusco LA
- Fusco P
- Fuster A
- Fyffe M
- Fynbo JPU
- Gabbard H
- Gabici S
- Gabovich AV
- Gadre BU
- Gaebel SM
- Gaensler BM
- Gaior R
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- Gaisser TK
- Gal-Yam A
- Galbany L
- Galicia JF Valdes
- Gallagher J
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- Gate F
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- Ghia PL
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- Ghosh Abhirup
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- Gianotti F
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- Goetz E
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- Goldschmidt A
- Goldstein A
- Goldstein DA
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- Golup G
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- Gu YD
- Guan J
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- Guelbenzu A Nicuesa
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- Guiriec S
- Guo CC
- Guo X
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- Gurovich S
- Gusai V
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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
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