15 research outputs found
Prognostic model to predict postoperative acute kidney injury in patients undergoing major gastrointestinal surgery based on a national prospective observational cohort study.
- Author
- Aamir A
- Abbas J
- Abbas N
- Abbott TEF
- Abdalla M
- Abdikadir H
- Abuhussein N
- Acquaah F
- Adamson R
- Adeleye O
- Adeogun A
- Adlan A
- Aftab R
- Afzal Z
- Agarwal M
- Aglan H
- Agnew CJF
- Agrawal R
- Ahern D
- Ahluwalia J
- Ahluwalia V
- Ahmad A
- Ahmad K
- Ahmed H
- Ahmed I
- Ahmed L
- Ahmed N
- Ahmed P
- Ainger E
- Ainsworth P
- Aishwarya G
- Ajibola-Taylor O
- Akhbari M
- Akhtar A
- Akhtar R
- Akpenyi O
- Al-Ausi M
- Al-Huneidi R
- Al-Khudairi R
- Al-Masri S
- Al-Mousawi A
- Al-Saadi N
- Alagappan A
- Alberts J
- Alfa-Wali M
- Ali A
- Ali B
- Ali I
- Ali M
- Ali Q
- Ali S
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- Alwandi A
- Amani L
- Amarnath T
- Amer M
- Amin H
- Amin MN
- Amoah R
- Amoah-Arko A
- Anandarajah C
- Ananthavarathan P
- Andah EJE
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- Appleton S
- Aquilina T
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- Arif T
- Arneill M
- Arnell S
- Arnold TJ
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- Ashwood J
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- Atkins B
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- Aubrey-Jones D
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- Auld F
- Auluck I
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- Renukanthan A
- Renwick P
- Reynolds J
- Reza N
- Richards C
- Richards T
- Richardson E
- Rickard L
- Rickards C
- Ridgway P
- Riley BJ
- Rimmer L
- Rinkoff S
- Riyat H
- Roberts B
- Roberts G
- Roberts J
- Robertson D
- Robinson A
- Robinson H
- Robinson K
- Robinson SD
- Rockall T
- Rodman L
- Roe T
- Rogers A
- Rogers D
- Roper L
- Roscoe HW
- Ross F
- Rothnie K
- Rothwell L
- Rotundo A
- Roy C
- Runkel M
- Rushd A
- Russell J
- Rutherford A
- Rutherford D
- Rutler L
- Ryan G
- Saad M
- Saat MI
- Sadanand KS
- Sadhra SS
- Sadiq S
- Saeed F
- Saggar S
- Sagoo H
- Saha A
- Sait MS
- Sait S
- Saito R
- Sajid M
- Salciccioli J
- Saleem H
- Salekin D
- Sales A
- Salman M
- Samaraweera S
- Sammut T
- Samuel R
- Sanders E
- Sandhu A
- Sandhu J
- Sandhu N
- Sandland-Taylor L
- Sangal P
- Sansome S
- Sarathy PP
- Saravanabavan S
- Sardar M
- Sarens N
- Sasapu K
- Sathiyakeerthy A
- Sattar M
- Sattar Z
- Saunders I
- Saunders M
- Sawers N
- Sawkins H
- Schade A
- Schinle P
- Schramm M
- Scotcher S
- Scott K
- Scott M
- Searle C
- Seehra H
- Seehra J
- Seelarbokus A
- Seetharam P
- Sellahewa C
- Selvadurai S
- Sen P
- Seraj SS
- Serry M
- Seth I
- Sethi R
- Shafi A
- Shafiq N
- Shaid M
- Shaman S
- Shang E
- Sharif I
- Sharkey E
- Sharma A
- Sharma E
- Sharma S
- Shaw A
- Shaw C
- Sheik-Ali S
- Sheikh A
- Sheikh S
- Sheikh Z
- Shergill M
- Shergill S
- Sherlock J
- Shields P
- Shingles C
- Shirazi S
- Shurovi BN
- Siddiqui A
- Siddiqui I
- Silke E
- Sim DPY
- Sim R
- Simmonds L
- Simon A
- Simpson L
- Simpson R
- Sinclair E
- Singagireson S
- Singh K
- Singh KKR
- Sinha C
- Sivagnanasithiyar T
- Sivakumar C
- Sivakumar R
- Skulsky S
- Slade G
- Slade RD
- Sleight S
- Small S
- Smallwood J
- Smart B
- Smart G
- Smart YW
- Smith ACD
- Smith C
- Smith F
- Smith H
- Smith J
- Smith M
- Smith R
- Sonagara V
- Song A
- Soonawalla Z
- Soor P
- Spencer R
- Spiers H
- Spoor H
- Springford LR
- Srikanthan M
- Sriram A
- Stageman N
- Standfield N
- Stanger S
- Stanier P
- STARSurg Collaborative Writing Committee, Data analysis, Steering committee, Advisory group, Regional leads, Collaborators and validators
- STARSurg Collaborative Writing Committee, Data analysis, Steering committee, Advisory group, Regional leads, Collaborators and validators, Nepogodiev, D
- Stechman M
- Stewart D
- Stewart E
- Stewart H
- Stewart R
- Stickler E
- Stoddart MT
- Stokes E
- Stott G
- Strang S
- Stringer H
- Stringfellow TD
- Stubbing-Moore A
- Sturrock S
- Subar D
- Subratty SM
- Sukirthan N
- Sukumar S
- Sulaiman SK
- Sultan S
- Sun L
- Sundaram K
- Suresh R
- Suresh S
- Sureshkumar A
- Suri A
- Svolkinas D
- Swan A
- Swan I
- Swaray A
- Swartbol T
- Symons L
- Szczap A
- Szuman A
- Tailor S
- Tam J
- Tam JP
- Tan CY
- Tan KL
- Tan L
- Tan LC
- Tan S
- Tan TSE
- Tang A
- Tang M
- Tanna A
- Taribagil P
- Tariq A
- Tate S
- Tayeh S
- Taylor K
- Taylor O
- Taylor R
- Taylor Z
- Telfer R
- Teng T
- Tenters F
- Teo R
- Thachettu A
- Thakrar D
- Thatcher A
- Theodoropoulou K
- Thomas A
- Thomas D
- Thomas M
- Thomas O
- Thomas S
- Thompson G
- Thompson J
- Thoms BL
- Thomson F
- Thorley N
- Thorn C
- Thornton T
- Thorpe O
- Tilliridou V
- Titu L
- Tod N
- Toellner H
- Toh C
- Toma T
- Tonks A
- Torrance HD
- Townsend D
- Traish M
- Trenear R
- Tresidder S
- Trevett J
- Triniman MC
- Trotter M
- Tsang JCH
- Tsang K
- Tseu B
- Tsui A
- Tullett A
- Tummon R
- Turlejski T
- Turner J
- Turner S
- Tyson N
- Ubhi HK
- Ujjal S
- Underhill R
- Vadgama N
- Vaidya A
- Vakharia A
- Van Den Berg N
- Van der Laan S
- Van Winsen K
- Vara S
- Varathan Y
- Varatharasasingam K
- Varcada M
- Vaughan R
- Vella-Baldacchino M
- Ventre C
- Venturini S
- Verma N
- Vernet G
- Victor L
- Vig S
- Vine M
- Vipond M
- Virani N
- Vizor R
- Vyas M
- Wadood Q
- Waite K
- Wakeford W
- Walford B
- Walker EY
- Walker G
- Walker K
- Walker L
- Walker NR
- Walls L
- Walsh T
- Wang H
- Wang L
- Wang X
- Ward AE
- Ward J
- Ward N
- Ward T
- Warren L
- Warren O
- Warusavitarne J
- Waterman A
- Waters S
- Watkinson G
- Watson L
- Watson N
- Waugh D
- Wayman J
- Webb E
- Webb R
- Weegenaar C
- Wei R
- Welsh K
- Whewell H
- Whitcroft I
- White C
- White F
- White P
- Whitham R
- Whyte M
- Widdison A
- Wiffen L
- Wigley C
- Wijeyaratne M
- Williams C
- Williams G
- Williams H
- Williams I
- Williams LM
- Williams P
- Williams S
- Wilson H
- Wilson J
- Wilson R
- Wilson V
- Wimalathasan A
- Woin E
- Wong C
- Wong E
- Wong J
- Wong MHY
- Wood CM
- Woodhams K
- Woolley A
- Wootton E
- Worley E
- Worsfold M
- Wright OW
- Wright R
- Wright S
- Wroe N
- Wynell-Mayow W
- Xu Y
- Yahaya AA
- Yalamarthi S
- Yang DD
- Yang N
- Yap J
- Yardimci E
- Yarham E
- Yasin IH
- Yasin T
- Yates J
- Ye W
- Yeo A
- Yeoh T
- Yeung J
- Yin ZD
- Yip J
- Yoganayagam N
- Yogeswara T
- York J
- Yousaf A
- Youssef H
- Yu T
- Yule A
- Zaat S
- Zanichelli D
- Zaver V
- Zeng R
- Zhang Y
- Zheleniakova T
- Zhu Y
- Zornoza A
- Zubikarai G
- Zulkifli A
- Zuzarte L
- Publication venue
- 'Wiley'
- Publication date
- 18/05/2018
- Field of study
Background: Acute illness, existing co-morbidities and surgical stress response can all contribute to postoperative acute kidney injury (AKI) in patients undergoing major gastrointestinal surgery. The aim of this study was prospectively to develop a pragmatic prognostic model to stratify patients according to risk of developing AKI after major gastrointestinal surgery. Methods: This prospective multicentre cohort study included consecutive adults undergoing elective or emergency gastrointestinal resection, liver resection or stoma reversal in 2-week blocks over a continuous 3-month period. The primary outcome was the rate of AKI within 7 days of surgery. Bootstrap stability was used to select clinically plausible risk factors into the model. Internal model validation was carried out by bootstrap validation. Results: A total of 4544 patients were included across 173 centres in the UK and Ireland. The overall rate of AKI was 14·2 per cent (646 of 4544) and the 30-day mortality rate was 1·8 per cent (84 of 4544). Stage 1 AKI was significantly associated with 30-day mortality (unadjusted odds ratio 7·61, 95 per cent c.i. 4·49 to 12·90; P < 0·001), with increasing odds of death with each AKI stage. Six variables were selected for inclusion in the prognostic model: age, sex, ASA grade, preoperative estimated glomerular filtration rate, planned open surgery and preoperative use of either an angiotensin-converting enzyme inhibitor or an angiotensin receptor blocker. Internal validation demonstrated good model discrimination (c-statistic 0·65). Discussion: Following major gastrointestinal surgery, AKI occurred in one in seven patients. This preoperative prognostic model identified patients at high risk of postoperative AKI. Validation in an independent data set is required to ensure generalizability
MHC-I peptides get out of the groove and enable a novel mechanism of HIV-1 escape
- Author
- A Schneidewind
- A Stryhn
- AJ McCoy
- Andrew G Brooks
- Anthony W Purcell
- AW Purcell
- Bosco K Ho
- C McMurtrey
- Corinne Hitchen
- CR Wang
- CS Clements
- D Chessman
- Daniel W McVicar
- David A Price
- EJ Collins
- F Bernardin
- FE Tynan
- G Alter
- G Alter
- GB Stewart-Jones
- Geraldine M O'Connor
- GM O'Connor
- H Crawford
- H Crawford
- H Escobar
- HG Rammensee
- IA Wilson
- J Martinez-Picado
- JA Speir
- Jamie Rossjohn
- JL Petersen
- JP Vivian
- JR Bailey
- Julian P Vivian
- K Deres
- K Ladell
- L Fadda
- L Kostenko
- M Carrington
- M Lichterfeld
- M Peruzzi
- M Seeger
- MA Saper
- MC Iglesias
- MP Martin
- MR Klein
- MS Malnati
- N Colaert
- NL Dudek
- NP Croft
- O Kutsch
- O Schwartz
- P Emsley
- P Evans
- Patricia T Illing
- PD Adams
- Phillip Pymm
- PJ Goulder
- PJ Goulder
- PM Saunders
- PT Illing
- QR Fan
- RA Kaslow
- RB Schittenhelm
- S Brackenridge
- S Hetherington
- S Jost
- S Mallal
- S Tenzer
- SA Migueles
- Sri H Ramarathinam
- T Miura
- TP Garrett
- V Novitsky
- VB Chen
- Victoria A Hughes
- VV Ganusov
- X Gao
- Y Qi
- Y Samino
- YC Liu
- Z Zhang
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 20/01/2017
- Field of study
Major histocompatibility complex class I (MHC-I) molecules play a crucial role in immunity by capturing peptides for presentation to T cells and natural killer (NK) cells. The peptide termini are tethered within the MHC-I antigen-binding groove, but it is unknown whether other presentation modes occur. Here we show that 20% of the HLA-B*57:01 peptide repertoire comprises N-terminally extended sets characterized by a common motif at position 1 (P1) to P2. Structures of HLA-B*57:01 presenting N-terminally extended peptides, including the immunodominant HIV-1 Gag epitope TW10 (TSTLQEQIGW), showed that the N terminus protrudes from the peptide-binding groove. The common escape mutant TSNLQEQIGW bound HLA-B*57:01 canonically, adopting a dramatically different conformation than the TW10 peptide. This affected recognition by killer cell immunoglobulin-like receptor (KIR) 3DL1 expressed on NK cells. We thus define a previously uncharacterized feature of the human leukocyte antigen class I (HLA-I) immunopeptidome that has implications for viral immune escape. We further suggest that recognition of the HLA-B*57:01-TW10 epitope is governed by a 'molecular tension' between the adaptive and innate immune systems
Reading the Early American Legal Profession: A Study of the First American Law Review
- Author
- ( Ross
- / Britain
- Adams V Storey
- Attorney-General V
- Bart V
- Baxter V
- Blewit V Marsden
- Blount V Chester
- Brown V
- Callahan V
- Carr V
- Coulter V Jones
- Coulter&apos
- Crittenden V Jones
- D C Stewart
- Davidson V Gray
- Dean Gilbert
- Duffie V Mathewson
- Evans V Weiss
- Fisher V
- Flury V
- Fogerty V Pratt
- Galt V
- Gilchrist V. Of Charleson
- Gill
- Grimball
- Groudson V Leonard
- Haskins V
- Hayton V Wilkinson
- Hitchen V Wilson
- Isaac Williams Case
- Jones V Smith
- Kirkpatrick V
- L&apos
- Lenox V
- Livingston V Jefferson
- Livingston V. Van Ingen
- M
- M&apos
- Managers President
- Marshall V. Delaware Insurance
- Maury V
- Mumford Murray
- Murray V Lane
- Odlin V. Ensurance Co
- Perrin V Blake
- President
- Rand
- Scott
- Scott V
- See
- Sinclair V Xavier
- Smith Mckim V
- Supra Hoeflich
- Supra Hulsebosch
- Talbott V
- The Saratoga
- Van Vechten V
- Wesley V Biays
- Zoey Orol
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2012
- Field of study
Geodynamic processes that are involved in the generation of the Northern Mid-Atlantic Ridge
- Author
- A. F. Byakov
- A.A. Koppers
- A.A. Shreider
- A.A. Shreider
- A.B. Watts
- A.C. Morton
- A.F. Byakov
- B. Lago
- B. Parsons
- B. Steinberger
- C. Gaina
- C. O’Neil
- D.A. Clague
- D.E. Hayes
- D.L. Turcotte
- D.P. McKenzie
- E. V. Verzhbitskii
- E.V. Verzhbitskii
- E.V. Verzhbitskii
- E.V. Verzhbitskii
- E.V. Verzhbitsky
- G.J. Golabek
- G.R. Foulger
- H. Becker
- H.S. Carslaw
- J. Escartin
- J. Hawkins
- J. Perice
- J.-G. Schilling
- J.A. Chalmers
- J.A. Keeton
- J.A. Tarduno
- J.C. Marty
- J.G. Sclater
- J.R. Smallwood
- J.T. Wilson
- K. Hitchen
- K.D. Klitgord
- L. Geli
- L.I. Lobkovskii
- M. Storey
- M. V. Kononov
- M. Wyss
- M.R. Fisk
- N.R.W. Weir
- P. Lonsdale
- P. Riisager
- P. Wessel
- P.D. Clift
- R.A. Duncan
- R.A. Duncan
- R.A. Duncan
- R.A. Duncan
- R.B. Whitmarsh
- R.D. Jarrard
- R.L. Carlson
- R.L. Parker
- R.P. Herzen Von
- R.P. Herzen Von
- R.S. White
- S. Douran Le
- S. Kodaira
- S. Kodaira
- S.G. Archer
- S.M. Jones
- T.A. Davies
- V.D. Kotelkin
- W. Schroeder
- W.D. Sharp
- W.J. Morgan
- W.R. Jacoby
- W.R. Roest
- W.S. Holdbrook
- X. Lenoir
- Yu.S. Genshaft
- Publication venue
- 'Pleiades Publishing Ltd'
- Publication date
- Field of study
Validation of the OAKS prognostic model for acute kidney injury after gastrointestinal surgery
- Author
- Ablett A.D.
- Ahmad K.
- Ahmed A.
- Ahmed K.
- Ahmed W.U.R.
- Ahmeidat A.
- Aitken G.
- Ajibola-Taylor O.
- Al-hadithi A.
- Ali A.
- Ali B.
- Ali Z.
- Alshakhs A.
- Aly M.H.
- Amin H.
- Amran M.A. bin
- Andah E.J.E.
- Ani C.
- Anilkumar A.
- Aromolaran O.
- Arthur J.
- Arulkumaran N.
- Atkin G.
- Attalla M.
- Azizi A.
- Babu V.S.
- Baker C.
- Baker D.
- Barai I.
- Barclay J.
- Basra M.
- Bath M.F.
- Beattie G.
- Beatty M.
- Belchos J.
- Bell S.
- Bennett J.
- Berry B.
- Bevan K.
- Bhangu A.
- Bhatia S.
- Bholah H.
- Blanco-Colino R.
- Bolton W.
- Borakati A.
- Boulton A.P.R.
- Bradley P.
- Brown F.S.
- Buari M.
- Burke J.
- Burns N.
- Busuttil A.
- Cabdi N.M.O.
- Campbell G.
- Cardus C.
- Cargill Z.
- Caroll P.
- Carroll L.
- Chan F.
- Chapman S.J.
- China Z.
- Chouari T.
- Christy S.
- Claireaux H.A.
- Collins J.
- Copeland M.
- Copley H.C.
- Corbridge O.
- Coulter C.
- Cresswell B.
- Davies J.
- Deekonda P.
- Delaugere L.P.
- Dennis Y.
- Dhillon A.K.
- Doherty C.
- Donaldson G.
- Doyle C.
- Drake T.M.
- Duggal A.
- Dunmore C.
- Dupaguntla Y.S.
- Durand C.
- Duthie F.
- Dwyer-Hemmings L.
- Dyal A.
- Dynes K.
- Edwin C.
- Elangovan S.
- Elliot J.
- Elliott D.
- Elst T. van
- Evans D.
- Evans R.
- Falamarzi A.
- Farhan-Alanie M.M.H.
- Fearnhead N.
- Finch E.
- Fitzgerald J.E.
- Foulkes A.
- Fox H.
- Francis A.A.
- Galea M.
- Gallagher P.
- Gallogly P.
- Gardner T.
- Gaze H.
- Ghaffar A.
- Gidwani A.
- Glasbey J.C.
- Goergen N.
- Graham S.
- Grant M.
- Greenan E.
- Gribbon C.
- Griffith J.
- Gruhn A.
- Gul W.
- Gundogan B.
- Gurung E.
- Harinath G.
- Harrison E.M.
- Haughey B.
- Hayashi E.
- Hayat F.
- Hayes J.D.B.
- Hayward J.
- Hensher C.
- Heywood E.
- Hirosue S.
- Hitchen C.
- Hodgson S.
- Holmes D.
- Hopkins M.
- Horne L.
- Hoskins T.
- Hossain S.
- Hughes B.
- Hughes J.
- Hungwe C.
- Hussain M.
- Hylands A.
- Ibrahim I.
- Islam Y.
- Isse M.
- Ito G.
- Jacob-Ramsdale B.
- Jain D.
- Jebakumar R.
- Johnston R.
- Joji N.
- Jones M.
- Jones N.
- Jones W.
- Joyce H.
- Jull P.
- Kamarajah S.K.
- Kanabar S.
- Kelly D.
- Kelly M.
- Kerr M.
- Khan M.
- Khatri C.
- Khaw R.
- Khoury G.
- Kidanu D.
- Kishore A.
- Klimach S.
- Knowles C.H.
- Komoriyama A.
- Kong C.
- Kwek I.
- Laan S. van der
- Lam J.
- Lang-Orsini M.
- Lau I.S.F.
- Laverty L.
- Lee J.
- Lee S.
- Leer M.
- Lehmann J.
- Leong S.H.
- Lewis E.
- Lim M.
- Lim S.
- Linn T.
- Liu H.
- Logan A.E.
- Long S.
- Looi W.L.
- Lovett B.
- Lowe-Zinola J.D.
- MacLeod C.S.
- Mah T.
- Maleyko I.
- Manikavasagar V.
- Martins T.
- McAllister R.
- McCann C.
- McCann E.
- McCartan N.
- McCormack R.
- McGuckin S.
- McHugh M.
- McKenna J.
- McKinley A.
- McKinstry S.
- McLean K.A.
- Mcnamara M.
- McNamee L.
- Millar Z.
- Miller F.A.
- Milligan W.
- Mills A.
- Mohan M.
- Moneim J.
- Monks M.
- Mookerjee S.
- Morley R.
- Mownah H.
- Mudalige G.
- Mullarkey L.
- Mushaini N.
- Nair M.
- Nakakande D.
- Naruka V.
- Nepogodiev D.
- Ng J.C.K.
- Ng L.
- Nigam N.
- Nirmalanantha A.
- Nixon G.
- Nourallah B.
- Ogunmwonyi I.
- Ojofeitimi O.
- Onyerindu C.
- Ooi L.
- Ormrod A.
- Pakenham A.
- Paola L. de
- Pata F.
- Patel M.
- Patel P.
- Pellino G.
- Perai K.G.
- Perera S.
- Phan V.
- Philomen J.
- Pillai S.
- Pinkney T.D.
- Powell J.
- Powell T.
- Pradhan A.
- Preece R.
- Prowle J.
- Qamar I.
- Qureshi A.
- Rafiq N.M.
- Ralston C.
- Ramsay G.
- Ransome M.
- Rao R.
- Reid N.
- Renju M.
- Reveendran D.
- Richards T.
- Rickards C.
- Ridgway P.
- Robi
- Robinson C.
- Rotimi O.
- Saggar S.
- Samaraweera S.
- Sammut T.
- Sangheli A.
- Scott M.
- Seetharam P.
- Sethi R.
- Sgro A.
- Shaman S.
- Shaw A.
- Sheikh Z.
- Siddiqui I.
- Sim D.P.Y.
- Sinclair E.
- Sivarajah S.
- Smart B.
- Smith M.
- Smith R.
- Soares A.
- Stewart R.
- Straten S. van
- Sun L.
- Suresh R.
- Suresh S.
- Teo R.
- Thomas M.
- Tie-Gill T.
- Titu L.
- Tsang J.C.H.
- Vara S.
- Vivian F.
- Walshe R.
- Wang X.
- Wcislo K.
- Wigley C.
- Wilson H.
- Woin E.
- Wong J.
- Yang D.D.
- Yeo Y.Q.
- Zaat S.
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 06/01/2022
- Field of study
Background Postoperative acute kidney injury (AKI) is a common complication of major gastrointestinal surgery with an impact on short- and long-term survival. No validated system for risk stratification exists for this patient group. This study aimed to validate externally a prognostic model for AKI after major gastrointestinal surgery in two multicentre cohort studies.Methods The Outcomes After Kidney injury in Surgery (OAKS) prognostic model was developed to predict risk of AKI in the 7 days after surgery using six routine datapoints (age, sex, ASA grade, preoperative estimated glomerular filtration rate, planned open surgery and preoperative use of either an angiotensin-converting enzyme inhibitor or an angiotensin receptor blocker). Validation was performed within two independent cohorts: a prospective multicentre, international study ('IMAGINE') of patients undergoing elective colorectal surgery (2018); and a retrospective regional cohort study ('Tayside') in major abdominal surgery (2011-2015). Multivariable logistic regression was used to predict risk of AKI, with multiple imputation used to account for data missing at random. Prognostic accuracy was assessed for patients at high risk (greater than 20 per cent) of postoperative AKI.Results In the validation cohorts, 12.9 per cent of patients (661 of 5106) in IMAGINE and 14.7 per cent (106 of 719 patients) in Tayside developed 7-day postoperative AKI. Using the OAKS model, 558 patients (9.6 per cent) were classified as high risk. Less than 10 per cent of patients classified as low-risk developed AKI in either cohort (negative predictive value greater than 0.9). Upon external validation, the OAKS model retained an area under the receiver operating characteristic (AUC) curve of range 0.655-0.681 (Tayside 95 per cent c.i. 0.596 to 0.714; IMAGINE 95 per cent c.i. 0.659 to 0.703), sensitivity values range 0.323-0.352 (IMAGINE 95 per cent c.i. 0.281 to 0.368; Tayside 95 per cent c.i. 0.253 to 0.461), and specificity range 0.881-0.890 (Tayside 95 per cent c.i. 0.853 to 0.905; IMAGINE 95 per cent c.i. 0.881 to 0.899).Conclusion The OAKS prognostic model can identify patients who are not at high risk of postoperative AKI after gastrointestinal surgery with high specificity.Presented to Association of Surgeons in Training (ASiT) International Conference 2018 (Edinburgh, UK), European Society of Coloproctology (ESCP) International Conference 2018 (Nice, France), SARS (Society of Academic and Research Surgery) 2020 (Virtual, UK).Nephrolog
Modulation of immune responses by targeting CD169/Siglec-1 with the glycan ligand
- Author
- Abaddi A
- Abdulkhalek S
- Abe H
- Acosta-Blanco I
- Adamczyk B
- Adams P
- Adams P
- Aderem A
- Adlercreutz D
- Aggeler R
- Agnew B
- Agravat S
- Akama TO
- Akita K
- Akutsu M
- Akçay G
- Albers SV
- Albiez RS
- Ali MF
- Allingham J
- Almeida I
- Alter G
- Amano J
- Amith SR
- Anastassiades T
- Andre S
- André S
- Angata K
- Angata K
- Angata K
- Aoki K
- Aoki K
- Apte A
- Arciniega-Fuentes MT
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- Zhou YD
- Zumwalt A
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2011
- Field of study
A fundamental role in the plant-bacterium interaction for
Gram-negative phytopathogenic bacteria is played by membrane
constituents, such as proteins, lipopoly- or lipooligosaccharides
(LPS, LOS) and Capsule Polysaccharides (CPS).
In the frame of the understanding the molecular basis of plant bacterium interaction, the Gram-negative bacterium Agrobacterium vitis was selected in this study. It is a phytopathogenic member of the Rhizobiaceae family and it induces the crown gall disease selectively on grapevines (Vitis vinifera).
A. vitis wild type strain F2/5, and its mutant in the quorum
sensing gene ΔaviR, were studied. The wild type produces biosurfactants; it is considered a model to study surface motility, and it causes necrosis on grapevine roots and HR (Hypersensitive
Response) on tobacco. Conversely, the mutant does not show any
surface motility and does not produce any surfactant material;
additionally, it induces neither necrosis on grape, nor HR on
tobacco. Therefore, the two strains were analyzed to shed some
light on the QS regulation of LOS structure and the consequent
variation, if any, on HR response. LOS from both strains were isolated and characterized: the two LOS structures maintained several common features and differed for few others.
With regards to the common patterns, firstly: the Lipid A region
was not phosphorylated at C4 of the non reducing glucosamine
but glycosylated by an uronic acid (GalA) unit, secondly: a third
Kdo and the rare Dha (3-deoxy-lyxo-2-heptulosaric acid) moiety
was present.
Importantly, the third Kdo and the Dha residues were substituted
by rhamnose in a not stoichiometric fashion, giving four different
oligosaccharide species.
The proportions among these four species, is the key difference
between the LOSs from both the two bacteria.
LOS from both strains and Lipid A from wild type A. vitis are
now examined for their HR potential in tobacco leaves and grapevine roots
Safety of Nonsteroidal Anti-inflammatory Drugs in Major Gastrointestinal Surgery: A Prospective, Multicenter Cohort Study
- Author
- Abbas Z
- Abburu S
- Abdelhadi M
- Abdikadir HR
- Abdulmajid A
- Abid A
- Abid H
- Abuhussein N
- Abul MH
- Acquaah F
- Acres M
- Adams R
- Adams RD
- Adebayo AA
- Adeleja I
- Adjei H
- Afzal Z
- Agarwal V
- Ahern N
- Ahmad K
- Ahmad S
- Ahmed F
- Ahmed H
- Ahmed M
- Ahmed N
- Ahmed S
- Ahmed S
- Ahn JS
- Aidoo-Micah GE
- Aildasani L
- Aithie JM
- Akhtar S
- Al-Mousawi A
- Al-Obaedi O
- Al-Obaedi O
- Al-Robeye A
- Ali A
- Ali B
- Ali H
- Ali M
- Ali S
- Alizadeh M
- Allan C
- Allen JLY
- Allot R
- Allot R
- Allot R
- Amajuoyi A
- Amin H
- Amin H
- Amin O
- Amphlett AH
- Anandarajah C
- Anderson L
- Anderson LB
- Anderson SM
- Ang A
- Angelov S
- Anilkumar A
- Anim-Addo N
- Ansari N
- Antoniou I
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2017
- Field of study
Background
Significant safety concerns remain surrounding the use of nonsteroidal anti-inflammatory drugs (NSAIDs) following gastrointestinal surgery, leading to wide variation in their use. This study aimed to determine the safety profile of NSAIDs after major gastrointestinal surgery.
Methods
Consecutive patients undergoing elective or emergency abdominal surgery with a minimum one-night stay during a 3-month study period were eligible for inclusion. The administration of any NSAID within 3 days following surgery was the main independent variable. The primary outcome measure was the 30-day postoperative major complication rate, as defined by the Clavien–Dindo classification (Clavien–Dindo III–V). Propensity matching with multivariable logistic regression was used to produce odds ratios (OR) and 95 % confidence intervals.
Results
From 9264 patients, 23.9 % (n = 2212) received postoperative NSAIDs. The overall major complication rate was 11.5 % (n = 1067). Following propensity matching and adjustment, use of NSAIDs were not significantly associated with any increase in major complications (OR 0.90, 0.60–1.34, p = 0.560).
Conclusions
Early use of postoperative NSAIDs was not associated with an increase in major complications following gastrointestinal surgery
Critical care usage after major gastrointestinal and liver surgery: a prospective, multicentre observational study
- Author
- Abbas Z.
- Abburu S.
- Abdelhadi M.
- Abdikadir H.R.
- Abdulmajid A.
- Abid A.
- Abid H.
- Abuhussein N.
- Abul M.H.
- Acquaah F.
- Acres M.
- Adams R.
- Adams R.D.
- Adebayo A.A.
- Adeleja I.
- Adjei H.
- Afzal Z.
- Agarwal V.
- Ahern N.
- Ahmad K.
- Ahmad S.
- Ahmed F.
- Ahmed H.
- Ahmed M.
- Ahmed N.
- Ahmed S.
- Ahn J.S.
- Aidoo-Micah G.E.
- Aildasani L.
- Aithie J.M.
- Akhtar S.
- Al-Mousawi A.
- Al-Obaedi O.
- Al-Robeye A.
- Ali A.
- Ali B.
- Ali H.
- Ali M.
- Ali S.
- Alizadeh M.
- Allan C.
- Allen J.L.Y.
- Allot R.
- Amajuoyi A.
- Amin H.
- Amin O.
- Amphlett A.H.
- Anandarajah C.
- Anderson L.
- Anderson L.B.
- Anderson S.M.
- Ang A.
- Angelov S.
- Anilkumar A.
- Anim-Addo N.
- Ansari N.
- Antoniou I.
- Archer C.H.
- Arif T.
- Asbjoernsen C.A.
- Ashfaq U.
- Ashken L.
- Ashraf S.
- Ashraf S.F.
- Ashton A.J.
- Ashwood J.
- Aslanyan A.
- Asmadi A.
- Assadullah S.
- Atayi A.
- Atraszkiewicz B.A.
- Attalla M.
- Austreng L.
- Auyoung E.
- Avery P.
- Axelson T.
- Aziz H.
- Aziz N.
- Baker A.N.
- Bakewell Z.R.
- Bakhsh A.
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- Wilson H.C.P.
- Wilson R.
- Wiltshire J.J.
- Winarski A.
- Wing V.C.
- Wingfield L.R.
- Winslow F.
- Woin E.
- Wong E.
- Wong V.
- Wood A.D.
- Woodcock N.
- Woodward H.
- Woon E.
- Wright A.
- Wright E.V.
- Wye J.
- Wylam D.
- Wylie J.
- Wynell-Mayow W.M.
- Xiao C.
- Xu G.X.
- Xylas D.
- Yan A.
- Yang T.
- Yates J.A.
- Yener A.
- Yim N.
- Yoganathan S.
- Yong C.S.
- Yong N.
- Yousif A.
- Yow L.
- Yuen R.
- Zegeye M.I.
- Zhao J.
- Ziff O.
- Ziprin P.
- Zuhair M.
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2019
- Field of study
Background
Patient selection for critical care admission must balance patient safety with optimal resource allocation. This study aimed to determine the relationship between critical care admission, and postoperative mortality after abdominal surgery.
Methods
This prespecified secondary analysis of a multicentre, prospective, observational study included consecutive patients enrolled in the DISCOVER study from UK and Republic of Ireland undergoing major gastrointestinal and liver surgery between October and December 2014. The primary outcome was 30-day mortality. Multivariate logistic regression was used to explore associations between critical care admission (planned and unplanned) and mortality, and inter-centre variation in critical care admission after emergency laparotomy.
Results
Of 4529 patients included, 37.8% (n=1713) underwent planned critical care admissions from theatre. Some 3.1% (n=86/2816) admitted to ward-level care subsequently underwent unplanned critical care admission. Overall 30-day mortality was 2.9% (n=133/4519), and the risk-adjusted association between 30-day mortality and critical care admission was higher in unplanned [odds ratio (OR): 8.65, 95% confidence interval (CI): 3.51–19.97) than planned admissions (OR: 2.32, 95% CI: 1.43–3.85). Some 26.7% of patients (n=1210/4529) underwent emergency laparotomies. After adjustment, 49.3% (95% CI: 46.8–51.9%, P<0.001) were predicted to have planned critical care admissions, with 7% (n=10/145) of centres outside the 95% CI.
Conclusions
After risk adjustment, no 30-day survival benefit was identified for either planned or unplanned postoperative admissions to critical care within this cohort. This likely represents appropriate admission of the highest-risk patients. Planned admissions in selected, intermediate-risk patients may present a strategy to mitigate the risk of unplanned admission. Substantial inter-centre variation exists in planned critical care admissions after emergency laparotomies
Body mass index and complications following major gastrointestinal surgery: A prospective, international cohort study and meta-analysis
- Author
- Aarts E
- Abbas Z
- Abburu S
- Abd Ghaffar Mk
- Abdelgalil R
- Abdelhadi M
- Abdikadir Hr
- Abdulmajid A
- Abdulrahman N
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- Abid H
- Abrisqueta Carrion J
- Abuhussein N
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- Agrawal M
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- Zuhair M
- Örhalmi J
- Özkan Bb
- Šimáčková B
- Široká M
- Žebrák R
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2018
- Field of study
Aim Previous studies reported conflicting evidence on the effects of obesity on outcomes after gastrointestinal surgery. The aims of this study were to explore the relationship of obesity with major postoperative complications in an international cohort and to present a metaanalysis of all available prospective data. Methods This prospective, multicentre study included adults undergoing both elective and emergency gastrointestinal resection, reversal of stoma or formation of stoma. The primary end-point was 30-day major complications (Clavien\u2013Dindo Grades III\u2013V). A systematic search was undertaken for studies assessing the relationship between obesity and major complications after gastrointestinal surgery. Individual patient meta-analysis was used to analyse pooled results. Results This study included 2519 patients across 127 centres, of whom 560 (22.2%) were obese. Unadjusted major complication rates were lower in obese vs normal weight patients (13.0% vs 16.2%, respectively), but this did not reach statistical significance (P = 0.863) on multivariate analysis for patients having surgery for either malignant or benign conditions. Individual patient meta-analysis demonstrated that obese patients undergoing surgery formalignancy were at increased risk of major complications (OR 2.10, 95% CI 1.49\u20132.96, P < 0.001), whereas obese patients undergoing surgery for benign indications were at decreased risk (OR 0.59, 95% CI 0.46\u20130.75, P < 0.001) compared to normal weight patients. Conclusions In our international data, obesity was not found to be associated with major complications following gastrointestinal surgery. Meta-analysis of available prospective data made a novel finding of obesity being associated with different outcomes depending on whether patients were undergoing surgery for benign or malignant disease
Body mass index and complications following major gastrointestinal surgery: a prospective, international cohort study and meta-analysis.
- Author
- 6rhalmi J
- 6zkan Bb
- \u160im\ue1\u10dkov\ue1 B
- \u160irok\ue1 M
- \u17debr\ue1k R
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- Atraszkiewicz Ba
- Attalla M
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- de Roy van Zuidewijn D
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- Lee J
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- Mahesh S
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- Martinez Rios Ce
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- Masood M
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- Mastandrea Bonaviri Gn
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- Matthews Jh
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- Mcgalliard Rj
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- Mcgarvie S
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- Mcgowan C
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- Mcgregor Rj
- Mcintyre Cj
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- Mckerr Cn
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- Mcrobbie Hd
- Medina-Fern\ue1ndez Fj
- Meek J
- Mehdi A
- Mehta Jk
- Meijerink Wjhj
- Menduni N
- Menon A
- Mensink G
- Mericliler M
- Mermer S
- Messina F
- Mestres Petit N
- Metcalf P
- Mian A
- Milana F
- Milazzo Lf
- Millan M
- Mills Ed
- Mills H
- Mills M
- Milne S
- Minhas M
- Mirallas Vi\uf1as O
- Miranda Bh
- Mirdavoudi V
- Mirza M
- Mishra A
- Mistry Bd
- Mistry S
- Mitchell H
- Mitha N
- Mithrakumar P
- Mitrasinovic S
- Mittapalli D
- Mitxelena Elosegi L
- Mizan Sr
- Mogan Yp
- Mohamed Us
- Mohamud M
- Mohan K
- Mohan M
- Mohite A
- Momoh Z
- Montanelli P
- Montuori M
- Monzonis Hernandez X
- Moody N
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- Moradzadeh J
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- Moratilla Lape\uf1a L
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- Morgan F
- Morino M
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- Moroni P
- Morris F
- Morris S
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- Morrison P
- Mortimer A
- Morton D
- Mosterd Cm
- Mugurtay Ys
- Mulder Im
- Muller S
- Mural-Krishnan S
- Muriel P
- Murkin C
- Muro M
- Murphy L
- Murray Se
- Murtaza A
- Murtaza Mi
- Mushtaq J
- Mustafa S
- Musters Gd
- Mutlu B
- Mutlu D
- Myers L
- Naccari P
- Naccari Pm
- Nachiappan R
- Nadanakumaran K
- Naqib S
- Narain A
- Naran P
- Narang Y
- Narayan P
- Narramore R
- Narwani V
- Navayogaarajah V
- Naveed H
- Nayee H
- Neary A
- Nehikhare I
- Nelaj S
- Nelli T
- Neo Yn
- Neophytou C
- Nepogodiev D.
- Nesargikar Pn
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- Ng Gs
- Ng Jck
- Ng Jq
- Ng K
- Ng L
- Ng S
- Ngaage M
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- Nixon G
- Noone Tm
- Norris Jm
- North As
- Norton J
- Nota Clma
- Notarnicola M
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- Pinkney Td
- Pinto R
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- Piran G
- Pistola I
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- Player C
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- Poelman M
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- Prado Perez R
- Prakash E
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- Punjabi N
- Qamar Ma
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- Radotra A
- Rafiq Nm
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- Raina V
- Rajan N
- Raji K
- Rakhimov I
- Raman Kp
- Ramana A
- Ramjeeawon N
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- Ramsay N
- Ramtoola T
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- Raut P
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- Ruiz Montesinos I
- Ruiz Em
- Russell G
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- Shoa M
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- Vanmali P
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- Xiao C
- Xu Gx
- Xylas D
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- Yauw S
- Yavuz G
- Yazkan Z
- Yekenkurul E
- Yener A
- Yeoh Tsl
- Yetiskin E
- Yildirim N
- Yildirim R
- Yildiz S
- Yildiz Ss
- Yildiz T
- Yilmaz I
- Yilmaz M
- Yilmaz S
- Yilmaz T
- Yim N
- Yoganathan S
- Yong Cs
- Yong N
- Yoruk I
- Yousif A
- Yow L
- Yuen R
- Yuksek B
- Yuksek Ma
- Yuksel A
- Yurdaor Ss
- Yurekli Am
- Zaidi R
- Zegeye Mi
- Zengin T
- Zhang Aa
- Zhao J
- Ziff O
- Zigiotto D
- Zijlmans Jl
- Zimmerman D
- Ziprin P
- Zope S
- Zuhair M
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2018
- Field of study
AIM:
Previous studies reported conflicting evidence on the effects of obesity on outcomes after gastrointestinal surgery. The aims of this study were to explore the relationship of obesity with major postoperative complications in an international cohort and to present a meta-analysis of all available prospective data.
METHODS:
This prospective, multicentre study included adults undergoing both elective and emergency gastrointestinal resection, reversal of stoma or formation of stoma. The primary end-point was 30-day major complications (Clavien-Dindo Grades III-V). A systematic search was undertaken for studies assessing the relationship between obesity and major complications after gastrointestinal surgery. Individual patient meta-analysis was used to analyse pooled results.
RESULTS:
This study included 2519 patients across 127 centres, of whom 560 (22.2%) were obese. Unadjusted major complication rates were lower in obese vs normal weight patients (13.0% vs 16.2%, respectively), but this did not reach statistical significance (P = 0.863) on multivariate analysis for patients having surgery for either malignant or benign conditions. Individual patient meta-analysis demonstrated that obese patients undergoing surgery for malignancy were at increased risk of major complications (OR 2.10, 95% CI 1.49-2.96, P < 0.001), whereas obese patients undergoing surgery for benign indications were at decreased risk (OR 0.59, 95% CI 0.46-0.75, P < 0.001) compared to normal weight patients.
CONCLUSIONS:
In our international data, obesity was not found to be associated with major complications following gastrointestinal surgery. Meta-analysis of available prospective data made a novel finding of obesity being associated with different outcomes depending on whether patients were undergoing surgery for benign or malignant disease