195 research outputs found
Association between acoustic features and brain volumes: the Framingham Heart Study
- Author
- Publication venue
- Frontiers Media S.A.
- Publication date
- 01/11/2023
- Field of study
IntroductionAlthough brain magnetic resonance imaging (MRI) is a valuable tool for investigating structural changes in the brain associated with neurodegeneration, the development of non-invasive and cost-effective alternative methods for detecting early cognitive impairment is crucial. The human voice has been increasingly used as an indicator for effectively detecting cognitive disorders, but it remains unclear whether acoustic features are associated with structural neuroimaging.MethodsThis study aims to investigate the association between acoustic features and brain volume and compare the predictive power of each for mild cognitive impairment (MCI) in a large community-based population. The study included participants from the Framingham Heart Study (FHS) who had at least one voice recording and an MRI scan. Sixty-five acoustic features were extracted with the OpenSMILE software (v2.1.3) from each voice recording. Nine MRI measures were derived according to the FHS MRI protocol. We examined the associations between acoustic features and MRI measures using linear regression models adjusted for age, sex, and education. Acoustic composite scores were generated by combining acoustic features significantly associated with MRI measures. The MCI prediction ability of acoustic composite scores and MRI measures were compared by building random forest models and calculating the mean area under the receiver operating characteristic curve (AUC) of 10-fold cross-validation.ResultsThe study included 4,293 participants (age 57 ± 13 years, 53.9% women). During 9.3 ± 3.7 years follow-up, 106 participants were diagnosed with MCI. Seven MRI measures were significantly associated with more than 20 acoustic features after adjusting for multiple testing. The acoustic composite scores can improve the AUC for MCI prediction to 0.794, compared to 0.759 achieved by MRI measures.DiscussionWe found multiple acoustic features were associated with MRI measures, suggesting the potential for using acoustic features as easily accessible digital biomarkers for the early diagnosis of MCI
The Constraints of Unitary on ππ Scattering Dispersion Relations
- Author
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2002
- Field of study
A new dispersion relation for the partial wave ππ scattering S matrix
is set up. Using the dispersion relation we generalize the single channel
unitarity condition, SS+=1, to the entire complex s plane, which is
equivalent to the generalized unitarity condition in quantum mechanics. The
pole positions of the σ resonance and the f0(980) resonance are
estimated based on the theoretical relations we obtained. The central value of
the σ pole position is Mσ≃410MeV, Γσ≃550MeV, obtained after including the the constraint of the Adler zero
condition.Comment: 10 pages with 4 figures, revised version to appear in Phys. Lett.
Recommended from our members
Minimal clinically important difference of the EORTC QLQ-CIPN20 for worsening peripheral neuropathy in patients receiving neurotoxic chemotherapy.
- Author
- Publication venue
- eScholarship, University of California
- Publication date
- 01/12/2019
- Field of study
Context/objectivesThis is the first study to determine the minimal clinically important difference (MCID) of the European Organisation of Research and Treatment of Cancer Quality of Life Questionnaire-CIPN twenty-item scale (EORTC QLQ-CIPN20), a validated instrument designed to elicit cancer patients' experience of symptoms and functional limitations related to chemotherapy-induced peripheral neuropathy.MethodsCancer patients receiving neurotoxic chemotherapy completed EORTC QLQ-CIPN20 and the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity [FACT/GOG-NTX] at baseline, second cycle of chemotherapy (T2, n = 287), and 12 months after chemotherapy (T3, n = 191). Anchor-based approach used the validated FACT/GOG-NTX neurotoxicity (Ntx) subscale to identify optimal MCID cutoff for deterioration. Distribution-based approach used one-third standard deviation (SD), half SD, and one standard error of measurement of the total EORTC QLQ-CIPN20 score.ResultsThere was a moderate correlation between the change scores of the Ntx subscale and sensory and motor subscales of QLQ-CIPN20 (T2: r = - 0.722, p < 0.001 and r = - 0.518, p < 0.001, respectively; T3: r = - 0.699; p < 0.001 and r = - 0.523, p < 0.001, respectively). The correlation between the change scores of the Ntx subscale and the QLQ-CIPN20 autonomic subscale was poor (T2: r = - 0.354, p < 0.001; T3: r = 0.286, p < 0.001). Based on the MCID derived using distribution-based method, the MCID for the QLQ-CIPN20 sensory subscale was 2.5-5.9 (6.9% to 16.4% of the subdomain score) and for motor subscale was 2.6-5.0 (8.1%-15.6% of the subdomain score).ConclusionThe MCID for the EORTC QLQ-CIPN20 established using distribution-based approaches was 2.5-5.9 for the sensory subscale and 2.6-5.0 for the motor subscale. When noted in assessments even with small change in scores, clinicians can be alerted for appropriate intervention
Augmented reliability analysis for estimating imprecise first excursion probabilities in stochastic linear dynamics
- Author
- Ang
- Au
- Au
- Au
- Beer
- Beer
- Bjerager
- Broggi
- Ching
- Ching
- Chopra
- Deodatis
- Der Kiureghian
- Deák
- Ditlevsen
- Faes
- Faes
- Faes
- Faes
- Faes
- Faes
- Faes
- Faes
- Ferson
- Gao
- Gautschi
- Howell
- Jensen
- Jensen
- Katafygiotis
- Koutsourelakis
- Misraji
- Moens
- Pradlwarter
- Sadeghi
- Schuëller
- Schuëller
- Schöbi
- Schöbi
- Shinozuka
- Song
- Stefanou
- Taflanidis
- Valdebenito
- Wei
- Wei
- Wu
- Xia
- Yin
- Yuan
- Zerva
- Zhang
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/05/2021
- Field of study
Determinants of suboptimal breastfeeding practices in Nigeria: evidence from the 2008 demographic and health survey
- Author
- A Patel
- AE Sadoh
- AM Qureshi
- AN Maduforo
- Andrew Page
- ANG Alutu
- AU Ukegbu
- B Maycock
- B Simkhada
- BA Aidam
- BW Yahya
- C Tawiah-Agyemang
- Center for Disease Control and Prevention
- D Filmer
- E Prior
- EN Ekure
- F Ladomenou
- Felix A Ogbo
- HA Agbo
- HT Akram
- J Grassley
- JO Ugboaja
- K Agho
- K Dearden
- Kenya National Bureau of Statistics MEASURE DHS, and ICF Macro
- Kingsley E Agho
- KM Edmond
- KR Bezner
- L Dubois
- L Salami
- M Aghaji
- M Kaunonen
- MS Kramer
- National Population Commission (NPC) [Nigeria] and ICF Macro
- National Population Commission (NPC) [Nigeria] and ICF Macro
- National Population Commission (NPC) [Nigeria] and ICF Macro
- National Population Commission (NPC) [Nigeria] and ICF Macro
- O Wole
- OM Agunbiade
- P Gertler
- R Black
- R Victor
- RE Black
- RM Dezoysa
- S Babalola
- S Ip
- S Olufowobi
- T Ogunlesi
- TA Ogunlesi
- United Nations Children’s Fund (UNICEF)
- V Khanal
- W Akmam
- WHO U., USAID, FANTA, AED, UC DAVIS, IFPRI
- World Health Organisation
- World Health Organisation
- World Health Organisation
- World Health Organization
- World Health Organization
- World Health Organization
- Y Van Der Meulen Rodgers
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Gender differences in the use of cardiovascular interventions in HIV-positive persons; the D:A:D Study
- Author
- Abeli C
- Abrams DI
- Abrescia N
- Acinapura R
- Ackens RP
- Aho I
- Aksak-Was B
- Albers M
- Alessandrini A
- Amele S
- Ammassari A
- Ammerlaan H
- Andreoni M
- André K
- Ang CW
- Angarano G
- Antinori A
- Arduino R
- Arends JE
- Aubert V
- Baas S
- Back N
- Bagella P
- Baker D
- Bakker Y
- Bakowska E
- Baldelli F
- Baldin G
- Balotta C
- Bandera A
- Barocci V
- Barth RE
- Bartsch G
- Bassetti M
- Battegay M
- Bauer MP
- Bax HI
- Baxter J
- Begovac J
- Bellecave P
- Belvisi V
- Benfield T
- Beniowski M
- Bergsma D
- Berkhout B
- Bermon N
- Bernard E
- Bernard N
- Bernasconi E
- Bezemer DO
- Bezemer M
- Bierman W
- Blaizeau MJ
- Blance A
- Blanco P
- Blaxhult A
- Bloch M
- Bloembergen P
- Blok WL
- Bobbio N
- Boender TS
- Boerg E
- Bogner J
- Bohlius J
- Bojesen A
- Bomers M
- Bonadies G
- Bonfanti P
- Bonnet F
- Bonora S
- Bont LJ
- Bor P
- Borderi M
- Borgia G
- Borodulina E
- Bos JC
- Bosch M
- Bosma AS
- Boucher C
- Bouchet S
- Bouwhuis JW
- Bower M
- Brandt RS
- Branger J
- Braun DL
- Bravo I
- Breilh D
- Brinkman K
- Brokking W
- Brouwer AE
- Brouwer CJ
- Bruinsma-Broekman FB
- Bruun J
- Bucher H
- Buiting A
- Burger D
- Burke M
- Böni J
- Cacopardo B
- Cadafalch J
- Caissotti C
- Calcagno A
- Caldeira L
- Calmy A
- Calvo G
- Calza L
- Capobianchi MR
- Capozzi M
- Caramello P
- Caramma I
- Carletti F
- Carr A
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- Cascio A
- Cassola G
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- Cattelan AM
- Caubet O
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- Cavassini M
- Cazanave C
- Ceccherini-Silberstein F
- Cecchetto M
- Celesia B
- Chiodera A
- Chirianni A
- Chkhartishvili N
- Chossat I
- Chêne G
- Cicalini S
- Cingolani A
- Cinque P
- Ciuffi A
- Claas E
- Claessen E
- Clarke A
- Clotet B
- Clumeck N
- Codina C
- Cohen Stuart J
- Cohn D
- Colomba C
- Conte V
- Cooper D
- Cornelissen M
- Costantini A
- Courjon J
- Courtault C
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- Crane LR
- Cristaudo A
- Cua E
- D'Arminio Monforte A.
- D'Ivernois C
- Dabis F.
- Damen M
- Dauchy FA
- de Boer M
- de Groot J
- de Groot L
- de Jong A
- de Lang A
- De Luca A
- de Munnik E
- de Oude-Lubbers A
- De Ruyter Ziekenhuis A
- De Salvador-Guillouet F
- de Vocht J
- de Weerd DA
- De Wit S.
- de Zeeuw-de Man M
- Decoin M
- Degen O
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- Del Cacho E
- Delforge M
- Dellamonica P
- Delsing CE
- Delveaux S
- den Berg JF
- den Berk G
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- Desjardin S
- Di Biagio A
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- Duffau P
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- Durant J
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- Duvivier C
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- Egger M
- El Berkaoui A
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- El-Sadr W.
- Elbirt D
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- Francisci D
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- Gabbuti A
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- Gennotte AF
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- Gentile I
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- Gerstoft J
- Giacometti A
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- Godfried MH
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- Grønborg Laut K
- Guaraldi G
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- Hirsch HH
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- Smith CJ
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- Sonnerborg A
- Sorin L
- Sozio F
- Speck R
- Spelbrink M
- Starnini G
- Staub T
- Stefan C
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- Stellbrink HJ
- Stelma FF
- Sthoeger ZM
- Stienstra Y
- Struik-Kalkman D
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- van der Prijt L
- van der Reijden WA
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- van Eden J
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- van Wijk M
- van Zonneveld LM
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- Vandenhende M
- Vandenhende MA
- Vaqué A
- Vareil MO
- Vassilenko A
- Vdoushkina E
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- Veenendaal D
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- Verbon A
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- Viallard JF
- Viard JP
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- Vlasblom DJ
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- Vrouenraets S
- Vullo V
- Wandeler G
- Wassenberg M
- Watson K
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- Weber R
- Weel J
- Wegdam M
- Weijenberg-Maes B
- Weijer S
- Weijsenfeld AM
- Wensing A
- Wessels E
- Wiersinga WJ
- Wiese L
- Wijnands S
- Wildenbeest GS
- Wille H
- Wilting KR
- Wirth G
- Wisse A
- Wit F
- Witte E
- Wittkop L
- Wojcik K
- Wolfhagen M
- Wolfs T
- Woudstra T
- Yakovlev A
- Yerly S.
- Yust I
- Zaaijer HL
- Zaccarelli M
- Zaheri S
- Ziekenhuis C
- Zilmer K
- Zomer BJ
- Åkerlund B
- Publication venue
- Publication date
- 01/01/2018
- Field of study
Peer reviewe
Pan-cancer analysis of whole genomes
- Author
- A. -L. rv
- A. -M. ma
- A. A. qj
- A. abp
- A. ak
- A. ak
- A. am
- A. am
- A. am
- A. av
- A. B. ry
- A. bb
- A. bg
- A. br
- A. bu
- A. cb
- A. cb
- A. ch
- A. ch
- A. ck
- A. D. b ey
- A. dg
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- wv abg
- wz Hupp
- x Eils
- x Yung
- X. abp
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- xy Visakorpi
- xz Whitaker
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- ya Al-Ahmadie
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- Yamaguchi T. N. k
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- zd Gershenwald
- Zenklusen
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- zf Ghossein
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang
- Zhang H. b
- Zhao
- Zheng
- Zhou
- Zhou
- Zhu
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- zi zj
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- Zou
- Zou
- zt Kim
- zw Lewis
- Ó. A. th
- Ø. sk
- Publication venue
- Publication date
- 11/12/2019
- Field of study
Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
Pooled analysis of WHO Surgical Safety Checklist use and mortality after emergency laparotomy
- Author
- Aahlin EK
- Aamer A
- Aaniana K
- Ababneh A
- Abaliksta T
- Abantanga F
- Abantanga F
- Abbas A
- Abbas M
- Abbasy J
- Abbo O
- Abbo O
- Abbott T
- Abbouch M
- 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-Elmawla M
- Abd-Elrasoul Y
- Abdallah E
- Abdallah E
- Abdel-Aty A
- Abdel-Hameed N
- Abdel-Kader SM
- Abdel-Wahab NYE
- Abdelaal A
- Abdelaty M
- Abdelazeam AR
- Abdelazim G
- Abdelaziz MA
- Abdelbadeai K
- Abdelfatah A
- AbdelFattah I
- Abdelgelil A
- Abdelghany S
- Abdelhady S
- Abdelhamed R
- Abdelhamid A
- Abdelhaq A
- Abdelkader M
- Abdelkader M
- Abdelkader O
- Abdelkareem A
- Abdelkhalek M
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- Abdelmotaleb I
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- Eduard P
- Edwards J
- Edye M
- Eid MM
- Eisner L
- Ekow M
- El Ashal G
- El Dahab AA
- El Deen KN
- El Gendy A
- El Gendy NH
- El Halawany M
- El Jamassi A
- El Kashash A
- El Kholy A
- El Magd AA
- El Mesery S
- El Sayed GS
- El Sayed IM
- El Shoura Y
- El-badawy HA
- El-Dien KS
- El-Dien KS
- El-Din RA
- El-Din SA
- El-Gizawy E
- El-Hamouly AS
- El-Kashef H
- El-Latif NK
- El-Ma'doul AS
- El-Rabaa S
- El-Sagheer N
- El-Sawy A
- El-Sehily A
- El-Shahat NS
- El-Sheemy H
- El-Taher E
- Elabdin HZ
- Elashmawy M
- Elashry R
- Elazab A
- Elazayem AA
- Elazoul M
- Elbanby E
- Elbanby ES
- Elbatahgy A
- Elbe P
- Elbermawy M
- Elbisomy KH
- Eldafrawy M
- Eldamaty L
- Eldeeb AZ
- Eldeen EA
- Eldin MAB
- EldosoukyMohammed A
- Elebute O
- Elebute O
- Elena G
- Elfarargy A
- Elfeki H
- Elfeki H
- Elfiky M
- Elfil M
- Elfouly N
- Elfouly N
- Elfouly Y
- Elfouly Y
- Elgebaly A
- Elgendy AH
- Elgendy FI
- Elgheriany M
- Elhadad A
- Elhadary NM
- Elhadry S
- Elhalawany E
- Elhamouly S
- Elhelbawy MS
- Elhendawy A
- Elhendawy AOA
- Elhoseny G
- Elhusseiny AAE
- Elizabeth Lopez C
- Elkadsh I
- Elkady F
- Elkelany A
- Elkelany A
- Elkelany A
- Elkelany A
- Elkhadrawi M
- Elkhalek EA
- Elkholy A
- Elkholy SS
- Elkolaly SS
- Elkorashy AM
- Ellison Q
- Elmashala A
- Elmasry M
- Elmelegy R
- Elmihy S
- Elnagar A
- Elnajjar MA
- Elnemr AE
- Elrazek AA
- Elsabbagh N
- Elsameea AA
- Elsawahly DME
- Elsawy A
- Elsayed M
- Elsayed M
- Elsayed N
- Elsayed NAR
- Elsayed ZM
- Elsebaaye AO
- Elsehimy M
- Elsemelawy R
- Elshaar M
- Elshaer K
- Elshaer M
- Elshaer M
- Elshafay AE
- Elshami M
- Elshanwany S
- Elsharkawy AA
- Elsheikh S
- Elsherbiney S
- Elsherbiny AS
- Elsherif FA
- Elshobary M
- Elsiddig M
- Elsobky S
- Elsorogy DEAA
- Elwaey A
- Elwakil H
- Elwan A
- Elwan A
- Elwy E
- Elzahed N
- Elzayat I
- Elzayat M
- Elzayyat I
- Elzowawi F
- Emadeldin D
- Emadeldin H
- Emara E
- Emile S
- Eng C
- English W
- Esam A
- Escalante Salas MDC
- Espin-Basany E
- Espinoza F
- Essam A
- Essam AA
- Essam M
- Essoun S
- Esteban E
- Estee MM
- Estupinian S
- Etchill E
- Etchill E
- Etienne S
- Etman M
- Etwire V
- Evajelista CV
- Evans D
- Evans E
- Eysa A
- Eyssartier E
- Ezzat E
- Ezzat T
- Faboya O
- Faccincani R
- Fadel A
- Fahiem A
- Fahim M
- Fahmy MAB
- Fahy C
- Fairfield C
- Fairfield C
- Fairfield C
- Fairfield C
- Fakher R
- Falaschi F
- Falco N
- Falzon M
- Farag A
- Farag S
- Farah A
- Farahat MM
- Faraz A
- Fares M
- Farhad M
- Farhan-Alanie MMH
- Farhangmehr N
- Farinella E
- Farmakis K
- Farooq T
- Farouk SAM
- Farquharson A
- Farrugia A
- Farrugia A
- Faruq A
- Fathy AM
- Fattah AA
- Fatuga A
- Faturoti O
- Faturoti O
- Faure A
- Fautz T
- Favero A
- Fawzy A
- Feidantsis T
- Felipe CO
- Fergany A
- Fergusson SJ
- Fergusson SJ
- Fergusson SJ
- Fergusson SJ
- Fermani C
- Fermani CG
- Fernandes C
- Fernandez C
- Fernandez-Bueno F
- Fernandez-Vega L
- Ferousis C
- Ferrero E
- Fievet L
- Filatau A
- Findlay-Cooper K
- Firdouse M
- Firdouse M
- Firdouse M
- Firwana A
- Fitsum A
- Fitzgerald JE
- Fitzgerald JE
- Florez Farfan ES
- Foco M
- Fok CYJ
- Fontana T
- Foo CC
- Forlin L
- Forno W
- Fouad A
- Fouad D
- Fouad D
- Fourcade L
- Fowler AJ
- Fozard T
- Fozard T
- Frade F
- Fraga GP
- Francisco Roxas M
- Franco H
- Francois P
- Francois-Coridon H
- Francone E
- Freitas AV
- Frey D
- Frisk B
- Fuentes-Rivera L
- Fujii F
- Furqan MM
- Gaafar S
- Gaarder T
- Gad A
- Gad MO
- Gadelkarim M
- Gadhvi V
- Gado A
- Gaignard E
- Gaignard E
- Gaizauskas V
- Gala T
- Gala T
- Galiqi G
- Galleano R
- Gallo G
- Galloway S
- Galvez CP
- Gamal D
- Gamal E
- Gamal H
- Gamal S
- Gamaly E
- Gamil D
- Gan C
- Gan YY
- Gani MA
- Garaycochea O
- Garcia Bernardo C
- Garcia Florez LJ
- Garcia Septiem J
- Garcia Torres CP
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- Garland A
- Gash K
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- Gastaldi P
- Gasteratos K
- Gaujoux S
- Gavagna L
- Gbessi DG
- Gemeah M
- Gemenetzis G
- Gemenetzis G
- George R
- Germanos S
- Germanos S
- Gerosa A
- Gerosa A
- Geuoshy A
- Ghaben A
- Ghandora N
- Ghanem A
- Ghanem E
- Ghanem S
- Ghanem S
- Ghannam M
- Gharib A
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- Ghazy AA
- Gheith A
- Ghetia M
- Ghetia M
- Ghonaim MA
- Ghoneem M
- Ghoneim O
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- Giardino FR
- Giavarini L
- Giglio MC
- Gilbert R
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- Giuliani S
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- Giuriato TF
- Gkiokas G
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- Glover-Addy H
- Glynn M
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- Goh W
- Gohar ME-SAM
- Gokani S
- Goldin E
- Golding D
- Gomaa A
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- Gonzales Montejo MS
- Gonzales Stuva JP
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- Grassi V
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- Grisin E
- Grizhja B
- Grobler DC
- Grosos C
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- Guevara Torres S
- Guevara R
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- Gul E
- Gulbinas A
- Gulcicek OB
- Gulielmi A
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- Gunawan R
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- Gyanchandani N
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- Hache-Marliere M
- Haddad N
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- Hafiz S
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- Hajeh H
- Hakim H
- Halhouli O
- Halhouli O
- Halicioglu I
- Hall E
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- Hamarshi A
- Hamasaki Hamaguchi JL
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- Hanley I
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- Hasheminia A
- Hashim A
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- Haslegrave A
- Hassaan A
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- Hassan I
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- Ibrahem AA
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- Ibrahim A
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- Ibrahim I
- Ibrahim K
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- Iqbal FM
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- Mizzi C
- Mizzi S
- Mlotshwa M
- Moaty M
- Mochet S
- Modolo MM
- Modolo MM
- 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
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- Mohammed AR
- Mohammed H
- Mohammed MM
- Mohammed MMH
- Mohammed S
- Mohan H
- Mohan M
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- Mok YT
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- Monrad-Hansen PW
- 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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- Morton D
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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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- Munipalle PC
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- Musowoya J
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- Mustafa M-A
- Musyoka CK
- Mutabazi A
- Mutabazi AZ
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- Mutlu V
- Muzio E
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- Nagy GS
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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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- Nasher O
- Nashidengo P
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- Nasir WNWM
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- Nassif D
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- Nataraja R
- Natili A
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- Nawara C
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- Nayel AR
- Nazir M
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- Ndegwa W
- Ndlovu SR
- Ndwambi P
- Negida A
- Negoi I
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- Neo YN
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- Neophytou C
- Nepogodiev D
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- Nesaratnam A
- Nessa A
- Nestorovic M
- Nevieraite V
- Newton T
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- Ngayu N
- Ngwa TE
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- Niyirera E
- Njokanma I
- Nnajiuba H
- Nocito A
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- Nofal E
- Noor F
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- Noukpozounkou B
- Novak A
- Nowers J
- Nsengimana VJP
- Nsengiyumva C
- Ntirenganya F
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- Nurqistan HD
- Nwabuoku E
- Nwinee V
- Nwokoro C
- Nyberg J
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- Palomino Castillo VD
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- Pasquali S
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- Pesenti G
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- Qureshi AU
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- Samalavicius NE
- Samaraweera DI
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- Tansoker I
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- Zakaria Y
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- Zalabia MF
- Zamarin K
- Zammit S
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- Zapata Ponze De Leon M
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- Zapata F
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- Zegarra S
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- Zelada Alvarez II
- Zerihun AB
- Zeta Solis LA
- Zhang Z
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- Zidan H
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- Zielinski M
- Ziff O
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- Zilinskas J
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- Zuk G
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- Zumbuhl L
- 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
Effects of hospital facilities on patient outcomes after cancer surgery: an international, prospective, observational study
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- A Yacoub M.
- A. Adam M.
- A. Nassar M.
- A. Nemer A.
- Aahlin E. K.
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- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2022
- Field of study
Background Early death after cancer surgery is higher in low-income and middle-income countries (LMICs) compared with in high-income countries, yet the impact of facility characteristics on early postoperative outcomes is unknown. The aim of this study was to examine the association between hospital infrastructure, resource availability, and processes on early outcomes after cancer surgery worldwide.Methods A multimethods analysis was performed as part of the GlobalSurg 3 study-a multicentre, international, prospective cohort study of patients who had surgery for breast, colorectal, or gastric cancer. The primary outcomes were 30-day mortality and 30-day major complication rates. Potentially beneficial hospital facilities were identified by variable selection to select those associated with 30-day mortality. Adjusted outcomes were determined using generalised estimating equations to account for patient characteristics and country-income group, with population stratification by hospital.Findings Between April 1, 2018, and April 23, 2019, facility-level data were collected for 9685 patients across 238 hospitals in 66 countries (91 hospitals in 20 high-income countries; 57 hospitals in 19 upper-middle-income countries; and 90 hospitals in 27 low-income to lower-middle-income countries). The availability of five hospital facilities was inversely associated with mortality: ultrasound, CT scanner, critical care unit, opioid analgesia, and oncologist. After adjustment for case-mix and country income group, hospitals with three or fewer of these facilities (62 hospitals, 1294 patients) had higher mortality compared with those with four or five (adjusted odds ratio [OR] 3.85 [95% CI 2.58-5.75]; p<0.0001), with excess mortality predominantly explained by a limited capacity to rescue following the development of major complications (63.0% vs 82.7%; OR 0.35 [0.23-0.53]; p<0.0001). Across LMICs, improvements in hospital facilities would prevent one to three deaths for every 100 patients undergoing surgery for cancer.Interpretation Hospitals with higher levels of infrastructure and resources have better outcomes after cancer surgery, independent of country income. Without urgent strengthening of hospital infrastructure and resources, the reductions in cancer-associated mortality associated with improved access will not be realised
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