27 research outputs found
Coping Strategies During Bereavement: The case of University of Botswana Students
- Author
- Publication venue
- Publication date
- 01/01/2010
- Field of study
South African HIV self-testing policy and guidance considerations
- Author
- Publication venue
- 'AOSIS'
- Publication date
- 01/01/2017
- Field of study
Examining the effects of HIV self-testing compared to standard HIV testing services in the general population: A systematic review and meta-analysis.
- Author
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/08/2021
- Field of study
BACKGROUND: We updated a 2017 systematic review and compared the effects of HIV self-testing (HIVST) to standard HIV testing services to understand effective service delivery models among the general population. METHODS: We included randomized controlled trials (RCTs) comparing testing outcomes with HIVST to standard testing in the general population and published between January 1, 2006 and June 4, 2019. Random effects meta-analysis was conducted and pooled risk ratios (RRs) were reported. The certainty of evidence was determined using the GRADE methodology. FINDINGS: We identified 14 eligible RCTs, 13 of which were conducted in sub-Saharan Africa. Support provided to self-testers ranged from no/basic support to one-on-one in-person support. HIVST increased testing uptake overall (RR:2.09; 95% confidence interval: 1.69-2.58; p < 0.0001;13 RCTs; moderate certainty evidence) and by service delivery model including facility-based distribution, HIVST use at facilities, secondary distribution to partners, and community-based distribution. The number of persons diagnosed HIV-positive among those tested (RR:0.81, 0.45-1.47; p = 0.50; 8 RCTs; moderate certainty evidence) and number linked to HIV care/treatment among those diagnosed (RR:0.95, 0.79-1.13; p = 0.52; 6 RCTs; moderate certainty evidence) were similar between HIVST and standard testing. Reported harms/adverse events with HIVST were rare and appeared similar to standard testing (RR:2.52: 0.52-12.13; p = 0.25; 4 RCTs; very low certainty evidence). INTERPRETATION: HIVST appears to be safe and effective among the general population in sub-Saharan Africa with a range of delivery models. It identified and linked additional people with HIV to care. These findings support the wider availability of HIVST to reach those who may not otherwise access testing
Determinants of recovery from post-COVID-19 dyspnoea: analysis of UK prospective cohorts of hospitalised COVID-19 patients and community-based controls
- Author
- Abel K
- Adamali H
- Adeloye D
- Adeyemi O
- Adrego R
- Aguilar Jimenez LA
- Ahmad Haider N
- Ahmad S
- Ahmed R
- Ahwireng N
- Ainsworth M
- Al-Sheklly B
- Alamoudi A
- Ali M
- Aljaroof M
- All AM
- Allan L
- Allen RJ
- Allerton L
- Allsop L
- Almeida P
- Altmann D
- Alvarez Corral M
- Amoils S
- Anderson D
- Antoniades C
- Arbane G
- Arias A
- Armour C
- Armstrong L
- Armstrong N
- Arnold D
- Arnold H
- Ashish A
- Ashworth A
- Ashworth M
- Aslani S
- Assefa-Kebede H
- Atkin C
- Atkin P
- Aul R
- Aung H
- Austin L
- Avram C
- Ayoub A
- Babores M
- Baggott R
- Bagshaw J
- Baguley D
- Bailey L
- Baillie JK
- Bain S
- Bakali M
- Bakau M
- Baldry E
- Baldwin D
- Baldwin M
- Ballard C
- Banerjee A
- Bang B
- Barker RE
- Barman L
- Barratt S
- Barrett F
- Basire D
- Basu N
- Bates A
- Bates M
- Batterham R
- Baxendale H
- Bayes H
- Beadsworth M
- Beckett P
- Beggs M
- Begum M
- Beirne P
- Bell D
- Bell R
- Bennett K
- Beranova E
- Bermperi A
- Berridge A
- Berry C
- Betts S
- Bevan E
- Bhui K
- Bingham M
- Birchall K
- Bishop L
- Bisnauthsing K
- Blaikely J
- Bloss A
- Bolger A
- Bolton CE
- Bonnington J
- Botkai A
- Bourne C
- Bourne M
- Bramham K
- Brear L
- Breen G
- Breeze J
- Briggs A
- Bright E
- Brightling CE
- Brightling CE
- Brill S
- Brindle K
- Broad L
- Broadley A
- Brookes C
- Broome M
- Brown A
- Brown CW
- Brown J
- Brown JS
- Brown JS
- Brown M
- Brown V
- Brugha T
- Brunskill N
- Buch M
- Buckley P
- Bularga A
- Bullmore E
- Burden L
- Burdett T
- Burn D
- Burns A
- Burns G
- Busby J
- Butcher R
- Butt A
- Byrne S
- Cairns P
- Calder PC
- Calvelo E
- Carborn H
- Card B
- Carr C
- Carr L
- Carson G
- Carter P
- Casey A
- Cassar M
- Cavanagh J
- Chablani M
- Chalder T
- Chalmers JD
- Chalmers JD
- Chambers RC
- Chan F
- Channon KM
- Chapman K
- Charalambou A
- Chaudhuri N
- Checkley A
- Chen J
- Cheng Y
- Chetham L
- Childs C
- Chilvers ER
- Chinoy H
- Chiribiri A
- Chong-James K
- Choudhury G
- Choudhury N
- Chowienczyk P
- Christie C
- Chrystal M
- Clark C
- Clark D
- Clarke J
- Clohisey S
- Coakley G
- Coburn Z
- Coetzee S
- Cole J
- Coleman C
- Conneh F
- Connell D
- Connolly B
- Connor L
- Cook A
- Cooper B
- Cooper J
- Cooper S
- Copeland D
- Cosier T
- Coulding M
- Coupland C
- Cox E
- Craig T
- Crisp P
- Cristiano D
- Crooks MG
- Cross A
- Cruz I
- Cullinan P
- Cuthbertson D
- D-C. Man W
- Daines L
- Daines L
- Dalton M
- Daly P
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- Dark P
- Dasgin J
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- Davies E
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- Davies G
- Davies GA
- Davies K
- Davies MJ
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- Daynes E
- De Soyza A
- De Soyza A
- Deakin B
- Deans A
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- Dell A
- Dempsey K
- Denneny E
- Dennis J
- Dewar A
- Dharmagunawardena R
- Diar-Bakerly N
- Dickens C
- Dipper A
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- Diwanji SN
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- Djukanovic R
- Dobson H
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- Docherty AB
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- Donaldson A
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- Dowling R
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- Drury HJC
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- Evenden C
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- Featherstone J
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- Greening NJ
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- Heaney LG
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- Holroyd-Hind B
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- Horsley A
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- Hosseini A
- Hotopf M
- Houchen-Wolloff L
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- Hurst J
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- Husain M
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- Kabir T
- Kaltsakas G
- Kamwa V
- Kanellakis N
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- Keenan N
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- Knighton A
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- Koprowska S
- Korszun A
- Koychev I
- Kurasz C
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- Laing C
- Lamlum H
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- Langenberg C
- Lasserson D
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- Macharia I
- Mackie J
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- Openshaw PJM
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- Ugwuoke R
- Upthegrove R
- Valabhji J
- Ventura M
- Vere J
- Vickers C
- Vinson B
- Vivaldi G
- Wade E
- Wade P
- Wain LV
- Wain LV
- Wainwright T
- Wajero LO
- Walder S
- Walker S
- Wall E
- Wallis T
- Walmsley S
- Walsh JA
- Walsh S
- Warburton L
- Ward TJC
- Warwick K
- Wassall H
- Waterson S
- Watson E
- Watson J
- Watson L
- Welch C
- Welch H
- Welsh B
- Wessely S
- West S
- Weston H
- Wheeler H
- White S
- Whitehead V
- Whitney J
- Whittaker S
- Whittam B
- Whitworth V
- Wight A
- Wild J
- Wilkins M
- Wilkinson D
- Williams B
- Williams J
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- Williams-Howard SA
- Willicombe M
- Willis G
- Willoughby J
- Wilson A
- Wilson D
- Wilson I
- Window N
- Witham M
- Wolf-Roberts R
- Wood C
- Woodhead F
- Woods J
- Wootton DG
- Wormleighton J
- Worsley J
- Wraith D
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- Wyles J
- Wynter I
- Xu M
- Yasmin N
- Yasmin S
- Yates T
- Yip KP
- Young A
- Young B
- Young S
- Yousuf AJ
- Zawia A
- Zeidan L
- Zhao B
- Zheng B
- Zheng B
- Zongo O
- Publication venue
- 'Elsevier BV'
- Publication date
- 27/03/2023
- Field of study
Background The risk factors for recovery from COVID-19 dyspnoea are poorly understood. We investigated determinants of recovery from dyspnoea in adults with COVID-19 and compared these to determinants of recovery from non-COVID-19 dyspnoea. Methods We used data from two prospective cohort studies: PHOSP-COVID (patients hospitalised between March 2020 and April 2021 with COVID-19) and COVIDENCE UK (community cohort studied over the same time period). PHOSP-COVID data were collected during hospitalisation and at 5-month and 1-year follow-up visits. COVIDENCE UK data were obtained through baseline and monthly online questionnaires. Dyspnoea was measured in both cohorts with the Medical Research Council Dyspnoea Scale. We used multivariable logistic regression to identify determinants associated with a reduction in dyspnoea between 5-month and 1-year follow-up. Findings We included 990 PHOSP-COVID and 3309 COVIDENCE UK participants. We observed higher odds of improvement between 5-month and 1-year follow-up among PHOSP-COVID participants who were younger (odds ratio 1.02 per year, 95% CI 1.01–1.03), male (1.54, 1.16–2.04), neither obese nor severely obese (1.82, 1.06–3.13 and 4.19, 2.14–8.19, respectively), had no pre-existing anxiety or depression (1.56, 1.09–2.22) or cardiovascular disease (1.33, 1.00–1.79), and shorter hospital admission (1.01 per day, 1.00–1.02). Similar associations were found in those recovering from non-COVID-19 dyspnoea, excluding age (and length of hospital admission). Interpretation Factors associated with dyspnoea recovery at 1-year post-discharge among patients hospitalised with COVID-19 were similar to those among community controls without COVID-19. Funding PHOSP-COVID is supported by a grant from the MRC-UK Research and Innovation and the Department of Health and Social Care through the National Institute for Health Research (NIHR) rapid response panel to tackle COVID-19. The views expressed in the publication are those of the author(s) and not necessarily those of the National Health Service (NHS), the NIHR or the Department of Health and Social Care. COVIDENCE UK is supported by the UK Research and Innovation, the National Institute for Health Research, and Barts Charity. The views expressed are those of the authors and not necessarily those of the funders
Cohort Profile: Post-Hospitalisation COVID-19 (PHOSP-COVID) study
- Author
- Abel K
- Adamali H
- Adeloye D
- Adeyemi O
- Adrego R
- Ahmad S
- Ahmed R
- Ahwireng N
- Ainsworth M
- Al-Sheklly B
- Alamoudi A
- Ali M
- Aljaroof M
- All AM
- Allan L
- Allen RJ
- Allerton L
- Allsop L
- Almeida P
- Altmann D
- Amoils S
- Anderson D
- Anifowose S
- Antoniades C
- Arbane G
- Arias A
- Armour C
- Armour C
- Armstrong L
- Armstrong N
- Armstrong N
- Arnold D
- Arnold H
- Ashish A
- Ashworth A
- Ashworth M
- Aslani S
- Assefa-Kebede H
- Atkin C
- Atkin P
- Atkins H
- Aul R
- Aul R
- Aul R
- Aung H
- Austin L
- Avram C
- Ayoub A
- Babores M
- Baggott R
- Bagshaw J
- Baguley D
- Bailey L
- Baillie JK
- Baillie JK
- Baillie JK
- Baillie JK
- Baillie JK
- Baillie JK
- Bain S
- Bakali M
- Bakau M
- Bakerly ND
- Bakerly ND
- Baldry E
- Baldwin D
- Baldwin M
- Baldwin M
- Ballard C
- Banerjee A
- Bang B
- Barker RE
- Barman L
- Barratt S
- Barrett F
- Barrett S
- Basire D
- Basu N
- Basu N
- Bates A
- Bates M
- Batterham R
- Baxendale H
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- MacGowan G
- Macharia I
- Mackie J
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- McMahon MJ
- McMorrow L
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- Window N
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- Wood C
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- Zawia A
- Zeidan L
- Zhao B
- Zheng B
- Zongo O
- Publication venue
- Oxford University Press (OUP)
- Publication date
- 18/12/2023
- Field of study
Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease
- Author
- Aaltonen M
- Abdur Rahman M
- Abell T
- Abide W. Jr
- Acheatel R
- Achiri P
- Acon J
- Adams T
- Affinito S
- Agarwal S
- Aggarwal K
- Aggarwal R
- Ahlström P
- Ahmad A
- Ahmed M
- Aillon C
- Airaksinen A
- Ait-sadi R
- Akers J
- Al-jumaily J
- Albers C
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- Alford C
- Algotsson L
- Allen T
- Allworth M
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- Aloisi A
- Alternburg C
- Alton M
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- Amundson A
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- Andersen M
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- Zhao L
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- Zhou Xingyu
- Zhou Yingyuan
- Zhu Wangqin
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- Zoghbi J
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- Zuchelkowski A
- Zulauf N
- Ågårdh A
- Öner A
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND:
Patients with atherosclerotic vascular disease remain at high risk for cardiovascular events despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels. The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels. However, trials of other CETP inhibitors have shown neutral or adverse effects on cardiovascular outcomes.
METHODS:
We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with atherosclerotic vascular disease who were receiving intensive atorvastatin therapy and who had a mean LDL cholesterol level of 61 mg per deciliter (1.58 mmol per liter), a mean non-HDL cholesterol level of 92 mg per deciliter (2.38 mmol per liter), and a mean HDL cholesterol level of 40 mg per deciliter (1.03 mmol per liter). The patients were assigned to receive either 100 mg of anacetrapib once daily (15,225 patients) or matching placebo (15,224 patients). The primary outcome was the first major coronary event, a composite of coronary death, myocardial infarction, or coronary revascularization.
RESULTS:
During the median follow-up period of 4.1 years, the primary outcome occurred in significantly fewer patients in the anacetrapib group than in the placebo group (1640 of 15,225 patients [10.8%] vs. 1803 of 15,224 patients [11.8%]; rate ratio, 0.91; 95% confidence interval, 0.85 to 0.97; P=0.004). The relative difference in risk was similar across multiple prespecified subgroups. At the trial midpoint, the mean level of HDL cholesterol was higher by 43 mg per deciliter (1.12 mmol per liter) in the anacetrapib group than in the placebo group (a relative difference of 104%), and the mean level of non-HDL cholesterol was lower by 17 mg per deciliter (0.44 mmol per liter), a relative difference of -18%. There were no significant between-group differences in the risk of death, cancer, or other serious adverse events.
CONCLUSIONS:
Among patients with atherosclerotic vascular disease who were receiving intensive statin therapy, the use of anacetrapib resulted in a lower incidence of major coronary events than the use of placebo. (Funded by Merck and others; Current Controlled Trials number, ISRCTN48678192 ; ClinicalTrials.gov number, NCT01252953 ; and EudraCT number, 2010-023467-18 .)