90 research outputs found
Effect of SGLT2 inhibitors on stroke and atrial fibrillation in diabetic kidney disease: Results from the CREDENCE trial and meta-analysis
- Author
- Abdallah J.
- Abdullah R.
- Abejuela Z.
- Abouglila K.
- Abramowitz M.
- Abusnana S.
- Acosta I.
- Agafyina A.
- Aggarwal N.
- Agra J.
- Ahmad N. N. F. N.
- Ahmed F.
- Aiello J.
- Ainsworth P.
- Aizenberg D.
- Akiyama H.
- Akright L.
- Akyea-Djamson A.
- Al-Karadsheh A.
- Alamartine E.
- Alappan R.
- Albisu J. P.
- Ali N.
- Ali Z.
- Alicic R.
- Allison D. C.
- Alonso R. D. V.
- Alva H.
- Alvarisqueta A.
- Amodeo C.
- Andreeva V.
- Angelescu L. M.
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- Aquitania G.
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- Zalunardo N.
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- Zaniewski-Singh M.
- Zanoli L.
- Zaoui P.
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- Zateyshshikov D.
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- Publication venue
- 'Ovid Technologies (Wolters Kluwer Health)'
- Publication date
- 01/01/2021
- Field of study
BACKGROUND AND PURPOSE: Chronic kidney disease with reduced estimated glomerular filtration rate or elevated albuminuria increases risk for ischemic and hemorrhagic stroke. This study assessed the effects of sodium glucose cotransporter 2 inhibitors (SGLT2i) on stroke and atrial fibrillation/flutter (AF/AFL) from CREDENCE (Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation) and a meta-Analysis of large cardiovascular outcome trials (CVOTs) of SGLT2i in type 2 diabetes mellitus. METHODS: CREDENCE randomized 4401 participants with type 2 diabetes mellitus and chronic kidney disease to canagliflozin or placebo. Post hoc, we estimated effects on fatal or nonfatal stroke, stroke subtypes, and intermediate markers of stroke risk including AF/AFL. Stroke and AF/AFL data from 3 other completed large CVOTs and CREDENCE were pooled using random-effects meta-Analysis. RESULTS: In CREDENCE, 142 participants experienced a stroke during follow-up (10.9/1000 patient-years with canagliflozin, 14.2/1000 patient-years with placebo; hazard ratio [HR], 0.77 [95% CI, 0.55-1.08]). Effects by stroke subtypes were: ischemic (HR, 0.88 [95% CI, 0.61-1.28]; n=111), hemorrhagic (HR, 0.50 [95% CI, 0.19-1.32]; n=18), and undetermined (HR, 0.54 [95% CI, 0.20-1.46]; n=17). There was no clear effect on AF/AFL (HR, 0.76 [95% CI, 0.53-1.10]; n=115). The overall effects in the 4 CVOTs combined were: Total stroke (HRpooled, 0.96 [95% CI, 0.82-1.12]), ischemic stroke (HRpooled, 1.01 [95% CI, 0.89-1.14]), hemorrhagic stroke (HRpooled, 0.50 [95% CI, 0.30-0.83]), undetermined stroke (HRpooled, 0.86 [95% CI, 0.49-1.51]), and AF/AFL (HRpooled, 0.81 [95% CI, 0.71-0.93]). There was evidence that SGLT2i effects on total stroke varied by baseline estimated glomerular filtration rate (P=0.01), with protection in the lowest estimated glomerular filtration rate (45 mL/min/1.73 m2]) subgroup (HRpooled, 0.50 [95% CI, 0.31-0.79]). CONCLUSIONS: Although we found no clear effect of SGLT2i on total stroke in CREDENCE or across trials combined, there was some evidence of benefit in preventing hemorrhagic stroke and AF/AFL, as well as total stroke for those with lowest estimated glomerular filtration rate. Future research should focus on confirming these data and exploring potential mechanisms
Effects of hospital facilities on patient outcomes after cancer surgery: an international, prospective, observational study
- Author
- A Yacoub M.
- A. Adam M.
- A. Nassar M.
- A. Nemer A.
- Aahlin E. K.
- Ab Rahim M. F.
- Abad Gurumeta A.
- Abad-Motos A.
- Abang Jamari D. Z. H.
- Abantanga F.
- Abarca S.
- Abazid E.
- Abbas A.
- Abbas K.
- Abbas M. M.
- Abbasy J.
- Abbosh A.
- Abd B.
- Abd Karim M. F. S.
- Abd Wahab H. H.
- Abdalei A.
- Abdalla Ahmed Elkamel A.
- Abdallah A.
- AbdAllah M. S. M.
- Abdel Malik A. B.
- Abdelhady Mousa H.
- Abdelhady S.
- Abdelhakim A.
- Abdelkader M.
- Abdelkawy S.
- Abdelkhalek M.
- Abdellatif E.
- Abdelmaksoud Tawakel N.
- Abdelmohsen N.
- Abdelmotaleb I.
- Abdelrazek A.
- Abdelsalam I.
- Abdelshakour M.
- Abdelwahed A. M.
- Abdou A.
- Abdou A. O.
- Abdou H.
- Abdul Aziz M. R.
- Abdul Aziz N.
- Abdulgawad Almogy M.
- Abdulla M. A.
- Abdullah M. T.
- Abdullahi L.
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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
Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy
- Author
- Abdallah J
- Abdul Ghani R
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- Zinman Bernard
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- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2019
- Field of study
BACKGROUND Type 2 diabetes mellitus is the leading cause of kidney failure worldwide, but few effective long-term treatments are available. In cardiovascular trials of inhibitors of sodium–glucose cotransporter 2 (SGLT2), exploratory results have suggested that such drugs may improve renal outcomes in patients with type 2 diabetes. METHODS In this double-blind, randomized trial, we assigned patients with type 2 diabetes and albuminuric chronic kidney disease to receive canagliflozin, an oral SGLT2 inhibitor, at a dose of 100 mg daily or placebo. All the patients had an estimated glomerular filtration rate (GFR) of 30 to 300 to 5000) and were treated with renin–angiotensin system blockade. The primary outcome was a composite of end-stage kidney disease (dialysis, transplantation, or a sustained estimated GFR of <15 ml per minute per 1.73 m 2), a doubling of the serum creatinine level, or death from renal or cardiovascular causes. Prespecified secondary outcomes were tested hierarchically. RESULTS The trial was stopped early after a planned interim analysis on the recommendation of the data and safety monitoring committee. At that time, 4401 patients had undergone randomization, with a median follow-up of 2.62 years. The relative risk of the primary outcome was 30% lower in the canagliflozin group than in the placebo group, with event rates of 43.2 and 61.2 per 1000 patient-years, respectively (hazard ratio, 0.70; 95% confidence interval [CI], 0.59 to 0.82; P=0.00001). The relative risk of the renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes was lower by 34% (hazard ratio, 0.66; 95% CI, 0.53 to 0.81; P<0.001), and the relative risk of end-stage kidney disease was lower by 32% (hazard ratio, 0.68; 95% CI, 0.54 to 0.86; P=0.002). The canagliflozin group also had a lower risk of cardiovascular death, myocardial infarction, or stroke (hazard ratio, 0.80; 95% CI, 0.67 to 0.95; P=0.01) and hospitalization for heart failure (hazard ratio, 0.61; 95% CI, 0.47 to 0.80; P<0.001). There were no significant differences in rates of amputation or fracture. CONCLUSIONS In patients with type 2 diabetes and kidney disease, the risk of kidney failure and cardiovascular events was lower in the canagliflozin group than in the placebo group at a median follow-up of 2.62 years
Outcomes from elective colorectal cancer surgery during the SARS-CoV-2 pandemic
- Author
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- Perotto L. O.
- Perra T.
- Persiani R.
- Pertile D.
- Petrillo A.
- Petropoulos K.
- Peyroteo M.
- Pezzuto A. P.
- Peña Ros E.
- Phan D. Townend D. (Lismore Base Hospital)
- Phillips E.
- Picardo A. L.
- Pickett L. (Connolly Hospital Blanchardstown)
- Picón Rodríguez R.
- Pieniowski E. (Stockholm South General Hospital)
- Piessen G.
- Pieve Emanuele (Mi))
- Pina S.
- Pinto J. Tojal A. (Centro Hospitalar Tondela-Viseu)
- Pipitone Federico N. S. (Edoardo Agnelli)
- Pisani Ceretti A. (ASST Santi Paolo E. Carlo)
- Pisanu A.
- Pizarro M. J.
- Pizzini P. (Ospedale Maggiore di Lodi)
- Pla Marti V. (Hospital Clínico Universitario de Valencia)
- Poch C.
- Pockney P. (John Hunter Hospital)
- Podda M. (Cagliari University Hospital)
- Poggioli G.
- Polydorou A.
- Popoola A. (University of Ilorin Teaching Hospital). Pakistan: Jamal A.
- Porcu A.
- Portinari M.
- Posadas-Trujillo O. E.
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- Presl J.
- Price C.
- Prieto Calvo M.
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- Provozina A. (Immanuel Kant Baltic Federal University
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- Ramcharan S.
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- Ravindrakumar S.
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- Raymond T.
- Razafindrahita J. B.
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- Rega D.
- Regional Clinical Hospital)
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- Reynolds I. S.
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- Ribeiro C. G.
- Ribeiro R.
- Ribeiro V. I.
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- Rice D.
- Richards T.
- Ridgway P. F.
- Righini E. (Azienda Unità Sanitaria Locale di Ferrara
- Riley C.
- Rimonda R.
- Ringressi M. N.
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- Risaliti M.
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- Robinson A.
- Rodimov S.
- Rodrigo V. S. D. (District General Hospital Chilaw)
- Rodriguez J. L.
- Rodríguez Gómez L. (Severo Ochoa University Hospital)
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- Rojo López J. A.
- Romano M.
- Romero de Diego A.
- Ronellenfitsch U. (University Hospital Halle (Saale))
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- Rose J.
- Roslani A. C. (University Malaya Medical Centre). Mexico: Buerba G. A.
- Rossi S.
- Rottoli M.
- Roy Mahapatra S.
- Royle T.
- Rozzano (Mi) and Humanitas University
- Rubio-Perez I.
- Ruivo A.
- Ruiz Escobar A. (Infanta Leonor University Hospital)
- Ruiz Soriano M.
- Ruiz-Marín M.
- Russ J.
- Rutegård M. (Umea University Hospital). Switzerland: Arigoni M.
- Rutherford D.
- Ruzzenente A.
- Ryan M. (University Hospital Waterford/University College Cork). Italy: Macina S. (ASST Mantua)
- Ryan É. (University Hospital Galway)
- Ryska O. (Royal Lancaster Infirmary)
- Río Lafuente F. D.
- Saad M. M.
- Saafan T.
- Saavedra J.
- Sabah)
- Sabratha)
- Sabry A.
- Saeed S.
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- Sagnotta A. (Ospedale San Filippo Neri)
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- Saleem A.
- Salem H.
- Salgado-Nesme N.
- Salimoğlu S.
- Salindera S.
- Sallam I.
- Samih A.
- Samir Abdelaal A.
- Samison L. H. (Joseph Ravoahangy Andrianavalona Hospital). Malaysia: Hamdan K. H.
- Samkari A.
- Sammarco G.
- Sammour T. (Royal Adelaide Hospital)
- Sampaio da Nóvoa Gomes Miguel I. I. (Centro Hospitalar Universitário do Algarve – Unidade de Portimão)
- Sampietro G. M. (Ospedale di Rho – ASST Rhodense)
- San Francisco (UCSF))
- Sanchez Cabezudo Noguera F.
- Sanchez Gonzalez J.
- Sanchez Jimenez R.
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- Sancho-Muriel J. (Hospital Universitario Y Politécnico la Fe)
- Sanchon L.
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- Santanach C.
- Santarrufina Martinez S.
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- Sarantitis I.
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- Sarjanoja E. (Länsi-Pohja Central Hospital)
- Sarma D. R.
- Sarre C. (Instituto Nacional de Ciencias Médicas y Nutrición ‘Salvador Zubirán’). Morocco: Amrani L.
- Sartarelli L.
- Sarveswaran J.
- Sasapu K. (Diana Princess of Wales Hospital Grimsby)
- Sasia D.
- Saudí S. (Hospital Universitario Miguel Servet)
- Sauvain M. (Pourtales Neuchatel Hospital)
- Sauvat F. (CHU Réunion). Romania: Bezede C.
- Savković N.
- Sayyed R. (Patel Hospital)
- Scabini S.
- Scalabre A. (Chu Saint Etienne)
- Scanu A. M. (Cliniche San Pietro
- Schiavo M. (Ospedale Vittorio Emanuele III – Carate Brianza)
- Schiergens T.
- Schineis C. (Charité University Medicine
- Schizas D.
- Schlesinger N.
- Schwartz P.
- Scott L. (Pinderfields Hospital)
- Scotton G. (St Moritz Hospital)
- Scrima O.
- Sechenov Medical State University)
- Seebah K.
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- Seguin-Givelet A.
- Sehgal T.
- Selmani J.
- Semina E. (Moscow Research and Educational Center
- Senossi O.
- Serevina O. L.
- Serralta de Colsa D. (Infanta Sofía University Hospital)
- Serrano González J. (Hospital Universitario de Torrejón de Ardoz)
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- Sert İ.
- Seymour Z. (Ysbyty Gwynedd). USA: Haynes A.
- Sganga G. (Fondazione Policlinico Universitario Agostino Gemelli IRCCS)
- Sgrò A.
- Shah J. (North Manchester General Hospital)
- Shah S. (The Whittington Hospital)
- Shah Z. A.
- Shaikh I.
- Shaikh S.
- Sharabiany S. (Amsterdam UMC
- Sharma P. (Aberdeen Royal Infirmary)
- Shehata S.
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- Sheridan K.
- Sherief M.
- Sherif A. (Misr Cancer Center)
- Sherif A. E. (National Liver Institute
- Sherif G. (National Cancer Institute)
- Shokuhi P.
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- Sian T.
- Sibilla M. G.
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- Silva M.
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- Silveira Nunes I.
- Simões J. (Centro Hospitalar e Universitário de Coimbra)
- Singh A.
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- Smith H. (Bispebjerg Hospital). Egypt: Al Sayed M.
- Smith L.
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- Soares A. P.
- Soh J. Y.
- Sohrabi C.
- Solari F.
- Soriero D. (IRCCS Ospedale Policlinico San Martino)
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- Soto Montesinos C. (Fundació Althaia – Xarxa Assistencial Universitària de Manresa)
- Souadka A. (Institut National d’Oncologie
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- Spampinato M. G. (Vito Fazzi
- Spartalis E.
- Spencer N.
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- Stavrinidou O.
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- Stylianidis G. (Evaggelismos General Hospital)
- Subhi M. T. (Alkhadra Hospital)
- Subocius A.
- Subramaniam S. (Queen Elizabeth Hospital and Universiti Malaysia Sabah
- Sundaram Venkatesan G. (Glan Clwyd Hospital)
- Suszták N. (Szent Borbála Kórház). India: Bhat G. A.
- Sutherland A. (Coffs Harbour Health Campus)
- Swinson B. (Royal Brisbane and Women’s Hospital). Austria: Messner F.
- Syed W. A. S.
- Syllaios A.
- Szatmary P.
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- Sánchez del Pueblo C.
- Sánchez Fuentes N.
- Sánchez- Pernaute A.
- Sánchez- Rubio M.
- Sánchez-García S.
- Taddei A.
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- Taibi A. (Chu Limoges)
- Talal El-Abur I.
- Talwar R. (Luton and Dunstable University Hospital)
- Tammaro P.
- Tan J. A.
- Tan X. S.
- Tanal M.
- Tang A. M.
- Tanzanu M.
- Tartaglia D. (Azienda Ospedaliero Universitaria Pisana)
- Tasis N. (Athens Naval and Veterans Hospital)
- Tatar O. C.
- Tavares F.
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- Tebala G. D.
- Teixeira J. (Centro Hospitalar Universitário do Algarve – Unidade de Faro)
- Teixeira M. (Centro Hospitalar do Tamega e Sousa)
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- Testa V. (Santa Croce E. Carle Hospital
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- Tezas S. (Furness General Hospital)
- Thaha M.
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- Theodosopoulos T.
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- Thulasiraman S. V.
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- TU Dresden)
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- Ugarte-Sierra B. (Hospital Universitario de Galdakao)
- Uludağ S. S.
- Umair M.
- Universiti Sains Malaysia)
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- Université Mohammed V Rabat). Netherlands: Hompes R.
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- Uslu G.
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- Velidedeoglu M.
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- Vervoort D.
- Vescio G. (University ‘Magna Graecia’ of Catanzaro)
- Vezakis A. (Aretaieion Hospital)
- Videira J. F. (IPO Porto). Réunion: Kassir R.
- Vieira B. (Centro Hospitalar de Trás-Os-Montes e Alto Douro
- Vieira Caroço T. (IPO Coimbra)
- Vieira Paiva Lopes A. C. (Hospital de Torres Vedras – Centro Hospitalar do Oeste)
- Vignali A. (San Raffaele Scientific Institute
- Vigorita V. (Álvaro Cunqueiro Hospital)
- Vijayan D. (Queen Elizabeth Hospital Birmingham)
- Villalabeitia Ateca I. (Hospital Universitario Cruces)
- Vimalachandran D. (Countess of Chester Hospital)
- Viswanath Y. K. S. (James Cook University Hospital)
- Vitali A. (Ospedale San Giovanni di Dio)
- Vitone L. (Royal Blackburn Hospital)
- Vives R. V. (Bellvitge University Hospital)
- Vo U. G. (Fiona Stanley Hospital)
- Von Papen M.
- Vovola F. (Ospedali Riuniti Azienda Ospedaliera Universitaria Foggia)
- Vucic N.
- Vázquez Fernández A. (Hospital Clínico Universitario de Valladolid)
- Wadham B. (The University Hospital of South Manchester)
- Walkes K. (Queen Elizabeth Hospital). Belgium: Flamey N.
- Wani R. (Sher-I-Kashmir Institute of Medical Sciences)
- Waqar S. H. (Pakistan Institute of Medical Sciences). Poland: Major P. (Jagiellonian University Medical College). Portugal: Azevedo C.
- Warren O. (Chelsea and Westminster Hospital)
- Watson L. J. (Sunderland Royal Hospital)
- Watson N. (King’s Mill Hospital)
- Weitz J.
- Welsch T. (Carl-Gustav-Carus University Hospital
- Werner J. (LMU Klinikum Campus Innenstadt)
- Westwood E. (James Paget University NHS Foundation Trust Hospital)
- Whelan M. (Tallaght University Hospital)
- Whitmore H. (Torbay and South Devon NHS Trust)
- Wilkin R. J. W. (South Warwickshire NHS Foundation Trust)
- Wilkins A. (Hull University Teaching Hospitals NHS Trust)
- Williams G. (Royal Gwent Hospital)
- Williams K. (St George’s Hospital)
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- Wong M.
- Worku D. (Queens Medical Centre)
- Wullschleger M. (Gold Coast University Hospital)
- Xavier R. G.
- Xenaki S.
- Xynos E. (University Hospital of Heraklion Crete and Interclinic Hospital of Crete). Hong Kong: Futaba K.
- Yang W.
- Yassin N. (Royal Wolverhampton NHS Trust)
- Ye G.
- Yesantharao P.
- Yetkin S. G. (Sisli Hamidiye Etfal Training and Research Hospital)
- Yeşilyurt D. (University of Health Sciences Tepecik Training and Research Hospital)
- Yiallourou A. (Nicosia General Hospital). Czechia: Martinek L.
- Yıldırım A.
- Yildiz A. (Yildirim Beyazit University Yenimahalle Training and Research Hospital). Uganda: Lule H.
- Young R. (York Teaching Hospitals NHS Trust)
- Yousof E. A. (Assiut University Hospital)
- Youssef M. (Norfolk and Norwich University Hospital)
- Yurttas C. (University Hospital Tuebingen)
- Yánez C. (Royo Villanova)
- Yüksel E. (Kocaeli University Teaching Hospital)
- Zafar S. N. (University of Wisconsin)
- Zakaria A. D.
- Zakaria Z. (School of Medical Sciences and Hospital
- Zambon M. (Policlinico Umberto I Sapienza University of Rome)
- Zanus G. (Ca’ Foncello Treviso – DISCOG – Università di Padova)
- Zegarac M. (Institute for Oncology and Radiology of Serbia)
- Zelić M. (University Hospital Center Rijeka)
- Zengin A. K. (Istanbul Universty – Cerrahpaşa Medical Faculty)
- Zerbib P. (CHU Lille)
- Zervas K.
- Zese M. (Santa Maria degli Angeli Hospital ULSS 5 – Adria)
- Zhang H. (Concord Repatriation General Hospital)
- Zizzo M. (Azienda Unità Sanitaria Locale – IRCCS di Reggio Emilia)
- Zografos C. (Laiko University Hospital)
- Zorrilla Ortúzar J. (Hospital General Universitario Gregorio Marañón)
- Zourntou S. (General Hospital of Larissa ‘Koutlimpaneio and Triantafylleio’)
- Zubaidi A. M. (King Saud University). Serbia: Aleksić L.
- Ângelo M.
- Çelebi F.
- Çolak E.
- Öfner D. (Medical University of Innsbruck)
- Öhlberger L.
- Özçelık M. F.
- Öğücü H.
- Überrück L.
- Ćoza I.
- Publication venue
- 'Wiley'
- Publication date
- 01/01/2020
- Field of study
This study aimed to describe the change in surgical practice and the impact of SARS-CoV-2 on mortality after surgical resection of colorectal cancer during the initial phases of the SARS-CoV-2 pandemic
Adolescent transport and unintentional injuries: a systematic analysis using the Global Burden of Disease Study 2019
- Author
- Abadi Kidanemariam Berhe
- Abbas Mosapour
- Abdallah M Samy
- Abdelrahman I Abushouk
- Abdiwahab Hashi
- Abdollah Mohammadian-Hafshejani
- Abdullah A Mamun
- Abdullah T Khoja
- Abhay Motiramji Gaidhane
- Abiy H Sinke
- Adam E Berman
- Adnan Kisa
- Adrian Otoiu
- Adrian Pana
- Afshin Maleki
- Agus Sudaryanto
- Ahamarshan Jayaraman Nagarajan
- Ahmad Ghashghaee
- Ahmad Zarei
- Ahmed I Hasaballah
- Ahmed Omar Bali
- Ai Koyanagi
- Ai-Min Wu
- Aidin Abedi
- Aisha Elsharkawy
- Akram Pourshams
- Akshaya Srikanth Bhagavathula
- Alberto Ortiz
- Alberto Raggi
- Alexander C Tsai
- Ali A Asadi-Pooya
- Ali Bijani
- Ali H Mokdad
- Ali Kabir
- Ali Koolivand
- Alireza Didarloo
- Amanda J Mason-Jones
- Amin Mousavi Khaneghah
- Amin Soheili
- Amir Abdoli
- Amir Almasi-Hashiani
- Amir Jalali
- Amir Radfar
- Amir Taherkhani
- Amira A Shaheen
- Amirhossein Sahebkar
- Amr Hassan
- Amy E Peden
- Anamika Pandey
- Anders O Larsson
- Andre Faro
- Andre M N Renzaho
- Andre Rodrigues Duraes
- Andreea Mirica
- Andrew T Olagunju
- André Karch
- Animut Tagele Tamiru
- Antonio Biondi
- Anurag Agrawal
- Anwar E Ahmed
- Arash Sarveazad
- Archith Boloor
- Arianna Maever L Amit
- Arielle Wilder Bell
- Aristidis Tsatsakis
- Artem Alekseevich Fomenkov
- Arvin Haj-Mirzaian
- Arya Aminorroaya
- Arya Haj-Mirzaian
- Asif Hanif
- Aso Mohammad Darwesh
- Assefa Ayalew Gebreslassie
- Assefa Desalew
- Ata Rafiee
- Atte Meretoja
- Ayesha Humayun
- Azeem Majeed
- Aziz Sheikh
- Azmeraw T Amare
- B Suresh Kumar Shetty
- Babak Eshrati
- Babak Moazen
- Bach Xuan Tran
- Bartosz Miazgowski
- Basema Saddik
- Beatriz Paulina Ayala Quintanilla
- Ben Lacey
- Bernhard T Baune
- Bhaskaran Unnikrishnan
- Biagio Simonetti
- Bing-Fang Hwang
- Bingyu Li
- Biresaw Wassihun Alemu
- Blessing Akombi-Inyang
- Bolajoko Olubukunola Olusanya
- Borhan Mansouri
- Boris Bikbov
- Brian J Hall
- Brigid Unim
- Budi Aji
- Carl Abelardo T Antonio
- Carlo Irwin Able Panelo
- Carlo La Vecchia
- Carlos A Castañeda-Orjuela
- Catalina Liliana Andrei
- Chandrashekhar T Sreeramareddy
- Chenkai Wu
- Chhabi Lal Ranabhat
- Chirag P Doshi
- Christian Kieling
- Christoph Nowak
- Christopher J L Murray
- Chuanhua Yu
- Chukwudi A Nnaji
- Claudio Alberto Dávila-Cervantes
- Claudiu Herteliu
- Cong Zhu
- Corina Benjet
- Dan J Stein
- Daniel Diaz
- Dara K Mohammad
- David C Schwebel
- David Edvardsson
- David Laith Rawaf
- Davide Sattin
- Davood Anvari
- Davoud Adham
- Deanna Anderlini
- Deborah Carvalho Malta
- Deepak Saxena
- Dejana Braithwaite
- Demelash Woldeyohannes Handiso
- Deniz Yuce
- Devasahayam J Christopher
- Dharmesh Kumar Lal
- Dian Kusuma
- Diana Dias da Silva
- Dickson A Amugsi
- Diego Augusto Santos Silva
- Diego De Leo
- Diep Ngoc Nguyen
- Dina Nur Anggraini Ningrum
- Dinh-Toi Chu
- Eduarda Fernandes
- Ehsan Sadeghi
- Elena V Gnedovskaya
- Elisabetta Pupillo
- Elvis Korku Avenyo
- Eman Abu-Gharbieh
- Emma U R Smith
- Emmanuel K Peprah
- Endalkachew Worku Mengesha
- Enrico Rubagotti
- Ensiyeh Jenabi
- Era Upadhyay
- Erkin M Mirrakhimov
- Ester Cerin
- Ettore Beghi
- Eugene Sobngwi
- Eun-Kee Park
- Fahad Mashhour Alanezi
- Faheem Hyder Pottoo
- Fakher Rahim
- Falk Schwendicke
- Farahnaz Joukar
- Fares Alahdab
- Farhad Ghamari
- Fariba Dorostkar
- Farshad Farzadfar
- Fatemeh Heydarpour
- Felix Akpojene Ogbo
- Felix Carvalho
- Feng Sha
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- Marco Vacante
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- Mariya Vladimirovna Titova
- Mark A Stokes
- Marwa Rashad Salem
- Maryam Khayamzadeh
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- Miriam Levi
- Mohamed Hsairi
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- Mohammad Abdollahi
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- Mohammad Ebrahimi Kalan
- Mohammad Hasan Rabiee
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- Mohammad Hossein Bakhshaei
- Mohammad Khammarnia
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- MohammadBagher Shamsi
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- Perminder S Sachdev
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- Pietro Ferrara
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- Raaj Kishore Biswas
- Rabia Hussain
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- Shuhei Nomura
- Siamak Sabour
- Silvano Gallus
- Silvia Schiavolin
- Simon I Hay
- Simon Øverland
- Sivan Yegnanarayana Iyer Saraswathy
- Soewarta Kosen
- Sofia Androudi
- Soheil Hassanipour
- Sojib Bin Zaman
- Somayeh Bohlouli
- Songhomitra Panda-Jonas
- Sonia Lewycka
- Sonia Saxena
- Soraya Siabani
- Sorin Hostiuc
- Soufiane Boufous
- Sowmya J Rao
- Srinivas Goli
- Srinivasa Rao Bolla
- Stanislav S Otstavnov
- Stefan Lorkowski
- Stephen S Lim
- Subramanian Senthilkumaran
- Supreet Kaur
- Suraj Bhattarai
- Susan Fred Rumisha
- Susan M Sawyer
- Suzanne Lyn Barker-Collo
- Syed Amir Gilani
- Syed Mohamed Aljunid
- Syed Saoud Zaidi
- Tahereh Javaheri
- Takahiro Tabuchi
- Takeshi Fukumoto
- Tanuj Kanchan
- Tanvir M Huda
- Taraneh Yousefinezhadi
- Tariku Tesfaye Bekuma
- Tauseef Ahmad
- Ted R Miller
- Teklehaimanot Gereziher Haile
- Tesega Tesega Mengistu Birhanu
- Teshome Gebre
- Theo Vos
- Thirunavukkarasu Sathish
- Till Winfried Bärnighausen
- Tomas Y Ferede
- Tomasz Miazgowski
- Tomislav Mestrovic
- Tommi Juhani Vasankari
- Traian Vasile Constantin
- Tuomo J Meretoja
- Turki M Alanzi
- Ulrich Otto Mueller
- Usman Iqbal
- Vafa Rahimi-Movaghar
- Vahid Rashedi
- Vahid Yazdi-Feyzabadi
- Valentin Yurievich Skryabin
- Valery L Feigin
- Van Charles Lansingh
- Vasily Vlassov
- Vegard Skirbekk
- Veincent Christian Filipino Pepito
- Vera Marisa Costa
- Victor Adekanmbi
- Vijay Kumar Chattu
- Vinay Nangia
- Vinod C Nayak
- Virendra Singh
- Virginia Nuñez-Samudio
- Vivekanand Jha
- Walter Mendoza
- Xiaochen Dai
- Xiu-Ju George Zhao
- Xuefeng Liu
- Yafeng Wang
- Yanzhong Wang
- Yared Asmare Aynalem
- Yasir Waheed
- Yong Yu
- Yordanos Gizachew Yeshitila
- Young-Eun Kim
- Yuan-Pang Wang
- Yuichiro Yano
- Yuming Guo
- Yun Jin Kim
- Yunquan Zhang
- Zahid A Butt
- Zahiruddin Quazi Syed
- Zelalem Nigussie Azene
- Zhi-Jiang Zhang
- Ziyad Al-Aly
- Zohra S Lassi
- Zubair Kabir
- Zulfiqar A Bhutta
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2022
- Field of study
Background: Globally, transport and unintentional injuries persist as leading preventable causes of mortality and morbidity for adolescents. We sought to report comprehensive trends in injury-related mortality and morbidity for adolescents aged 10–24 years during the past three decades. Methods: Using the Global Burden of Disease, Injuries, and Risk Factors 2019 Study, we analysed mortality and disability-adjusted life-years (DALYs) attributed to transport and unintentional injuries for adolescents in 204 countries. Burden is reported in absolute numbers and age-standardised rates per 100 000 population by sex, age group (10–14, 15–19, and 20–24 years), and sociodemographic index (SDI) with 95% uncertainty intervals (UIs). We report percentage changes in deaths and DALYs between 1990 and 2019. Findings: In 2019, 369 061 deaths (of which 214 337 [58%] were transport related) and 31·1 million DALYs (of which 16·2 million [52%] were transport related) among adolescents aged 10–24 years were caused by transport and unintentional injuries combined. If compared with other causes, transport and unintentional injuries combined accounted for 25% of deaths and 14% of DALYs in 2019, and showed little improvement from 1990 when such injuries accounted for 26% of adolescent deaths and 17% of adolescent DALYs. Throughout adolescence, transport and unintentional injury fatality rates increased by age group. The unintentional injury burden was higher among males than females for all injury types, except for injuries related to fire, heat, and hot substances, or to adverse effects of medical treatment. From 1990 to 2019, global mortality rates declined by 34·4% (from 17·5 to 11·5 per 100 000) for transport injuries, and by 47·7% (from 15·9 to 8·3 per 100 000) for unintentional injuries. However, in low-SDI nations the absolute number of deaths increased (by 80·5% to 42 774 for transport injuries and by 39·4% to 31 961 for unintentional injuries). In the high-SDI quintile in 2010–19, the rate per 100 000 of transport injury DALYs was reduced by 16·7%, from 838 in 2010 to 699 in 2019. This was a substantially slower pace of reduction compared with the 48·5% reduction between 1990 and 2010, from 1626 per 100 000 in 1990 to 838 per 100 000 in 2010. Between 2010 and 2019, the rate of unintentional injury DALYs per 100 000 also remained largely unchanged in high-SDI countries (555 in 2010 vs 554 in 2019; 0·2% reduction). The number and rate of adolescent deaths and DALYs owing to environmental heat and cold exposure increased for the high-SDI quintile during 2010–19. Interpretation: As other causes of mortality are addressed, inadequate progress in reducing transport and unintentional injury mortality as a proportion of adolescent deaths becomes apparent. The relative shift in the burden of injury from high-SDI countries to low and low–middle-SDI countries necessitates focused action, including global donor, government, and industry investment in injury prevention. The persisting burden of DALYs related to transport and unintentional injuries indicates a need to prioritise innovative measures for the primary prevention of adolescent injury. Funding: Bill & Melinda Gates Foundation
Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019
- Author
- Abbafati Cristiana
- Abbas Kaja M.
- Abbasi Mohammad
- Abbasi-Kangevari Mohsen
- Abbasifard Mitra
- Abbastabar Hedayat
- Abd El Razek Hassan Magdy
- Abd El Razek Muhammed Magdy
- Abd-Allah Foad
- Abdelalim Ahmed
- Abdollahi Mohammad
- Abdollahpour Ibrahim
- Abdulkader Rizwan Suliankatchi
- Abdullah Kanaan Hamagharib
- Abedi Aidin
- Abedi Parisa
- Abegaz Kedir Hussein
- Abolhassani Hassan
- Abosetugn Akine Eshete
- Aboyans Victor
- Abrams Elissa M.
- Abreu Lucas Guimaraes
- Abrigo Michael R. M.
- Abu Haimed Abdulaziz Khalid
- Abu-Gharbieh Eman
- Abu-Raddad Laith Jamal
- Abualhasan Ahmed
- Abushouk Abdelrahman I.
- Acebedo Alyssa
- Ackerman Ilana N.
- Adabi Maryam
- Adair Tim
- Adamu Abdu A.
- Adebayo Oladimeji M.
- Adedeji Isaac Akinkunmi
- Adekanmbi Victor
- Adelson Jaimie D.
- Adeoye Abiodun Moshood
- Adetokunboh Olatunji O.
- Adham Davoud
- Advani Shailesh M.
- Afarideh Mohsen
- Afshari Mahdi
- Afshin Ashkan
- Agardh Emilie E.
- Agarwal Gina
- Agasthi Pradyumna
- Agesa Kareha M.
- Aghaali Mohammad
- Aghamir Seyed Mohammad Kazem
- Agrawal Anurag
- Ahmad Tauseef
- Ahmadi Alireza
- Ahmadi Keivan
- Ahmadi Mehdi
- Ahmadieh Hamid
- Ahmadpour Ehsan
- Ahmed Muktar Beshir
- Aji Budi
- Akalu Temesgen Yihunie
- Akinyemi Rufus Olusola
- Akinyemiju Tomi
- Akombi Blessing
- Akunna Chisom Joyqueenet
- Al-Aly Ziyad
- Al-Mekhlafi Hesham M.
- Al-Raddadi Rajaa M.
- Alahdab Fares
- Alam Khurshid
- Alam Noore
- Alam Samiah
- Alam Tahiya
- Alanezi Fahad Mashhour
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- Alcalde-Rabanal Jacqueline Elizabeth
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- Ali Saqib
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- Alizade Hesam
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- Yu Yong
- Yuan Chun-Wei
- Yuce Deniz
- Yusefzadeh Hasan
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- Zamani Mohammad
- Zamanian Maryam
- Zandian Hamed
- Zangeneh Alireza
- Zarafshan Hadi
- Zastrozhin Mikhail Sergeevich
- Zewdie Kaleab Alemayehu
- Zhang Jianrong
- Zhang Yunquan
- Zhang Zhi-Jiang
- Zhao Jeff T.
- Zhao Xiu-Ju George
- Zhao Yingxi
- Zheleva Bistra
- Zheng Peng
- Zhou Maigeng
- Zhu Cong
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- Publication venue
- Publication date
- 01/01/2020
- Field of study
Background: In an era of shifting global agendas and expanded emphasis on non-communicable diseases and injuries along with communicable diseases, sound evidence on trends by cause at the national level is essential. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) provides a systematic scientific assessment of published, publicly available, and contributed data on incidence, prevalence, and mortality for a mutually exclusive and collectively exhaustive list of diseases and injuries. Methods: GBD estimates incidence, prevalence, mortality, years of life lost (YLLs), years lived with disability (YLDs), and disability-adjusted life-years (DALYs) due to 369 diseases and injuries, for two sexes, and for 204 countries and territories. Input data were extracted from censuses, household surveys, civil registration and vital statistics, disease registries, health service use, air pollution monitors, satellite imaging, disease notifications, and other sources. Cause-specific death rates and cause fractions were calculated using the Cause of Death Ensemble model and spatiotemporal Gaussian process regression. Cause-specific deaths were adjusted to match the total all-cause deaths calculated as part of the GBD population, fertility, and mortality estimates. Deaths were multiplied by standard life expectancy at each age to calculate YLLs. A Bayesian meta-regression modelling tool, DisMod-MR 2.1, was used to ensure consistency between incidence, prevalence, remission, excess mortality, and cause-specific mortality for most causes. Prevalence estimates were multiplied by disability weights for mutually exclusive sequelae of diseases and injuries to calculate YLDs. We considered results in the context of the Socio-demographic Index (SDI), a composite indicator of income per capita, years of schooling, and fertility rate in females younger than 25 years. Uncertainty intervals (UIs) were generated for every metric using the 25th and 975th ordered 1000 draw values of the posterior distribution. Findings: Global health has steadily improved over the past 30 years as measured by age-standardised DALY rates. After taking into account population growth and ageing, the absolute number of DALYs has remained stable. Since 2010, the pace of decline in global age-standardised DALY rates has accelerated in age groups younger than 50 years compared with the 1990–2010 time period, with the greatest annualised rate of decline occurring in the 0–9-year age group. Six infectious diseases were among the top ten causes of DALYs in children younger than 10 years in 2019: lower respiratory infections (ranked second), diarrhoeal diseases (third), malaria (fifth), meningitis (sixth), whooping cough (ninth), and sexually transmitted infections (which, in this age group, is fully accounted for by congenital syphilis; ranked tenth). In adolescents aged 10–24 years, three injury causes were among the top causes of DALYs: road injuries (ranked first), self-harm (third), and interpersonal violence (fifth). Five of the causes that were in the top ten for ages 10–24 years were also in the top ten in the 25–49-year age group: road injuries (ranked first), HIV/AIDS (second), low back pain (fourth), headache disorders (fifth), and depressive disorders (sixth). In 2019, ischaemic heart disease and stroke were the top-ranked causes of DALYs in both the 50–74-year and 75-years-and-older age groups. Since 1990, there has been a marked shift towards a greater proportion of burden due to YLDs from non-communicable diseases and injuries. In 2019, there were 11 countries where non-communicable disease and injury YLDs constituted more than half of all disease burden. Decreases in age-standardised DALY rates have accelerated over the past decade in countries at the lower end of the SDI range, while improvements have started to stagnate or even reverse in countries with higher SDI. Interpretation: As disability becomes an increasingly large component of disease burden and a larger component of health expenditure, greater research and developm nt investment is needed to identify new, more effective intervention strategies. With a rapidly ageing global population, the demands on health services to deal with disabling outcomes, which increase with age, will require policy makers to anticipate these changes. The mix of universal and more geographically specific influences on health reinforces the need for regular reporting on population health in detail and by underlying cause to help decision makers to identify success stories of disease control to emulate, as well as opportunities to improve. Funding: Bill & Melinda Gates Foundation. © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 licens
Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study
- Author
- Abduljalal Maryam
- Abdullaev Alisher A.
- Abdullaeva Guzal J.
- Abifadel Marianne
- Acevedo Rivera Karina J.
- Adamidis Petros-Spyridon
- Aguilar Humberto Garcia
- Aguilar-Salinas Carlos A.
- Al-Khateeb Alyaa
- Al-Rasadi Khalid
- Al-Sarraf Ahmad
- Al-Sayed Nasreen
- Alammari Dalal
- Alareedh Mohammed
- Alcala Hector Garcia
- Alfil Sarmad
- Alhabib Khalid
- Alieva Rano B.
- Alkhnifsawi Mutaz
- Almahmeed Wael
- Almeida Ana Filipa
- Alnouri Fahad
- Alonso Rodrigo
- Alrowaily Nawal Lafi
- Alsahari Atif
- Alvarado Rocio Martinez
- Alvarez Jose A.
- Alves Ana Catarina
- Amezcua Martinez Jose C.
- Anagnostis Panagiotis
- Anastasiou Georgia
- Antonio-Villa Neftali Eduardo
- Antza Christina
- Aouchiche Karine
- Aparicio Berenice Pe~na
- Arca Marcello
- Arjona Villica~na Ruy D.
- Arriaga Cazares Hector E.
- Ashavaid Tester F.
- Ates Sara
- Attilakos Achilleas
- Averna Maurizio
- Ayoub Carine
- Balligand Jean-Luc
- Banach Maciej
- Barrera Bustillo Manuel de los Reyes
- Bartkova Ivana
- Batool Hijab
- Battelino Tadej
- Baumgartner-Kaut Margot
- Bañares Virginia
- Bendary Ahmed
- Benn Marianne
- Benso Andrea
- Berteotti Martina
- Bertolini Stefano
- Bielecka-Dąbrowa Agata
- Bilhoto Carla
- Binder Christoph
- Biolo Gianni Biolo
- Bizjan Barbara Jenko
- Blom Dirk
- Boccara Franck
- Bogsrud Martin P.
- Bonanni Luca
- Borghi Claudio
- Borowiec-Wolna Justyna
- Bossi Antonio Carlo
- Bourbon Mafalda
- Branchi Adriana
- Brandts Julia M.
- Bruckert Eric
- Brunham Liam
- Buganova Ingrid
- Buonuomo Paola Sabrina
- Buresova Kristyna
- Béliard Sophie
- Calabrò Paolo
- Calandra Sebastiano
- Capra Maria Elena
- Cariou Bertrand
- Carrera Ricardo Allende
- Carrié Alain
- Casula Manuela
- Catapano Alberico L.
- Cavallaro Raimondo
- Cefalù Angelo Baldassare
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- Chlebus Izabela
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- Chmara Magdalena
- Chua Yung-An
- Cipollone Francesco
- Citroni Nadia
- Coelho Raquel
- Cohen Hofit
- Cooremans Elizabeth Ramirez
- Corral Pablo
- Correia Susana
- Cottin Yves
- Cruz Diogo
- Cuevas Ada
- Dalal Jamshed J.
- Davletov Kairat
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- Dieplinger Hans
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- Durst Ronen
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- Jamialahmadi Tannaz
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- Kolovou Genovefa
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- Konopka Agnieszka
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- Muntoni Sandro
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- März Winfried
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- Petakov Ana
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- Pipolo Antonio
- Pirro Matteo
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- Valdez Talavera Luis A.
- Valero René
- Vallejo-Vaz Antonio J.
- Varga Tibor
- Vargas Gonzalo Carazo
- Vargas-Vazquez Arsenio
- Vasanwala Rashida Farhan
- Venkatesh Sreedharan Aravind
- Vera Arroyo Luis E.
- Verges Bruno
- Verma Ishwar C.
- Viigimaa Margus
- Virtuoso Maria João
- Vohnout Branislav
- Vrablik Michal
- Vázquez Cárdenas Alejandra
- Wang Luya
- Wasąg Bartosz
- Watts Gerald F.
- Weigman Albert
- Werba José Pablo
- Wojtecka Agnieszka
- Yamashita Shizuya
- Yelnik Cecile
- Yotov Yoto
- Zacharis Evangelos
- Zakirova Daria V.
- Zambon Alberto
- Zazueta Alejandro Romero
- Zdrojewski Tomasz
- Zenti Maria Grazia
- Zepeda Carrillo Eloy A.
- Zubieta Victoria Mendoza
- Šaligova Jana
- Żarczyńska-Buchowiecka Marta
- Publication venue
- Publication date
- 01/01/2024
- Field of study
Background: Approximately 450 000 children are born with familial hypercholesterolaemia worldwide every year, yet only 2·1% of adults with familial hypercholesterolaemia were diagnosed before age 18 years via current diagnostic approaches, which are derived from observations in adults. We aimed to characterise children and adolescents with heterozygous familial hypercholesterolaemia (HeFH) and understand current approaches to the identification and management of familial hypercholesterolaemia to inform future public health strategies. Methods: For this cross-sectional study, we assessed children and adolescents younger than 18 years with a clinical or genetic diagnosis of HeFH at the time of entry into the Familial Hypercholesterolaemia Studies Collaboration (FHSC) registry between Oct 1, 2015, and Jan 31, 2021. Data in the registry were collected from 55 regional or national registries in 48 countries. Diagnoses relying on self-reported history of familial hypercholesterolaemia and suspected secondary hypercholesterolaemia were excluded from the registry; people with untreated LDL cholesterol (LDL-C) of at least 13·0 mmol/L were excluded from this study. Data were assessed overall and by WHO region, World Bank country income status, age, diagnostic criteria, and index-case status. The main outcome of this study was to assess current identification and management of children and adolescents with familial hypercholesterolaemia. Findings: Of 63 093 individuals in the FHSC registry, 11 848 (18·8%) were children or adolescents younger than 18 years with HeFH and were included in this study; 5756 (50·2%) of 11 476 included individuals were female and 5720 (49·8%) were male. Sex data were missing for 372 (3·1%) of 11 848 individuals. Median age at registry entry was 9·6 years (IQR 5·8-13·2). 10 099 (89·9%) of 11 235 included individuals had a final genetically confirmed diagnosis of familial hypercholesterolaemia and 1136 (10·1%) had a clinical diagnosis. Genetically confirmed diagnosis data or clinical diagnosis data were missing for 613 (5·2%) of 11 848 individuals. Genetic diagnosis was more common in children and adolescents from high-income countries (9427 [92·4%] of 10 202) than in children and adolescents from non-high-income countries (199 [48·0%] of 415). 3414 (31·6%) of 10 804 children or adolescents were index cases. Familial-hypercholesterolaemia-related physical signs, cardiovascular risk factors, and cardiovascular disease were uncommon, but were more common in non-high-income countries. 7557 (72·4%) of 10 428 included children or adolescents were not taking lipid-lowering medication (LLM) and had a median LDL-C of 5·00 mmol/L (IQR 4·05-6·08). Compared with genetic diagnosis, the use of unadapted clinical criteria intended for use in adults and reliant on more extreme phenotypes could result in 50-75% of children and adolescents with familial hypercholesterolaemia not being identified. Interpretation: Clinical characteristics observed in adults with familial hypercholesterolaemia are uncommon in children and adolescents with familial hypercholesterolaemia, hence detection in this age group relies on measurement of LDL-C and genetic confirmation. Where genetic testing is unavailable, increased availability and use of LDL-C measurements in the first few years of life could help reduce the current gap between prevalence and detection, enabling increased use of combination LLM to reach recommended LDL-C targets early in life
Global burden of 369 diseases and injuries in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019
- Author
- Abbafati C
- Abbas KM
- Abbasi M
- Abbasi-Kangevari M
- Abbasifard M
- Abbastabar H
- Abd El Razek HM
- Abd El Razek MM
- Abd-Allah F
- Abdelalim A
- Abdollahi M
- Abdollahpour I
- Abdulkader RS
- Abdullah KH
- Abedi A
- Abedi P
- Abegaz KH
- Abolhassani H
- Abosetugn AE
- Aboyans V
- Abrams EM
- Abreu LG
- Abrigo MRM
- Abu Haimed AK
- Abu-Gharbieh E
- Abu-Raddad LJ
- Abualhasan A
- Abushouk AI
- Acebedo A
- Ackerman IN
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- Mumford JE
- Munro SB
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- Nguyen DN
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- Nigatu D
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- Nikbakhsh R
- Nikpoor AR
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- Nnaji CA
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- Norheim OF
- Norrving B
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- Nowak C
- Nsoesie EO
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- Oancea B
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- Ogbo FA
- Oghenetega OB
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- Oladnabi M
- Olagunju AT
- Olusanya BO
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- Oluwasanu MM
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- Truelsen TC
- Tsai AC
- Tsatsakis A
- Tyrovolas S
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- Ullah I
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- Umeokonkwo CD
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- Upadhyay E
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- Wickramasinghe ND
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- Wolfe CDA
- Wondmeneh TG
- Wondmieneh AB
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- Wu A-M
- Wu C
- Wu J
- Wunrow HY
- Xie Y
- Xu G
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- Yamagishi K
- Yaminfirooz M
- Yano Y
- Yaya S
- Yazdi-Feyzabadi V
- Yearwood JA
- Yeheyis TY
- Yeshitila YG
- Yilgwan CS
- Yilma MT
- Yip P
- Yonemoto N
- Yoon S-J
- York HW
- Younis MZ
- Younker TP
- Yousefi B
- Yousefi Z
- Yousefifard M
- Yousefinezhadi T
- Yousuf AY
- Yu C
- Yu Y
- Yuan C-W
- Yuce D
- Yusefzadeh H
- Zadey S
- Zahabi SS
- Zaidi SS
- Zaki L
- Zaki MES
- Zakzuk J
- Zamani M
- Zamanian M
- Zandian H
- Zangeneh A
- Zarafshan H
- Zastrozhin MS
- Zewdie KA
- Zhang J
- Zhang Y
- Zhang Z-J
- Zhao JT
- Zhao X-JG
- Zhao Y
- Zheleva B
- Zheng P
- Zhou M
- Zhu C
- Ziapour A
- Zimsen SRM
- Zlavog BS
- Zodpey S
- Publication venue
- 'Elsevier BV'
- Publication date
- 17/10/2020
- Field of study
Five insights from the Global Burden of Disease Study 2019
- Author
- Abbafati C
- Abbas KM
- Abbasi M
- Abbasi-Kangevari M
- Abbasifard M
- Abbastabar H
- Abd El Razek HM
- Abd El Razek MM
- Abd-Allah F
- Abdelalim A
- Abdollahi M
- Abdollahpour I
- Abdulkader RS
- Abdullah KH
- Abedi A
- Abedi P
- Abegaz KH
- Abolhassani H
- Abosetugn AE
- Aboyans V
- Abrams EM
- Abreu LG
- Abrigo MRM
- Abu Haimed AK
- Abu-Gharbieh E
- Abu-Raddad LJ
- Abualhasan A
- Abushouk AI
- Acebedo A
- Ackerman IN
- Adabi M
- Adair T
- Adamu AA
- Adebayo OM
- Adedeji IA
- Adekanmbi V
- Adelson JD
- Adeoye AM
- Adetokunboh OO
- Adham D
- Advani SM
- Afarideh M
- Afshari M
- Afshin A
- Agardh EE
- Agarwal G
- Agasthi P
- Agesa KM
- Aghaali M
- Aghamir SMK
- Agrawal A
- Ahmad T
- Ahmadi A
- Ahmadi K
- Ahmadi M
- Ahmadieh H
- Ahmadpour E
- Ahmed MB
- Aji B
- Akalu TY
- Akinyemi RO
- Akinyemiju T
- Akombi B
- Akunna CJ
- Al-Aly Z
- Al-Mekhlafi HM
- Al-Raddadi RM
- Alahdab F
- Alam K
- Alam N
- Alam S
- Alam T
- Alanezi FM
- Alanzi TM
- Albertson SB
- Alcalde-Rabanal JE
- Alema NM
- Alemu BW
- Alemu YM
- Alhabib KF
- Alhassan RK
- Ali M
- Ali S
- Alicandro G
- Alijanzadeh M
- Alinia C
- Alipour V
- Alizade H
- Aljunid SM
- Alla F
- Allebeck P
- Almadi MAH
- Almasi A
- Almasi-Hashiani A
- Almasri NA
- Almulhim AM
- Alonso J
- Altirkawi KA
- Alumran AK
- Alvis-Guzman N
- Alvis-Zakzuk NJ
- Amare AT
- Amare B
- Amini S
- Amini-Rarani M
- Aminorroaya A
- Amiri F
- Amit AML
- Amugsi DA
- Amul GGH
- Anbesu EW
- Ancuceanu R
- Anderlini D
- Anderson JA
- Andrei CL
- Andrei T
- Androudi S
- Angus C
- Anjomshoa M
- Ansari F
- Ansari I
- Ansari-Moghaddam A
- Antonazzo IC
- Antonio CAT
- Antony CM
- Antriyandarti E
- Anvari D
- Anwer R
- Appiah SCY
- Arab-Zozani M
- Arabloo J
- Aravkin AY
- Arba AAK
- Aremu O
- Ariani F
- Aripov T
- Armoon B
- Arnlov J
- Arowosegbe OO
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- Arzani A
- Asaad M
- Asadi-Aliabadi M
- Asadi-Pooya AA
- Asgari S
- Asghari B
- Ashbaugh C
- Assmus M
- Atafar Z
- Athari SS
- Atnafu DD
- Atout MMW
- Atre SR
- Atteraya MS
- Ausloos F
- Ausloos M
- Avila-Burgos L
- Avokpaho EFGA
- Ayano G
- Ayanore MA
- Aynalem GL
- Aynalem YA
- Ayza MA
- Azari S
- Azarian G
- Azene ZN
- Azhar G
- Azzopardi PS
- Babaee E
- Badawi A
- Badiye AD
- Bagherzadeh M
- Bagli E
- Bahrami MA
- Baig AA
- Bairwa M
- Bakhshaei MH
- Bakhtiari A
- Bakkannavar SM
- Balachandran A
- Balakrishnan S
- Balalla S
- Balassyano S
- Baldasseroni A
- Bali AO
- Ball K
- Ballew SH
- Balzi D
- Banach M
- Bandpei MAM
- Banerjee SK
- Banik PC
- Bannick MS
- Bante AB
- Bante SA
- Baraki AG
- Barboza MA
- Barker-Collo SL
- Barnighausen TW
- Barrero LH
- Barthelemy CM
- Barua L
- Barzegar A
- Basaleem H
- Bassat Q
- Basu S
- Baune BT
- Bayati M
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- Becker JS
- Bedi N
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- Benziger CP
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- Bernabe E
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- Bhageerathy R
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- Bhat AG
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- Bhattarai S
- Bhutta ZA
- Bibi S
- Bicer BK
- Biehl MH
- Bijani A
- Bikbov B
- Bilano V
- Bin Sayeed MS
- Bin Zaman S
- Biondi A
- Birihane BM
- Bisanzio D
- Bisignano C
- Biswas RK
- Bitew H
- Bjorge T
- Bockarie MJ
- Bohlouli S
- Bohluli M
- Bojia HA
- Bolla SR
- Boloor A
- Boon-Dooley AS
- Borges G
- Borzi AM
- Borzouei S
- Bose D
- Bosetti C
- Boston S
- Boufous S
- Bourne R
- Brady OJ
- Braithwaite D
- Brauer M
- Brayne C
- Breitborde NJK
- Breitner S
- Brenner H
- Breusov AV
- Briant PS
- Briggs AM
- Briko AN
- Briko NI
- Britton GB
- Brugha T
- Bryazka D
- Buchbinder R
- Bumgarner BR
- Burkart K
- Burnett RT
- Busse R
- Butt ZA
- Caetano dos Santos FL
- Cahill LE
- Cahuana-Hurtado L
- Cai T
- Callender CSKH
- Camera LA
- Campos-Nonato IR
- Cao J
- Car J
- Car LT
- Cardenas R
- Carreras G
- Carrero JJ
- Carvalho F
- Castaldelli-Maia JM
- Castaneda-Orjuela CA
- Castelpietra G
- Castle CD
- Castro E
- Castro F
- Catala-Lopez F
- Causey K
- Cederroth CR
- Cercy KM
- Cerin E
- Chalek J
- Chandan JS
- Chang AR
- Chang AY
- Chang J-C
- Chang K-L
- Charan J
- Charlson FJ
- Chattu VK
- Chaturvedi S
- Cherbuin N
- Chimed-Ochir O
- Chin KL
- Chirinos-Caceres JL
- Cho DY
- Choi J-YJ
- Christensen H
- Chu D-T
- Chung MT
- Chung S-C
- Cicuttini FM
- Ciobanu LG
- Cirillo M
- Cislaghi B
- Classen TKD
- Cohen AJ
- Collins EL
- Comfort H
- Compton K
- Conti S
- Cooper OR
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- Cortesi PA
- Costa VM
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- Cowie BC
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- Cross M
- Crowe CS
- Cruz JA
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- Cunningham M
- D'Amico E
- da Silva DD
- Dahlawi SMA
- Dai H
- Dai H
- Damasceno AAM
- Damiani G
- Dandona L
- Dandona R
- Daneshpajouhnejad P
- Dangel WJ
- Danielsson A-K
- Dargan PI
- Darshan BB
- Darwesh AM
- Daryani A
- Das Gupta R
- Das Neves J
- Das JK
- Dash AP
- Davey G
- Davila-Cervantes CA
- Davis AC
- Davitoiu DV
- Davletov K
- De Leo D
- De Neve J-W
- Dean FE
- DeCleene NK
- Deen A
- Defo BK
- Degenhardt L
- DeLang M
- Dellavalle RP
- Demeke FM
- Demoz GT
- Demsie DG
- Denova-Gutierrez E
- Dereje ND
- Deribe K
- Dervenis N
- Desai R
- Desalew A
- Dessie GA
- Deuba K
- Dharmaratne SD
- Dhungana GP
- Dianatinasab M
- Diaz D
- Dichgans M
- Didarloo A
- Dingels ZV
- Dippenaar IN
- Dirac MA
- Djalalinia S
- Do HT
- Dokova K
- Doku DT
- Dolecek C
- Dolgert AJ
- Dorostkar F
- Doshi CP
- Doshi PP
- Doshmangir L
- Douiri A
- Doxey MC
- Doyle KE
- Driscoll TR
- Dubljanin E
- Dunachie SJ
- Duncan BB
- Duraes AR
- Eagan AW
- Ebrahimi H
- Edvardsson D
- Effiong A
- Ehrlich JR
- El Nahas N
- El Sayed I
- El Tantawi M
- El-Jaafary SI
- Elbarazi I
- Elgendy IY
- Elhabashy HR
- Elsharkawy A
- Elyazar IRF
- Emamian MH
- Emmons-Bell S
- Erskine HE
- Eshrati B
- Eskandari K
- Eskandarieh S
- Esmaeilnejad S
- Esmaeilzadeh F
- Esteghamati A
- Esteghamati S
- Estep K
- Etemadi A
- Etisso AE
- Ezekannagha O
- Fanzo J
- Farag T
- Farahmand M
- Faraj A
- Faraon EJA
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- Faridnia R
- Farinha CSES
- Farioli A
- Faris PS
- Faro A
- Faruque M
- Farzadfar F
- Fattahi N
- Fazaeli AA
- Fazlzadeh M
- Feigin VL
- Feldman R
- Fereshtehnejad S-M
- Fernandes E
- Ferrara G
- Ferrara P
- Ferrari AJ
- Ferreira ML
- Feyissa GT
- Filip I
- Fischer F
- Fisher JL
- Fitzgerald R
- Flohr C
- Flor LS
- Foigt NA
- Folayan MO
- Fomenkov AA
- Force LM
- Fornari C
- Forooshani ZSD
- Foroutan M
- Fox JT
- Francis JM
- Frank TD
- Franklin RC
- Freitas M
- Fu W
- Fukumoto T
- Fukutaki K
- Fuller JE
- Fullman N
- Furtado JM
- Gad MM
- Gaidhane AM
- Gakidou E
- Galles NC
- Gallus S
- Gamkrelidze A
- Garcia-Basteiro AL
- Gardner WM
- Geberemariyam BS
- Gebrehiwot AM
- Gebremedhin KB
- Gebremeskel GG
- Gebremeskel LG
- Gebresillassie BM
- Gebreslassie AAAA
- Gela JD
- Geramo YCD
- Geremew A
- Gesesew HA
- Gething PW
- Gezae KE
- Ghadimi M
- Ghadiri K
- Ghaffarifar F
- Ghafourifard M
- Ghajar A
- Ghamari F
- Ghashghaee A
- Ghiasvand H
- Ghith N
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- Giampaoli S
- Gilani SA
- Gill PS
- Gill TK
- Gillum RF
- Ginawi IA
- Ginindza TG
- Gitimoghaddam M
- Giussani G
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- Glushkova EV
- Gnedovskaya EV
- Godinho MA
- Goharinezhad S
- Golechha M
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- Gopalani SV
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- Gorini G
- Gorman TM
- Gottlich HC
- Goudarzi H
- Goudarzian AH
- Goulart AC
- Goulart BNG
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- Grosso G
- Gubari MIM
- Gudi N
- Gugnani HC
- Guimaraes ALS
- Guimaraes RA
- Guled RA
- Gultie T
- Guo G
- Guo Y
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- Hachinski V
- Haddock B
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- Hafiz A
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- Publication venue
- Publication date
- 01/01/2020
- Field of study
The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 provides a rules-based synthesis of the available evidence on levels and trends in health outcomes, a diverse set of risk factors, and health system responses. GBD 2019 covered 204 countries and territories, as well as first administrative level disaggregations for 22 countries, from 1990 to 2019. Because GBD is highly standardised and comprehensive, spanning both fatal and non-fatal outcomes, and uses a mutually exclusive and collectively exhaustive list of hierarchical disease and injury causes, the study provides a powerful basis for detailed and broad insights on global health trends and emerging challenges. GBD 2019 incorporates data from 281 586 sources and provides more than 3.5 billion estimates of health outcome and health system measures of interest for global, national, and subnational policy dialogue. All GBD estimates are publicly available and adhere to the Guidelines on Accurate and Transparent Health Estimate Reporting. From this vast amount of information, five key insights that are important for health, social, and economic development strategies have been distilled. These insights are subject to the many limitations outlined in each of the component GBD capstone papers.Peer reviewe
Global, regional, and national mortality among young people aged 10–24 years, 1950–2019: a systematic analysis for the Global Burden of Disease Study 2019
- Author
- Abd-Allah F
- Abdoli A
- Abdollahi M
- Abdullah KH
- Abedi A
- Abolhassani H
- Abreu LG
- Abrigo MRM
- Abu-Gharbieh E
- Abushouk AI
- Adebayo OM
- Adekanmbi V
- Adham D
- Advani SM
- Afshari K
- Agrawal A
- Ahmad T
- Ahmadi K
- Ahmed AE
- Aji B
- Akombi-Inyang B
- Al-Aly Z
- Al-Hajj S
- Al-Mekhlafi HM
- Al-Raddadi RM
- Alahdab F
- Alam K
- Alanezi FM
- Alanzi TM
- Alcalde-Rabanal JE
- Alemu BW
- Alhassan RK
- Ali S
- Alicandro G
- Alijanzadeh M
- Aljunid SM
- Almasi-Hashiani A
- Almasri NA
- Alonso J
- Altirkawi KA
- Alvis-Guzman N
- Amare AT
- Amini S
- Aminorroaya A
- Amit AML
- Amugsi DA
- Ancuceanu R
- Anderlini D
- Andrei CL
- Androudi S
- Ansari F
- Ansari I
- Antonio CAT
- Anvari D
- Anwer R
- Appiah SCY
- Arab-Zozani M
- Arabloo J
- Asaad M
- Asadi-Aliabadi M
- Asadi-Pooya AA
- Atout MMW
- Ausloos M
- Avenyo EK
- Avila-Burgos L
- Ayano G
- Aynalem YA
- Azari S
- Azene ZN
- Azzopardi PS
- Bakhshaei MH
- Bakkannavar SM
- Bali AO
- Banach M
- Banik PC
- Barboza MA
- Barker-Collo SL
- Basu S
- Baune BT
- Bayati M
- Bedi N
- Beghi E
- Bekuma TT
- Bell AW
- Bell ML
- Benjet C
- Bensenor IM
- Berhe AK
- Berhe K
- Berman AE
- Bhagavathula AS
- Bhardwaj N
- Bhardwaj P
- Bhattacharyya K
- Bhattarai S
- Bhutta ZA
- Bijani A
- Bikbov B
- Bin Zaman S
- Biondi A
- Birhanu TTM
- Biswas RK
- Bohlouli S
- Bolla SR
- Boloor A
- Borschmann R
- Boufous S
- Bragazzi NL
- Braithwaite D
- Breitborde NJK
- Brenner H
- Britton GB
- Burns RA
- Butt ZA
- Bärnighausen TW
- Campos-Nonato IR
- Car LT
- Carreras G
- Carrero JJ
- Carvalho F
- Castaldelli-Maia JM
- Castañeda-Orjuela CA
- Castelpietra G
- Catalá-López F
- Cerin E
- Chandan JS
- Chang H-Y
- Chang J-C
- Charan J
- Chattu VK
- Chaturvedi S
- Choi J-YJ
- Chowdhury MAK
- Christopher DJ
- Chu D-T
- Chung MT
- Chung S-C
- Cicuttini FM
- Collaborators GAM
- Constantin TV
- Costa VM
- Cámera LA
- Cárdenas R
- da Silva DD
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- Dai H
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- Damiani G
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- Zastrozhin MS
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- Zhang Z-J
- Zhao X-JG
- Zhu C
- Ärnlöv J
- Øverland S
- Publication venue
- eCommons@AKU
- Publication date
- 01/01/2021
- Field of study
Summary: Background Documentation of patterns and long-term trends in mortality in young people, which reflect huge changes in demographic and social determinants of adolescent health, enables identification of global investment priorities for this age group. We aimed to analyse data on the number of deaths, years of life lost, and mortality rates by sex and age group in people aged 10–24 years in 204 countries and territories from 1950 to 2019 by use of estimates from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019. Methods We report trends in estimated total numbers of deaths and mortality rate per 100 000 population in young people aged 10–24 years by age group (10–14 years, 15–19 years, and 20–24 years) and sex in 204 countries and territories between 1950 and 2019 for all causes, and between 1980 and 2019 by cause of death. We analyse variation in outcomes by region, age group, and sex, and compare annual rate of change in mortality in young people aged 10–24 years with that in children aged 0–9 years from 1990 to 2019. We then analyse the association between mortality in people aged 10–24 years and socioeconomic development using the GBD Socio-demographic Index (SDI), a composite measure based on average national educational attainment in people older than 15 years, total fertility rate in people younger than 25 years, and income per capita. We assess the association between SDI and all-cause mortality in 2019, and analyse the ratio of observed to expected mortality by SDI using the most recent available data release (2017). Findings In 2019 there were 1·49 million deaths (95% uncertainty interval 1·39–1·59) worldwide in people aged 10–24 years, of which 61% occurred in males. 32·7% of all adolescent deaths were due to transport injuries, unintentional injuries, or interpersonal violence and conflict; 32·1% were due to communicable, nutritional, or maternal causes; 27·0% were due to non-communicable diseases; and 8·2% were due to self-harm. Since 1950, deaths in this age group decreased by 30·0% in females and 15·3% in males, and sex-based differences in mortality rate have widened in most regions of the world. Geographical variation has also increased, particularly in people aged 10–14 years. Since 1980, communicable and maternal causes of death have decreased sharply as a proportion of total deaths in most GBD super-regions, but remain some of the most common causes in sub-Saharan Africa and south Asia, where more than half of all adolescent deaths occur. Annual percentage decrease in all-cause mortality rate since 1990 in adolescents aged 15–19 years was 1·3% in males and 1·6% in females, almost half that of males aged 1–4 years (2·4%), and around a third less than in females aged 1–4 years (2·5%). The proportion of global deaths in people aged 0–24 years that occurred in people aged 10–24 years more than doubled between 1950 and 2019, from 9·5% to 21·6%. Interpretation Variation in adolescent mortality between countries and by sex is widening, driven by poor progress in reducing deaths in males and older adolescents. Improving global adolescent mortality will require action to address the specific vulnerabilities of this age group, which are being overlooked. Furthermore, indirect effects of the COVID-19 pandemic are likely to jeopardise efforts to improve health outcomes including mortality in young people aged 10–24 years. There is an urgent need to respond to the changing global burden of adolescent mortality, address inequities where they occur, and improve the availability and quality of primary mortality data in this age group
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