Medicine (Western Health) - Research Publications

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    Chronic disease IMPACT (chronic disease early detection and improved management in primary care project): An Australian stepped wedge cluster randomised trial
    Jones, JL ; Simons, K ; Manski-Nankervis, J-A ; Lumsden, NG ; Fernando, S ; de Courten, MP ; Cox, N ; Hamblin, PS ; Janus, ED ; Nelson, CL (SAGE PUBLICATIONS LTD, 2023)
    BACKGROUND: Interrelated chronic vascular diseases (chronic kidney disease (CKD), type 2 diabetes (T2D) and cardiovascular disease (CVD)) are common with high morbidity and mortality. This study aimed to assess if an electronic-technology-based quality improvement intervention in primary care could improve detection and management of people with and at risk of these diseases. METHODS: Stepped-wedge trial with practices randomised to commence intervention in one of five 16-week periods. Intervention included (1) electronic-technology tool extracting data from general practice electronic medical records and generating graphs and lists for audit; (2) education regarding chronic disease and the electronic-technology tool; (3) assistance with quality improvement audit plan development, benchmarking, monitoring and support. De-identified data analysis using R 3.5.1 conducted using Bayesian generalised linear mixed model with practice and time-specific random intercepts. RESULTS: At baseline, eight included practices had 37,946 active patients (attending practice ≥3 times within 2 years) aged ≥18 years. Intervention was associated with increased OR (95% CI) for: kidney health checks (estimated glomerular filtration rate, urine albumin:creatinine ratio (uACR) and blood pressure) in those at risk 1.34 (1.26-1.42); coded diagnosis of CKD 1.18 (1.09-1.27); T2D diagnostic testing (fasting glucose or HbA1c) in those at risk 1.15 (1.08-1.23); uACR in patients with T2D 1.78 (1.56-2.05). Documented eye checks within recommended frequency in patients with T2D decreased 0.85 (0.77-0.96). There were no significant changes in other assessed variables. CONCLUSIONS: This electronic-technology-based intervention in primary care has potential to help translate guidelines into practice but requires further refining to achieve widespread improvements across the interrelated chronic vascular diseases.
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    B-Type Natriuretic Peptide and Long-Term Cardiovascular Mortality in Patients With Coronary Heart Disease.
    Stewart, RAH ; Kirby, A ; White, HD ; Marschner, SL ; West, M ; Thompson, PL ; Sullivan, D ; Janus, E ; Hunt, D ; Kritharides, L ; Keech, A ; Simes, J ; Tonkin, AM (Ovid Technologies (Wolters Kluwer Health), 2022-07-05)
    Background The plasma concentration of B-type natriuretic peptide (BNP) is a strong predictor of adverse cardiovascular events. The aim of this study was to determine whether the association between plasma BNP concentration and cardiovascular mortality is sustained or diminishes with increasing time after BNP is measured. Methods and Results Six thousand seven hundred forty patients with a history of myocardial infarction or unstable angina who participated in the LIPID (Long-Term Intervention with Pravastatin in Ischemic Disease) trial had plasma BNP concentration measured at baseline and after 1 year. Associations with cardiovascular mortality were evaluated in landmark analyses 1 to <5, 5 to <10, and 10 to 16 years after randomization. There were 1640 cardiovascular deaths. The cardiovascular mortality rate increased progressively from 10.2 to 19.1 to 26.3/1000 patient-years from 1 to <5, 5 to <10, and 10 to 16 years after baseline, respectively. The average of baseline and 1-year BNP concentration was more strongly associated with cardiovascular mortality compared with baseline or 1-year BNP only. The hazard ratio (HR) for cardiovascular death associated with each doubling of average BNP concentration was similar during years 1 to <5 (HR, 1.53 [95% CI, 1.44-1.63]), years 5 to <10 (HR, 1.52 [95% CI, 1.44-1.60]), and years 10-16 (HR, 1.43 [95% CI, 1.36-1.50]), P<0.0001 for all. Conclusions BNP concentration remains an independent predictor of cardiovascular mortality more than a decade after it is measured. Because of random variation in plasma concentrations, the average of >1 BNP measurement improves long-term risk prediction.
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    Depression: An Important Comorbidity With Metabolic Syndrome in a General Population
    Dunbar, JA ; Reddy, P ; Davis-Lameloise, N ; Philpot, B ; Laatikainen, T ; Kilkkinen, A ; Bunker, SJ ; Best, JD ; Vartiainen, E ; Lo, SK ; Janus, ED (AMER DIABETES ASSOC, 2008-12)
    OBJECTIVE: There is a recognized association among depression, diabetes, and cardiovascular disease. The aim of this study was to examine in a sample representative of the general population whether depression, anxiety, and psychological distress are associated with metabolic syndrome and its components. RESEARCH DESIGN AND METHODS: Three cross-sectional surveys including clinical health measures were completed in rural regions of Australia during 2004-2006. A stratified random sample (n = 1,690, response rate 48%) of men and women aged 25-84 years was selected from the electoral roll. Metabolic syndrome was defined by the Third Report of the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults, Adult Treatment Panel III (NCEP ATP III), and International Diabetes Federation (IDF) criteria. Anxiety and depression were assessed by the Hospital Anxiety and Depression Scale and psychological distress by the Kessler 10 measure. RESULTS: Metabolic syndrome was associated with depression but not psychological distress or anxiety. Participants with the metabolic syndrome had higher scores for depression (n = 409, mean score 3.41, 95% CI 3.12-3.70) than individuals without the metabolic syndrome (n = 936, mean 2.95, 95% CI 2.76-3.13). This association was also present in 338 participants with the metabolic syndrome and without diabetes (mean score 3.37, 95% CI 3.06-3.68). Large waist circumference and low HDL cholesterol showed significant and independent associations with depression. CONCLUSIONS: Our results show an association between metabolic syndrome and depression in a heterogeneous sample. The presence of depression in individuals with the metabolic syndrome has implications for clinical management.
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    Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants
    Zhou, B ; Carrillo-Larco, RM ; Danaei, G ; Riley, LM ; Paciorek, CJ ; Stevens, GA ; Gregg, EW ; Bennett, JE ; Solomon, B ; Singleton, RK ; Sophiea, MK ; Iurilli, MLC ; Lhoste, VPF ; Cowan, MJ ; Savin, S ; Woodward, M ; Balanova, Y ; Cifkova, R ; Damasceno, A ; Elliott, P ; Farzadfar, F ; He, J ; Ikeda, N ; Kengne, AP ; Khang, Y-H ; Kim, HC ; Laxmaiah, A ; Lin, H-H ; Margozzini Maira, P ; Miranda, JJ ; Neuhauser, H ; Sundstrom, J ; Varghese, C ; Widyahening, IS ; Zdrojewski, T ; Ezzati, M ; Abarca-Gomez, L ; Abdeen, ZA ; Rahim, HFA ; Abu-Rmeileh, NM ; Acosta-Cazares, B ; Adams, RJ ; Aekplakorn, W ; Afsana, K ; Afzal, S ; Agdeppa, IA ; Aghazadeh-Attari, J ; Aguilar-Salinas, CA ; Agyemang, C ; Ahmad, NA ; Ahmadi, A ; Ahmadi, N ; Ahmadi, N ; Ahmadizar, F ; Ahmed, SH ; Ahrens, W ; Ajlouni, K ; Al-Raddadi, R ; Alarouj, M ; AlBuhairan, F ; AlDhukair, S ; Ali, MM ; Alkandari, A ; Alkerwi, A ; Allin, K ; Aly, E ; Amarapurkar, DN ; Amougou, N ; Amouyel, P ; Andersen, LB ; Anderssen, SA ; Anjana, RM ; Ansari-Moghaddam, A ; Ansong, D ; Aounallah-Skhiri, H ; Araujo, J ; Ariansen, I ; Aris, T ; Arku, RE ; Arlappa, N ; Aryal, KK ; Aspelund, T ; Assah, FK ; Assuncao, MCF ; Auvinen, J ; Avdicova, M ; Azevedo, A ; Azimi-Nezhad, M ; Azizi, F ; Azmin, M ; Babu, BV ; Bahijri, S ; Balakrishna, N ; Balanova, Y ; Bamoshmoosh, M ; Banach, M ; Banadinovic, M ; Bandosz, P ; Banegas, JR ; Baran, J ; Barbagallo, CM ; Barcelo, A ; Barkat, A ; Barreto, M ; Barros, AJD ; Gomes Barros, MV ; Bartosiewicz, A ; Basit, A ; Bastos, JLD ; Bata, I ; Batieha, AM ; Batyrbek, A ; Baur, LA ; Beaglehole, R ; Belavendra, A ; Ben Romdhane, H ; Benet, M ; Bennett, JE ; Benson, LS ; Berkinbayev, S ; Bernabe-Ortiz, A ; Bettiol, H ; Bezerra, J ; Bhagyalaxmi, A ; Bhargava, SK ; Bia, D ; Biasch, K ; Lele, ECB ; Bikbov, MM ; Bista, B ; Bjerregaard, P ; Bjertness, E ; Bjertness, MB ; Bjorkelund, C ; Bloch, KV ; Blokstra, A ; Bo, S ; Bobak, M ; Boeing, H ; Boggia, JG ; Boissonnet, CP ; Bojesen, SE ; Bongard, V ; Bonilla-Vargas, A ; Bopp, M ; Borghs, H ; Bovet, P ; Boyer, CB ; Braeckman, L ; Brajkovich, I ; Branca, F ; Breckenkamp, J ; Brenner, H ; Brewster, LM ; Briceno, Y ; Brito, M ; Bruno, G ; Bueno-de-Mesquita, HB ; Bueno, G ; Bugge, A ; Burns, C ; Bursztyn, M ; Cabrera de Leon, A ; Cacciottolo, J ; Cameron, C ; Can, G ; Candido, APC ; Capanzana, MV ; Capkova, N ; Capuano, E ; Capuano, V ; Cardoso, VC ; Carlsson, AC ; Carvalho, J ; Casanueva, FF ; Censi, L ; Cervantes-Loaiza, M ; Chadjigeorgiou, CA ; Chamukuttan, S ; Chan, AW ; Chan, Q ; Chaturvedi, HK ; Chaturvedi, N ; Chee, ML ; Chen, C-J ; Chen, F ; Chen, H ; Chen, S ; Chen, Z ; Cheng, C-Y ; Cheraghian, B ; Dekkaki, IC ; Chetrit, A ; Chien, K-L ; Chiolero, A ; Chiou, S-T ; Chirita-Emandi, A ; Chirlaque, M-D ; Cho, B ; Christensen, K ; Christofaro, DG ; Chudek, J ; Cifkova, R ; Cinteza, E ; Claessens, F ; Clarke, J ; Clays, E ; Cohen, E ; Concin, H ; Cooper, C ; Coppinger, TC ; Costanzo, S ; Cottel, D ; Cowell, C ; Craig, CL ; Crampin, AC ; Crujeiras, AB ; Cruz, JJ ; Csilla, S ; Cui, L ; Cureau, FV ; Cuschieri, S ; D'Arrigo, G ; d'Orsi, E ; Dallongeville, J ; Damasceno, A ; Danaei, G ; Dankner, R ; Dantoft, TM ; Dauchet, L ; Davletov, K ; De Backer, G ; De Bacquer, D ; De Curtis, A ; de Gaetano, G ; De Henauw, S ; de Oliveira, PD ; De Ridder, D ; De Smedt, D ; Deepa, M ; Deev, AD ; DeGennaro, VJ ; Delisle, H ; Demarest, S ; Dennison, E ; Deschamps, V ; Dhimal, M ; Di Castelnuovo, AF ; Dias-da-Costa, JS ; Diaz, A ; Dickerson, TT ; Dika, Z ; Djalalinia, S ; Do, HTP ; Dobson, AJ ; Donfrancesco, C ; Donoso, SP ; Doering, A ; Dorobantu, M ; Doerr, M ; Doua, K ; Dragano, N ; Drygas, W ; Duante, CA ; Duboz, P ; Duda, RB ; Dulskiene, V ; Dushpanova, A ; Dzakula, A ; Dzerve, V ; Dziankowska-Zaborszczyk, E ; Eddie, R ; Eftekhar, E ; Eggertsen, R ; Eghtesad, S ; Eiben, G ; Ekelund, U ; El-Khateeb, M ; El Ati, J ; Eldemire-Shearer, D ; Eliasen, M ; Elliott, P ; Elosua, R ; Erasmus, RT ; Erbel, R ; Erem, C ; Eriksen, L ; Eriksson, JG ; Escobedo-de la Pena, J ; Eslami, S ; Esmaeili, A ; Evans, A ; Faeh, D ; Fakhretdinova, AA ; Fall, CH ; Faramarzi, E ; Farjam, M ; Farzadfar, F ; Fattahi, MR ; Fawwad, A ; Felix-Redondo, FJ ; Felix, SB ; Ferguson, TS ; Fernandes, RA ; Fernandez-Berges, D ; Ferrante, D ; Ferrao, T ; Ferrari, M ; Ferrario, MM ; Ferreccio, C ; Ferreira, HS ; Ferrer, E ; Ferrieres, J ; Figueiro, TH ; Fink, G ; Fischer, K ; Foo, LH ; Forsner, M ; Fouad, HM ; Francis, DK ; Franco, MDC ; Frikke-Schmidt, R ; Frontera, G ; Fuchs, FD ; Fuchs, SC ; Fujita, Y ; Fumihiko, M ; Furdela, V ; Furer, A ; Furusawa, T ; Gaciong, Z ; Galbarczyk, A ; Galenkamp, H ; Galvano, F ; Gao, J ; Gao, P ; Garcia-de-la-Hera, M ; Garcia, P ; Gareta, D ; Garnett, SP ; Gaspoz, J-M ; Gasull, M ; Gazzinelli, A ; Gehring, U ; Geleijnse, JM ; George, R ; Ghanbari, A ; Ghasemi, E ; Gheorghe-Fronea, O-F ; Ghimire, A ; Gialluisi, A ; Giampaoli, S ; Gieger, C ; Gill, TK ; Giovannelli, J ; Gironella, G ; Giwercman, A ; Gkiouras, K ; Goldberg, M ; Goldsmith, RA ; Gomez, LF ; Gomula, A ; Cordeiro da Silva, BG ; Goncalves, H ; Goncalves, M ; Gonzalez-Chica, DA ; Gonzalez-Gross, M ; Gonzalez-Rivas, JP ; Gonzalez-Villalpando, C ; Gonzalez-Villalpando, M-E ; Gonzalez, AR ; Bonet Gorbea, M ; Gottrand, F ; Graff-Iversen, S ; Grafnetter, D ; Grajda, A ; Grammatikopoulou, MG ; Gregor, RD ; Grodzicki, T ; Grosso, G ; Gruden, G ; Gu, D ; Guan, OP ; Gudmundsson, EF ; Gudnason, V ; Guerrero, R ; Guessous, I ; Guimaraes, AL ; Gulliford, MC ; Gunnlaugsdottir, J ; Gunter, MJ ; Gupta, PC ; Gupta, R ; Gureje, O ; Gurzkowska, B ; Gutierrez, L ; Gutzwiller, F ; Ha, S ; Hadaegh, F ; Haghshenas, R ; Hakimi, H ; Halkjaer, J ; Hambleton, IR ; Hamzeh, B ; Hange, D ; Hanif, AAM ; Hantunen, S ; Hao, J ; Hardman, CM ; Kumar, RH ; Hashemi-Shahri, SM ; Hata, J ; Haugsgjerd, T ; Hayes, AJ ; He, J ; He, Y ; Heier, M ; Hendriks, ME ; Henrique, RDS ; Henriques, A ; Cadena, LH ; Herrala, S ; Heshmat, R ; Hill, AG ; Ho, SY ; Ho, SC ; Hobbs, M ; Holdsworth, M ; Homayounfar, R ; Dinc, GH ; Horimoto, ARVR ; Hormiga, CM ; Horta, BL ; Houti, L ; Howitt, C ; Htay, TT ; Htet, AS ; Htike, MMT ; Hu, Y ; Huerta, JM ; Huhtaniemi, IT ; Huiart, L ; Huisman, M ; Husseini, AS ; Huybrechts, I ; Hwalla, N ; Iacoviello, L ; Iannone, AG ; Ibrahim, MM ; Wong, NI ; Ikeda, N ; Ikram, MA ; Iotova, V ; Irazola, VE ; Ishida, T ; Isiguzo, GC ; Islam, M ; Islam, SMS ; Iwasaki, M ; Jackson, RT ; Jacobs, JM ; Jaddou, HY ; Jafar, T ; James, K ; Jamrozik, K ; Janszky, I ; Janus, E ; Jarvelin, M-R ; Jasienska, G ; Jelakovic, A ; Jelakovic, B ; Jennings, G ; Jha, AK ; Jiang, CQ ; Jimenez, RO ; Joeckel, K-H ; Joffres, M ; Johansson, M ; Jokelainen, JJ ; Jonas, JB ; Jorgensen, T ; Joshi, P ; Joukar, F ; Jozwiak, J ; Juolevi, A ; Jurak, G ; Juresa, V ; Kaaks, R ; Kafatos, A ; Kajantie, EO ; Kalmatayeva, Z ; Kalpourtzi, N ; Kalter-Leibovici, O ; Kampmann, FB ; Kannan, S ; Karaglani, E ; Karhus, LL ; Karki, KB ; Katibeh, M ; Katz, J ; Kauhanen, J ; Kaur, P ; Kavousi, M ; Kazakbaeva, GM ; Keil, U ; Boker, LK ; Keinanen-Kiukaanniemi, S ; Kelishadi, R ; Kemper, HCG ; Kengne, AP ; Keramati, M ; Kerimkulova, A ; Kersting, M ; Key, T ; Khader, YS ; Khalili, D ; Khang, Y-H ; Khaw, K-T ; Kheiri, B ; Kheradmand, M ; Khosravi, A ; Kiechl-Kohlendorfer, U ; Kiechl, S ; Killewo, J ; Kim, DW ; Kim, HC ; Kim, J ; Klakk, H ; Klimek, M ; Klumbiene, J ; Knoflach, M ; Kolle, E ; Kolsteren, P ; Kontto, JP ; Korpelainen, R ; Korrovits, P ; Kos, J ; Koskinen, S ; Kouda, K ; Kowlessur, S ; Koziel, S ; Kratenova, J ; Kriaucioniene, V ; Kristensen, PL ; Krokstad, S ; Kromhout, D ; Kruger, HS ; Kubinova, R ; Kuciene, R ; Kujala, UM ; Kulaga, Z ; Kumar, RK ; Kurjata, P ; Kusuma, YS ; Kutsenko, V ; Kuulasmaa, K ; Kyobutungi, C ; Laatikainen, T ; Lachat, C ; Laid, Y ; Lam, TH ; Landrove, O ; Lanska, V ; Lappas, G ; Larijani, B ; Latt, TS ; Laxmaiah, A ; Le Coroller, G ; Khanh, LNB ; Le, TD ; Lee, J ; Lee, J ; Lehmann, N ; Lehtimaki, T ; Lemogoum, D ; Levitt, NS ; Li, Y ; Lilly, CL ; Lim, W-Y ; Lima-Costa, MF ; Lin, H-H ; Lin, X ; Lin, Y-T ; Lind, L ; Lingam, V ; Linneberg, A ; Lissner, L ; Litwin, M ; Lo, W-C ; Loit, H-M ; Lopez-Garcia, E ; Lopez, T ; Lotufo, PA ; Lozano, JE ; Lovrencic, IL ; Lukrafka, JL ; Luksiene, D ; Lundqvist, A ; Lundqvist, R ; Lunet, N ; Lustigova, M ; Luszczki, E ; Ma, G ; Ma, J ; Machado-Coelho, GLL ; Machado-Rodrigues, AM ; Macia, E ; Macieira, LM ; Madar, AA ; Maggi, S ; Magliano, DJ ; Magriplis, E ; Mahasampath, G ; Maire, B ; Majer, M ; Makdisse, M ; Malekzadeh, F ; Malekzadeh, R ; Malhotra, R ; Mallikharjuna, K ; Malyutina, SK ; Maniego, LV ; Manios, Y ; Mann, JI ; Mansour-Ghanaei, F ; Manzato, E ; Marcil, A ; Margozzini, P ; Marild, SB ; Glavic, MM ; Marques-Vidal, P ; Marques, LP ; Marrugat, J ; Martorell, R ; Mascarenhas, LP ; Matasin, M ; Mathiesen, EB ; Mathur, P ; Matijasevich, A ; Matlosz, P ; Matsha, TE ; Mavrogianni, C ; Mbanya, JCN ; Mc Donald Posso, AJ ; McFarlane, SR ; McGarvey, ST ; McLachlan, S ; McLean, RM ; McLean, SB ; McNulty, BA ; Benchekor, SM ; Medzioniene, J ; Mehdipour, P ; Mehlig, K ; Mehrparvar, AH ; Meirhaeghe, A ; Meisinger, C ; Mendoza Montano, C ; Menezes, AMB ; Menon, GR ; Mereke, A ; Meshram, II ; Metspalu, A ; Meyer, HE ; Mi, J ; Michels, N ; Mikkel, K ; Milkowska, K ; Miller, JC ; Minderico, CS ; Mini, GK ; Miranda, JJ ; Mirjalili, MR ; Mirrakhimov, E ; Misigoj-Durakovic, M ; Modesti, PA ; Moghaddam, SS ; Mohajer, B ; Mohamed, MK ; Mohamed, SF ; Mohammad, K ; Mohammadi, MR ; Mohammadi, Z ; Mohammadifard, N ; Mohammadpourhodki, R ; Mohan, V ; Mohanna, S ; Yusoff, MFM ; Mohebbi, I ; Mohebi, F ; Moitry, M ; Mollehave, LT ; Molnar, D ; Momenan, A ; Mondo, CK ; Monterrubio-Flores, E ; Monyeki, KDK ; Moon, JS ; Moosazadeh, M ; Moreira, LB ; Morejon, A ; Moreno, LA ; Morgan, K ; Moschonis, G ; Mossakowska, M ; Mostafa, A ; Mostafavi, S-A ; Mota, J ; Motlagh, ME ; Motta, J ; Andre Moura-dos-Santos, M ; Mridha, MK ; Msyamboza, KP ; Mu, TT ; Muhihi, AJ ; Muiesan, ML ; Muller-Nurasyid, M ; Murphy, N ; Mursu, J ; Musa, KI ; Milanovic, SM ; Musil, V ; Mustafa, N ; Nabipour, I ; Naderimagham, S ; Nagel, G ; Naidu, BM ; Najafi, F ; Nakamura, H ; Namesna, J ; Nang, EEK ; Nangia, VB ; Narake, S ; Ndiaye, NC ; Neal, WA ; Nejatizadeh, A ; Nenko, I ; Neovius, M ; Neuhauser, HK ; Nguyen, CT ; Nguyen, ND ; Nguyen, QV ; Quang, NN ; Nieto-Martinez, RE ; Niiranen, TJ ; Nikitin, YP ; Ninomiya, T ; Nishtar, S ; Njelekela, MA ; Noale, M ; Noboa, OA ; Noorbala, AA ; Norat, T ; Nordendahl, M ; Nordestgaard, BG ; Noto, D ; Nowak-Szczepanska, N ; Al Nsour, M ; Nunes, B ; O'Neill, TW ; O'Reilly, D ; Ochimana, C ; Oda, E ; Odili, AN ; Oh, K ; Ohara, K ; Ohtsuka, R ; Olie, V ; Olinto, MTA ; Oliveira, IO ; Omar, MA ; Onat, A ; Ong, SK ; Ono, LM ; Ordunez, P ; Ornelas, R ; Ortiz, PJ ; Osmond, C ; Ostojic, SM ; Ostovar, A ; Otero, JA ; Overvad, K ; Owusu-Dabo, E ; Paccaud, FM ; Padez, C ; Pahomova, E ; de Paiva, KM ; Pajak, A ; Palli, D ; Palmieri, L ; Pan, W-H ; Panda-Jonas, S ; Panza, F ; Paoli, M ; Papandreou, D ; Park, S-W ; Park, S ; Parnell, WR ; Parsaeian, M ; Pasquet, P ; Patel, ND ; Pavlyshyn, H ; Pecin, I ; Pednekar, MS ; Pedro, JM ; Peer, N ; Peixoto, SV ; Peltonen, M ; Pereira, AC ; Peres, KGDA ; Peres, MA ; Peters, A ; Petkeviciene, J ; Peykari, N ; Son, TP ; Pichardo, RN ; Pigeot, I ; Pikhart, H ; Pilav, A ; Pilotto, L ; Pitakaka, F ; Piwonska, A ; Pizarro, AN ; Plans-Rubio, P ; Polasek, O ; Porta, M ; Poudyal, A ; Pourfarzi, F ; Pourshams, A ; Poustchi, H ; Pradeepa, R ; Price, AJ ; Price, JF ; Providencia, R ; Puhakka, SE ; Puiu, M ; Punab, M ; Qasrawi, RF ; Qorbani, M ; Queiroz, D ; Tran, QB ; Radic, I ; Radisauskas, R ; Rahimikazerooni, S ; Rahman, M ; Raitakari, O ; Raj, M ; Rakhimova, EM ; Rao, SR ; Ramachandran, A ; Ramos, E ; Rampal, L ; Rampal, S ; Rangel Reina, DA ; Rarra, V ; Rech, CR ; Redon, J ; Reganit, PFM ; Regecova, V ; Revilla, L ; Rezaianzadeh, A ; Ribeiro, R ; Riboli, E ; Richter, A ; Rigo, F ; de Wit, TFR ; Ritti-Dias, RM ; Robitaille, C ; Rodriguez-Artalejo, F ; del Cristo Rodriguez-Perez, M ; Rodriguez-Villamizar, LA ; Roggenbuck, U ; Rojas-Martinez, R ; Romaguera, D ; Romeo, EL ; Rosengren, A ; Roy, JGR ; Rubinstein, A ; Ruidavets, J-B ; Sandra Ruiz-Betancourt, B ; Ruiz-Castell, M ; Rusakova, IA ; Russo, P ; Rutkowski, M ; Sabanayagam, C ; Sabbaghi, H ; Sachdev, HS ; Sadjadi, A ; Safarpour, AR ; Safi, S ; Safiri, S ; Saidi, O ; Sakarya, S ; Saki, N ; Salanave, B ; Salazar Martinez, E ; Salmeron, D ; Salomaa, V ; Salonen, JT ; Salvetti, M ; Sanchez-Abanto, J ; Sans, S ; Santos, DA ; Santos, IS ; Santos, LC ; Santos, MP ; Santos, R ; Saramies, JL ; Sardinha, LB ; Sarganas, G ; Sarrafzadegan, N ; Sathish, T ; Saum, K-U ; Savva, S ; Sawada, N ; Sbaraini, M ; Scazufca, M ; Schaan, BD ; Schargrodsky, H ; Schipf, S ; Schmidt, CO ; Schnohr, P ; Schoettker, B ; Schramm, S ; Schultsz, C ; Schutte, AE ; Sebert, S ; Sein, AA ; Sen, A ; Senbanjo, IO ; Sepanlou, SG ; Servais, J ; Shalnova, SA ; Shamah-Levy, T ; Shamshirgaran, M ; Shanthirani, CS ; Sharafkhah, M ; Sharma, SK ; Shaw, JE ; Shayanrad, A ; Shayesteh, AA ; Shi, Z ; Shibuya, K ; Shimizu-Furusawa, H ; Shin, DW ; Shirani, M ; Shiri, R ; Shrestha, N ; Si-Ramlee, K ; Siani, A ; Siantar, R ; Sibai, AM ; de Moura Silva, CR ; Santos Silva, DA ; Simon, M ; Simons, J ; Simons, LA ; Sjostrom, M ; Slowikowska-Hilczer, J ; Slusarczyk, P ; Smeeth, L ; So, H-K ; Soares, FC ; Sobngwi, E ; Soderberg, S ; Soemantri, A ; Sofat, R ; Solfrizzi, V ; Somi, MH ; Sonestedt, E ; Song, Y ; Sorensen, TIA ; Sorgjerd, EP ; Soric, M ; Jerome, CS ; Soumare, A ; Sparboe-Nilsen, B ; Sparrenberger, K ; Staessen, JA ; Starc, G ; Stavreski, B ; Steene-Johannessen, J ; Stehle, P ; Stein, AD ; Stergiou, GS ; Stessman, J ; Stieber, J ; Stoeckl, D ; Stocks, T ; Stokwiszewski, J ; Stronks, K ; Strufaldi, MW ; Suka, M ; Sun, C-A ; Sundstrom, J ; Sung, Y-T ; Suriyawongpaisal, P ; Sy, RG ; Syddall, HE ; Sylva, RC ; Szklo, M ; Tai, ES ; Tammesoo, M-L ; Tamosiunas, A ; Tan, EJ ; Tang, X ; Tanser, F ; Tao, Y ; Tarawneh, MR ; Tarqui-Mamani, CB ; Taylor, A ; Taylor, J ; Tebar, WR ; Tell, GS ; Tello, T ; Tham, YC ; Thankappan, KR ; Theobald, H ; Theodoridis, X ; Thijs, L ; Thinggaard, M ; Thomas, N ; Thorand, B ; Thuesen, BH ; Timmermans, EJ ; Tjandrarini, DH ; Tjonneland, A ; Toft, U ; Tolonen, HK ; Tolstrup, JS ; Topbas, M ; Topor-Madry, R ; Jose Tormo, M ; Tornaritis, MJ ; Torrent, M ; Torres-Collado, L ; Touloumi, G ; Traissac, P ; Triantafyllou, A ; Trichopoulos, D ; Trichopoulou, A ; Trinh, OTH ; Trivedi, A ; Tshepo, L ; Tsugane, S ; Tuliakova, AM ; Tulloch-Reid, MK ; Tullu, F ; Tuomainen, T-P ; Tuomilehto, J ; Turley, ML ; Twig, G ; Tynelius, P ; Tzourio, C ; Ueda, P ; Ugel, E ; Ulmer, H ; Uusitalo, HMT ; Valdivia, G ; Valvi, D ; van Dam, RM ; van den Born, B-J ; Van der Heyden, J ; van der Schouw, YT ; Van Herck, K ; Hoang, VM ; Van Schoor, NM ; van Valkengoed, IGM ; van Zutphen, EM ; Vanderschueren, D ; Vanuzzo, D ; Varbo, A ; Vasan, SK ; Vega, T ; Veidebaum, T ; Velasquez-Melendez, G ; Veronesi, G ; Verschuren, WMM ; Verstraeten, R ; Victora, CG ; Viet, L ; Villalpando, S ; Vineis, P ; Vioque, J ; Virtanen, JK ; Visvikis-Siest, S ; Viswanathan, B ; Vlasoff, T ; Vollenweider, P ; Voutilainen, A ; Wade, AN ; Walton, J ; Wambiya, EOA ; Bebakar, WMW ; Mohamud, WNW ; Wanderley Junior, RDS ; Wang, M-D ; Wang, N ; Wang, Q ; Wang, X ; Wang, YX ; Wang, Y-W ; Wannamethee, SG ; Wareham, N ; Wei, W ; Weres, A ; Werner, B ; Whincup, PH ; Widhalm, K ; Widyahening, IS ; Wiecek, A ; Wilks, RJ ; Willeit, J ; Willeit, P ; Williams, EA ; Wilsgaard, T ; Wojtyniak, B ; Wong-McClure, RA ; Wong, A ; Wong, TY ; Woo, J ; Woodward, M ; Wu, FC ; Wu, S ; Wyszynska, J ; Xu, H ; Xu, L ; Yaacob, NA ; Yan, W ; Yang, L ; Yang, X ; Yang, Y ; Yasuharu, T ; Ye, X ; Yiallouros, PK ; Yoosefi, M ; Yoshihara, A ; You, S-L ; Younger-Coleman, NO ; Yusoff, AF ; Zainuddin, AA ; Zakavi, SR ; Zamani, F ; Zambon, S ; Zampelas, A ; Elisa Zapata, M ; Zaw, KK ; Zdrojewski, T ; Zejglicova, K ; Vrkic, TZ ; Zeng, Y ; Zhang, L ; Zhang, Z-Y ; Zhao, D ; Zhao, M-H ; Zhen, S ; Zheng, Y ; Zholdin, B ; Zhu, D ; Zins, M ; Zitt, E ; Zocalo, Y ; Zoghlami, N ; Zuniga Cisneros, J (ELSEVIER SCIENCE INC, 2021-09-11)
    BACKGROUND: Hypertension can be detected at the primary health-care level and low-cost treatments can effectively control hypertension. We aimed to measure the prevalence of hypertension and progress in its detection, treatment, and control from 1990 to 2019 for 200 countries and territories. METHODS: We used data from 1990 to 2019 on people aged 30-79 years from population-representative studies with measurement of blood pressure and data on blood pressure treatment. We defined hypertension as having systolic blood pressure 140 mm Hg or greater, diastolic blood pressure 90 mm Hg or greater, or taking medication for hypertension. We applied a Bayesian hierarchical model to estimate the prevalence of hypertension and the proportion of people with hypertension who had a previous diagnosis (detection), who were taking medication for hypertension (treatment), and whose hypertension was controlled to below 140/90 mm Hg (control). The model allowed for trends over time to be non-linear and to vary by age. FINDINGS: The number of people aged 30-79 years with hypertension doubled from 1990 to 2019, from 331 (95% credible interval 306-359) million women and 317 (292-344) million men in 1990 to 626 (584-668) million women and 652 (604-698) million men in 2019, despite stable global age-standardised prevalence. In 2019, age-standardised hypertension prevalence was lowest in Canada and Peru for both men and women; in Taiwan, South Korea, Japan, and some countries in western Europe including Switzerland, Spain, and the UK for women; and in several low-income and middle-income countries such as Eritrea, Bangladesh, Ethiopia, and Solomon Islands for men. Hypertension prevalence surpassed 50% for women in two countries and men in nine countries, in central and eastern Europe, central Asia, Oceania, and Latin America. Globally, 59% (55-62) of women and 49% (46-52) of men with hypertension reported a previous diagnosis of hypertension in 2019, and 47% (43-51) of women and 38% (35-41) of men were treated. Control rates among people with hypertension in 2019 were 23% (20-27) for women and 18% (16-21) for men. In 2019, treatment and control rates were highest in South Korea, Canada, and Iceland (treatment >70%; control >50%), followed by the USA, Costa Rica, Germany, Portugal, and Taiwan. Treatment rates were less than 25% for women and less than 20% for men in Nepal, Indonesia, and some countries in sub-Saharan Africa and Oceania. Control rates were below 10% for women and men in these countries and for men in some countries in north Africa, central and south Asia, and eastern Europe. Treatment and control rates have improved in most countries since 1990, but we found little change in most countries in sub-Saharan Africa and Oceania. Improvements were largest in high-income countries, central Europe, and some upper-middle-income and recently high-income countries including Costa Rica, Taiwan, Kazakhstan, South Africa, Brazil, Chile, Turkey, and Iran. INTERPRETATION: Improvements in the detection, treatment, and control of hypertension have varied substantially across countries, with some middle-income countries now outperforming most high-income nations. The dual approach of reducing hypertension prevalence through primary prevention and enhancing its treatment and control is achievable not only in high-income countries but also in low-income and middle-income settings. FUNDING: WHO.
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    Circulating Cystatin C Is an Independent Risk Marker for Cardiovascular Outcomes, Development of Renal Impairment, and Long-Term Mortality in Patients With Stable Coronary Heart Disease: The LIPID Study.
    West, M ; Kirby, A ; Stewart, RA ; Blankenberg, S ; Sullivan, D ; White, HD ; Hunt, D ; Marschner, I ; Janus, E ; Kritharides, L ; Watts, GF ; Simes, J ; Tonkin, AM ; LIPID Study Group *, (Ovid Technologies (Wolters Kluwer Health), 2022-03)
    Background Elevated plasma cystatin C levels reflect reduced renal function and increased cardiovascular risk. Less is known about whether the increased risk persists long-term or is independent of renal function and other important biomarkers. Methods and Results Cystatin C and other biomarkers were measured at baseline (in 7863 patients) and 1 year later (in 6106 patients) in participants in the LIPID (Long-Term Intervention with Pravastatin in Ischemic Disease) study, who had a previous acute coronary syndrome. Outcomes were ascertained during the study (median follow-up, 6 years) and long-term (median follow-up, 16 years). Glomerular filtration rate (GFR) was estimated using Chronic Kidney Disease Epidemiology Collaboration equations (first GFR-creatinine, then GFR-creatinine-cystatin C). Over 6 years, in fully adjusted multivariable time-to-event models, with respect to the primary end point of coronary heart disease mortality or nonfatal myocardial infarction, for comparison of Quartile 4 versus 1 of baseline cystatin C, the hazard ratio was 1.37 (95% CI, 1.07-1.74; P=0.01), and for major cardiovascular events was 1.47 (95% CI, 1.19-1.82; P<0.001). Over 16 years, the association of baseline cystatin C with coronary heart disease, cardiovascular, and all-cause mortality persisted (each P<0.001) and remained significant after adjustment for estimated GFR-creatinine-cystatin C. Cystatin C also predicted the development of chronic kidney disease for 6 years (odds ratio, 6.61; 95% CI, 4.28-10.20) independently of estimated GFR-creatinine and other risk factors. However, this association was no longer significant after adjustment for estimated GFR-creatinine-cystatin C. Conclusions Cystatin C independently predicted major cardiovascular events, development of chronic kidney disease, and cardiovascular and all-cause mortality. Prediction of long-term mortality was independent of improved estimation of GFR. Registration URL: https://anzctr.org.au; Unique identifier: ACTRN12616000535471.
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    Asia-Pacific Consensus Statement on the Management of Peripheral Artery Disease: A Report from the Asian Pacific Society of Atherosclerosis and Vascular Disease Asia-Pacific Peripheral Artery Disease Consensus Statement Project Committee.
    Abola, MTB ; Golledge, J ; Miyata, T ; Rha, S-W ; Yan, BP ; Dy, TC ; Ganzon, MSV ; Handa, PK ; Harris, S ; Zhisheng, J ; Pinjala, R ; Robless, PA ; Yokoi, H ; Alajar, EB ; Bermudez-Delos Santos, AA ; Llanes, EJB ; Obrado-Nabablit, GM ; Pestaño, NS ; Punzalan, FE ; Tumanan-Mendoza, B (Japan Atherosclerosis Society, 2020-08-01)
    BACKGROUND: Peripheral artery disease (PAD) is the most underdiagnosed, underestimated and undertreated of the atherosclerotic vascular diseases despite its poor prognosis. There may be racial or contextual differences in the Asia-Pacific region as to epidemiology, availability of diagnostic and therapeutic modalities, and even patient treatment response. The Asian Pacific Society of Atherosclerosis and Vascular Diseases (APSAVD) thus coordinated the development of an Asia-Pacific Consensus Statement (APCS) on the Management of PAD. OBJECTIVES: The APSAVD aimed to accomplish the following: 1) determine the applicability of the 2016 AHA/ACC guidelines on the Management of Patients with Lower Extremity Peripheral Artery Disease to the Asia-Pacific region; 2) review Asia-Pacific literature; and 3) increase the awareness of PAD. METHODOLOGY: A Steering Committee was organized to oversee development of the APCS, appoint a Technical Working Group (TWG) and Consensus Panel (CP). The TWG appraised the relevance of the 2016 AHA/ACC PAD Guideline and proposed recommendations which were reviewed by the CP using a modified Delphi technique. RESULTS: A total of 91 recommendations were generated covering history and physical examination, diagnosis, and treatment of PAD-3 new recommendations, 31 adaptations and 57 adopted statements. This Asia-Pacific Consensus Statement on the Management of PAD constitutes the first for the Asia-Pacific Region. It is intended for use by health practitioners involved in preventing, diagnosing and treating patients with PAD and ultimately the patients and their families themselves.
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    Growth Environment and Sex Differences in Lipids, Body Shape and Diabetes Risk
    Schooling, CM ; Lam, TH ; Thomas, GN ; Cowling, BJ ; Heys, M ; Janus, ED ; Leung, GM ; Miranda, JJ (PUBLIC LIBRARY SCIENCE, 2007-10-24)
    BACKGROUND: Sex differences in lipids and body shape, but not diabetes, increase at puberty. Hong Kong Chinese are mainly first or second generation migrants from China, who have shared an economically developed environment for years, but grew up in very different environments in Hong Kong or contemporaneously undeveloped Guangdong, China. We assessed if environment during growth had sex-specific associations with lipids and body shape, but not diabetes. METHODOLOGY AND PRINCIPAL FINDINGS: We used multivariable regression in a population-based cross-sectional study, undertaken from 1994 to 1996, of 2537 Hong Kong Chinese residents aged 25 to 74 years with clinical measurements of ischaemic heart disease (IHD) risk, including HDL-cholesterol, ApoB, diabetes and obesity. Waist-hip ratio was higher (mean difference 0.01, 95% CI 0.001 to 0.02) in men, who had grown up in an economically developed rather than undeveloped environment, as was apolipoprotein B (0.05 g/L, 95% CI 0.001 to 0.10), adjusted for age, socio-economic status and lifestyle. In contrast, the same comparison was associated in women with lower waist-hip ratio (-0.01, 95% CI -0.001 to -0.02) and higher HDL-cholesterol (0.05 mmol/L, 95% CI 0.0004 to 0.10). The associations in men and women were significantly different (p-values<0.001). There were no such differences for diabetes. CONCLUSIONS: Growth in a developed environment with improved nutrition may promote higher sex-steroids at puberty producing an atherogenic lipid profile and male fat pattern in men but the opposite in women, with tracking of increased male IHD risk into adult life.
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    Using electronic medical record data to assess chronic kidney disease, type 2 diabetes and cardiovascular disease testing, recognition and management as documented in Australian general practice: a cross-sectional analysis
    Jones, JL ; Lumsden, NG ; Simons, K ; Ta'eed, A ; de Courten, MP ; Wijeratne, T ; Cox, N ; Neil, CJA ; Manski-Nankervis, J-A ; Hamblin, PS ; Janus, ED ; Nelson, CL (BMJ PUBLISHING GROUP, 2022-02)
    OBJECTIVES: To evaluate the capacity of general practice (GP) electronic medical record (EMR) data to assess risk factor detection, disease diagnostic testing, diagnosis, monitoring and pharmacotherapy for the interrelated chronic vascular diseases-chronic kidney disease (CKD), type 2 diabetes (T2D) and cardiovascular disease. DESIGN: Cross-sectional analysis of data extracted on a single date for each practice between 12 April 2017 and 18 April 2017 incorporating data from any time on or before data extraction, using baseline data from the Chronic Disease early detection and Improved Management in PrimAry Care ProjecT. Deidentified data were extracted from GP EMRs using the Pen Computer Systems Clinical Audit Tool and descriptive statistics used to describe the study population. SETTING: Eight GPs in Victoria, Australia. PARTICIPANTS: Patients were ≥18 years and attended GP ≥3 times within 24 months. 37 946 patients were included. RESULTS: Risk factor and disease testing/monitoring/treatment were assessed as per Australian guidelines (or US guidelines if none available), with guidelines simplified due to limitations in data availability where required. Risk factor assessment in those requiring it: 30% of patients had body mass index and 46% blood pressure within guideline recommended timeframes. Diagnostic testing in at-risk population: 17% had diagnostic testing as per recommendations for CKD and 37% for T2D. Possible undiagnosed disease: Pathology tests indicating possible disease with no diagnosis already coded were present in 6.7% for CKD, 1.6% for T2D and 0.33% familial hypercholesterolaemia. Overall prevalence: Coded diagnoses were recorded in 3.8% for CKD, 6.6% for T2D, 4.2% for ischaemic heart disease, 1% for heart failure, 1.7% for ischaemic stroke, 0.46% for peripheral vascular disease, 0.06% for familial hypercholesterolaemia and 2% for atrial fibrillation. Pharmaceutical prescriptions: the proportion of patients prescribed guideline-recommended medications ranged from 44% (beta blockers for patients with ischaemic heart disease) to 78% (antiplatelets or anticoagulants for patients with ischaemic stroke). CONCLUSIONS: Using GP EMR data, this study identified recorded diagnoses of chronic vascular diseases generally similar to, or higher than, reported national prevalence. It suggested low levels of extractable documented risk factor assessments, diagnostic testing in those at risk and prescription of guideline-recommended pharmacotherapy for some conditions. These baseline data highlight the utility of GP EMR data for potential use in epidemiological studies and by individual practices to guide targeted quality improvement. It also highlighted some of the challenges of using GP EMR data.
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    Recommendations for promoting healthier lifestyles in postpartum women after gestational diabetes
    Lim, SS ; O'Reilly, S ; Versace, V ; Janus, E ; Skinner, TC ; Best, JD ; Dunbar, J ; Teede, H (WILEY, 2020-04)
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