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1  risk but have not yet had a vascular event (primary prevention).
2  early adulthood to inform discussions about primary prevention.
3  essential in developing strategies aimed at primary prevention.
4 nalyses among patients receiving statins for primary prevention.
5 in-related risks and benefits is critical in primary prevention.
6 concerning prescription of statin therapy in primary prevention.
7  or lifestyle were identified as targets for primary prevention.
8 ure CHD and may benefit from more aggressive primary prevention.
9 entify adults eligible for statin therapy as primary prevention.
10             They were started on statins for primary prevention.
11    Prophylactic HPV vaccine is available for primary prevention.
12 l-based evidence supports statin efficacy in primary prevention.
13 alance the risks and benefits of therapy for primary prevention.
14 t and effective, but understudied, tools for primary prevention.
15 ible cancer plans, including initiatives for primary prevention.
16 ear-old man considering starting aspirin for primary prevention.
17 of appropriate therapy than those placed for primary prevention.
18  randomized to egg were not amenable to this primary prevention.
19 ealth score (ICHS) is recommended for use in primary prevention.
20  recommendations for using statin therapy in primary prevention.
21 evidence supporting these recommendations in primary prevention.
22                     The need to scale-up the primary prevention actions is urgent.
23 ater numbers of high-risk women eligible for primary prevention after BBD diagnosis are identified us
24               Future efforts could intensify primary prevention aimed at young adults, adolescents, a
25                                  Coverage of primary prevention alone saved 3.6 million disability-ad
26 per DALY averted, when compared with that of primary prevention alone.
27  The Justification for the Use of Statins in Primary Prevention: An Intervention Trial Evaluating Ros
28 TER [Justification for the Use of Statins in Primary Prevention: An Intervention Trial Evaluating Ros
29  are possible from sufficient uptake of both primary prevention and ART, but with continuation of the
30                                              Primary prevention and early detection are integral stra
31 rability of MESA with target populations for primary prevention and possibility of missed events in M
32                                              Primary prevention and screening among children and adol
33 ions was dominated by a strategy of covering primary prevention and tertiary treatment, which prevent
34 ey suggest novel pharmacological methods for primary prevention and treatment of posttraumatic stress
35  abolish reductions in function with ageing (primary prevention) and/or improve function or slow furt
36 ntion strategies that include biomedical and primary prevention approaches add complexity to the task
37 gent need to identify novel risk factors and primary prevention approaches for CVD in HIV.
38 inappropriate aspirin use was determined for primary prevention (aspirin use in those with 10-year CV
39 ions include secondary prevention, high-risk primary prevention based on formal risk assessment, and
40  both recommend lipid-lowering treatment for primary prevention based on global risk for cardiovascul
41                                  Statins for primary prevention based on low-density lipoprotein chol
42 vention based on formal risk assessment, and primary prevention based on single risk factor measureme
43 underwent first-time device implantation for primary prevention between April 2006 and December 2009.
44 o had previously undergone ICD placement for primary prevention but subsequently never received appro
45 liferative breast lesions are candidates for primary prevention, but few risk models incorporate beni
46 ted with cause-specific cardiac mortality in primary-prevention candidates with ischemic cardiomyopat
47                                          The primary prevention cohort comprised individuals >/=50 ye
48                           Pooled analyses of primary prevention cohort studies showed that compared w
49   Forty patients had no prior history of VT (primary prevention cohort).
50           Conclusion In this community-based primary prevention cohort, guideline-based statin eligib
51                      In this community-based primary prevention cohort, the ACC/AHA guidelines for de
52 ata from intervention trials that included a primary prevention cohort.
53 ere similarly increased in the secondary and primary prevention cohorts (HR, 2.07; 95% CI, 1.43-3.00
54  were similarly reduced in the secondary and primary prevention cohorts, respectively.
55  or greater expected benefit from statins in primary prevention compared with higher-risk individuals
56 eline also provides a new risk estimator for primary prevention decisions, including stroke outcomes
57 ricular arrhythmias (VAs) occur in a current primary prevention defibrillator (implantable cardiovert
58 iduals benefit from long-term statin use for primary prevention depends more on the disutility associ
59                                              Primary prevention efforts are being guided by study of
60  the importance of consistent primordial and primary prevention efforts throughout midlife to late li
61  whether they could therefore be targets for primary prevention efforts.
62 table cardioverter defibrillators (ICDs) for primary prevention enrolled a limited number of women.
63                                              Primary prevention exceeds secondary prevention for CHD
64              Guidelines recommend initiating primary prevention for atherosclerotic cardiovascular di
65 ernment should make great efforts to provide primary prevention for those on high-risk cluster as a p
66 68,808 unique patients receiving aspirin for primary prevention from 119 U.S. practices.
67 esidents potentially eligible for statins in primary prevention from the National Health and Nutritio
68 secondary prevention group compared with the primary prevention group (36.9 versus 15.7/1000 patient-
69 ege of Cardiology/American Heart Association primary prevention guidelines are mainly on the basis of
70                                              Primary prevention guidelines focus on risk, often assum
71    Purpose: To systematically review current primary prevention guidelines on adult cardiovascular ri
72                                              Primary prevention had higher New York Heart Association
73                                              Primary prevention has several advantages: the effective
74           Each has their place, but upstream primary prevention has the largest effect on reduction o
75 ersal public health system, which focuses on primary prevention, has contributed to this achievement.
76 atins are projected to be cost-effective for primary prevention; however, even a small increase in ge
77  approximately one fourth of patients with a primary prevention ICD and no previous therapy have EF >
78         Prescription fills for recipients of primary prevention ICD between 2007 and 2011 were examin
79 herapy can be predicted in ICM patients with primary prevention ICD by quantifying the LGE border zon
80 and could inform clinical decision making on primary prevention ICD candidacy.
81 care patients with heart failure receiving a primary prevention ICD had frailty (10%) or dementia (1%
82 ta Registry ICD Registry who underwent first primary prevention ICD implantation between 2006 and 200
83               Rates of GDMT for HFrEF before primary prevention ICD implantation were low, and failur
84 l population of Medicare patients undergoing primary prevention ICD implantation were stable between
85 is relationship between age and outcome of a primary prevention ICD in patients with nonischemic syst
86 ns for continued device therapy in pediatric primary prevention ICD patients might be reconsidered af
87                                        Among primary prevention ICD patients, 40.0% had an improved L
88 d beta-blocker [HFBB]) within 90 days before primary prevention ICD placement in patients with HFrEF.
89                              We assessed all primary prevention ICD recommendations listed in both do
90  430 women with heart failure who received a primary prevention ICD to 430 women who did not; we furt
91 educed left ventricular ejection fraction, a primary prevention ICD was associated with a significant
92         Among 19,733 patients with HFrEF and primary prevention ICD, 61.1% filled any GDMT before imp
93 g women with heart failure with or without a primary prevention ICD.
94 nalysis investigates the association between primary prevention ICDs and mortality among Medicare, ra
95 ty and dementia among older adults receiving primary prevention ICDs and to determine the impact of m
96                                              Primary prevention ICDs are associated with lower mortal
97                                              Primary prevention ICDs are efficacious at reducing all-
98 review of patients undergoing replacement of primary prevention ICDs at 2 tertiary Veterans Affairs M
99                                Patients with primary prevention ICDs from the National Cardiovascular
100 e beneficiaries with heart failure receiving primary prevention ICDs have frailty or dementia.
101 e findings support guideline-directed use of primary prevention ICDs in eligible patients.
102 justed comparative effectiveness analysis of primary prevention ICDs in Medicare, racial/ethnic minor
103    Approximately 25% of patients who receive primary prevention ICDs may no longer meet guideline ind
104              Before data collection started, primary prevention ICDs were hypothesized to reduce all-
105            To investigate the association of primary prevention ICDs with all-cause mortality in pati
106  primary prevention of sudden cardiac death (primary prevention ICDs) in patients with nonischemic ca
107 ng patients who are unlikely to benefit from primary prevention ICDs.
108 ess likely to derive a survival benefit from primary prevention ICDs.
109 icular ejection fraction </=35% referred for primary prevention implantable cardioverter defibrillato
110 ful for understanding risk stratification of primary prevention implantable cardioverter defibrillato
111 ts with ischemic cardiomyopathy referred for primary prevention implantable cardioverter defibrillato
112                                              Primary prevention implantable cardioverter defibrillato
113 that women and black patients eligible for a primary prevention implantable cardioverter-defibrillato
114 ilated cardiomyopathy patients evaluated for primary prevention implantable cardioverter-defibrillato
115  rates occurred despite a low rate (4.0%) of primary prevention implantable cardioverter-defibrillato
116 ction fraction (HFrEF) is recommended before primary prevention implantable cardioverter-defibrillato
117                  Heart failure patients with primary prevention implantable cardioverter-defibrillato
118 he risks of death or rehospitalization after primary prevention implantable cardioverter-defibrillato
119  are under-represented in clinical trials of primary prevention implantable cardioverter-defibrillato
120  sought to determine how often patients with primary prevention implantable cardioverter-defibrillato
121 ose with DCM may not benefit from additional primary prevention implantable cardioverter-defibrillato
122 lator indications for patients with CHD were primary prevention in 1943 (61.9%) and secondary prevent
123                       The ICD indication was primary prevention in 67% and secondary in 33% patients.
124 ary prevention in 10 patients (9.6%) and for primary prevention in 94 patients (90.4%).
125 Task Force recommendations for statin use in primary prevention in a cohort of adults who experienced
126 l variation in inappropriate aspirin use for primary prevention in a large U.S. nationwide registry.
127                            Evidence to guide primary prevention in adults aged 75 years or older is l
128             Limited trial evidence targeting primary prevention in adults aged 75 years or older.
129                                              Primary prevention in adults aged younger than 60 years
130 ioverter-defibrillator (ICD) indications for primary prevention in Brugada syndrome (BrS) are still d
131 s the literature on the topic of aspirin for primary prevention in general, and in subjects with diab
132 he decision to initiate statin treatment for primary prevention in older adults requires further inve
133             However, the role of aspirin for primary prevention in patients with no overt cardiovascu
134 ardiovascular disease risk factor control as primary prevention in patients with type 2 diabetes mell
135 Cardioverter-Defibrillators in Patients with Primary Prevention Indication to Prolong Time to First S
136 ction fraction was 43 +/- 18%, and 65% had a primary prevention indication.
137                     Lifetime aspirin use for primary prevention initiated at younger ages (40 to 69 y
138 t such a reduction requires a combination of primary prevention interventions and preventative effect
139 essing family history and suggest that early primary prevention interventions may be warranted at you
140 syndrome and 2) whether ICD implantation for primary prevention is associated with improved outcomes
141                          However, aspirin as primary prevention is debated because of the risk of hem
142                      Evidence for aspirin in primary prevention is heterogeneous and limited by rare
143 njuries is needed, and greater investment in primary prevention is needed.
144 der patients, so the use of these agents for primary prevention is possible.
145 CC/AHA guideline for expanded statin use for primary prevention is projected to treat more people, to
146 mation to cardiovascular risk prediction for primary prevention, is not currently recommended.
147 nd four randomised controlled trials of both primary prevention (JUPITER and ASCOT) and secondary pre
148  of benefits from risk-reducing therapies in primary prevention may help target therapies to those in
149                                              Primary prevention measures should be strengthened to pr
150           The decision to treat a patient in primary prevention must be a careful one because the ben
151 evaluate the effectiveness of synbiotics for primary prevention of AD.
152 sponse is logical for interventions aimed at primary prevention of allergic disease.
153 s will ultimately provide a road map for the primary prevention of allergic disease.
154 mmendations on initiating statin therapy for primary prevention of ASCVD (net 221 individuals appropr
155 ein cholesterol (LDL-C)-lowering therapy for primary prevention of ASCVD events.
156 mance of the ACC/AHA risk-based approach for primary prevention of ASCVD with statins was superior to
157 n before initiating a statin, especially for primary prevention of ASCVD.
158 ance induction is an attractive approach for primary prevention of asthma.
159                 Statins are effective in the primary prevention of atherosclerotic cardiovascular dis
160                            Their role in the primary prevention of atherothrombosis remains controver
161  the absence of proven interventions for the primary prevention of atrial fibrillation, this post hoc
162 corporated into clinical assessments for the primary prevention of cardiac emergencies in basketball
163 ded "initiating low-dose aspirin use for the primary prevention of cardiovascular disease (CVD) and c
164  indicates that aspirin is effective for the primary prevention of cardiovascular disease (CVD) and c
165 long-term benefits of lowering LDL-C for the primary prevention of cardiovascular disease among indiv
166 ued a guideline titled, "Aspirin Use for the Primary Prevention of Cardiovascular Disease and Colorec
167 s and harms of behavioral counseling for the primary prevention of cardiovascular disease in adults w
168 st for screening and risk assessment for the primary prevention of cardiovascular disease in apparent
169  benefit-risk profile of low-dose aspirin in primary prevention of cardiovascular disease is unclear.
170  Current guidelines recommend statins in the primary prevention of cardiovascular disease on the basi
171 o 75 years, who initiated statin therapy for primary prevention of cardiovascular disease.
172 ive Services Task Force endorsed aspirin for primary prevention of cardiovascular disease.
173 ll included trials evaluated aspirin for the primary prevention of cardiovascular events.
174                                      For the primary prevention of CHD, Multi-Ethnic Study of Atheros
175 g from birth represents a first step towards primary prevention of childhood obesity.
176 gen and progestin has no net benefit for the primary prevention of chronic conditions for most postme
177 at estrogen alone has no net benefit for the primary prevention of chronic conditions for most postme
178                      Hormone therapy for the primary prevention of chronic conditions in menopausal w
179 ds against the use of estrogen alone for the primary prevention of chronic conditions in postmenopaus
180 e of combined estrogen and progestin for the primary prevention of chronic conditions in postmenopaus
181 he use of menopausal hormone therapy for the primary prevention of chronic conditions.
182 hough the effects of supplementation for the primary prevention of clinical cardiovascular events in
183                              Aspirin for the primary prevention of coronary heart disease (CHD) is on
184                         This paper discusses primary prevention of coronary heart disease that may be
185 ends initiating low-dose aspirin use for the primary prevention of CVD and CRC in adults aged 50 to 5
186 ion to initiate low-dose aspirin use for the primary prevention of CVD and CRC in adults aged 60 to 6
187  and harms of initiating aspirin use for the primary prevention of CVD and CRC in adults aged 70 year
188  and harms of initiating aspirin use for the primary prevention of CVD and CRC in adults younger than
189 ewed 5 additional studies of aspirin for the primary prevention of CVD and several additional analyse
190     The beneficial effect of aspirin for the primary prevention of CVD is modest and occurs at doses
191               According to the guidelines on primary prevention of CVD, aspirin use is considered app
192 ed eligibility for each of 10 major RCTs for primary prevention of CVD.
193 o improve evidence-based aspirin use for the primary prevention of CVD.
194  help guide initiation of statin therapy for primary prevention of CVD.
195  deepens the need for clinicians to focus on primary prevention of de novo humoral allosensitization.
196 e ICD therapy with conventional care for the primary prevention of death of various causes in adults
197      The decrease in disability onset due to primary prevention of diabetes could play an important p
198 evaluation of antibiotic recommendations and primary prevention of exposure to Salmonella.
199 benefit in using nutritional supplements for primary prevention of eye disease.
200 o provide evidence-based recommendations for primary prevention of food allergy.
201 cines may reduce the economic burden through primary prevention of influenza and reduction in illness
202  intervention that seems justifiable for the primary prevention of Parkinson's disease is the promoti
203        The ICD therapy is routinely used for primary prevention of SCD in patients with cardiomyopath
204 risk stratification of patients with HCM for primary prevention of SCD, and calculating an individual
205 dioverter-defibrillator implantation for the primary prevention of SCD.
206 s are performed in asymptomatic patients for primary prevention of stroke, it is incumbent upon clini
207 an implantable cardiac defibrillator for the primary prevention of sudden cardiac arrest after baseli
208 table cardioverter defibrillators (ICDs) for primary prevention of sudden cardiac death (primary prev
209  cardioverter defibrillators (ICDs) used for primary prevention of sudden cardiac death (SCD) conclud
210 patients with dilated cardiomyopathy for the primary prevention of sudden cardiac death (SCD) in thos
211  implantable cardioverter defibrillators for primary prevention of sudden cardiac death are less like
212             The rate of ICD implantation for primary prevention of sudden cardiac death in this patie
213  LVEF assessments after ICD implantation for primary prevention of sudden cardiac death.
214 e appropriate implantation of an ICD for the primary prevention of sudden cardiac death.
215 table cardioverter-defibrillators (ICDs) for primary prevention of sudden death in patients with an e
216 able selection of patients likely to achieve primary prevention of sudden death with implantable defi
217 Previously, hormone therapy was used for the primary prevention of these chronic conditions.
218         These shared origins are targets for primary prevention of type 2 diabetes.
219  available regarding their potential role in primary prevention of type 2 diabetes.
220                                      Data on primary prevention of zinc status and diabetes risk are
221 ated with a Biventricular ICD [RELEVANT] and Primary Prevention Parameters Evaluation [PREPARE]).
222                                              Primary prevention participants (N=3486; 34%) were young
223  atherosclerotic cardiovascular disease in a primary prevention patient; screening for familial lipid
224 and updated 10-year ASCVD risk estimates for primary prevention patients adhering to the appropriate
225 he cohort includes approximately 9.4 million primary prevention patients and approximately 400,000 se
226 ing heart disease, in a large study group of primary prevention patients with heart failure.
227  the use of ezetimibe or PCSK9 inhibitors in primary prevention patients with LDL-C <190 mg/dL with o
228                      Designed especially for primary prevention patients, this process of shared deci
229 tion it might be more suitable for high-risk primary prevention patients, though future combinations
230 mulations, might be more suited to high-risk primary prevention patients.
231 ed with low-dose aspirin in secondary versus primary prevention patients.
232 of cardiovascular outcomes compared with the primary prevention patients.
233 l ASCVD and in a smaller number of high-risk primary prevention patients.
234 rted of $5588 when compared with coverage of primary prevention plus tertiary treatment.
235 eed for population-wide health promotion and primary prevention policies is emphasized.
236                                 Among the US primary prevention population represented by 3416 indivi
237         Among the 8.9% of individuals in the primary prevention population who would be recommended f
238 iovascular effects of LDL-C lowering among a primary prevention population with LDL-C >/=190 mg/dL.
239                            In a contemporary primary prevention population, baseline cardiac troponin
240 tatins, and reflect response to therapy in a primary prevention population.
241 ompensated by the lower baseline risk in the primary prevention population.
242                                       In CVD primary prevention populations, aspirin's effect on tota
243 iated with adverse cardiovascular outcome in primary prevention populations.
244 n implantable cardioverter-defibrillator for primary prevention purposes.
245 aimed to confirm this observation in a third primary prevention randomized controlled trial.
246 lysis across the WOSCOPS, ASCOT, and JUPITER primary prevention, relative risk reduction in those at
247                      The place of aspirin in primary prevention remains controversial, with North Ame
248 s of risk factor modification are a focus of primary prevention research.
249 act of expanding national insurance to cover primary prevention, secondary prevention, and tertiary t
250 , sudden, any cardiac, or noncardiac) in the primary prevention setting.
251 TnT to outcomes are limited, particularly in primary prevention settings.
252                                              Primary prevention should remain a priority for cancer c
253 ention) and for two blood pressure ranges in primary prevention (stage one, 140-159/90-99 mm Hg; stag
254 k threshold considered sufficient to warrant primary prevention statin therapy, and the decision not
255  lower number of individuals recommended for primary prevention statin therapy, including many younge
256                              Eligibility for primary prevention statin therapy.
257  determine the difference in eligibility for primary prevention statin treatment among US adults, ass
258 to medication, yet most patients discontinue primary prevention statins within 3 years.
259   These findings could have implications for primary prevention strategies and help target at-risk ad
260 d might support the development of effective primary prevention strategies for allergy and asthma in
261  eating occasions, are potential targets for primary prevention strategies with large health impacts.
262 onal limitation or cognitive impairment, all primary prevention strategies would prevent MIs and CHD
263 ty may be a crucial factor in the success of primary prevention strategies, and a range of options, a
264 would contribute greatly to inform effective primary prevention strategies.
265 ear period, supporting the wider adoption of primary prevention strategies.
266 ality and provide an opportunity for testing primary prevention strategies.
267 y complementary regular supplementation in a primary prevention strategy rather than secondary preven
268  at early stages of the disease process in a primary prevention strategy.
269 ial infarction nor ischemic stroke, yet most primary prevention studies focus on these presentations.
270                    Several observational and primary prevention studies have investigated these relat
271                                       Future primary prevention studies might explore medication disu
272 ith cardiovascular disease (CVD) outcomes in primary prevention studies.
273 ested cohort within the 1995 Canadian Asthma Primary Prevention Study intervention study was performe
274 ealth Study) and CAPPS/SAGE (Canadian Asthma Primary Prevention Study/Study of Asthma, Genetics and E
275              Despite significant progress in primary prevention, the rate of MI has not declined in y
276                                 Ranging from primary prevention to end-of-life care, the scope for ne
277 icular Dysfunction, Non-ischemic Etiology in Primary Prevention Treated with a Biventricular ICD [REL
278                                    One large primary prevention trial found that a Mediterranean diet
279  of Scotland Coronary Prevention Study was a primary prevention trial in 45- to 64-year-old men with
280 Trial Evaluating Rosuvastatin), a randomized primary prevention trial that compared rosuvastatin trea
281  events, including coronary death or MI) for primary prevention trials (1.5% lower event rate [95% CI
282 ever, in analyses of 2 randomized controlled primary prevention trials (ASCOT [Anglo-Scandinavian Car
283                          Data Synthesis: Two primary prevention trials found no difference in all-cau
284 et autoimmunity is initiated in infancy, and primary prevention trials require children at high genet
285 ose that targeted communities or clinicians, primary prevention trials, and trials that reported even
286                                       In CVD primary prevention trials, cancer mortality (relative ri
287                         Specifically, in the primary prevention trials, the number needed to treat to
288 vent one coronary heart disease event in the primary prevention trials.
289  Current algorithms for statin allocation in primary prevention use epidemiologic estimates of absolu
290 e randomized clinical trials have found that primary prevention use of an implantable cardioverter-de
291  of cardiovascular disease (secondary versus primary prevention) were prespecified for evaluation.
292 ss IIb assessment and is most appropriate in primary prevention when clinical decisions to initiate s
293        This goal is only fully achieved with primary prevention, which requires us to identify and pr
294 egies for the prevention of FA might include primary prevention, which seeks to prevent the onset of
295               Consideration of the safety of primary prevention with aspirin requires an individualiz
296                                     Overall, primary prevention with ICD therapy versus conventional
297 ipants from a randomized controlled trial of primary prevention with statin therapy (WOSCOPS [West of
298 Heart Association (AHA) guidelines recommend primary prevention with statins for individuals with >/=
299  receiving inappropriate aspirin therapy for primary prevention, with significant practice-level vari
300 her to provide a complementary public health primary prevention zinc strategy.

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