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1  and without pretreatment with enalapril, an angiotensin converting enzyme inhibitor.
2 d were more often on diuretics, digoxin, and angiotensin converting enzyme inhibitors.
3 roteinuric angiotensin receptor blockers and angiotensin-converting enzyme inhibitors.
4 system with angiotensin receptor blockers or angiotensin-converting enzyme inhibitors.
5 ence to angiotensin II receptor blockers and angiotensin-converting enzyme inhibitors.
6 red thiazide or thiazide-like diuretics over angiotensin-converting enzyme inhibitors.
7 ives (eOC), hormonal replacement therapy, or angiotensin-converting enzyme inhibitors.
8 , 378 (9.2%) were taking azathioprine and an angiotensin-converting enzyme inhibitor, 171 (12.9%) wer
9 et, 53% versus 66%; statins, 40% versus 52%; angiotensin-converting enzyme inhibitors, 20% versus 29%
10 [CI]: 49%-64%) of patients were treated with angiotensin-converting enzyme inhibitors, 34% (95% CI: 2
11                We then imaged the effects of angiotensin-converting enzyme inhibitor (5 mg/kg enalapr
12         The occurrence of the casein-derived angiotensin converting enzyme-inhibitor (ACE-I) peptides
13 hypertensive medications included diuretics, angiotensin-converting enzyme inhibitors (ACE), and beta
14 lled trial planned to evaluate the impact of angiotensin-converting enzyme inhibitors (ACE-i) on the
15 al of the study was to assess the effects of angiotensin-converting enzyme inhibitors (ACE-Is) and an
16 geting the renin-angiotensin system, such as angiotensin-converting enzyme inhibitors (ACE-Is) and an
17  appropriate initiation of beta blockers and angiotensin-converting-enzyme inhibitors (ACE-Is) or ang
18                There is no consensus whether angiotensin-converting enzyme inhibitor (ACEI) and angio
19                                          The angiotensin-converting enzyme inhibitor (ACEi) enalapril
20 and an angiotensin receptor blocker (ARB) or angiotensin-converting enzyme inhibitor (ACEI) has demon
21 conflicting regarding whether chronic use of angiotensin-converting enzyme inhibitor (ACEI) or angiot
22 ation Trial (BENEDICT), all of whom received angiotensin-converting enzyme inhibitor (ACEI) therapy a
23 remental cost-effectiveness ratios (ICER) of angiotensin-converting enzyme inhibitor (ACEI), beta-blo
24 ective was to assess the association between angiotensin-converting enzyme inhibitor (ACEI)/angiotens
25 ications to medical therapy, use and dose of angiotensin-converting enzyme inhibitor (ACEI)/angiotens
26 kground drug therapy, that is, high doses of angiotensin-converting enzyme inhibitor (ACEi, or angiot
27                      The association between angiotensin-converting enzyme inhibitors (ACEI) and angi
28                                              Angiotensin-converting enzyme inhibitors (ACEi) for reni
29 vestigated continued and discontinued use of angiotensin-converting enzyme inhibitors (ACEi) or angio
30 round clinician-directed therapy with either angiotensin-converting enzyme inhibitors (ACEI) or angio
31                                              Angiotensin-converting enzyme inhibitors (ACEI) or angio
32 e first mechanistic evidence that the use of angiotensin-converting enzyme inhibitors (ACEI) or angio
33                            Although statins, angiotensin-converting enzyme inhibitors (ACEI) or angio
34                                We focused on angiotensin-converting enzyme inhibitors (ACEI), angiote
35 re with reduced ejection fraction, including angiotensin-converting enzyme inhibitors (ACEI), angiote
36 eatment doses of beta-blockers, statins, and angiotensin-converting enzyme inhibitors (ACEI)/angioten
37 al trials of antihypertensive therapy (ARBs, angiotensin-converting-enzyme inhibitors [ACEi], beta bl
38 CI], -1.46 to -0.02; P = 0.01), specifically angiotensin-converting enzyme inhibitors (ACEIs) (beta =
39        Reduced potassium excretion caused by angiotensin-converting enzyme inhibitors (ACEis) and ang
40                                  The role of angiotensin-converting enzyme inhibitors (ACEIs) and ang
41 schemic heart disease, the pattern of use of angiotensin-converting enzyme inhibitors (ACEIs) in coro
42                                              Angiotensin-converting enzyme inhibitors (ACEIs) may ret
43                                              Angiotensin-converting enzyme inhibitors (ACEIs) or angi
44 hough several studies have shown that use of angiotensin-converting enzyme inhibitors (ACEIs) potenti
45 ion, that thiazide diuretics are superior to angiotensin-converting enzyme inhibitors (ACEIs), calciu
46 rm use of calcium channel blockers (CCBs) or angiotensin-converting enzyme inhibitors (ACEis), respec
47  promulgated as an acceptable alternative to angiotensin-converting enzyme inhibitors (ACEIs).
48                It has been hypothesized that angiotensin-converting enzyme inhibitors (ACEIs)/angiote
49 dication use (antiplatelet therapy, statins, angiotensin-converting enzyme inhibitors [ACEIs] or angi
50 ondition for which the medication was taken (angiotensin-converting enzyme inhibitors [ACEIs], angiot
51 ics showed better primary effectiveness than angiotensin-converting enzyme inhibitors: acute myocardi
52 .50; 95% confidence interval, 0.48-0.52), or angiotensin-converting enzyme inhibitors (adjusted odds
53 but an increased risk was found for users of angiotensin-converting enzyme inhibitors (adjusted OR 1
54                                              Angiotensin-converting enzyme inhibitor also significant
55               Pairwise matching (1:1) of the angiotensin-converting enzyme inhibitor and angiotensin
56 2009 and 2010 in appropriate prescription of angiotensin-converting enzyme inhibitor and beta-blocker
57 ere -4.38 mm Hg (95% CI, -7.27 to -2.16) for angiotensin-converting enzyme inhibitors and -3.07 mm Hg
58  100 person-years for the patients receiving angiotensin-converting enzyme inhibitors and 2.87 per 10
59 orrhagic shock, 4) shocked mice treated with angiotensin-converting enzyme inhibitors and a single bo
60 prescribed drugs in the same year, including angiotensin-converting enzyme inhibitors and angiotensin
61 view that found high-certainty evidence that angiotensin-converting enzyme inhibitors and angiotensin
62    This study aimed to compare the effect of angiotensin-converting enzyme inhibitors and angiotensin
63 e for CKD treatment benefit is strongest for angiotensin-converting enzyme inhibitors and angiotensin
64 ssessed for each of 6 drug classes: statins, angiotensin-converting enzyme inhibitors and angiotensin
65     On admission, medical therapy, including angiotensin-converting enzyme inhibitors and angiotensin
66                               Uptitration of angiotensin-converting enzyme inhibitors and beta blocke
67                                              Angiotensin-converting enzyme inhibitors and beta-blocke
68 ic, but not asymptomatic, heart failure with angiotensin-converting enzyme inhibitors and beta-blocke
69 -receptor blockers and statins, moderate for angiotensin-converting enzyme inhibitors and beta-blocke
70                                              Angiotensin-converting enzyme inhibitors and beta-blocke
71                         We hypothesized that angiotensin-converting enzyme inhibitors and beta-blocke
72 ons known to be unsafe in pregnancy, such as angiotensin-converting enzyme inhibitors and statins, sh
73 de or thiazide-like diuretics superiority to angiotensin-converting enzyme inhibitors and the inferio
74                Current standard therapy with angiotensin-converting enzyme inhibitors and/or angioten
75 rgic receptor blockers (beta-blockers), ACE (angiotensin-converting enzyme) inhibitors and ANG (angio
76 n, renal function, medication (beta-blocker, angiotensin converting enzyme inhibitor, and angiotensin
77  antiplatelet, antithrombotic, beta blocker, angiotensin-converting enzyme inhibitor, and statin agen
78 itration of beta-adrenergic blocking agents, angiotensin-converting enzyme inhibitors, and angiotensi
79 he use of thiazide diuretics, beta-blockers, angiotensin-converting enzyme inhibitors, and angiotensi
80               Concomitant therapy with ARBs, angiotensin-converting enzyme inhibitors, and antiarrhyt
81 upporting the use of aspirin, beta-blockers, angiotensin-converting enzyme inhibitors, and lipid-lowe
82 r disease medicines (aspirin, beta blockers, angiotensin-converting enzyme inhibitors, and statins) i
83 0.8 [95% confidence interval, 0.64-0.98] for angiotensin-converting enzyme inhibitors; and relative r
84 to support initiating drug treatment with an angiotensin-converting enzyme inhibitor, angiotensin rec
85 scharge included the following: medications (angiotensin-converting enzyme inhibitors, angiotensin II
86                                              Angiotensin-converting enzyme inhibitors, angiotensin re
87 atio [UPCR] 500-5000 mg/g) and taking stable angiotensin-converting enzyme inhibitors, angiotensin re
88 zine for 48 hours, and rapid up-titration of angiotensin-converting enzyme inhibitors, angiotensin re
89 classes thiazide or thiazide-like diuretics, angiotensin-converting enzyme inhibitors, angiotensin re
90 g or higher on permitted background drugs of angiotensin-converting enzyme inhibitors, angiotensin-re
91         The medication classes examined were angiotensin-converting enzyme inhibitors, angiotensin-re
92               No class of medications (i.e., angiotensin-converting enzyme inhibitors, angiotensin-re
93 ential introduction of medications including angiotensin-converting-enzyme inhibitors, angiotensin-re
94 f amlodipine 5 mg/day, a standard dose of an angiotensin converting enzyme inhibitor/angiotensin rece
95     Pivotal trials of beta-blockers (BB) and angiotensin converting enzyme inhibitors/angiotensin rec
96 nary intervention, in-hospital and discharge angiotensin-converting enzyme inhibitor/angiotensin II r
97 to receive treatment with a beta-blocker, an angiotensin-converting enzyme inhibitor/angiotensin II r
98 nts' baseline characteristics (shock, use of angiotensin-converting enzyme inhibitor/angiotensin II r
99 s a combination of statin, beta-blocker, and angiotensin-converting enzyme inhibitor/angiotensin rece
100 antiplatelet drug, statin, beta-blocker, and angiotensin-converting enzyme inhibitor/angiotensin rece
101 B-type natriuretic peptide, pkVO2, NYHA, and angiotensin-converting enzyme inhibitor/angiotensin rece
102  and statins but were less likely to receive angiotensin-converting enzyme inhibitor/angiotensin rece
103 thin 24 hours, (2) aspirin at discharge, (3) angiotensin-converting enzyme inhibitor/angiotensin rece
104                                              Angiotensin-converting enzyme inhibitor/angiotensin rece
105 l/L increase, P<0.001; CI: 0.31-0.85), using angiotensin-converting enzyme inhibitor/angiotensin rece
106       Medications including statin, fibrate, angiotensin-converting enzyme inhibitor/angiotensin rece
107 Statin use was reported in only 30.5+/-2.5%, angiotensin-converting enzyme inhibitor/angiotensin rece
108 no statistically significant improvements in angiotensin-converting enzyme inhibitor/angiotensin rece
109 98% of patients were on >50% target dose for angiotensin-converting enzyme inhibitor/angiotensin rece
110 idence, clinical characteristics, treatment (angiotensin-converting enzyme inhibitor/angiotensin rece
111 445-patient subset received at least 1 GDMT (angiotensin-converting enzyme inhibitor/angiotensin rece
112 current smoking, chronic kidney disease, and angiotensin-converting enzyme inhibitors/angiotensin II
113 current smoking, chronic kidney disease, and angiotensin-converting enzyme inhibitors/angiotensin II
114 e of and patient adherence to beta-blockers, angiotensin-converting enzyme inhibitors/angiotensin rec
115 vention with a combination of beta-blockers, angiotensin-converting enzyme inhibitors/angiotensin rec
116 f 85 017 individuals, 55%, 76%, and 61% used angiotensin-converting enzyme inhibitors/angiotensin rec
117 ethnicity, but women were less likely to use angiotensin-converting enzyme inhibitors/angiotensin rec
118                  Rates of patients receiving angiotensin-converting enzyme inhibitors/angiotensin rec
119 escription rates ranged from 44% to 100% for angiotensin-converting enzyme inhibitors/angiotensin rec
120             Practice rates of treatment with angiotensin-converting enzyme inhibitors/angiotensin rec
121 .11 (95% confidence interval, 1.08-1.18) for angiotensin-converting enzyme inhibitors/angiotensin rec
122         Successive eras had greater usage of angiotensin-converting enzyme inhibitors/angiotensin rec
123 ational level, history of eczema, the use of angiotensin-converting enzyme inhibitors/angiotensin rec
124            In multivariable analyses, use of angiotensin-converting enzyme inhibitors/angiotensin rec
125 D not taking statins, 5.4 million not taking angiotensin-converting enzyme inhibitors/angiotensin rec
126   Utilization of statins, beta-blockers, and angiotensin-converting enzyme inhibitors/angiotensin rec
127 al therapy including statins, beta-blockers, angiotensin-converting enzyme inhibitors/angiotensin rec
128 and 0.86 (0.74-1.01) in patients on statins, angiotensin-converting enzyme inhibitors/angiotensin rec
129 ficial effects of treatment with statins and angiotensin-converting enzyme inhibitors/angiotensin rec
130 , and 66.4% of the patients were on statins, angiotensin-converting enzyme inhibitors/angiotensin rec
131 es were treatment at discharge with statins, angiotensin-converting enzyme inhibitors/angiotensin rec
132 versus 57% in rural; P=0.1) and reversed for angiotensin-converting enzyme inhibitors/angiotensin rec
133 , documentation of ejection fraction, use of angiotensin-converting enzyme inhibitors/angiotensin rec
134 fills for beta-blockers, antiplatelet drugs, angiotensin-converting enzyme inhibitors/angiotensin-2 r
135               Use of antiplatelet agents and angiotensin-converting enzyme inhibitors/angiotensin-2 r
136                                              Angiotensin-converting enzyme inhibitors are associated
137         Because the pharmacologic effects of angiotensin-converting enzyme inhibitors are partly medi
138  reduced ejection fraction (HFrEF) receiving angiotensin-converting enzyme inhibitors are well-docume
139 eurohormonal activity (like beta-blockers or angiotensin-converting enzyme inhibitors) are considered
140 leroderma Clinical Trials Consortium confirm angiotensin-converting enzyme inhibitors as first-line t
141 edema, acquired C1 inhibitor deficiency, and angiotensin-converting enzyme inhibitor-associated angio
142 ocked mice treated with ramipril for 7 days (angiotensin-converting enzyme inhibitors) before hemorrh
143 d and then subsequently filled prescriptions angiotensin-converting enzyme inhibitors, beta-blockers,
144 ar complications have also been treated with angiotensin-converting enzyme inhibitors, beta-blockers,
145                 Suitable genetic proxies for angiotensin-converting enzyme inhibitors, beta-blockers,
146  that promoted antiplatelet agents, statins, angiotensin-converting enzyme inhibitors, blood pressure
147 angiotensin type 1 receptor blocker (ARB) or angiotensin-converting enzyme inhibitor can induce regre
148                                              Angiotensin-converting enzyme inhibitors can delay the p
149 , statins, angiotensin II receptor blockers, angiotensin-converting enzyme inhibitors) can modify the
150                    Combining THR-123 and the angiotensin-converting enzyme inhibitor captopril had an
151 ptor blockers losartan and valsartan and the angiotensin-converting enzyme inhibitor captopril on wou
152 wer of DPM, three effect categories, namely, angiotensin-converting enzyme inhibitor, cyclooxygenase
153 ium oxide nanoparticles for the detection of angiotensin-converting enzyme inhibitor drug, captopril,
154 sin inhibitor LCZ696 (400 mg daily) with the angiotensin-converting enzyme inhibitor enalapril (20 mg
155 ejection fraction (HFrEF), compared with the angiotensin-converting enzyme inhibitor enalapril, and i
156  be prescribed lipid-lowering medication and angiotensin-converting enzyme inhibitors, especially if
157  should include calcium channel blockers and angiotensin-converting enzyme inhibitors for cardiovascu
158 lasses: aspirin, statins, beta-blockers, and angiotensin-converting enzyme inhibitors given to patien
159 ant prevented blood pressure lowering in the angiotensin-converting enzyme inhibitor group (p < 0.001
160 ume withdrawn was significantly lower in the angiotensin-converting enzyme inhibitor group than in th
161 lood lactate was significantly higher in the angiotensin-converting enzyme inhibitor group than in th
162 ation before the index date, those receiving angiotensin-converting enzyme inhibitors had a higher ri
163          In addition, the patients receiving angiotensin-converting enzyme inhibitors had a higher ri
164          Patients receiving beta-blockers or angiotensin-converting enzyme inhibitors had a higher ri
165                  Many vasodilators including angiotensin-converting enzyme inhibitors have been evalu
166                                Intracoronary angiotensin-converting enzyme inhibitors have been shown
167 giotensin II receptor blockers compared with angiotensin-converting enzyme inhibitors (HR, 1.33; 95%
168 ant (HOE-140) immediately before anesthesia (angiotensin-converting enzyme inhibitors + icatibant), a
169 n, clopidogrel, beta-blocker, statin, and an angiotensin-converting enzyme inhibitor in patients with
170 nist-neprilysin inhibitor was superior to an angiotensin-converting enzyme inhibitor in reducing mort
171 s support the need to reevaluate the role of angiotensin-converting enzyme inhibitors in humans with
172 ith lower rates of sepsis and mortality than angiotensin-converting enzyme inhibitors in the patients
173 s a metabolite significantly associated with angiotensin-converting-enzyme inhibitors in our metabolo
174 ioedema, hereditary angioedema type III, and angiotensin converting enzyme inhibitor-induced angioede
175 II and III), acquired C1-INH deficiency, and angiotensin-converting enzyme inhibitor-induced angioede
176                                          The angiotensin converting enzyme inhibitor lisinopril and m
177 neficial ACE10 phenotype was reversed by the angiotensin-converting enzyme inhibitor (lisinopril) and
178 get (95/60 to 110/75 mm Hg) and to either an angiotensin-converting-enzyme inhibitor (lisinopril) plu
179 erior compared with the 24-h BP reduction of angiotensin-converting enzyme inhibitors (mean BP reduct
180 harmacologic therapy that includes either an angiotensin-converting enzyme inhibitor (moderate-qualit
181 nsin II type 1 receptor antagonists (n=6) or angiotensin-converting enzyme inhibitors (n=6) exhibited
182  patients more often received beta-blockers, angiotensin-converting enzyme inhibitors, nitrates, and
183                                 Moreover, an angiotensin-converting enzyme inhibitor normalized CXCR4
184 tes mellitus and overt nephropathy receiving angiotensin converting enzyme inhibitor or angiotensin r
185 e, primary renal disease classification, and angiotensin converting enzyme inhibitor or angiotensin r
186  the renin-angiotensin system with either an angiotensin-converting enzyme inhibitor or a mineralocor
187 ent with a glomerular disease with either an angiotensin-converting enzyme inhibitor or an angiotensi
188 without diabetes who are currently taking an angiotensin-converting enzyme inhibitor or an angiotensi
189 -angiotensin-aldosterone pathway, such as an angiotensin-converting enzyme inhibitor or an angiotensi
190 ack patients and 18.2% of patients not on an angiotensin-converting enzyme inhibitor or angiotensin I
191 mol), who had been receiving stable doses of angiotensin-converting enzyme inhibitor or angiotensin I
192 or without saxagliptin, given in addition to angiotensin-converting enzyme inhibitor or angiotensin I
193 oup had worse baseline renal function, lower angiotensin-converting enzyme inhibitor or angiotensin r
194 d as prescription of beta-blocker and either angiotensin-converting enzyme inhibitor or angiotensin r
195 l or add-on antihypertensive therapy with an angiotensin-converting enzyme inhibitor or angiotensin r
196 ssociation (NYHA) classification, and use of angiotensin-converting enzyme inhibitor or angiotensin r
197                  Most patients (84%) used an angiotensin-converting enzyme inhibitor or angiotensin r
198 ection fraction (93.4% versus 88.8%), use of angiotensin-converting enzyme inhibitor or angiotensin r
199                                              Angiotensin-converting enzyme inhibitor or angiotensin r
200              Of these patients, 40% received angiotensin-converting enzyme inhibitor or angiotensin r
201 ith symptomatic decreased LVEF, 67% received angiotensin-converting enzyme inhibitor or angiotensin r
202 th asymptomatic decreased LVEF, 31% received angiotensin-converting enzyme inhibitor or angiotensin r
203  (<140 mm Hg systolic, <90 mm Hg diastolic), angiotensin-converting enzyme inhibitor or angiotensin r
204  every 1, 2, 5, or 10 years, with subsequent angiotensin-converting enzyme inhibitor or beta-blocker
205  arm, patients on active therapy with either angiotensin-converting enzyme inhibitor or beta-blockers
206 estin 2, but not in MFS mice treated with an angiotensin-converting enzyme inhibitor or lacking angio
207                            Treatment with an angiotensin-converting enzyme inhibitor or mineralocorti
208 atory profile, and were less likely to be on angiotensin-converting enzyme inhibitors or aldosterone
209  clinical evidence does not support stopping angiotensin-converting enzyme inhibitors or angiotensin
210 ck patients and patients with intolerance to angiotensin-converting enzyme inhibitors or angiotensin
211 elet P2Y12 receptor inhibitors, statins, and angiotensin-converting enzyme inhibitors or angiotensin
212 bing, indications, and contraindications for angiotensin-converting enzyme inhibitors or angiotensin
213 vention medications (statins, beta-blockers, angiotensin-converting enzyme inhibitors or angiotensin
214 giotensin-aldosterone system with the use of angiotensin-converting enzyme inhibitors or angiotensin
215 ary discharge diagnosis of HF, initiation of angiotensin-converting enzyme inhibitors or angiotensin
216 ose eligible at discharge were not receiving angiotensin-converting enzyme inhibitors or angiotensin
217 and 88% were receiving beta-blockers and 81% angiotensin-converting enzyme inhibitors or angiotensin
218 ves as the portal for infection, the role of angiotensin-converting enzyme inhibitors or angiotensin
219 0.017) but not among those only treated with angiotensin-converting enzyme inhibitors or angiotensin
220                               beta-blockers, angiotensin-converting enzyme inhibitors or angiotensin
221 e of antihypertensive medications other than angiotensin-converting enzyme inhibitors or angiotensin
222                    Time-dependent effects of angiotensin-converting enzyme inhibitors or angiotensin
223 re, where use of beta-blockers, statins, and angiotensin-converting enzyme inhibitors or angiotensin
224 95% CI, 0.75-0.99; P = 0.030) and trends for angiotensin-converting enzyme inhibitors or angiotensin
225 ng diuretics (95.9%), beta-blockers (82.5%), angiotensin-converting enzyme inhibitors or angiotensin
226 R, 4.17; [95% CI, 1.42-12.23]; P=0.009), and angiotensin-converting enzyme inhibitors or angiotensin
227  microalbuminuria followed by treatment with angiotensin-converting enzyme inhibitors or angiotensin
228 79) and the following discharge medications: angiotensin-converting enzyme inhibitors or angiotensin
229 h above 10 cm (p = 0.023), no treatment with angiotensin-converting enzyme inhibitors or angiotensin
230                   Three randomized trials of angiotensin-converting enzyme inhibitors or angiotensin
231 ends in the uptake of key medical therapies (angiotensin-converting enzyme inhibitors or angiotensin
232                                              Angiotensin-converting enzyme inhibitors or angiotensin
233                 At entry, 91% were receiving angiotensin-converting enzyme inhibitors or angiotensin
234 e management), treatment of albuminuria (eg, angiotensin-converting enzyme inhibitors or angiotensin
235 c obstructive pulmonary disease who received angiotensin-converting enzyme inhibitors or angiotensin
236  were receiving insulin, and 84% were taking angiotensin-converting enzyme inhibitors or angiotensin
237 opathy and proteinuria >1 g/d, maintained on angiotensin-converting enzyme inhibitors or angiotensin
238 sting), prescribing appropriate medications (angiotensin-converting enzyme inhibitors or angiotensin-
239               All patients were treated with angiotensin-converting enzyme inhibitors or angiotensin-
240 giotensin system (RAS) blockade therapy with angiotensin-converting enzyme inhibitors or angiotensin-
241                 Patients who were prescribed angiotensin-converting enzyme inhibitors or angiotensin-
242 sting), prescribing appropriate medications (angiotensin-converting enzyme inhibitors or angiotensin-
243 th literacy and less likely to be prescribed angiotensin-converting enzyme inhibitors or beta-blocker
244 rpose of this study was to determine whether angiotensin-converting enzyme inhibitors or beta-blocker
245 between angiotensin II receptor blockers and angiotensin-converting enzyme inhibitors or between diur
246 he renin- angiotensin system, either an ACE (angiotensin-converting enzyme) inhibitor or an ARB (angi
247 on <40% (OR, 0.97 [95% CI, 0.69-1.35]), ACE (angiotensin-converting enzyme) inhibitor or angiotensin
248 um testing within 30 days of initiating ACE (angiotensin-converting enzyme) inhibitor or angiotensin
249          Results Combination therapy of ACE (angiotensin-converting enzyme) inhibitors or ARBs (angio
250 vely low-cost heart failure medication (ACE [angiotensin-converting enzyme] inhibitor or angiotensin
251 300 mg daily) or placebo as an adjunct to an angiotensin-converting-enzyme inhibitor or an angiotensi
252 or blockers (OR = 0.70, 95% CI 0.54-0.92) or angiotensin-converting enzyme inhibitors (OR = 0.69, 95%
253 tion fraction (HFrEF), who tolerate an ACEI (angiotensin-converting enzyme inhibitor) or ARB (angiote
254                RAAS inhibition by enalapril (angiotensin-converting enzyme inhibitor) or losartan (an
255 n angiotensin receptor-neprilysin inhibitor, angiotensin-converting enzyme inhibitor, or angiotensin
256 ary coverage for all statins, beta-blockers, angiotensin-converting enzyme inhibitors, or angiotensin
257 10 patients) for all statins, beta-blockers, angiotensin-converting-enzyme inhibitors, or angiotensin
258      Her medications include a beta-blocker, angiotensin-converting enzyme inhibitor, oral antidiabet
259  marital status, and baseline beta-blockers, angiotensin-converting enzyme inhibitors, oral anticoagu
260 g proportion of days covered for statins and angiotensin-converting enzyme inhibitors, patients were
261    As predicted, BALB/c mice pretreated with angiotensin-converting enzyme inhibitors potentiated IFN
262                                     Further, angiotensin-converting enzyme inhibitors potentiated TCT
263 blockers, angiotensin receptor blockers, and angiotensin-converting enzyme inhibitors; prophylactic s
264                                              Angiotensin-converting enzyme inhibitors reduced mortali
265 s indicated that angiotensin II (Ang II) and angiotensin converting enzyme inhibitors regulated blood
266                                              Angiotensin-converting enzyme inhibitors (relative risk,
267 hereas 91% and 54% were on beta-blockers and angiotensin-converting enzyme inhibitors, respectively.
268 in-II-antagonists, calcium-channel blockers, angiotensin-converting-enzyme inhibitors, serotonin-spec
269                                              Angiotensin-converting enzyme inhibitor significantly de
270 ption of antiplatelet agents, beta-blockers, angiotensin-converting enzyme inhibitor, statins at disc
271                                     It is an angiotensin-converting enzyme inhibitor that operates vi
272 tments consider the use of beta-blockers and angiotensin-converting enzyme inhibitors that are sympto
273  treatment of avascular necrosis, and use of angiotensin-converting enzyme inhibitor therapy for micr
274 ia could identify patients with COPD in whom angiotensin-converting enzyme inhibitor therapy improves
275 effectiveness of sacubitril-valsartan versus angiotensin-converting enzyme inhibitor therapy in patie
276 hod to follow the immunomodulatory impact of angiotensin-converting enzyme inhibitor therapy on myelo
277 who derive significant clinical benefit from angiotensin-converting enzyme inhibitor therapy regardle
278                               The ability of angiotensin-converting enzyme inhibitor therapy to prese
279 lled in the PEACE (Prevention of Events With Angiotensin-Converting Enzyme Inhibitor Therapy) trial.
280 nts who derive greater clinical benefit from angiotensin-converting enzyme inhibitor therapy.
281 patients who derive significant benefit from angiotensin-converting enzyme inhibitor therapy.
282 giotensin Receptor-Neprilysin Inhibitor With Angiotensin Converting Enzyme Inhibitor to Determine Imp
283 tensin Receptor-Neprilysin Inhibitor With an Angiotensin-Converting Enzyme Inhibitor to Determine Imp
284 re use was high, ranging from 78% for use of angiotensin-converting enzyme inhibitors to 96% for use
285 in-receptor-neprilysin inhibitor) with ACEI (angiotensin-converting enzyme inhibitor) to Determine Im
286 in Receptor-Neprilysin Inhibitor] with ACEI [Angiotensin-Converting-Enzyme Inhibitor] to Determine Im
287 in Receptor-Neprilysin Inhibitor] with ACEI [Angiotensin-Converting-Enzyme Inhibitor] to Determine Im
288 in Receptor-Neprilysin Inhibitor] With ACEI [Angiotensin-Converting-Enzyme Inhibitor] to Determine Im
289 eceptor blockade during hemorrhagic shock in angiotensin-converting enzyme inhibitor-treated mice.
290         This benefit could be of interest in angiotensin-converting enzyme inhibitor-treated patients
291 nuates the deleterious hemodynamic effect of angiotensin-converting enzyme inhibitor treatment in mic
292 resent findings support the possibility that angiotensin-converting enzyme inhibitor treatment might
293  with HF; however, retrospective analysis of angiotensin-converting enzyme inhibitor trials and prosp
294 sure, and no angiotensin II receptor blocker/angiotensin-converting enzyme inhibitor use were associa
295 rular status, birth weight, premature birth, angiotensin-converting enzyme inhibitor use, angiotensin
296 body mass index, diabetes, hypertension, and angiotensin-converting enzyme inhibitor use, BB intake w
297  associated with calcium channel blocker and angiotensin-converting enzyme inhibitor use.
298 n, other lipid-lowering agents, aspirin, and angiotensin-converting enzyme inhibitors was identified.
299 The benefit of sacubitril/valsartan, over an angiotensin-converting enzyme inhibitor, was consistent
300 m, as evidenced by trials that have compared angiotensin-converting enzyme inhibitors with drugs that

 
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