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1 ct of empagliflozin in combination with loop diuretics.
2 c shock includes inotropes, vasopressors and diuretics.
3 ving dialysis and 847 discharged on thiazide diuretics.
4 thier patients are simply more responsive to diuretics.
5 aemia may lead to the creation of uricosuric diuretics.
6 imilar after the exclusion of individuals on diuretics.
7 es of GS with a blunted response to thiazide diuretics.
8 blockers, angiotensin receptor blockers, and diuretics.
9 l outcomes than those not discharged on loop diuretics.
10 estinal bleeding, and patients that required diuretics.
11 istry, 9,866 (39%) received no pre-admission diuretics.
12 e management, typically addressed using loop diuretics.
13 d overload despite significant doses of loop diuretics.
14 the target of the clinically important loop diuretics.
15 ngiotensin-converting enzyme inhibitors, and diuretics.
16 es of antihypertensive medications, thiazide diuretics.
17 randomized to ultrafiltration or intravenous diuretics.
18 miloride 40 mg was as effective as the other diuretics.
19 randomized to ultrafiltration or intravenous diuretics.
20 oportion of instructions given for fluid and diuretics.
21 of SPIRO and a potential target for thiazide diuretics.
22 cluding vasopressors, intravenous fluids, or diuretics.
23 o in addition to standard therapy, including diuretics.
24 bitors plus diuretics and beta-blockers plus diuretics.
25 diabetes development than beta-blockers and diuretics.
26 risk of CVD mortality vs beta-blockers plus diuretics.
27 es to the cytoprotection afforded by osmotic diuretics.
28 U-50488H and bremazocine are analgesics and diuretics.
29 erting enzyme inhibitors, beta blockers, and diuretics.
30 nce of treatment effect modification by loop diuretics.
31 lance and related this to renal clearance of diuretics.
32 ervative care and was started on digoxin and diuretics.
33 beta-blockers, calcium channel blockers, or diuretics.
34 and the available data on the optimal use of diuretics.
35 was confirmed by the natriuretic response to diuretics.
36 positive effect, such as glaucoma, or act as diuretics.
37 ir actions on glycemic control or as osmotic diuretics.
38 el approach to potentiate the action of loop diuretics.
39 , 0.80-1.08), CCBs (1.27%; 0.96, 0.82-1.11), diuretics (1.30%; 0.98, 0.84-1.13), other controls (1.43
40 , 0.88-1.07), CCBs (2.11%; 1.05, 0.96-1.13), diuretics (2.02%; 1.00, 0.90-1.11), or other controls (1
41 uded; at baseline, 3352 (50.5%) did not have diuretics, 2195 (33.1%) had diuretic doses between 1 and
42 agliflozin group reported intensification of diuretics (297 versus 414 [HR, 0.67; 95% CI, 0.56-0.78;
43 therapy (23.0% vs. 4.9% and 9.2%, p mu .01), diuretics (4.2% vs. 2.6% and 0.8%, p mu .001), or vasopr
44 0%) of beta-blockers, 10 of 11 RCTs (91%) of diuretics, 5 of 7 RCTs (71%) of calcium channel blockers
45 s 43.8%), ivabradine (8.3% versus 3.6%), and diuretics (94.2% versus 78.6%) and less often renin-angi
46 At randomization, patients were receiving diuretics (95.9%), beta-blockers (82.5%), angiotensin-co
48 he compounds currently in clinical trials as diuretics, a series of 1,4-substituted 8-cyclohexyl and
49 for a particular drug (PPIs, NSAIDs, SSRIs, diuretics, ACE inhibitors) in the 6 months prior to the
52 el antihypertensive therapy (mostly thiazide diuretics) added as needed to control blood pressure.
55 diuretic doses, and delays in the timing of diuretics among patients with acute decompensated heart
56 .35, and to have been treated optimally with diuretics and angiotensin-converting enzyme inhibitors u
57 nction, and are on background treatment with diuretics and angiotensin-converting enzyme inhibitors.
59 ally in part by overcoming the resistance to diuretics and atrial-natriuretic-peptide and inhibiting
61 n separate classes, with lowest adherence to diuretics and beta-blockers and highest adherence to ang
64 d LVSD therapies (neurohormonal antagonists, diuretics and cardiac resynchronization in appropriate c
65 s to determine the relationship between loop diuretics and clinical outcomes in patients with HF.
66 ation of incontinence, medications including diuretics and estrogen, obstetric history, physical exam
68 of BP response of thiazide and thiazide-like diuretics and help identify the patients better suited f
69 es most strongly support the use of thiazide diuretics and long-acting calcium channel blockers as fi
71 ss by exercise training, sodium retention by diuretics and monitoring devices, myocardial nitric oxid
72 ckers, calcium-channel blockers, or thiazide diuretics and the likelihood of a positive or negative r
73 sms and sites of action of loop and thiazide diuretics and the similarity of their chronic effects to
74 of clinically important drugs including loop diuretics and their disruption has been implicated in pa
76 summarizes available data on the use of both diuretics and UF in ADHF patients and identifies challen
77 in 11 patients we withdrew beta-blockers and diuretics and used phenylephrine and albumin infusion to
79 lcohol consumption, hypertension, and use of diuretics and was inversely associated with physical act
80 hibitors, angiotensin-receptor blockers, and diuretics and/or beta blockers in the prevention of hear
81 uncontrolled hypertension (P=0.049), need of diuretics, and age <60 years (P=0.016) were associated w
82 mic beta blockers, calcium channel blockers, diuretics, and angiotensin receptor antagonists), smokin
86 selection and doses of thiazide and similar diuretics, and the association of antihypertensive drug
88 uric, nonsteroidal anti-inflammatories, loop diuretics, angiotensin II receptor antagonists, and beta
89 y used antihypertensive medications included diuretics, angiotensin-converting enzyme inhibitors (ACE
90 At 1 year, use of added open-label atenolol, diuretics, angiotensin-converting enzyme inhibitors, and
92 Routine therapy included use of digoxin, diuretics, angiotensin-converting enzyme inhibitors, and
93 -line drug classes thiazide or thiazide-like diuretics, angiotensin-converting enzyme inhibitors, ang
94 lure often progresses despite treatment with diuretics, angiotensin-converting enzyme inhibitors, bet
95 io to receive optimal pharmacologic therapy (diuretics, angiotensin-converting-enzyme inhibitors, bet
96 erapeutically important compounds, including diuretics, anticonvulsants and antidepressants, many of
97 commonly prescribed drugs (e.g. penicillins, diuretics, antivirals, methotrexate, and non-steroidal a
105 l hypertension remains unknown, but thiazide diuretics are frequently recommended as first-line treat
110 The initial ALLHAT conclusion, that thiazide diuretics are superior to angiotensin-converting enzyme
122 dence, and future trials should use low-dose diuretics as the standard for clinically useful comparis
123 erenone would lead clinicians to reduce loop diuretics, as a consequence of the improvement in patien
124 s were found between groups for use of other diuretics, aspirin, antidepressants, antiepileptics, ant
127 : (1) observational: patients receiving loop diuretics at the Yale Transitional Care Center (N=162) a
129 ALLHAT conclusion that thiazide and similar diuretics (at evidence-based doses) are the preferred fi
130 -1.66; 95% CI, -2.57 to -0.75; P < 0.001) or diuretics (beta = -1.38; 95% CI, -2.59 to -0.17; P < 0.0
131 -2.44; 95% CI, -3.99 to -0.89; P = 0.002) or diuretics (beta = -2.76; 95% CI, -4.76 to -0.76; P = 0.0
132 ontrast media, antiinflamatory, cytostatics, diuretics, beta blockers, anesthetics, analgesics, antie
133 total energy intake, body mass index, use of diuretics, beta-blockers, allopurinol, and uricosuric ag
135 iabetes, hypertension medications, including diuretics, blood lead levels, and hyperlipidemia, the od
138 ce NKCC2 is the molecular target of the loop diuretics bumetanide and furosemide, we asked about thei
139 lkalosis impairs the natriuretic response to diuretics, but the underlying mechanisms are unclear.
141 I receptor blockers, beta-blockers, thiazide diuretics, calcium channel blockers, and metformin.
142 c therapy using any of several thiazide-type diuretics can more than double daily urine sodium excret
143 better suited for thiazide and thiazide-like diuretics compared to beta-blockers for improved BP mana
144 onger median time to the second dose of loop diuretics compared with long call patients (17.9 hours v
146 tense neurohumoral antagonism, limitation of diuretics, correction of hypokalemia, exercise, and diet
147 and right ventricular stroke volume, whereas diuretics decreased right ventricular preload and right
150 decreased albuminuria significantly, whereas diuretics did significantly reduce urinary angiotensinog
151 angiotensin-converting enzyme inhibitor and diuretics, digoxin had no effect on natural history end
152 nce of comorbidities, and were more often on diuretics, digoxin, and angiotensin converting enzyme in
153 herapy for congestive heart failure, such as diuretics, digoxin, angiotensin-converting enzyme inhibi
155 uretic resistance, ultrafiltration before IV diuretics effectively and safely decreases length of sta
156 Using propensity scores for receipt of loop diuretics estimated for each of the 7,936 patients, a ma
158 pensation (HF hospitalization or intravenous diuretics for HF without hospitalization), and with elev
160 ould represent a target for new and improved diuretics for the treatment of hypertension and heart fa
165 o received a discharge prescription for loop diuretics had significantly better 30-day clinical outco
166 decompensated heart failure (ADHF), and loop diuretics have historically been the cornerstone of trea
167 that men using NSAIDs, statins, and thiazide diuretics have reduced PSA levels by clinically relevant
170 .57; 95% confidence interval, 1.38 to 1.79), diuretics (HR, 1.95; 95% confidence interval, 1.73 to 2.
172 ely with standard medical therapy, including diuretics, if they develop symptoms suggestive of heart
174 an in addition to standard therapy including diuretics improved many, though not all, heart failure s
175 7 +/- 3.5 h of hospitalization and before IV diuretics in 20 heart failure patients with volume overl
176 ded transient dasatinib interruption in 83%, diuretics in 71%, pulse steroids in 27%, and thoracentes
178 trial (SGLT2 Inhibition in Combination With Diuretics in Heart Failure) was a randomized, double-bli
180 our study demonstrate increased use of loop diuretics in patients with BP before the development of
181 e if ultrafiltration before intravenous (IV) diuretics in patients with decompensated heart failure a
182 tration may be an alternative to intravenous diuretics in patients with decompensated HF and volume o
183 luating the combination of loop and thiazide diuretics in patients with heart failure in order to des
186 acokinetics is essential for skillful use of diuretics in the management of heart failure in both the
188 are not understood, including the action of diuretics in the treatment of ascites and the ability of
189 ous antiarrhythmic drug use, previous use of diuretics, increased left atrial diameter, increased lef
190 and NF-kappaB activation produced by osmotic diuretics, indicating a role of adenosine metabolites in
192 ons of the current therapeutic regimens with diuretics, intravenous vasodilators (ie, nitroglycerin,
193 el mechanisms of nephroprotection by osmotic diuretics, involving both activation and induction of th
195 hen administration of moderate doses of loop diuretics is not sufficient, patients can be treated wit
197 weight loss needs clarification, the role of diuretics is uncertain, and which surgical intervention
198 oconcentration received higher doses of loop diuretics, lost more weight/fluid, and had greater reduc
199 that inexpensive and well-tolerated thiazide diuretics may be especially effective in preventing the
200 in cells expressing NCC, indicating thiazide diuretics may be particularly effective for lowering BP
203 beta-receptor blockers, digoxin and thiazide diuretics may worsen sexual dysfunction owing to medicat
204 s for HFpEF but evidence supports the use of diuretics, mineralocorticoid antagonists and lifestyle i
206 = 437), calcium-channel blockers (n = 223), diuretics (n = 226), and combinations (n = 1,442), beta-
210 rs, beta-blockers, calcium channel blockers, diuretics, nitrates, statins, insulin, biguanides, sulfo
211 1.17-2.62), and IV fluids, electrolytes, or diuretics (odds ratio, 1.73; 95% CI, 1.21-2.48) at trans
213 rate (eGFR) less than 50 mL/min, and taking diuretics or cyclosporine were associated with hyperuric
215 bate cardiovascular problems from overuse of diuretics or inotropes because of the unusual loading co
216 , are usually treated with potassium-sparing diuretics or nonsteroidal anti-inflammatory drugs and or
218 te MI was present among nonusers of alcohol, diuretics, or aspirin and among those who did not have m
220 iles also favoured thiazide or thiazide-like diuretics over angiotensin-converting enzyme inhibitors.
221 ic patients were more likely to be receiving diuretics (p < 0.0001) and have a lower mean corpuscular
222 t loss (p < 0.001), later transition to oral diuretics (p = 0.03), and shorter length of stay (p < 0.
223 with truly resistant hypertension, thiazide diuretics, particularly chlorthalidone, should be consid
224 when prescribing long-term beta-blockers and diuretics, particularly in patients at high risk of deve
225 correcting for relevant variables (including diuretics, pH, potassium levels and renal sodium excreti
226 events of coronary heart disease or stroke, diuretics plus ACE inhibitors or calcium channel blocker
228 glycerides at baseline, high blood pressure, diuretics, pre-enrollment weight change, dieting, total
231 it from the use of chronic diuretic therapy, diuretics rapidly improve symptoms associated with volum
233 eater weight and fluid loss than intravenous diuretics, reduces 90-day resource utilization for HF, a
234 0.7 [95% confidence interval, 0.57-0.82] for diuretics; relative risk, 0.8 [95% confidence interval,
235 inition that excluded the intensification of diuretics resulted in a lower event rate but a stronger
236 uresis, particularly when combined with loop diuretics, resulting in an improvement in blood volume.
237 eta-blockers, calcium channel blockers, loop diuretics, selective serotonin reuptake inhibitors, stat
238 pressin receptor antagonists, urea, and loop diuretics serve this purpose, but received different rec
239 tors' original conclusion that thiazide-type diuretics should remain the preferred first-step drug cl
240 classes; however, thiazide or thiazide-like diuretics showed better primary effectiveness than angio
241 The combination of statins and thiazide diuretics showed the greatest reduction in PSA levels: 3
243 ymptomatic management may include the use of diuretics, statins, infection prophylaxis and anticoagul
244 unds (mixture of anabolics, beta-2 agonists, diuretics, stimulants, narcotics, and beta-blockers) spi
245 the K-Cl cotransporter is dominated by loop diuretics such as furosemide and bumetanide, molecules u
247 h the exception of thiazide or thiazide-like diuretics superiority to angiotensin-converting enzyme i
249 was confirmed by the natriuretic response to diuretics targeting the thick ascending limb, the distal
251 2 inhibitors are proximal tubule and osmotic diuretics that reduce volume retention and blood pressur
254 ts otherwise resistant to high doses of loop diuretics, this strategy has not been subjected to large
255 nitroglycerin, or nesiritide in addition to diuretics to achieve hemodynamic and symptomatic improve
256 e enhancing drugs in sports as athletes take diuretics to dilute the concentration of drugs in their
257 uggest that administration of high-dose loop diuretics to patients with HF yields meaningful increase
258 Treatment strategies include the use of diuretics to relieve symptoms and application of an expa
259 in converting enzyme (ACE) inhibitor or loop diuretics to those 75 years or older without assessment
261 UT-B inhibitors represent a new class of diuretics, "urearetics," which are predicted to increase
262 od pressure less than 140/90 mm Hg; thiazide diuretics used in multidrug hypertensive regimen; athero
263 ass regimen of calcium channel blockers plus diuretics was associated with a higher risk of CVD morta
264 Monotherapy with calcium channel blockers vs diuretics was associated with greater risk of CVD death
266 roups, respectively (HR when the use of loop diuretics was compared with nonuse: 0.73; 95% CI: 0.57 t
268 reduction in office SBP produced by the two diuretics was identical, further strengthening the case
269 enal function (p = 0.01), whereas total dose diuretics was lower in patients with hemoconcentration (
270 ding intravenous treatment with inotropes or diuretics was the most common adverse event (in 20 [2%]
272 n, adiposity, weight gain, hypertension, and diuretics were all found to be independent risk factors
273 more antihypertensive medications, ACEI, and diuretics were associated with a loss of structural mark
282 calcium channel blockers (CCB), insulin, and diuretics were significantly higher in the periodontitis
287 of the kidney and is the target of thiazide diuretics, which are commonly prescribed to treat hypert
288 Disease features are reversed by thiazide diuretics, which inhibit the Na-Cl cotransporter in the
289 ulating blood decreases with the use of loop diuretics, which might result in less immediate transloc
291 ept for NSAIDs, ACE inhibitors, and thiazide diuretics, which were more prevalent in black patients.
292 between the two groups with the exception of diuretics, which were used more often in the DWGF group.
293 re likely to be treated with higher doses of diuretics, while higher filling pressures, N-terminal pr
295 bitors are first in their class salt-sparing diuretics with potential clinical indications in volume-
297 n reuptake inhibitors, statins, and thiazide diuretics), with evaluation of how often drugs were wide
298 r more effective fluid removal compared with diuretics, with improved quality of life and reduced reh
299 ive management includes salt restriction and diuretics, with thoracentesis and transjugular intrahepa
300 study treatment in the following subgroups: diuretics (yes/no), digitalis glycoside (yes/no), minera