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1 ojections, as produced by septal infusion of anticholinergics.
2 nd treatment centred on early institution of anticholinergics.
3 nasal decongestant, saline douches and nasal anticholinergics.
4 tilation, and receipt of benzodiazepines and anticholinergics.
6 rected] of the patients treated with inhaled anticholinergics (2.1%) and 108 [corrected] of the contr
9 is treated with medications that raise serum anticholinergic activity and are known to adversely affe
10 hors examined the relationship between serum anticholinergic activity and baseline cognitive performa
20 ddition of tiotropium bromide (a long-acting anticholinergic agent approved for the treatment of chro
21 nt of patients < or =1 yr of age received an anticholinergic agent before ET intubation compared with
22 f salmeterol with those of albuterol and the anticholinergic agent ipratropium in 20 patients with st
25 atients (1.9%) [corrected] receiving inhaled anticholinergics and 83 of 6661 [corrected] patients (1.
26 ee classes of bronchodilators-beta agonists, anticholinergics, and theophylline-are available and can
27 took part in five drug challenges using the anticholinergic antinicotinic agent mecamylamine (MECA)
29 These studies provided good evidence that anticholinergics are effective at improving both urodyna
30 consists of medical therapy, primarily with anticholinergics as well as behavioral therapy to modify
31 response to botulinum toxin is not adequate, anticholinergics, benzodiazepines, baclofen and other me
32 dase type B inhibitors [MAOBIs], amantadine, anticholinergics, beta-blockers, or dopamine agonists) m
34 ve demonstrated the benefit of a long-acting anticholinergic bronchodilator in addition to beta(2)-ag
36 a; Ba679BR) is a new-generation, long-acting anticholinergic bronchodilator that has muscarinic M(1)
37 beta-agonists, compared with ipratropium, an anticholinergic bronchodilator, and placebo in patients
39 eceptor assay, quantifies a person's overall anticholinergic burden caused by all drugs and their met
43 exposure to prescriptions with a cumulative Anticholinergic Cognitive Burden (ACB) score of 3 or hig
44 exposure to prescriptions with a cumulative Anticholinergic Cognitive Burden (ACB) score of 3 or hig
45 A approval; these are the antimuscarinic and anticholinergic/direct smooth muscle relaxant drugs.
47 ted for each patient based on the sum of the Anticholinergic Drug Scale score for each medication adm
48 for confounding, a one-unit increase in the Anticholinergic Drug Scale score resulted in a nonsignif
50 nticholinergic properties, as defined by the Anticholinergic Drug Scale, does not increase the probab
54 rmed obstruction supports the assertion that anticholinergic drugs are safe in men with bladder outle
55 mention of the possible therapeutic role of anticholinergic drugs for treating storage symptoms in s
57 ergic systems, and central administration of anticholinergic drugs in dependent rats has been shown t
59 ndomized controlled trial recently evaluated anticholinergic drugs in men with lower urinary tract sy
60 Should symptoms fail to resolve, addition of anticholinergic drugs may be considered in the absence o
61 the possibility that some of the effects of anticholinergic drugs on placticity and learning may be
64 domains of cognition and require less use of anticholinergic drugs, which impair memory, for treatmen
68 rent autonomic failure; dramatic response to anticholinergics; early or atypical L-dopa-induced dyski
69 rease in extrapyramidal symptoms, or central anticholinergic effects were found at any olanzapine dos
70 se and anxiety disorders, antidepressant and anticholinergic exposure, lifetime exposure to electroco
72 jections for overactive bladder and an adult anticholinergic for overactive bladder that underwent te
73 evidence on the effectiveness and safety of anticholinergics for male lower urinary tract symptoms.
74 esting in children; enuresis topics included anticholinergics for treating monosyptomatic enuresis re
75 eline average of 5.0 per day, was 3.4 in the anticholinergic group and 3.3 in the onabotulinumtoxinA
80 nd new or broadened indications for existing anticholinergics, in treating the overactive bladder in
81 QSAR) study is presented for quaternary soft anticholinergics including two distinctly different clas
83 ptor agonist (salbutamol) and a short-acting anticholinergic (ipratropium bromide), in COPD is encour
85 ose with detrusor overactivity refractory to anticholinergics, is, however, evidenced increasingly.
87 e in vitro and clinically derived indexes of anticholinergic load in predicting these cognitive impai
90 lly evaluation of various inhaled therapies (anticholinergics, long-acting beta-agonists, and cortico
91 ation inhaled therapies (long-acting inhaled anticholinergics, long-acting inhaled beta-agonists, or
92 e who were not receiving inhaled long-acting anticholinergic medication (difference in composite at 5
93 cipants were randomly assigned to daily oral anticholinergic medication (solifenacin, 5 mg initially,
94 idol-treated subjects to require concomitant anticholinergic medication after 4 weeks (20% versus 63%
95 , have potential implications for the use of anticholinergic medication in elderly Parkinson's diseas
97 s on recent data determining the efficacy of anticholinergic medication in men with lower urinary tra
98 he ICU is frequent, the relationship between anticholinergic medication use and delirium in this sett
99 garding the role of invasive urodynamics and anticholinergic medication, and further large-scale pros
100 asthma and those not receiving a long-acting anticholinergic medication, newly prescribed LABA and in
101 use of antihypertensive, lipid-lowering, or anticholinergic medication; and apolipoprotein E genotyp
105 s the key neurochemical impairment in PD and anticholinergic medications are used for symptomatic tre
106 ich is reflected in an increased efficacy of anticholinergic medications during acute asthma attacks.
109 s are most affected by the administration of anticholinergic medications to patients with schizophren
110 gonists working alone or in conjunction with anticholinergic medications will improve clinical sympto
111 U medications, especially some sedatives and anticholinergic medications, and keeping patients more a
112 nd oxybutynin treatment, a new generation of anticholinergic medications, such as tolterodine, has be
115 acting anticholinergics (n = 7), long-acting anticholinergics (n = 10), long-acting beta2-agonists (n
116 CTs examined inhaled therapies: short-acting anticholinergics (n = 7), long-acting anticholinergics (
117 pain control, minimizing benzodiazepines and anticholinergics, normalizing the sleep-wake cycle, prov
118 tention, because of the inhibitory effect of anticholinergics on bladder contraction in the presence
119 Pharmacologic interventions include use of anticholinergics or antipsychotic medications for dement
120 monotherapy using either long-acting inhaled anticholinergics or long-acting inhaled beta-agonists fo
122 n the proper clinical situation such as pure anticholinergic overdose with severe symptoms, physostig
123 een shown to be useful in cases of confirmed anticholinergic poisoning by controlling agitation and r
125 yperthermia, neuroleptic malignant syndrome, anticholinergic poisoning, sympathomimetic poisoning, an
126 ically useful standard index of the relative anticholinergic potency of psychiatric medications; 2) t
127 , paroxetine has approximately one-fifth the anticholinergic potential of nortriptyline in older pati
128 ase delirium risk and use of medication with anticholinergic properties in the ICU is frequent, the r
129 stigated whether exposure to medication with anticholinergic properties increases the probability of
131 T3 receptor antagonists, antihistamines, and anticholinergics reduce the incidence of PONV, whereas m
136 components of the primary end point, inhaled anticholinergics significantly increased the risk of MI
139 therapy with inhaled beta-agonists, inhaled anticholinergics, systemic corticosteroids, and intraven
142 nists salmeterol and formeterol, and the new anticholinergic tiotropium bromide provide a better ther
145 lection when rats were tested off-drug, both anticholinergic treatments were effective in disrupting
147 MI, or stroke (2.9% of patients treated with anticholinergics vs 1.8% of the control patients; RR, 1.
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