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1 erapy (topical, regionally injected, or oral corticosteroid therapy).
2 all patients, and none responded to topical corticosteroid therapy.
3 % in ED visits, and 46% in the need for oral corticosteroid therapy.
4 asthma in spite of high-dose inhaled or oral corticosteroid therapy.
5 epartment (ED) visits, and the need for oral corticosteroid therapy.
6 less responsive to the beneficial effects of corticosteroid therapy.
7 mately 20% of icteric AIH presentations fail corticosteroid therapy.
8 lowing intravenous gamma globulin (IVIG) and corticosteroid therapy.
9 Both subtypes respond to corticosteroid therapy.
10 nize estrogen-promoted events in response to corticosteroid therapy.
11 osis of asthma, identifying those in need of corticosteroid therapy.
12 engraftment period and favorable response to corticosteroid therapy.
13 the diagnosis, especially before initiating corticosteroid therapy.
14 but aggressive disease that responds well to corticosteroid therapy.
15 ocular hypertensive response with the use of corticosteroid therapy.
16 patients do not respond well to conventional corticosteroid therapy.
17 solved disease and was unrelated to systemic corticosteroid therapy.
18 pients remain without the need for long-term corticosteroid therapy.
19 resses in only a minority of patients during corticosteroid therapy.
20 kin of the abdominal wall that resolved with corticosteroid therapy.
21 roids, and 20 (56%) were able to discontinue corticosteroid therapy.
22 ascular protective effect of acute high-dose corticosteroid therapy.
23 was reversed with the prompt institution of corticosteroid therapy.
24 grade I and IIA and were fully reversed with corticosteroid therapy.
25 nce oral corticosteroid use while on inhaled corticosteroid therapy.
26 ients (38%) developed diabetes during pulsed corticosteroid therapy.
27 month and 2 gm thereafter; and conventional corticosteroid therapy.
28 tient was successfully treated using topical corticosteroid therapy.
29 tructive pulmonary disease (COPD) respond to corticosteroid therapy.
30 0.20, n = 19, p < 0.001) and normalizes with corticosteroid therapy.
31 s documented in patients receiving long-term corticosteroid therapy.
32 veitis, which are often managed with chronic corticosteroid therapy.
33 nd one of complications related to long-term corticosteroid therapy.
34 ion of the effusion after the institution of corticosteroid therapy.
35 rease risk for this blinding complication of corticosteroid therapy.
36 evere pain, and a rapid response to systemic corticosteroid therapy.
37 loped clinical skin GVHD, which responded to corticosteroid therapy.
38 ation at 90 and 180 days after initiation of corticosteroid therapy.
39 commonly in patients who deteriorated during corticosteroid therapy.
40 It appears unresponsive to corticosteroid therapy.
41 ation of cyclophosphamide and institution of corticosteroid therapy.
42 pneumonitis is reversible and may respond to corticosteroid therapy.
43 of a 58-year-old patient undergoing empiric corticosteroid therapy.
44 t, or by differences in the use of antenatal corticosteroid therapy.
45 iving patients required maintenance low-dose corticosteroid therapy.
46 erlying chronic inflammatory disease or from corticosteroid therapy.
47 Nine patients received corticosteroid therapy.
48 sis, especially when treated with adjunctive corticosteroid therapy.
49 ion are important potential complications of corticosteroid therapy.
50 due to DRESS is poor and was not improved by corticosteroid therapy.
51 Six patients improved with corticosteroid therapy.
52 c and visual recovery was attained following corticosteroid therapy.
53 within 24 h of initiating high-dose systemic corticosteroid therapy.
54 dermatitis that was unresponsive to topical corticosteroid therapy.
55 COVID-19 patients, following tocilizumab and corticosteroid therapy.
56 1%) patients also having concurrent systemic corticosteroid therapy.
57 sed neutrophils and often poorly responds to corticosteroid therapy.
58 OR, 2.12; 95% CI, 1.36-3.29) associated with corticosteroid therapy.
59 symptomatic and endoscopic remission without corticosteroid therapy.
60 overlap syndrome might benefit from inhaled corticosteroid therapy.
61 to inhaled beta-agonist, antimuscarinic, and corticosteroid therapy.
62 on (n = 1), which resolved following topical corticosteroid therapy.
63 erage 5.5 months following the initiation of corticosteroid therapy.
64 oimmune-like hepatitis that is responsive to corticosteroid therapy.
65 subfield volume in humans receiving chronic corticosteroid therapy.
66 arter of patients with SAH do not respond to corticosteroid therapy.
67 Single and multiple courses of antenatal corticosteroid therapy.
68 linical examination as well as with systemic corticosteroid therapy.
69 or had contraindications to bevacizumab and corticosteroid therapies.
71 1 of 27, 40.7%), dialysis (22 of 27, 81.5%), corticosteroid therapy (12 of 27, 44.4%), intensive care
72 layed resistance to combined vinblastine and corticosteroid therapy (21.9% v 3.3%; P = .001), showed
73 7 (3.2%) continued to receive long-term oral corticosteroid therapy, 5 (2.3%) received biologic thera
78 ral nutrition therapy is more effective than corticosteroid therapy alone in patients with severe AH.
79 compare the efficacy and safety of systemic corticosteroid therapy alone versus corticosteroid plus
84 erage 4.2 months following the initiation of corticosteroid therapy and 8% (9/105) were intolerant to
85 p avoid unnecessary morbidity from high-dose corticosteroid therapy and allow the most appropriate an
87 be a biomarker for responsiveness to inhaled corticosteroid therapy and may help identify patients as
88 patitis of undetermined cause can respond to corticosteroid therapy and represent autoantibody-negati
89 ts with severe asthma are less responsive to corticosteroid therapy and show increased airway remodel
91 ray of effector T cells that persist despite corticosteroid therapy and sustain chronic, smoldering v
94 in both blood and lung tissue in relation to corticosteroid therapy and vitamin D levels, especially
96 myopathy who had not responded adequately to corticosteroid therapy and whose clinical course was fur
97 udesonide (Nefecon) or reduced-dose systemic corticosteroid therapy and, in Chinese patients, mycophe
99 ntaneously--only to relapse after receipt of corticosteroid therapy, and clear again, 8.5 years later
100 ICI therapy cessation, prompt initiation of corticosteroid therapy, and escalation of therapy are al
101 but aggressive disease that responds well to corticosteroid therapy, and human leukocyte antigen DR4
102 Autoimmune hepatitis commonly relapses after corticosteroid therapy, and long-term management strateg
103 ed trends in the use of ventilatory support, corticosteroid therapy, antibiotic therapy, and patient
105 ity evidence that periocular and intraocular corticosteroid therapies are effective and safe for the
106 ith severe asthma who require long-term oral corticosteroid therapy are at risk of unwanted effects.
107 infusion (IVIG), with or without additional corticosteroid therapy, are common options, but optimal
108 y high-volume saline irrigation with topical corticosteroid therapy as a first-line therapy for chron
109 The second case outlines the use of topical corticosteroid therapy as an adjunct to non-surgical per
110 y biliary cirrhosis entered remission during corticosteroid therapy as commonly as individuals with d
111 portion of patients who discontinued inhaled corticosteroid therapy as part of a phased-reduction pro
112 logical cirrhosis at presentation respond to corticosteroid therapy as well as patients without cirrh
113 whether benefit exists to combination NSAID/corticosteroid therapy, as well as whether NSAIDS can re
114 sits, and 44% reduction in the need for oral corticosteroid therapy at 48 months, the model simulated
117 is not needed, but using concomitant pulsed corticosteroid therapy beyond 3 to 5 days requires an in
118 toms and infiltrates regressed after topical corticosteroid therapy, but recurred after each adalimum
120 Autoimmune hepatitis may fail to respond to corticosteroid therapy, but the frequency and bases for
121 articularly following exposure cessation and corticosteroid therapy, but the time course to improveme
122 ho had persistent asthma and were prescribed corticosteroid therapy by the physician were also signif
123 conclusion, patients who respond to initial corticosteroid therapy can achieve a sustained remission
126 utcomes in subjects randomized to continuous corticosteroid therapy (CCS) or early corticosteroid wit
127 ompare patterns of weight gain under chronic corticosteroid therapy (CCST) with that observed under e
132 t high risk for asthma, two years of inhaled-corticosteroid therapy did not change the development of
133 compared with a single course, of antenatal corticosteroid therapy did not increase or decrease the
134 hil count is a promising biomarker to direct corticosteroid therapy during COPD exacerbations, but la
136 , and systemic corticosteroid ( sCS systemic corticosteroid ) therapy effects were assessed in compar
137 adequately controlled asthma despite inhaled corticosteroid therapy, especially in periostin-high pat
138 systemic side effects compared with regional corticosteroid therapy, except for greater antibiotic us
139 s 50 years or older (or 40 years or older on corticosteroid therapy) expected to require NSAIDs for 1
140 ion, defined as inactive uveitis and no oral corticosteroid therapy for 2 consecutive study visits >=
142 gh in patients without and with sCS systemic corticosteroid therapy for 5 days or fewer (area under t
145 that children who receive long-term inhaled corticosteroid therapy for asthma have height deficits 1
149 s, with important limitations, suggests that corticosteroid therapy for presumed influenza-associated
150 observational studies investigating systemic corticosteroid therapy for presumed influenza-associated
151 spine occurred in association with long-term corticosteroid therapy for systemic lupus erythematosus.
153 t-line therapy for mild to moderate UC, with corticosteroid therapy for those who fail to achieve rem
154 was identified in 7 articles on intravitreal corticosteroid therapy for treatment of DME: triamcinolo
155 rance that the potential benefits of topical corticosteroid therapy, for treating pain and discomfort
157 ly completed randomized, controlled studies, corticosteroid therapy has proven to be efficacious in t
159 suppressive measures, particularly high-dose corticosteroid therapy, has been reported variably, but
161 sts considering a 6-month course of systemic corticosteroid therapy; however, the efficacy of systemi
163 all investigated periocular and intraocular corticosteroid therapies improved VA, macular structure,
169 spitalizations, ED visits, and need for oral corticosteroid therapy in childhood asthma for planning
172 earch of trials that evaluated the effect of corticosteroid therapy in patients hospitalized with CAP
174 placebo-controlled trial the effects of oral corticosteroid therapy in patients with exacerbations of
175 nse prompted us to examine the role of early corticosteroid therapy in patients with moderate to seve
177 f pIPA requires Aspergillus culture or prior corticosteroid therapy in this cohort of critically ill
179 ed the risk of UGIB; concomitant nsNSAID and corticosteroid therapies increased the IRR to the greate
187 intervention; long-term therapy with inhaled corticosteroid therapy is safer than frequent bursts of
191 le airway obstruction, withdrawal of inhaled corticosteroid therapy leads to a deterioration in venti
194 wing the institution of cyclophosphamide and corticosteroid therapy, longer-term management issues ca
196 in animals and children have suggested that corticosteroid therapy may be a useful adjunct to conven
200 ds on cytokine synthesis in T cells, chronic corticosteroid therapy may indirectly exacerbate the lon
203 For hospitalized adults with CAP, systemic corticosteroid therapy may reduce mortality by approxima
206 ting that retinal vasculitis unresponsive to corticosteroid therapy maybe a poor prognostic sign.
208 ed assay, those seropositive by ELISA failed corticosteroid therapy more commonly (24% vs. 3%, P = .0
210 derate asthma controlled by low-dose inhaled corticosteroid therapy (n = 114 assigned to physician as
211 ALF, aspiration is more likely if there's no corticosteroid therapy, negative Aspergillus culture, an
212 tional symptoms, prompt response to systemic corticosteroid therapy, neutrophilia, and abrupt onset o
213 which suggested an adverse association with corticosteroid therapy (odds ratio, 3.90; 95% CI, 2.31-6
214 ients and assess the effect of ribavirin and corticosteroid therapy on the case-fatality rate, strati
218 ated with bolus impaction: swallowed topical corticosteroid therapy (OR 0.411, 95%-CI 0.203-0.835, P
219 istic regression modeling: swallowed topical corticosteroid therapy (OR 0.503, 95%-CI 0.255-0.993, P
220 itial pneumonia generally responds poorly to corticosteroid therapy, other forms of interstitial pneu
222 han those without to have received intensive corticosteroid therapy (P<0.007), had virus isolated fro
225 restimated in children who are responsive to corticosteroid therapy prescribed for a suspicion of min
231 years, systemic adverse effects from inhaled corticosteroid therapy remains a complicated and controv
234 echanistic basis of the variable response to corticosteroid therapy seen in patients with AAH and to
235 tion of ipratropium bromide to albuterol and corticosteroid therapy significantly decreases the hospi
236 al insufficiency animal model, we found that corticosteroid therapy significantly improved the surviv
237 atment with elimination diets and/or topical corticosteroid therapy slow disease progression, but are
238 henotype, as treatment, including daily oral corticosteroid therapy, suppresses eosinophilic inflamma
239 domized controlled trial has been published, corticosteroid therapy, surgical decompression or observ
240 l II study and 6 level III studies) explored corticosteroid therapy that did not have uniformly bette
241 Patients were also randomly assigned to corticosteroid therapy that included either dexamethason
242 a within the first month after initiation of corticosteroid therapy that is attenuated during the sub
243 In all IAC patients, after 4 and 8 weeks of corticosteroid therapy the contribution of these IgG4+ c
244 eria (eg, lack of exacerbations and systemic corticosteroid therapy), the proposed definitions diverg
245 tent asthma controlled with low-dose inhaled corticosteroid therapy, the use of either biomarker-base
246 60 eyes in 40 patients who received topical corticosteroid therapy, there was a dose-dependent incre
247 ving tacrolimus/sirolimus and withdrawn from corticosteroid therapy three months after transplantatio
248 eases after more than 5 days of sCS systemic corticosteroid therapy; thus, imaging should not be dela
252 pulmonary fibrosis that was unresponsive to corticosteroid therapy to receive subcutaneous interfero
253 Treatment can be improved by continuing corticosteroid therapy until normal liver test results a
254 ortion in whom complete cessation of inhaled corticosteroid therapy was achieved (17.4 percent in the
259 Using a Cox proportional hazards model, corticosteroid therapy was associated with similar 30-da
261 risk of death or disability associated with corticosteroid therapy was inversely associated with the
263 t reported the occurrence of adverse events, corticosteroid therapy was not associated with an increa
265 children with bacterial meningitis, adjuvant corticosteroid therapy was not associated with time to d
272 on showed that younger age, higher MELD, and corticosteroid therapy were independently associated wit
274 omen (N = 46) receiving chronic prescription corticosteroid therapy were randomized to memantine or p
275 tis patients aged >or=50 years (or >or=40 on corticosteroid therapy) were randomly assigned to rofeco
276 to 4 acute GVHD, 91% responded to front-line corticosteroid therapy, whereas 50% responded in the SOC
277 -host disease (GVHD) from receiving systemic corticosteroid therapy, which impairs cellular immunity.
278 e anterior segment and manageable with local corticosteroid therapy, which justified the continuation
279 ce and predictors of AKI, the association of corticosteroid therapy with AKI risk, and factors associ
281 zed, controlled trials, comparing adjunctive corticosteroid therapy with the standard of care alone f
282 to severe UC should undergo a course of oral corticosteroid therapy, with transition to 5-ASA, thiopu
283 ng-term sustained complete remission without corticosteroid therapy without any additional maintenanc
284 ifying children who are likely responders to corticosteroid therapy would be a major benefit in the m