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1 by volume of the magnesium silicate mineral, talc.
2 CI, 50 to 199; p = 0.004) were greater after talc.
3 duced more systemic inflammation than graded talc.
4 ant effusions received tetracycline or mixed talc.
5 86 +/- 191 versus 85 +/- 37 microm) than did talc.
6 when compared with intrapleural injection of talc.
7 after, whereas a control group received only talc.
8 nt Effusion Trial [TIME2]) comparing IPC and talc (1:1) for which 106 patients with malignant pleural
10 inflammation (change in C-reactive protein, talc 198 SD 79.2 vs. tetracycline 74 SD 79.4 microg/L; d
11 abbits received an intrapleural injection of talc (400 mg/kg) and an intramuscular injection of triam
12 were given TGF-beta(2) (1.7 or 5.0 microg), talc (400 mg/kg), doxycycline (10 mg/kg), or buffer intr
13 g inflammation (change in isotope clearance, talc -9.26, SD 14.3 vs. tetracycline 4.10, SD 13.8 minut
15 Conventional pleurodesing agents such as talc act by inducing pleural injury, which results in ac
19 ight inducible protein (hli), transaldolase (talC) and ribonucleotide reductase (nrd)--are transcribe
21 y decreases the inflammatory reaction to the talc, and essentially prevents a pleurodesis from develo
22 Second, 48 patients received mixed or graded talc, and gas exchange was assessed from changes in the
23 an detect binders and fillers such as chalk, talc, and starch not revealed by traditional chromatogra
25 s significant, as the frictional strength of talc at elevated temperatures is sufficiently low to mee
28 he present study was designed to evaluate if talc directly effects cell death of malignant mesothelio
31 We conclude that the routine use of graded talc for pleurodesis would reduce the morbidity of this
33 experienced adverse events vs 7 of 54 in the talc group (OR, 4.70; 95% CI, 1.75-12.60; P = .002).
34 e in VAS score between the IPC group and the talc group of -14.0 mm (95% CI, -25.2 to -2.8 mm; P = .0
37 0-1 day) and 4 days (IQR, 2-6 days) for the talc group, with a difference of -3.5 days (95% CI, -4.8
38 m) and 24.4 mm (95% CI, 19.4-29.4 mm) in the talc group, with a difference of 0.16 mm (95% CI, -6.82
40 perature synthesis of 10 angstrom phase from talc + H(2)O to be observed in situ in a multianvil appa
49 tion of triamcinolone (0.8 mg/kg) 1 d before talc instillation and weekly thereafter, whereas a contr
61 at although TGF-beta was more effective than talc or doxycycline, it induced transient production of
65 ersus ten (14%) of 73 patients who completed talc pleurodesis (p=0.019), as were respiratory complica
66 s no significant difference between IPCs and talc pleurodesis at relieving patient-reported dyspnea.
67 randomly assigned (1:1) to either VAT-PP or talc pleurodesis by computer-generated random numbers, s
68 ) in the VAT-PP group and 57% (46-66) in the talc pleurodesis group (hazard ratio 1.04 [95% CI 0.76-1
69 of overall survival, and cost, of VAT-PP and talc pleurodesis in patients with malignant pleural meso
70 n due to malignant pleural mesothelioma, and talc pleurodesis might be preferable considering the few
73 ed 196 patients, of whom 175 (88 assigned to talc pleurodesis, 87 assigned to VAT-PP) had confirmed m
74 ficantly more common after VAT-PP than after talc pleurodesis, occurring in 24 (31%) of 78 patients w
76 article size of less than 15 microm ("mixed" talc) produces more lung and systemic inflammation than
77 shear at depth can become localized along a talc-rich principal-slip surface within serpentinite ent
78 dded), mottled deposits containing saponite, talc-saponite, Fe-rich mica (for example, glauconite-non
80 pleurodesis in rabbits at a rate faster than talc slurry and all other pleurodesing agents investigat
85 at the use of corticosteroids at the time of talc-slurry pleurodesis markedly decreases the inflammat
86 he concurrent use of steroids at the time of talc-slurry pleurodesis would influence the development
88 ive of this study was to investigate whether talc stimulates pleural mesothelial cells (PMC) to relea
90 bdominal wall tissue showed that five of six talc-treated animals given placebo expressed mRNA for th
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