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1 (ADL) limitations (transferring, eating, and dressing).
2 sts, and no evidence supports one particular dressing.
3 incisions received either NPWT or a standard dressing.
4 he photo-oxidation of vegetable oil in salad dressing.
5 mbined action of dipole excitation and field dressing.
6 presentation, cross-presentation, and cross-dressing.
7 erse and depended on type of herring and its dressing.
8 h berberine (Beri) as the DFU-specific wound dressing.
9 activated by a third mechanism, called cross-dressing.
10 cells requires both cross-priming and cross-dressing.
11 ten causes discomfort and leakage from stoma dressing.
12 with and without added a standardised salad dressing.
13 receive prophylactic NPWT or standard gauze dressing.
14 for type of surgery using a large abdominal dressing.
15 f 2700 cP, similar to the viscosity of salad dressing.
16 pply and can be used as any other disposable dressing.
17 n SSI rate when compared with standard gauze dressing.
18 octasulfate dressing and 114 to the control dressing.
19 function, pharmaceutical delivery and wound dressings.
20 opical applications such as wound rinses and dressings.
21 tronics and the emerging area of smart wound dressings.
22 t previously treated with silver-impregnated dressings.
23 orhexidine gluconate-impregnated transparent dressings.
24 ation of chlorhexidine gluconate-impregnated dressings.
25 cies of S. aureus and P. aeruginosa in wound dressings.
26 susceptible to the irritant effects of these dressings.
27 ssed by the use of chlorhexidine-impregnated dressings.
28 illion per day, continually infiltrate wound dressings.
29 al wound care, and alternative antimicrobial dressings.
30 ), Italian (I) and Thousand Island (T) salad dressings.
31 lorhexidine versus standard nonchlorhexidine dressings.
32 ve several advantages over traditional wound dressings.
33 cytotoxic concentrations of silver in these dressings.
34 s antisepsis and silver alginate-impregnated dressings.
35 procedure eliminates bandages, sutures, and dressings.
36 orhexidine rinses, systemic antibiotics, and dressings.
37 tiles to composites, and waveguides to wound dressings.
38 zed studies that compared iNPWT with control dressings.
39 heir sensory acceptance were tested in salad dressings.
40 enting clinical studies with electroceutical dressings.
41 driven use of skin antiseptics and occlusive dressings.
42 gic tissue have performed well as wound care dressings.
43 ich may range from smart filtration to smart dressings.
44 Among 54 RCTs evaluating absorbent wound dressings, 1 found calcium alginate dressings improved h
45 t previously treated with silver-impregnated dressings: (1) the appearance of pseudo-ochronotic fiber
47 s [n = 562]; high consistency), radiant heat dressings (4 studies [n = 160]; moderate consistency), a
51 are and low-strength evidence for biological dressing and a biological skin equivalent compared with
52 with a bioabsorbable collagen wound-healing dressing and a coronally advanced flap (CAF) to a subepi
54 patients assigned to the sucrose octasulfate dressing and four (4%) assigned to the control dressing
55 n between the amount of soybean oil in salad dressing and the absorption of 1) carotenoids, phylloqui
57 leg ulcer healing compared with usual care (dressings and bandages without antimicrobials) or an alt
59 ) with chlorhexidine versus nonchlorhexidine dressings and catheter colonization rate with highly adh
61 sensors embedded in care products like wound dressings and diapers to track wound and urinary infecti
66 entiate to cytolytic effectors through cross-dressing, and indeed which DC subset would be responsibl
71 red chlorhexidine dressings, highly adhesive dressings, and standard dressings from May 2010 to July
73 crobial-impregnated catheters, catheter site dressings, antibiotic lock solutions, anticoagulation, c
74 in vitro experiments demonstrate that cross-dressing APCs do not acquire peptide-MHC complexes in th
78 CTG and rhPDGF-BB + beta-TCP + wound-healing dressing are effective treatment modalities for clinical
84 dings support the use of sucrose octasulfate dressing as a local treatment for neuroischaemic diabeti
85 Here we describe the use of discarded wound dressings as a novel, cost effective, accessible, and no
86 of wound infection identified standard wound dressings as the only significant predictor of SSI devel
87 nce of wound infections, the total number of dressings at 8 weeks, and the percentage of change in ar
88 f concomitant IADL and ADL, with bathing and dressing being the earliest ADL losses, and finally tota
89 ailure to induce T cell proliferation, cross-dressing by donor DCs contributes to generation of the i
91 An alternative way, referred to as 'cross-dressing', by which an uninfected APC could present anti
92 for the first time that recipient APC cross-dressing can be transiently detected in the circulation
94 36/40 [90%] versus 9/40 [23%]; P<0.001), and dressing change skills (19/20 [95%] versus 0/20; P<0.001
95 h the 3-day chlorhexidine-impregnated sponge dressing change strategy, and $83 with the 7-day standar
97 f-care skills (controller, power source, and dressing change), then viewed videos and participated in
99 r thousand catheter days, and that scheduled dressing changes every 7 days was not inferior to schedu
103 each consumed 5 vegetable salads with salad dressings containing 0, 2, 4, 8, or 32 g soybean oil.
104 a-TCP + bioabsorbable collagen wound-healing dressing; contralateral control sites were treated with
106 hysiological function, compared to occlusive dressing control wounds that showed formation of tortuou
111 er, they mediate their effect through "cross-dressing." Cross-dressing, or peptide-MHC (pMHC) transfe
114 onstrated that chlorhexidine-gel-impregnated dressings decreased the CRI rate in patients in the ICU
116 -0.868; P = 0.02) than with nonchlorhexidine dressings; decreases were noted in catheter colonization
118 dies utilizing a modified collagen gel (MCG) dressing demonstrated improved vascularization of ischem
120 wound therapy, compared with standard wound dressing, did not significantly reduce the risk of surgi
121 essing and four (4%) assigned to the control dressing died, but none of the deaths were related to tr
122 g through the use of tourniquets, hemostatic dressings, direct pressure, or pressure devices; the use
123 sed by more than three-fold after the second dressing disruption and by more than ten-fold if the fin
126 nsertion site and enhanced efforts to reduce dressing disruption in postinsertion bundles of care.
128 rmed in order to determine the importance of dressing disruption on the risk for development of cathe
135 ified four-wave mixing (PA-FWM) process with dressing effects in a three-level "double-Lambda" config
136 etraacetate (EDTA)] in a sunflower oil salad dressing emulsion (SOSDE) and shelf life affecting condi
140 levels of the atomic ground state, where the dressing field is spatially modulated by inductive effec
142 mechanobiology studies demonstrate the TRIM dressing film with a critical dimension for surface feat
143 xtent to which donor sEVs might induce cross-dressing following liver and kidney transplantation.
147 rn patients who had received living pig-skin dressings for up to 8 wk for the presence of PERV as wel
152 bricated hierarchical copper- and zinc- buds dressing gamma-AlOOH mesostrands (Cu- and Zn-AMSs) with
153 ted that hierarchical copper- and zinc- buds dressing gamma-AlOOH mesostrands, which are oriented in
154 bility (two or more difficulties in bathing, dressing, going to the toilet, transferring, feeding, an
155 g group and 34 patients (30%) in the control dressing group (18 percentage points difference, 95% CI
157 ifference in dehiscence between NPWT and dry dressing group (36.4% vs 29.7%; P = 0.54) or mean time t
158 pressure group and 27 (3.4%) in the standard dressing group (difference, 0.36%; 95% CI, -1.46% to 2.1
159 % (50 of 749 patients) of the standard wound dressing group (odds ratio, 0.87 [95% CI, 0.57 to 1.33];
160 dly reduced in the chlorhexidine-impregnated dressing group (random effects relative risk, 0.52; 95%
161 gnificantly reduced in the negative pressure dressing group [6.1 vs 14.7 days, P = 0.019 (2-sided)].
162 patients randomized to the negative pressure dressing group and 25 to the standard dressing group.
163 60 patients (48%) in the sucrose octasulfate dressing group and 34 patients (30%) in the control dres
164 ) patients of 126 in the sucrose octasulfate dressing group and 36 in 32 (28%) patients of 114 in the
166 one (1%) patient in the sucrose octasulfate dressing group and two (2%) patients in the control dres
167 6.8% of the NPWT group and 13.5% of the dry dressing group developed wound infection, but this was n
173 % [78 of 590 patients] in the standard wound dressing group; odds ratio, 0.84 [95% CI, 0.59 to 1.19];
179 in 12 French ICUs, we compared chlorhexidine dressings, highly adhesive dressings, and standard dress
181 nt wound dressings, 1 found calcium alginate dressings improved healing compared with dextranomer pas
183 the nanoemulsions was similar to the control dressing in appearance, consistency and colour terms.
184 Despite the importance of thymic DC cross-dressing in negative selection, the factors that regulat
186 ffect of chlorhexidine gluconate-impregnated dressings in critically ill patients has not been descri
187 nds that clinicians use hydrocolloid or foam dressings in patients with pressure ulcers to reduce wou
189 ity of hydrogels in soft contact lens, wound dressings, intraocular lens, vitreous substitutes, vitre
193 lysis shows that a chlorhexidine-impregnated dressing is beneficial in preventing catheter colonizati
194 ericardial collagen matrix (sPCM) wound care dressing is flexible cross-linked proteolytic enzyme deg
195 PWT, as compared with standard postoperative dressings, is associated with a reduction in the rate of
196 ndogenous antimicrobial defense systems, the dressing itself has properties that minimize biofilm for
197 cy linewidth, measured relative to the Raman dressing laser, that is less than that of single-particl
199 on of the chlorhexidine gluconate-containing dressings, local wound care, and alternative antimicrobi
202 (Putty P15 and bioabsorbable collagen wound dressing material) or control (bioabsorbable collagen wo
205 monstrating that a collagen-based wound-care dressing may influence wound macrophage function and the
206 orhexidine-impregnated and strongly adherent dressings may decrease catheter colonization and CRI rat
208 rs vs. 34 hrs; p = 0.05) and less protective dressings (n = 2, 9.5% vs. n = 8, 53.3%; p = 0.007).
209 e pressure over the wound, vs standard wound dressing not involving negative pressure (n = 763).
210 2.19; 95% CI, 1.00-4.82], performing a wound dressing [odds ratio, 8.35; 95% CI, 2.07-33.63] and inte
211 The effect of prophylactic negative pressure dressing of closed incisional wounds on SSI rate is unkn
214 s rich, including ponderomotive interaction, dressing of the electronic states, creation of coherent
215 l space before closing, and a post-operative dressing of the incisional surgical wound with a sterile
217 murine models of transplantation, the "cross-dressing" of recipient antigen presenting cells (APCs) w
219 onal guides for ultracold atoms through the 'dressing' of hyperfine sublevels of the atomic ground st
220 s (95% CIs) were 0.95 (0.87, 1.04) for salad dressing olive oil and 0.85 (0.74, 0.98) for olive oil a
221 with bilateral incisions randomly received a dressing on one incision and the opposite dressing on th
222 e such as red cabbage with and without salad dressing on the intestinal cellular bioaccessibility (cB
224 ucrose octasulfate dressing versus a control dressing on wound closure in patients with neuroischaemi
226 any sublethal effects of neonicotinoid seed dressings on Bombus colonies are potentially offset by t
227 the effect of prophylactic negative pressure dressings on postoperative surgical site infection (SSI)
228 ing the use of prophylactic NPWT to standard dressings on primarily closed laparotomy incisions follo
230 ment with either a sucrose octasulfate wound dressing or a control dressing (the same dressing withou
231 ood transfusion; hematoma requiring pressure dressing or change in anticoagulation therapy; or prolon
233 infection, utilizing devices imbedded within dressings or as point-of-care techniques to allow for co
234 their effect through "cross-dressing." Cross-dressing, or peptide-MHC (pMHC) transfer, involves the g
238 .C. (KCI, San Antonio, TX) or a standard dry dressing over their incision at the conclusion of surger
239 ed with a clinically approved collagen wound dressing, peptide-free hydrogel, or blank wound controls
240 versus 71.9% (P < 0.0001) and the number of dressings per catheter to two (one to four) versus three
242 alternating-pressure surfaces, hydrocolloid dressings, platelet-derived growth factor, and light the
243 eatment of injured skin with a semiocclusive dressing preserves the hydration of the skin and results
244 s covered with a rapidly absorbable collagen dressing (RACD) (Group B) in function of a panel of radi
245 e patients who had NPWT compared to standard dressings; relative risk (RR) 0.56 (95% confidence inter
249 An adhesive yet easily removable burn wound dressing represents a breakthrough in second-degree burn
250 ted cell and an uninfected APC, termed cross-dressing, represents an important mechanism of Ag presen
252 wound therapy, compared with standard wound dressing, resulted in no significant difference in the r
253 atient consultation rooms, laboratories, and dressing rooms, and categorised infection prevention and
254 virgin olive oil in commercial vinaigrettes, dressing salad and in-house reference materials (i-HRM)
255 e compounds and peroxide values of the salad dressing samples simultaneously decreased with the addit
256 College of Surgeons (bathing, transferring, dressing, shopping, and meals), history of falling or ga
257 argyria or treatment with silver-impregnated dressings should be considered before treatment with fra
259 y substituting other types of fats and salad dressings (stick margarine, butter, and mayonnaise) with
264 ng interest in the development of absorbable dressings that can be left in the injury site and degrad
265 developing electronically controllable wound dressings that can deliver drugs with desired temporal p
266 dration status and that the use of occlusive dressings that prevent water loss from wounds decreases
267 ying interactions between ultracold atoms by dressing the bare atomic states with light, creating an
268 rose octasulfate wound dressing or a control dressing (the same dressing without sucrose octasulfate)
272 ted subspace, obtained by applying microwave dressing to a clock transition of the ground-state elect
275 a neutral atomic Bose-Einstein condensate by dressing two atomic spin states with a pair of lasers.
277 rapy (n = 785), which involved a specialized dressing used to create negative pressure over the wound
279 red for female, nonchlorhexidine-impregnated dressings users, and when catheters are left in place mo
280 o assess the effect of a sucrose octasulfate dressing versus a control dressing on wound closure in p
285 ption and by more than ten-fold if the final dressing was disrupted, independently of other risk fact
289 The wound healing efficacy of the fabricated dressings was evaluated in streptozotocin-induced diabet
290 acquire viral peptide-MHC complexes by cross-dressing, we show that such presentation can promote the
291 inistration-cleared wireless electroceutical dressing (WED) was tested in an established porcine chro
292 mmune responses induced exclusively by cross-dressing were as strong as those induced exclusively thr
295 id not compromise the physical properties of dressing, while improving the biological activities.
296 ractive ground-state potential and adiabatic dressing with an excited state whose potential is engine
300 und dressing or a control dressing (the same dressing without sucrose octasulfate) for 20 weeks.