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1 ral line, intracranial hemorrhage, and blood transfusion).
2 lerated tumor growth which was halted by PMP transfusion.
3 RBCs) and subsequent lung inflammation after transfusion.
4 in lower platelet count increments following transfusion.
5 revious transplantation, pregnancy, or blood transfusion.
6 e development of lung injury following blood transfusion.
7 iming as well as the location of the initial transfusion.
8 t count increment 10 to 90 minutes following transfusion.
9 an section requires donor (allogeneic) blood transfusion.
10 requiring treatment and postprocedural blood transfusion.
11 s measured before and at defined times after transfusion.
12 own to contribute to lung inflammation after transfusion.
13 higher (7 d) primaquine dose required blood transfusion.
14 r parameters and microvascular changes after transfusion.
15 25 x 10(9) platelets per L or greater after transfusion.
16 the potential to replace donor platelets for transfusion.
17 -day survival than delayed transfusion or no transfusion.
18 age duration for red cells to 5 weeks before transfusion.
19 re may exacerbate vascular injury during RBC transfusion.
20 een hemorrhagic shock patients requiring RBC transfusion.
21 clinical requirement to prevent any risks in transfusion.
22 were the most common indications for massive transfusion.
23 row failure, requiring prophylactic platelet transfusion.
24 platelet function for prophylactic platelet transfusion.
25 linical improvement and outweigh the risk of transfusion.
26 t, lung, and stem-cell transplant, and blood transfusion.
27 r and an intended recipient prior to a blood transfusion.
28 Patients were followed from first blood transfusion.
29 is confounded by potential concomitant blood transfusion.
30 rk Field imaging device before and after RBC transfusion.
31 erum ERFE levels, which decrease after blood transfusion.
32 Israel, and the USA and expected to need RBC transfusions.
33 s of less than 10 x 10(9) per L; or platelet transfusions.
34 resonance imaging before and after exchange transfusions.
35 n plasma (6 [2, 10] vs 6 [2, 12], P = 0.032) transfusions.
36 incurable diseases, immunotherapy and blood transfusions.
37 that aim to reduce or eliminate unnecessary transfusions.
38 d blood loss, fluid resuscitation, and blood transfusions.
39 undergoing major surgery often receive PRBC transfusions.
40 n may be an alternative to fully HLA-matched transfusions.
41 ology/oncology patients in spite of platelet transfusions.
42 ects of restrictive transfusion protocols on transfusions.
43 tervention Triage) and requirement for blood transfusions.
44 requently become dependent on red blood cell transfusions.
46 ury (20.8% vs 13.8%, P < .001), 30-day blood transfusion (3.4% vs 2.7%, P < .01), and 1-year readmiss
47 bleeding (14.0% versus 0.9%; P<0.001), blood transfusion (3.7% versus 0.2%; P<0.001), and death (10.0
48 1.00; 95% CI: 0.50 to 1.99; p = 0.99), blood transfusions (4.8% vs. 4.5%; HR: 1.09; 95% CI: 0.51 to 2
49 than 8 (31.5% vs 10.7%; P < .001), 4 or more transfusions (51.4% vs 17.6%; P < .001), operation time
50 injury (54.8% vs 25.3%; P < .001), 4 or more transfusions (74.2% vs 39.6%; P < .001), operation time
52 aT is a lifelong dependence on regular blood transfusions, a consequence of which is systemic iron ov
53 sk, 1.34; 95% CI, 1.10 to 1.62; P=0.001) and transfusion (absolute risk, 1.8% vs. 1.5%; relative risk
54 nt with asplenia and multiple red blood cell transfusions acquired babesiosis infection with Babesia
56 d, autologous, leukoreduced, packed red cell transfusion after 1, 2, 3, 4, 5, or 6 weeks of storage (
57 lation-based cohort of patients who received transfusions, allowing detection of small yet clinically
61 tissue cryopreservation for transplantation, transfusion and basic biomedical research, as well as te
62 effect with those who both received a blood transfusion and developed sepsis having even worse survi
64 Conventional management primarily relies on transfusion and iron-chelation therapy, as well as splen
67 otently impact immune outcomes following RBC transfusion and suggest that RBCs with altered Ag levels
70 To examine the association of prehospital transfusion and time to initial transfusion with injury
71 The sensitivity analysis including daily transfusions and fluid balance (in a subset of 518 patie
72 sitivity analysis further adjusted for daily transfusions and fluid balance in a subset of our patien
73 urrently available treatments are limited to transfusions and hydroxycarbamide, although stem cell tr
74 es, 30-day acute kidney injury, 30-day blood transfusion, and 1-year readmission rates for myocardial
76 ospital length of stay, hemorrhage requiring transfusion, and permanent pacemaker implantation (P<0.0
78 Bleeding complication was defined as any transfusion, any hemorrhage or hematoma, or the need for
84 n enabling platform to mechanistically study transfusion-associated pulmonary vascular complications
86 t experienced centers may receive a platelet transfusion at the first sign of bleeding, rather than p
87 125-0.5 mg/kg vs 0.75-1.75 mg/kg); pre-study transfusion burden (high transfusion burden vs low trans
89 cell units over 8 weeks versus pre-treatment transfusion burden in high transfusion burden patients.
90 r from baseline for 14 days or longer in low transfusion burden patients, and a reduction in red bloo
92 5 mg/kg); pre-study transfusion burden (high transfusion burden vs low transfusion burden, defined as
93 usion burden (high transfusion burden vs low transfusion burden, defined as >/=4 vs <4 red blood cell
94 (and baseline haemoglobin <10 g/dL), or high transfusion burden, defined as requiring 4 or more red b
95 olled patients were classified as having low transfusion burden, defined as requiring less than 4 red
96 ransfusion protocols to reduce avoidable RBC transfusions, but evidence of their effectiveness in pra
97 graft and new red cell antibodies induced by transfusion can lead to immunohaematological complicatio
100 ible alternative for fractionating blood for transfusion, cellular therapy and blood-based diagnostic
101 The change in microvascular perfusion after transfusion correlated negatively with baseline microvas
102 of-of-principle study, we determined whether transfusion could augment cerebral oxygen delivery, part
103 intravenous fluids, vasopressors, and blood transfusion decreases mortality among Zambian adults wit
104 stem and the randomisation was stratified by transfusion dependence and by baseline total symptom sco
111 2% female) who received 59320 red blood cell transfusions exclusively from 1 of 3 types of donors (88
112 ixture cohort (ie, either all red blood cell transfusions exclusively from male donors, or all exclus
113 an arterial pressure (>/=65 mm Hg) and blood transfusion (for patients with a hemoglobin level <7 g/d
115 ed red blood cell transfusions, receipt of a transfusion from an ever-pregnant female donor, compared
116 ntify the association between red blood cell transfusion from female donors with and without a histor
118 cipient dogs received up to 8 weekly treated transfusions from a single donor (a highly immunogenic s
120 ssociation between mortality and exposure to transfusions from ever-pregnant or never-pregnant female
123 ictive transfusion group than in the liberal transfusion group (mean difference -1.73 units, 95% CI -
124 nits transfused was lower in the restrictive transfusion group than in the liberal transfusion group
126 e colon cancer disease-specific survival [(+)transfusion: hazard ratio (HR) 1.19, 95% confidence inte
128 cardiovascular disease-specific survival [(+)transfusion: HR 1.18, 95% CI 1.04-1.33; (+)sepsis: HR 1.
129 95% CI 1.58-2.63], and overall survival [(+)transfusion: HR 1.21, 95% CI 1.14-1.29; (+)sepsis: HR 1.
130 perioperative factors, including anesthesia, transfusions, hypothermia, and postoperative complicatio
133 mplications occurred in 7.0% of cases, blood transfusion in 17.5%, clinical stroke in 1.8%, and pacem
136 protocols independently reduced the odds of transfusion in moderate anemia with an odds ratio of 0.5
139 ines (the use of leukoreduction and platelet transfusion in solid tumors or chronic, stable severe th
140 a previous recommendation involved platelet transfusion in the setting of hematopoietic stem-cell tr
141 ese data suggest that greater than 1:2 ratio transfusion in the setting of massive hemorrhage may not
145 nt with immunosuppressive agents, leading to transfusion independence or complete recovery of periphe
146 t of patients treated with decitabine became transfusion independent compared with 16% of patients tr
152 ood sampling (FBS) and intrauterine platelet transfusions (IUPT), as well as weekly maternal IV immun
153 and in estimated blood loss, intraoperative transfusion, length of stay, and postoperative complicat
155 eic SCT or chemotherapy and because platelet transfusions may not prevent bleeding, other risk factor
156 and thrombosis, and different thresholds for transfusion, may be appropriate subjects of future trial
157 The restrictive group received fewer blood transfusions: mean 20.3 +/- 32.7 units, median = 8 (inte
158 bility could be explored for applications in transfusion medicine but also for delivery of nucleic ac
159 AABB and the International Collaboration for Transfusion Medicine Guidelines (the use of leukoreducti
162 Among female recipients of red blood cell transfusions, mortality rates for an ever-pregnant femal
165 ciated with 23% lower odds of receiving PRBC transfusion (odds ratio = 0.77, 95% confidence interval
166 ivariable analysis, only receiving 4 or more transfusions (odds ratio [OR], 3.47; 95% CI, 2.04-5.91),
168 g for confounders on multivariable analysis, transfusion of "older" blood remained independently asso
169 d an adjusted odds ratio for receiving blood transfusion of 1.93 (95% CI, 1.21-3.07) compared with wo
170 patients, and a reduction in red blood cell transfusion of 4 or more red blood cell units or a 50% o
185 times the lethal dose (LD50) of BoNT/A, and transfusion of these red blood cells into naive mice aff
186 ressible hemorrhage still heavily depends on transfusion of whole blood or blood's hemostatic compone
188 g inflammation was studied in mice receiving transfusions of pRBCs and microparticles isolated from t
189 tient-level analyses were conducted with RBC transfusion on day of enrollment as the outcome and admi
195 ect of PRBC age (ie, storage duration before transfusion) on perioperative surgical outcomes remains
197 incidence of bleeding (blood loss requiring transfusion or intracranial hemorrhage) and thrombosis d
199 95% CI 1.09-1.91), and intraoperative blood transfusion (OR 1.45, 95% CI 1.15-1.83) were weak predic
200 ore widespread implementation of restrictive transfusion policies for adults with acute upper gastroi
202 scitation has become integrated into massive transfusion practice, there is a paucity of evidence sup
203 the impact of implementing a PBM program on transfusion practices and perioperative clinical outcome
205 oglobin values and suggests that restrictive transfusion practices may not be appropriate in this pop
206 at causalities in Afghanistan, blood product transfusion prehospital or within minutes of injury was
207 ed a priori, to compare rates of donor blood transfusion (primary outcome) and fetomaternal haemorrha
211 ld (hematocrit, > 30%) anemia in restrictive transfusion protocol ICUs was 67%, 19%, and 4%, respecti
214 Of the 59 study ICUs, 24 had an restrictive transfusion protocol; 2,510 patients (41.6%) were in an
216 justing for confounding factors, restrictive transfusion protocols independently reduced the odds of
218 ports the efficacy and safety of restrictive transfusion protocols to reduce avoidable RBC transfusio
219 udy is a retrospective review of all massive transfusions provided in an urban academic hospital from
226 against RBC non-ABO Ags can cause hemolytic transfusion reactions and limit availability of compatib
227 he probability of life-threatening hemolytic transfusion reactions, not all patients generate anti-RB
230 Among patients who received red blood cell transfusions, receipt of a transfusion from an ever-preg
231 Retrospective cohort study of first-time transfusion recipients at 6 major Dutch hospitals enroll
236 assess whether a restrictive strategy of RBC transfusion reduces 28-day mortality when compared with
237 fusion and time from MEDEVAC rescue to first transfusion, regardless of location (ie, prior to or dur
239 ury (acute respiratory distress syndrome and transfusion-related acute lung injury), for assessment o
242 examic acid (TXA) in reducing blood loss and transfusion requirements during liver transplantation.
243 appears effective in reducing red blood cell transfusion requirements without increasing the risk of
244 re, surgery length, operative blood loss, or transfusion requirements, but was positively associated
245 cute kidney injury, atrial fibrillation, and transfusion requirements, whereas TAVR had higher rates
250 study has investigated the association among transfusion, sepsis, and disease-specific survival in po
251 33; (+)sepsis: HR 1.63, 95% CI 1.14-2.31; (+)transfusion/(+)sepsis: HR 2.04, 95% CI 1.58-2.63], and o
252 30; (+)sepsis: HR 1.84, 95% CI 1.44-2.35; (+)transfusion/(+)sepsis: HR 2.27, 95% CI 1.87-2.76], cardi
253 29; (+)sepsis: HR 1.76, 95% CI 1.48-2.09; (+)transfusion/(+)sepsis: HR 2.36, 95% CI 2.07-2.68] relati
257 comes of a restrictive to a liberal red cell transfusion strategy in 20% or more total body surface a
259 observed a survival trend favoring a liberal transfusion strategy in patients with septic shock when
260 ect of a restrictive versus liberal red-cell transfusion strategy on clinical outcomes in patients un
264 in the screening period of 4 weeks: platelet transfusion, symptomatic bleeding, or platelet count of
265 ere hypoxemia are expected outcomes from RBC transfusion that need to be weighted with its benefits i
267 complications of iron overload, arising from transfusions that represent the basis of disease managem
268 defined as the absence of rebleeding, blood transfusion, therapeutic intervention, 28 day readmissio
269 enty-one children with SCA receiving chronic transfusion therapy (CTT) underwent magnetic resonance i
270 s whereby both increased iron absorption and transfusion therapy contribute to the iron overload.
272 r cardiac surgery) to a restrictive red-cell transfusion threshold (transfuse if hemoglobin level was
273 duction of anesthesia) or a liberal red-cell transfusion threshold (transfuse if hemoglobin level was
274 Zika virus in semen, the potential for blood-transfusion transmission, mother-to-child transmission,
276 currently the number one cause of reportable transfusion-transmitted infection in the United States.
277 ssociated with fewer patients receiving PRBC transfusion using a liberal trigger hemoglobin concentra
279 io for mortality associated with prehospital transfusion was 0.26 (95% CI, 0.08 to 0.84, P = .02) ove
286 h, a restrictive strategy regarding red-cell transfusion was noninferior to a liberal strategy with r
287 verall, in our cohort of 6,016 patients, RBC transfusion was not associated with death (hazard ratio,
288 njury severity, nonrecipients of prehospital transfusion were frequency matched to recipients by mech
291 e and postoperative complications, and blood transfusion when undergoing a hysterectomy later in life
292 t 28 days who either required red blood cell transfusions while on ruxolitinib or ruxolitinib dose re
293 should be considered for patients requiring transfusion with a very high risk of alloimmunization an
296 or grade 4 thrombocytopenia before platelet transfusion, with 25 x 10(9) platelets per L or greater
299 leading indication for red blood cell (RBC) transfusion worldwide, although optimal thresholds for t
301 and management of refractoriness to platelet transfusion ( www.asco.org/supportive-care-guidelines an
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