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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.
45 tation (2.9% versus 8.0%; P<0.001) and blood transfusion (12.8% versus 22.9%; P<0.001).
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
51 enced grade 4 thrombocytopenia that required transfusion, a dose-limiting toxicity.
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
55 rrin-bound iron (P < 0.001) as compared with transfusion after 1 to 5 weeks of storage.
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
58  of red-cell storage affects mortality after transfusion among critically ill adults.
59                         The frequency of RBC transfusion among patients with severe (hematocrit, < 21
60        Among 24,230 patients, 29% received a transfusion and 4% developed sepsis.
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
63                         However, receiving a transfusion and developing sepsis has an additive effect
64  Conventional management primarily relies on transfusion and iron-chelation therapy, as well as splen
65         Secondary outcomes included red-cell transfusion and other clinical outcomes.
66                       After risk adjustment, transfusion and sepsis were associated with worse colon
67 otently impact immune outcomes following RBC transfusion and suggest that RBCs with altered Ag levels
68 ching was used to account for confounders of transfusion and thrombotic risk.
69                    Initiation of prehospital transfusion and time from MEDEVAC rescue to first transf
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
75 fety outcomes included major bleeding, blood transfusion, and hospitalization for bleeding.
76 ospital length of stay, hemorrhage requiring transfusion, and permanent pacemaker implantation (P<0.0
77 collected included demographics, infections, transfusions, and outcomes.
78     Bleeding complication was defined as any transfusion, any hemorrhage or hematoma, or the need for
79 n worldwide, although optimal thresholds for transfusion are debated.
80                          Perioperative blood transfusions are associated with infectious complication
81                          Perioperative blood transfusions are associated with shorter survival, indep
82                         Red blood cell (RBC) transfusions are of vital importance in patients with si
83                                        Blood transfusions are the mainstay of stroke prevention in pe
84 n enabling platform to mechanistically study transfusion-associated pulmonary vascular complications
85                        Prophylactic platelet transfusion at defined platelet count thresholds is stil
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
88 etic features, profound cytopenias, and high transfusion burden are candidates for HSCT.
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
91 sus pre-treatment transfusion burden in high transfusion burden patients.
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
98                                 Although RBC transfusion can result in the development of anti-RBC al
99                Sequential expansion of blood transfusion capability after 2012 to deployed military m
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
105                                              Transfusion dependency was the only clinical variable as
106                                          RBC transfusion did not affect overall mortality in critical
107 o define which patients can benefit from RBC transfusion during cardiovascular resuscitation.
108 aboratory sampling is a major contributor to transfusion during ECMO.
109 tegy (hemoglobin threshold, < 7 g/dL) of RBC transfusion during ICU stay.
110 a, who account for nearly 90% of all massive transfusion events.
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
114                               For receipt of transfusion from a never-pregnant female donor vs male 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
117          854 862 adult patients who received transfusions from 2003 to 2012.
118 cipient dogs received up to 8 weekly treated transfusions from a single donor (a highly immunogenic s
119                               Red blood cell transfusions from ever-pregnant or never-pregnant female
120 ssociation between mortality and exposure to transfusions from ever-pregnant or never-pregnant female
121  female donors, compared with red blood cell transfusions from male donors.
122                                              Transfusions from never-pregnant female donors were not
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
125 ates and replaces the previous ASCO platelet transfusion guideline published initially in 2001.
126 e colon cancer disease-specific survival [(+)transfusion: hazard ratio (HR) 1.19, 95% confidence inte
127                                        After transfusion, hemoglobin rose from 9.6 +/- 1.4 to 10.8 +/
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
131             This study demonstrates that RBC transfusion improves cerebral oxygen delivery globally a
132                                          RBC transfusion improves sublingual microcirculation indepen
133 mplications occurred in 7.0% of cases, blood transfusion in 17.5%, clinical stroke in 1.8%, and pacem
134 6%, and was the sole reason for at least one transfusion in 42.2% of patients.
135  childhood, requiring >/=1 blood or platelet transfusion in 78% of cases.
136  protocols independently reduced the odds of transfusion in moderate anemia with an odds ratio of 0.5
137       Other recommendations address platelet transfusion in patients with hematologic malignancies or
138 idence-based guidance on the use of platelet transfusion in people with cancer.
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
142             The findings support prehospital transfusion in this setting.
143                    Prehospital blood product transfusion in trauma care remains controversial due to
144                                              Transfusions increased hemoglobin (Hb; from 9.1 to 10.3
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
147                                          PMP transfusion inhibited growth of both lung and colon carc
148 NL-parasitized red blood cells (pRBCs) after transfusion into naive or acutely infected mice.
149                                          RBC transfusion is often required in patients with sepsis.
150                                     Platelet transfusion is often used to restore hemostasis during o
151 donors on patient outcome following platelet transfusion is unknown.
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
154                    This approach to platelet transfusion may be particularly important when supportin
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
160 AABB and the International Collaboration for Transfusion Medicine Guidelines.
161                            In a dog platelet transfusion model, we have evaluated other methods of pr
162    Among female recipients of red blood cell transfusions, mortality rates for an ever-pregnant femal
163 atients with perforation including bleeding, transfusion, myocardial infarction, and death.
164                                     Red-cell transfusion occurred in 52.3% of the patients in the res
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),
167                                              Transfusion of "older" blood products may contribute to
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
171                                              Transfusion of aged pRBCs or microparticles isolated fro
172       Massive transfusion was defined as the transfusion of at least 10 U of RBCs in the first 24 hou
173       After 6 weeks of refrigerated storage, transfusion of autologous red cells to healthy human vol
174                                              Transfusion of blood products should not be withheld fro
175                                              Transfusion of either platelets or red blood cells (RBCs
176                         We hypothesized that transfusion of leukocytes loaded ex vivo with the lipoph
177                                        After transfusion of one unit of RBC, hemoglobin concentration
178                                              Transfusion of one unit of RBCs.
179                                              Transfusion of platelets poses significant challenges of
180                    This was attenuated after transfusion of pRBCs treated with amitriptyline or from
181                                              Transfusion of RBC significantly decreased the flow hete
182                                              Transfusion of RBC significantly increased microcirculat
183                                              Transfusion of red blood cells expressing self-antigen e
184                                              Transfusion of red blood cells from female donors has be
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
187                                              Transfusion of wild-type platelets into platelet-specifi
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
190  of traumatic brain injury (TBI) and massive transfusion on fibrinolysis status.
191 those seeking to assess effects of anemia or transfusion on lung function).
192                           The effects of RBC transfusion on microvascular perfusion are not well docu
193            We investigated the effect of RBC transfusion on sublingual microcirculation in hemorrhagi
194                       The effect of platelet transfusions on IGF-1R was explored.
195 ect of PRBC age (ie, storage duration before transfusion) on perioperative surgical outcomes remains
196  treatments (MISC), whereas 697 received RBC transfusions only.
197  incidence of bleeding (blood loss requiring transfusion or intracranial hemorrhage) and thrombosis d
198 ter 24-hour and 30-day survival than delayed transfusion or no transfusion.
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
201                         Red blood cell (RBC) transfusion poses significant risks to critically ill pa
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
204                    Restrictive perioperative transfusion practices are a possible strategy to reduce
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
208                                   During RBC transfusion, production of alloantibodies against RBC no
209                Extravascular hemolysis after transfusion progressively increased with increasing stor
210 e and admission to an ICU with a restrictive transfusion protocol as the exposure of interest.
211 ld (hematocrit, > 30%) anemia in restrictive transfusion protocol ICUs was 67%, 19%, and 4%, respecti
212 s (41.6%) were in an ICU with an restrictive transfusion protocol.
213  2% for those in ICUs without an restrictive transfusion protocol.
214  Of the 59 study ICUs, 24 had an restrictive transfusion protocol; 2,510 patients (41.6%) were in an
215 munization and may benefit from personalized transfusion protocols and/or targeted therapies.
216 justing for confounding factors, restrictive transfusion protocols independently reduced the odds of
217 essed the independent effects of restrictive transfusion protocols on transfusions.
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
220 adverse events have been associated with RBC transfusion, raising safety concerns.
221                                  Donor blood transfusion rate was 3.5% in the control group versus 2.
222          In a planned subgroup analysis, the transfusion rate was 4.6% in women assigned to control v
223                       The practice of a high transfusion ratio of fresh frozen plasma (FFP) to red bl
224                                 High FFP:RBC transfusion ratios are applied mostly to patients withou
225                       Examination of FFP:RBC transfusion ratios for patients without trauma.
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
228 can cause life-threatening delayed hemolytic transfusion reactions.
229 ating a risk for Vel blood typing errors and transfusion reactions.
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
232                                          All transfusion recipients in Sweden and Denmark.
233 62 recipients vs 68 deaths among 324 delayed transfusion recipients or nonrecipients).
234                                              Transfusion recipients were compared with nonrecipients
235                           At all thresholds, transfusions reduced the volume of peak OEF found in the
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
238                              Time to initial transfusion, regardless of location (prehospital or duri
239 ury (acute respiratory distress syndrome and transfusion-related acute lung injury), for assessment o
240  the highest rate of acceptance for platelet transfusions reported in either animals or man.
241           Laboratory sampling contributed to transfusion requirement in 56.6%, and was the sole reaso
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
246 ith major burns have major (>1 blood volume) transfusion requirements.
247 latelet counts, and ten had reduced platelet transfusion requirements.
248 (33.3%) and 9 of 282 (3.4%) receiving 2 or 3 transfusions, respectively.
249                 In vulnerable brain regions, transfusion resulted in a greater (16%) rise in oxygen d
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
254 s: HR 2.36, 95% CI 2.07-2.68] relative to (-)transfusion/(-)sepsis.
255  the liberal (n = 149) or to the restrictive transfusion strategy (n = 151) group.
256                                A restrictive transfusion strategy halved blood product utilization.
257 comes of a restrictive to a liberal red cell transfusion strategy in 20% or more total body surface a
258                                  The optimal transfusion strategy in major burn injury is thus needed
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
261 7-8 g/dL) or liberal (hemoglobin 10-11 g/dL) transfusion strategy throughout hospitalization.
262 d had anaemia with or without red blood cell transfusion support.
263 omes were complications, death, and need for transfusions, surgery, or angiography.
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
266 ed specific tolerance to 8 more weekly donor transfusions that had not been treated.
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.
271             However, a major complication of transfusion therapy is alloimmunization.
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,
275             This is believed to be the first transfusion-transmitted case and the fifth documented ca
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
278 perative central venous pressure and greater transfusion volumes.
279 io for mortality associated with prehospital transfusion was 0.26 (95% CI, 0.08 to 0.84, P = .02) ove
280                                        Blood transfusion was administered to 195 women (2.5%).
281                                 However, RBC transfusion was associated with increased occurrence of
282                                  Restrictive transfusion was associated with lower risk of all-cause
283                                      Massive transfusion was defined as the transfusion of at least 1
284 ared with nonrecipients (unexposed) for whom transfusion was delayed or not given.
285       After 6 weeks of refrigerated storage, transfusion was followed by increases in AUC for serum i
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
289                                  Only 27% of transfusions were associated with a hematocrit less than
290                                Most of these transfusions were received by patients without trauma (7
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
294  prehospital transfusion and time to initial transfusion with injury survival.
295                           In these patients, transfusions with platelets showing low HLA class I expr
296  or grade 4 thrombocytopenia before platelet transfusion, with 25 x 10(9) platelets per L or greater
297         Overall, 282 of 318 (88.7%) received transfusions, with 94 of 282 (33.3%) and 9 of 282 (3.4%)
298            All patients who received massive transfusions within the study period and survived more t
299  leading indication for red blood cell (RBC) transfusion worldwide, although optimal thresholds for t
300                We hypothesized that exchange transfusions would decrease CBF and OEF by increasing Ca
301 and management of refractoriness to platelet transfusion ( www.asco.org/supportive-care-guidelines an

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