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1 to undergo an MRI scan, or had a history of splenectomy.
2 ed with 1.7% in patients who did not undergo splenectomy.
3 ate (>/=90 days; HR 1.5 [CI, 0.9-2.6]) after splenectomy.
4 iesis-dependent iron consumption by means of splenectomy.
5 ents with refractory disease usually require splenectomy.
6 76 patients with ITP, 1762 of whom underwent splenectomy.
7 of response to rituximab and the response to splenectomy.
8 -8.5]) and late (HR 2.7 [CI, 1.9-3.8]) after splenectomy.
9 nosis of accessory spleens in patients after splenectomy.
10 cancers, granulomatous disease, or previous splenectomy.
11 , 1.39-2.01) among the 19 states in rates of splenectomy.
12 sthesia, instrumentation for monitoring, and splenectomy.
13 gths, and more commonly involved concomitant splenectomy.
14 nts were incidences of treatment failure and splenectomy.
15 ents develop massive splenomegaly or undergo splenectomy.
16 extramedullary hematopoiesis and preventing splenectomy.
17 of IgM(+) CD27(+) memory B cells found after splenectomy.
18 ell ablative therapies such as anti-CD20 and splenectomy.
19 , but fails to protect septic mice following splenectomy.
20 ear lower following rituximab than following splenectomy.
21 y is before splenectomy, or after failure of splenectomy.
22 ti-D, intravenous immunoglobulin (IVIG), and splenectomy.
23 patient), AMR was treated with laparoscopic splenectomy.
24 cannot tolerate, or are unwilling to undergo splenectomy.
25 to standard therapy (ST) who resolved after splenectomy.
26 ease from bone marrow, a process enhanced by splenectomy.
27 n the outcomes of ITP patients refractory to splenectomy.
28 9.6% (88 of 921 patients) with laparoscopic splenectomy.
29 ) had gastric variceal bleeding and required splenectomy.
30 t an ITP second-line treatment: Rituximab or splenectomy.
31 reported consistently predicted response to splenectomy.
32 Overall, 9 (20%) donors underwent splenectomy.
33 Nissen fundoplication, cholecystectomy, and splenectomy.
34 if MCC vaccination occurred <10 years after splenectomy.
35 ous congenital anemias who underwent partial splenectomy.
36 n causing severe infection in patients after splenectomy.
37 of severe sepsis and septic shock following splenectomy.
38 This defect resolved after splenectomy.
39 o patients who received observation required splenectomy.
40 patient underwent total pancreatectomy with splenectomy.
41 nd 1 patient had a distal pancreatectomy and splenectomy.
42 nd stress the relevance of vaccination after splenectomy.
43 mplications and mortality following elective splenectomy.
44 rocedural management, angioembolization, and splenectomy.
45 asive bacterial infection, notably following splenectomy.
46 onset, intravascular hemolysis, and previous splenectomy.
47 ent urgent right hepatic artery ligation and splenectomy.
48 plenectomy and depends on the indication for splenectomy.
49 e common for all other procedures, including splenectomy (0.7% MIS), common bile duct exploration (24
50 twenty-three children underwent laparoscopic splenectomy (211 total; 12 partial) by the lateral appro
51 management strategy (195 patients undergoing splenectomy [23.6%], 70 undergoing angioembolism [23.9%]
52 index hospitalization, 825 (21.8%) underwent splenectomy, 293 (7.7%) underwent angioembolization, and
53 05) with a trend toward worsened response to splenectomy (3 of 18, 17%; vs 36 of 86, 42%; P = .06).
55 leen in ischemic injury, we found that prior splenectomy (-7d) or chemical sympathectomy of the splee
57 led hypertension, previous aneurysm surgery, splenectomy, acute aortic dissection, aneurysm type, old
58 1), trocar site hernia (1), subsequent total splenectomy after an initial partial (1), and recurrent
62 afts with this severe AMR phenotype by using splenectomy alone (n=14), eculizumab alone (n=5), or spl
63 very high load of PCs may not be rescued by splenectomy alone and may need additional treatments.
65 udies show that corticosteroid treatment and splenectomy, alone or together, increase platelet counts
66 There was more chronic glomerulopathy in the splenectomy-alone and eculizumab-alone groups at 1 year,
67 At a median follow-up of 533 days, 4 of 14 splenectomy-alone patients experienced graft loss (media
69 s 11.1% among the ITP patients who underwent splenectomy and 10.1% among the patients who did not.
70 Gender, age, ABO blood-type, cold ischemia, splenectomy and allograft type were significant DSA pred
72 is high in patients who previously underwent splenectomy and depends on the indication for splenectom
73 defined as a normal platelet count following splenectomy and for the duration of follow-up with no ad
74 ecommended only in patients at high risk for splenectomy and in those not willing to undergo surgery.
78 discuss criteria for treatment, the roles of splenectomy and other treatment options along with their
79 variate analysis suggested an interaction of splenectomy and perioperative transfusion in their effec
82 the treatment of the disease has changed as splenectomy and rituximab have been shown to have unexpe
86 und in patients (n=3) who did not respond to splenectomy and subsequently underwent bortezomib treatm
87 sly defined as lack of a minimum response to splenectomy and the requirement for long-term treatment
90 All patients in group 1 underwent emergent splenectomy, and all patients in group 2 were initially
92 ncluding gastrojejunostomy, cholecystectomy, splenectomy, and distal pancreatectomy have been perform
93 nt correlation between methemoglobin levels, splenectomy, and factors that modify the degree of globi
94 rpura for more than 3 months, had a previous splenectomy, and had a platelet count less than 50 x 10(
95 use of rituximab, increased plasma exchange, splenectomy, and immunosuppressive options, including cy
98 he increased thrombotic risk associated with splenectomy, and patients with hemoglobinopathies is a p
99 orbidity (including leaks, wound dehiscence, splenectomy, and postoperative hemorrhage) occurred in 2
100 s, type of immunosuppression, recipient age, splenectomy, and treatment of rejection were significant
101 imus and sirolimus maintenance therapy, with splenectomy, anti-CD20 and daily alpha-Gal polymer.
102 ren with hereditary spherocytosis, a partial splenectomy appears to control hemolysis while retaining
103 rituximab leads to response rates similar to splenectomy ( approximately 70%), but rituximab-induced
105 raft recipients, and particularly those with splenectomy are at high risk of developing GVHD after tr
113 included transfusion-dependent anemia until splenectomy at age 3 and increasing muscle weakness, wit
115 eadmitted patients (4.5%) who did not have a splenectomy at their index hospitalization, leading to a
119 erm risk of sepsis in patients who underwent splenectomy before, during, and after implementation of
120 arious hematological disorders who underwent splenectomy between 1998 and 2009 were followed until de
121 uality Improvement Program data for elective splenectomy between January 1, 2005, and December 31, 20
122 a risk of splenic injury, which may require splenectomy, but predictors of such events remain uncert
123 spleens in oncologic patients who underwent splenectomy can be misinterpreted as a recurrence, espec
124 resent time, the use of immunotherapy before splenectomy can be recommended only in patients at high
126 n and antibody removal, without rituximab or splenectomy, can achieve long-term outcomes comparable t
127 Moreover, the hypothesis that incidental splenectomy carries a worse prognosis deserves attention
128 boembolic events, palpable splenomegaly, and splenectomy; chemotherapy exposure; leukemic transformat
130 he alloimmune response to the lymph nodes by splenectomy conferred the ability of B6.muMT(-/-) CD4 T
132 y), thymic irradiation (700 cGy), and native splenectomy (day 0), and received a 45-day course of int
134 th splenic injury, progression to incidental splenectomy decreased by 92% during the study period.
135 erioperative transfusion but did not undergo splenectomy demonstrated the worst prognosis on multivar
136 large datasets indicate contrasting rates of splenectomy depending on the expertise of the institutio
137 ing pneumococcal bacteremia after undergoing splenectomy despite having received numerous doses of PP
138 urrent guidelines recommend consideration of splenectomy, despite the known risks associated with sur
140 of Hbb-b2(Plt12/Plt12) mice was normal, and splenectomy did not correct the thrombocytopenia, sugges
141 hree patients required surgery: laparoscopic splenectomy due to infarct and abscess for 1 patient and
142 who were declared brain-dead or had emergent splenectomy due to trauma; control lungs (n = 20) were o
144 19% of whom underwent pre- or peritransplant splenectomy, experienced twice the adjusted risk of earl
145 nditioning regimen that included thymectomy, splenectomy, extracorporeal immunoadsorption of anti-alp
146 We studied 114 patients with ITP for whom splenectomy failed and who required additional therapy;
148 In regression analyses adjusting for age at splenectomy, follow-up time, sex, and calendar year of s
152 uraging evidence suggests that the effect of splenectomy for children is durable in the long term.
153 zed with rheumatoid vasculitis or to undergo splenectomy for Felty's syndrome, cervical spine fusion
154 nt the cases of three patients who underwent splenectomy for gastric carcinoid, gastric adenocarcinom
155 e pertaining to vascular complications after splenectomy for hematologic conditions and attempts to d
157 rdingly, the adverse effects and benefits of splenectomy for hematologic disorders and other conditio
158 ibed 15 or more consecutive patients who had splenectomy for ITP and that had data for 1 of these 3 o
159 Follow-up of patients who have undergone splenectomy for ITP reveals significant potential risks
164 Current evidence supports alternatives to splenectomy for second-line management of patients with
165 scopic splenectomy as an alternative to open splenectomy for splenomegaly is regarded as controversia
167 onferred by C1 stimulation was eliminated by splenectomy, ganglionic-blocker administration or beta2-
168 oup for Nissen fundoplication, appendectomy, splenectomy, gastrostomy/jejunostomy, orchidopexy, and c
169 ary outcome-free survival rate was higher in splenectomy groups (84% for OS, 86% for LS) than Rituxim
172 efractory antibody-mediated rejection (AMR), splenectomy has been associated with surprisingly rapid
180 spective cohort study of patients undergoing splenectomy in 2008 and 2009 using data from the America
181 1.9% (37.1% operable, 23.5% nonoperable) and splenectomy in 3.4% of patients (1.9% operable, 5.7% non
183 ospitalization for rheumatoid vasculitis and splenectomy in Felty's syndrome decreased progressively
184 ospitalization for rheumatoid vasculitis and splenectomy in Felty's syndrome have decreased over the
187 No study has directly compared rituximab to splenectomy in patients with chronic immune thrombocytop
191 ests an interaction of blood transfusion and splenectomy in their effect on survival paralleling the
194 nts, rituximab was found to be equivalent to splenectomy, indicating that this invasive surgical proc
195 time less than 60 min, absence of recipient splenectomy, interleukin-2 receptor antagonist induction
205 sses diverse underlying conditions for which splenectomy is performed, diverse thrombotic complicatio
208 se, lower incidence of treatment failure and splenectomy, less bleeding and fewer blood transfusions,
211 LDLT followed by thymoglobulin induction and splenectomy, maintenance with tacrolimus/cyclosporine (F
213 al bacteremia in patients who have undergone splenectomy may indicate a genetically regulated failure
217 inage, and intra-abdominal bleeding (n = 3), splenectomy (n = 1), acute pancreatitis (n = 2), gastric
218 ng iron-chelating treatment and a history of splenectomy need regular ophthalmic checkups because the
219 and hospital characteristics, the choice of splenectomy (odds ratio, 0.93; 95% CI, 0.66-1.31) vs ang
221 ertook this study to determine the impact of splenectomy on transfusion requirements in patients with
224 previously reported, 3 Gy of TBI with either splenectomy or CD154 blockade induced mixed chimerism an
227 In peripheral blood from patients after splenectomy or in patients with sickle cell disease (SCD
231 ed the risk of splenic injury and incidental splenectomy (OR: 0.58; 95% CI: 0.41-0.80; and OR: 0.41;
233 reference characteristics (no chemotherapy, splenectomy, or radiation therapy; male; attained age 28
236 patients with TI and TM, age (P = 0.001) and splenectomy (P = 0.001) had the strongest association wi
240 omy alone (n=14), eculizumab alone (n=5), or splenectomy plus eculizumab (n=5), in addition to plasma
242 t for patients manifesting early severe AMR, splenectomy plus eculizumab may provide an effective int
243 d eculizumab-alone groups at 1 year, whereas splenectomy plus eculizumab patients had almost no trans
245 sk of surgery is an important consideration, splenectomy provides a high frequency of durable respons
246 usive trauma systems had significantly lower splenectomy rate (RR 0.79; 95% CI, 0.68-0.92) and lower
250 ivariate regression was performed to compare splenectomy rates, inpatient mortality, and costs betwee
254 ltirefractory ITP, defined as no response to splenectomy, rituximab, romiplostim, and eltrombopag.
255 e review 11 recipients, who underwent rescue splenectomy (RS) as a treatment of AMR within 3 months a
258 ality and severe infections after incidental splenectomy should be kept in mind during surgery, and w
259 lihood of gastric variceal bleeding and that splenectomy should be performed to prevent hemorrhage.
262 platelet counts, concomitant ITP drugs, and splenectomy status) or by the number of previous ITP tre
263 re significant univariate risk factors, with splenectomy surfacing as the dominant risk factor over t
265 or those who received rituximab or underwent splenectomy, the overall graft survival was 94.5% (95% C
266 y, follow-up time, sex, and calendar year of splenectomy, there were no significant risk decreases af
267 options for symptomatic patients ranges from splenectomy to rituximab alone or combined with chemothe
269 mune thrombocytopenia, who had not undergone splenectomy, to receive the standard of care (77 patient
271 ared with 1% in patients who did not undergo splenectomy; venous thromboembolism (VTE) (deep venous t
272 ble living donor kidney transplantation with splenectomy versus a protocol involving intensive posttr
273 nous thrombosis and pulmonary embolus) after splenectomy was 4.3% compared with 1.7% in patients who
275 er of > or =8 was observed if the reason for splenectomy was a medical cause or if MCC vaccination oc
277 nd 50% of children under the age of 6 years; splenectomy was associated with a significant improvemen
279 y developed grade 3 or 4 hematotoxicity, and splenectomy was inversely associated with the incidence
282 protection was abolished in animals in which splenectomy was performed 7 days before VNS and IRI.
287 nts, and conventional evisceration including splenectomy was performed in remaining six recipients.
292 as hampered by ineffective chemotherapy, and splenectomy was the major therapeutic approach to improv
294 ic artery ligation, hemiportocaval shunt, or splenectomy) was performed at the discretion of the oper
295 Predictors of splenic injury and incidental splenectomy were analyzed using multivariable logistic r
300 cient evidence to support the replacement of splenectomy with rituximab as a second-line treatment of
301 owever, risks depended on the indication for splenectomy, with SIRs varying from 3.4 (95% CI, 3.0-3.8
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