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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).
54          Of 33,131 patients, 26.2% underwent splenectomy, 6.1% died, and median hospital costs were $
55 leen in ischemic injury, we found that prior splenectomy (-7d) or chemical sympathectomy of the splee
56                                     Finally, splenectomy abrogated the enhancing effects of poly (I:C
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
59       However, the chance of readmission for splenectomy after initial nonoperative management was 1.
60  predicted sustained responses whereas prior splenectomy, age, sex, and duration of ITP did not.
61 the frequency of surgical complications with splenectomy all remain uncertain.
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.
64                      These data suggest that splenectomy alone may not be the sole reason for loss of
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
68                                              Splenectomy also was performed less frequently in patien
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
71                                     However, splenectomy and anti-CD20 is associated with an increase
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.
75 actors that improved platelet responses were splenectomy and increasing patient age.
76 ), and 4 months after transplantation (after splenectomy and on maintenance immunosuppression).
77                         The interval between splenectomy and OPSI was 6 years (range, 1 month-50 year
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
80              Associations between incidental splenectomy and risk of mortality and severe infections
81                      As second-line therapy, splenectomy and Rituximab are both recommended.
82  the treatment of the disease has changed as splenectomy and rituximab have been shown to have unexpe
83 est triage model for decision making between splenectomy and SAE (AUC, 0.84).
84                        Unlike adrenalectomy, splenectomy and splenic neurectomy prevent the anti-infl
85 cells promote MPE formation, as indicated by splenectomy and splenocyte restoration experiments.
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
88  of studies comparing second-line options to splenectomy and to each other.
89  were retreated with cladribine, 3 underwent splenectomy, and 1 received pentostatin.
90   All patients in group 1 underwent emergent splenectomy, and all patients in group 2 were initially
91 ry spleen) and laparoscopic in 2 (completion splenectomy, and cyst excision).
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
96 cium, pre-transfusion hemoglobin, history of splenectomy, and liver iron concentration.
97 onor-specific antibody, absence of recipient splenectomy, and liver-inclusive graft type.
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
104                         Patients who undergo splenectomy are at greatly increased risk for overwhelmi
105 raft recipients, and particularly those with splenectomy are at high risk of developing GVHD after tr
106           We conclude that ITP patients post splenectomy are at increased risk for AbVTE, VTE, and se
107          Because patients who have undergone splenectomy are considered at increased risk of bacteria
108 , vincristine, or cyclosporine A; or salvage splenectomy are considered.
109 erm risks, the indications for and timing of splenectomy are debated in the medical community.
110                             Advanced age and splenectomy are risk factors for PAH in this patient pop
111                                 Laparoscopic splenectomy as an alternative to open splenectomy for sp
112       Because subjects with autoimmunity had splenectomy at a significantly older age than participan
113  included transfusion-dependent anemia until splenectomy at age 3 and increasing muscle weakness, wit
114 l involving pretransplant plasmapheresis and splenectomy at the time of transplant (n=23).
115 eadmitted patients (4.5%) who did not have a splenectomy at their index hospitalization, leading to a
116 ft outcomes when compared most frequently to splenectomy-based protocols.
117                                    Moreover, splenectomy before RSD blocked monocyte trafficking to t
118                                              Splenectomy before subthreshold stress attenuated macrop
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
125                                 Laparoscopic splenectomy can be safely performed during pregnancy.
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
129                      The overall PR or CR to splenectomy combined with medical therapy was 84%.
130 he alloimmune response to the lymph nodes by splenectomy conferred the ability of B6.muMT(-/-) CD4 T
131                                              Splenectomy continues to provide the highest cure rate (
132 y), thymic irradiation (700 cGy), and native splenectomy (day 0), and received a 45-day course of int
133                      Thirteen pigs underwent splenectomy (day 0); all received a blood transfusion.
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
139       None of the patients with a history of splenectomy developed grade 3 or 4 hematotoxicity, and s
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
143                                              Splenectomy eliminated both the survival benefit of 6-hy
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;
147               Median time to remission after splenectomy failure was 46 months (range, 1-437 months).
148  In regression analyses adjusting for age at splenectomy, follow-up time, sex, and calendar year of s
149                                 Furthermore, splenectomy following RSD prevented the recurrence of an
150              Patients underwent laparoscopic splenectomy for a range of hematological disorders betwe
151  help with patient selection before elective splenectomy for certain patients.
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
156                                     Elective splenectomy for hematologic conditions.
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
160                             We observed that splenectomy for ITP second-line treatment was more effec
161                                              Splenectomy for massive splenomegaly (>1500 g) provides
162                                              Splenectomy for massive splenomegaly can be performed sa
163                                              Splenectomy for massive splenomegaly was performed most
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
166 utation in their granulocytes and undergoing splenectomy for therapeutical reasons.
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
170                                 Laparoscopic splenectomy has become the procedure of choice for most
171                                              Splenectomy has been a standard treatment for adult pati
172 efractory antibody-mediated rejection (AMR), splenectomy has been associated with surprisingly rapid
173                                  The role of splenectomy has been controversial in this patient popul
174                                         Age, splenectomy, hepatitis C, and smoking are significant un
175                                 A history of splenectomy, hepatitis C, smoking, or high white blood c
176                  These beneficial effects of splenectomy hold true even for the most profoundly throm
177                                              Splenectomy, however, had no effect on monocyte accumula
178 ated with 2 or more therapy lines, including splenectomy, immunosuppressants, and rituximab.
179 h national inpatient register, who underwent splenectomy in 1970-2009.
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
182 que group (0% vs. 10.5%; P=.03), requiring a splenectomy in 4 patients (4.7%).
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
185              The risk of hospitalization for splenectomy in Felty's syndrome was 71% lower in 1998-20
186                                              Splenectomy in mice with established HF reversed patholo
187  No study has directly compared rituximab to splenectomy in patients with chronic immune thrombocytop
188  was to compare the efficacy of Rituximab to splenectomy in persistent or chronic ITP patients.
189 y because of long-term immunosuppression and splenectomy in refractory cases.
190 usion and iron-chelation therapy, as well as splenectomy in specific cases.
191 ests an interaction of blood transfusion and splenectomy in their effect on survival paralleling the
192                              Indications for splenectomy included: thrombocytopenia refractory to (64
193                        Incidental accidental splenectomy increased the overall risk of mortality (HR:
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
196                                              Splenectomy is a commonly performed operation; however,
197                                    A partial splenectomy is an alternative procedure, although its ut
198                                              Splenectomy is considered acceptable for patients with r
199                                 Laparoscopic splenectomy is feasible in patients with giant spleens.
200                                 Nonetheless, splenectomy is invasive, irreversible, associated with p
201 and persistent severe thrombocytopenia after splenectomy is minimal.
202                                              Splenectomy is not essential for successful ABO-incompat
203 s in only 4% of patients; therefore, routine splenectomy is not recommended.
204 The most widely recognized long-term risk of splenectomy is overwhelming bacterial infection.
205 sses diverse underlying conditions for which splenectomy is performed, diverse thrombotic complicatio
206                                              Splenectomy is usually proposed when a second-line thera
207 patible kidney transplantation have employed splenectomy, its utility is unproven.
208 se, lower incidence of treatment failure and splenectomy, less bleeding and fewer blood transfusions,
209                                              Splenectomy, loss of SIGN-R1(+) cells in the splenic mar
210 stinction between open (OS) and laparoscopic splenectomy (LS) was analyzed.
211 LDLT followed by thymoglobulin induction and splenectomy, maintenance with tacrolimus/cyclosporine (F
212 rs contributing to myelosuppression, whereas splenectomy may exert a protective effect.
213 al bacteremia in patients who have undergone splenectomy may indicate a genetically regulated failure
214                                              Splenectomy may play a role in the treatment of AMR refr
215                                              Splenectomy may remove an important antigen reservoir an
216                                              Splenectomy may reverse AMR by debulking PCs.
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
220  per 1-year increase; 95% CI, 1.06-1.15) and splenectomy (odds ratio, 9.31; 95% CI, 2.57-33.7).
221 ertook this study to determine the impact of splenectomy on transfusion requirements in patients with
222                        Age (two studies) and splenectomy (one study) had the strongest association wi
223 on without long-term B-cell suppression from splenectomy or anti-CD20.
224 previously reported, 3 Gy of TBI with either splenectomy or CD154 blockade induced mixed chimerism an
225                                              Splenectomy or depletion of splenic macrophages by lipos
226                                              Splenectomy or high-dose cortisone treatment had no effe
227      In peripheral blood from patients after splenectomy or in patients with sickle cell disease (SCD
228 plenomegaly and constitutional symptoms, and splenectomy or radiotherapy in selected patients.
229                                              Splenectomy or radiotherapy offers benefit, but careful
230  than OS, irrespective of the indication for splenectomy or the patient's clinical status.
231 ed the risk of splenic injury and incidental splenectomy (OR: 0.58; 95% CI: 0.41-0.80; and OR: 0.41;
232 he optimal timing for this therapy is before splenectomy, or after failure of splenectomy.
233  reference characteristics (no chemotherapy, splenectomy, or radiation therapy; male; attained age 28
234 ced- or conventional-intensity conditioning, splenectomy, or radiotherapy.
235  rates of in-hospital mortality, concomitant splenectomy, or total charges.
236 patients with TI and TM, age (P = 0.001) and splenectomy (P = 0.001) had the strongest association wi
237 ns of patients who received rituximab before splenectomy (P=0.0004).
238                    In patients who underwent splenectomy, perioperative transfusion had no effect on
239 l antibody (Ab), four of whom also underwent splenectomy perioperatively.
240 omy alone (n=14), eculizumab alone (n=5), or splenectomy plus eculizumab (n=5), in addition to plasma
241                     No patients treated with splenectomy plus eculizumab experienced graft loss.
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
244             In the hematologic malignancies, splenectomy produces a significant and longlasting resto
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
247 spitalization, leading to an overall delayed splenectomy rate of 1.2% (36 of 2967 patients).
248 m outcomes, such as readmissions and delayed splenectomy rate, are not well understood.
249                Secondary outcome was delayed splenectomy rate.
250 ivariate regression was performed to compare splenectomy rates, inpatient mortality, and costs betwee
251                                              Splenectomy reproduced antiinflammatory effects of enala
252                                              Splenectomy resulted in a dramatic enhancement of G-CSF-
253               Immunosuppression consisted of splenectomy, Rituximab (Anti-CD20), tacrolimus, sirolimu
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
256                                              Splenectomy should be avoided.
257                                              Splenectomy should be considered safe and efficacious fo
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.
260                In this study, we report that splenectomy significantly reduces systemic HMGB1 release
261 01, 25 consecutive adults with SLE underwent splenectomy specifically for thrombocytopenia.
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
264 ression to assess the adjusted effect of the splenectomy technique on outcomes.
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
268                              The addition of splenectomy to this protocol only modestly added to the
269 mune thrombocytopenia, who had not undergone splenectomy, to receive the standard of care (77 patient
270 ty, rates of perioperative complications and splenectomy, total charges, and length of stay.
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
274   Early partial or complete response rate to splenectomy was 88%.
275 er of > or =8 was observed if the reason for splenectomy was a medical cause or if MCC vaccination oc
276                                              Splenectomy was associated with a higher adjusted risk o
277 nd 50% of children under the age of 6 years; splenectomy was associated with a significant improvemen
278                               Indication for splenectomy was hereditary spherocytosis (111), immune t
279 y developed grade 3 or 4 hematotoxicity, and splenectomy was inversely associated with the incidence
280                                           No splenectomy was needed.
281                              After May 2003, splenectomy was not performed and a protocol that involv
282 protection was abolished in animals in which splenectomy was performed 7 days before VNS and IRI.
283 er an average of 11 days of ST, laparoscopic splenectomy was performed for rescue.
284                                              Splenectomy was performed in 1344 patients (78.4%) for b
285 antation, 88 patients received chemotherapy; splenectomy was performed in 24 patients.
286                                              Splenectomy was performed in 36 of 799 readmitted patien
287 nts, and conventional evisceration including splenectomy was performed in remaining six recipients.
288 D) 3, HLA-DSA remained negative but a rescue splenectomy was performed.
289 ressure monitoring and blood sampling, and a splenectomy was performed.
290                                  Response to splenectomy was rated as: complete (CR: platelets >/=150
291                    The presence of recipient splenectomy was significantly associated with the incide
292 as hampered by ineffective chemotherapy, and splenectomy was the major therapeutic approach to improv
293                                              Splenectomy was then performed.
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
296 ered activity, and the protective effects of splenectomy were of particular interest.
297  with hematologic malignancies who underwent splenectomy were reviewed.
298 5 x 10(9)/L, more previous therapies, and/or splenectomy were somewhat lower.
299                                     Avoiding splenectomy while controlling hypersplenism by using cor
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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