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Bone Marrow Examination

Bone Marrow Examination: A comprehensive diagnostic procedure that evaluates the cellular composition and function of bone marrow.
This examination provides crucial insights into hematological disorders, cancer metastasis, and other medical conditions.
PubCompare.ai, an AI-driven platform, can elevate this process by helping researchers and clinicians locate the best protocols from literature, pre-prints, and patents.
Leverage data-driven comparisons to optimize your research and identify the most effective protocols and products for bone marrow examinations.

Most cited protocols related to «Bone Marrow Examination»

Enrolled patients were randomly assigned, in a 1:1 ratio, to receive standard chemotherapy plus either midostaurin or placebo. Randomization was performed with a block size of 6 and was stratified according to the subtype of FLT3 mutation: TKD, or ITD with either a high ratio (>0.7) or a low ratio (0.05 to 0.7) of mutant to wild-type alleles (ITD [high] and ITD [low], respectively).
Therapy consisted of induction therapy with daunorubicin (at a dose of 60 mg per square meter of body-surface area per day, administered by rapid intravenous injection on days 1, 2, and 3) and cytarabine (at a dose of 200 mg per square meter, administered by continuous intravenous infusion on days 1 through 7). Midostaurin or placebo was administered in a double-blind fashion, at a dose of 50 mg orally twice daily, on days 8 through 21. Midostaurin or placebo was not administered if the patient had a corrected QT interval above 500 msec or a grade 3 or 4 non-hematologic toxic effect (for further details, see the Supplementary Appendix). A missed dose of midostaurin or placebo was not made up. A bone marrow examination was to be performed on day 21. If there was definitive evidence of clinically significant residual leukemia, a second cycle of induction therapy that was identical to the first, including midostaurin or placebo, was administered.
Patients who achieved complete remission after induction therapy received four 28-day cycles of consolidation therapy with high-dose cytarabine (at a dose of 3000 mg per square meter, administered over a period of 3 hours every 12 hours on days 1, 3, and 5). Midostaurin or placebo was administered at a dose of 50 mg orally twice daily on days 8 through 21. Patients who remained in remission after completion of consolidation therapy entered a maintenance phase in which they received midostaurin or placebo, administered at a dose of 50 mg orally twice daily, for twelve 28-day cycles. Complete remission was defined as the presence of less than 5% blasts in the marrow or extramedullary leukemia, an absolute neutrophil count of more than 1000 per microliter, a platelet count of more than 100,000 per microliter, and the absence of blasts in the peripheral blood; in addition, per protocol, the complete remission had to have occurred by day 60. Transplantation was not mandated in the protocol but was performed at the discretion of the investigator.
Publication 2017
Alleles BLOOD Body Surface Area Bone Marrow Examination Cytarabine Daunorubicin FLT3 protein, human Intravenous Infusion Leukemia Marrow midostaurin Mutation Neoadjuvant Therapy Neutrophil Patients Pharmacotherapy Placebos Platelet Counts, Blood Remission Induction Therapeutics Transplantation
Eligible patients were either untreated or had no more than one cycle of prior therapy for symptomatic MM fulfilling CRAB criteria. Subjects up to the age of 75 years were eligible, provided they had adequate cardio-pulmonary functions; liver function tests could not exceed twice normal values. Treatment assignment was done once GEP results were available.
In addition to commonly employed MM marker analysis and bone marrow morphological examinations, we documented GEP70-based risk scores and molecular subgroups as well as fluorescence in situ hybridization-based del17p.12 (link) Seventy-four patients were screened, of whom 50 were eligible for the enrollment into the study; 24 patients treated on the protocol were excluded from the final analysis because they were classified as low risk by GEP70. The treatment consisted of eight-drug combinations for induction (M-VTD-PACE; melphalan, bortezomib, thalidomide, dexamethasone; and four-day continuous infusions of cisplatin, doxorubicin, cyclophosphamide, etoposide), both transplants (MEL80-VRD-PACE (R, lenalidomide)), and two inter-transplant cycles with Mel20-VTD-PACE; followed by 3 years of maintenance with VRD (V=bortezomib, R=lenalidomide, D= dexamethasone) alternating with VMD (M=melphalan) (Figure 1). Owing to cumulative hematological toxicity from the VMD component seen with the first patients initiating the maintenance phase, VRD was later employed as the sole maintenance, with provision for bortezomib escalation to 1.5 mg/m2 weekly and of lenalidomide to 25 mg for 21 days of a 28-day cycle. The protocol and its revisions had been approved by the institutional review board. All patients signed a written informed consent acknowledging the investigational nature of the protocol, in keeping with institutional, federal and Helsinki Declaration guidelines. A Data Safety and Monitoring Board conducted annual reviews. A team of experts provided semiannual audits for protocol adherence, toxicities and efficacy data. Toxicities were graded according to Version 3 of the NCI Common Terminology Criteria for Adverse Events.
Publication 2016
Bone Marrow Examination Bortezomib Brachyura Cisplatin Clinical Trials Data Monitoring Committees Cyclophosphamide Dexamethasone Doxorubicin Drug Combinations Ethics Committees, Research Etoposide Fluorescent in Situ Hybridization Grafts Lenalidomide Liver Function Tests Lung Melphalan Patients Thalidomide Vision
Primary end points were safety and tolerability (phase Ib) and CR rate of pola-BR
versus BR (phase II), as measured by [18F]fluorodeoxyglucose positron
emission tomography-computed tomography (PET-CT) using modified Lugano Response
Criteria22 (link) (Appendix,
online only) at the end of treatment (EOT; 6-8 weeks after cycle 6 day 1 or last
dose of study treatment) by an independent review committee (IRC). If no scans
were performed, the IRC considered the patient missing or unevaluable and he or
she was treated as a nonresponder. Secondary end points included ORR at EOT,
best overall response, DOR, and PFS as assessed by the IRC. Exploratory end
points included biomarker evaluation of efficacy by cell of origin (COO),
determined by either NanoString (NanoString Technologies, Seattle, WA) or Hans
criteria, and immunohistochemical staining for DEL, investigator-assessed (INV)
DOR and PFS, and OS.
Responses were assessed by CT, PET-CT, and bone marrow examination (if required
to confirm CR) after 3 cycles (interim) and at EOT (primary response
assessment). Follow-up CT scans were performed every 6 months for 2 years or
until progressive disease (PD) or patient withdrawal.
The National Cancer Institute Common Terminology Criteria for Adverse Events
(version 4.03) was used to assess and grade all adverse events (AEs) throughout
the study. All AEs, including serious AEs (SAEs), were reported from cycle 1 day
1 until 90 days after last dose of study drug, regardless of relationship to
treatment. All SAEs were reported indefinitely.
Publication 2019
Biological Markers Bone Marrow Examination Cells F18, Fluorodeoxyglucose Patients Safety Tomography X-Ray Computed Tomography

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Publication 2019
Adrenal Cortex Hormones Adult Blood Platelets Bone Marrow Examination Cells Compassionate Use Conferences Creatinine Cytotoxin Eligibility Determination End Stage Liver Disease Ethics Committees, Research Females Fever Fibrinogen Deficiency Hemoglobin Hepatic Insufficiency Hepatitis C virus HIV Infections Hyperferritinemia Hypertriglyceridemia Interleukin 2 Receptor Involuntary Treatment Kidney Failure Liver Cirrhosis Lymphohistiocytosis, Hemophagocytic Malabsorption Syndrome Malignant Neoplasms Megakaryocytes Natural Killer Cells Neutrophil Patient Participation Patients ruxolitinib Safety Syndrome, Myelodysplastic Thrombocytopenia Tissues
The details of this cohort and their natural history have been described previously.8 (link) In brief, we identified 1395 persons with MGUS who resided in the 11 counties of southeastern Minnesota and who had a serum M protein concentration of 3 g per deciliter or less and 10% or fewer plasma cells in the bone marrow (if assessed). Patients with light-chain MGUS were not included, since this entity was defined after the establishment of the cohort at the inception of the study.9 (link) In accordance with our clinical practice, bone marrow examination was deemed unnecessary unless the patient had unexplained anemia, renal insufficiency, or bone pain. The patients were evaluated at the Mayo Clinic from January 1, 1960, through December 31, 1994. A total of 11 patients who had previously signed a form prohibiting review of their medical records for any type of research at the Mayo Clinic were excluded.8 (link),10 (link) Of the remaining 1384 patients, 514 (37%) resided in Olmsted County, which had a population of 92,006 persons in 1980, and the remaining 870 patients resided in the other counties of southeastern Minnesota (1980 population, 312,559 persons). The medical-records-linkage system of the Rochester Epidemiology Project11 (link) makes it possible to obtain complete case ascertainment among the residents of Olmsted County.
Follow-up included the review of each patient’s inpatient and outpatient medical records at the Mayo Clinic and the review of death certificates for patients who had died. Death certificates can be currently obtained from only 10 states; however, in almost all other patients we were able to ascertain survival status by contacting the patient’s family or primary care physician. For the purposes of this study, the follow-up of the original cohort was extended by more than 15 years to December 31, 2015; this change yielded an increase by a factor of 1.3 in the number of person-years of follow-up and in the number of observed progressions.
The M proteins were identified and quantitated by means of cellulose acetate or agarose-gel electrophoresis.12 If there was an abnormal band or equivocal pattern, immunoelectrophoresis or immunofixation was performed to confirm the presence of M protein and to ascertain the type. Patients were advised to undergo serum protein electrophoresis annually.
There was no commercial funding for this study. All the authors participated in the study concept, study design, and data collection; two of the authors conducted the data analysis. The authors vouch for the accuracy of the data and analyses presented and for the fidelity of the study to the protocol.
Publication 2018
acetylcellulose Anemia Bone Marrow Cells Bone Marrow Examination Bones Disease Progression Electrophoresis Electrophoresis, Agar Gel factor A Immunoelectrophoresis Inpatient Monoclonal Gammopathy of Undetermined Significance M protein, multiple myeloma Pain Patients Plasma Primary Care Physicians Renal Insufficiency Serum Proteins TNFSF14 protein, human

Most recents protocols related to «Bone Marrow Examination»

After review by the hospital’s institutional review committee, the patients were exempted from the requirement to obtain informed consent. We retrospectively analysed the CT and MRI data of 399 patients with thoracic/lumbar compression fractures diagnosed and treated in our hospital between April 2016 and April 2022. The inclusion criteria were as follows: ① diagnosis of benign VCFs, including traumatic or osteoporotic fractures; and ② complete original data, including CT and MRI vertebral examinations, with an interval between the two examinations of less than 3 days. Exclusion criteria: ① suspected infection or tumour-related pathological fractures; ② poor image quality or presence of foreign body artifacts; ③ patients with uncertain health status or acute or chronic VCFs. Acute VCFs was defined as sudden onset of chest and back pain and bone marrow oedema within 4 weeks of MRI examination [16 ]. The chronic phase was defined as the absence of bone marrow oedema, which was evaluated by two senior doctors with 6 years and 10 years of experience in skeletal and muscle imaging who made a diagnosis of acute or chronic VCFs. When their results are inconsistent, a final conclusion will be reached through their consultation. The detailed screening process is shown in Fig. 1. The flowchart and DLR workflow of this study (Figs. 2 and 3) shows the case collection and grouping, image preprocessing, feature extraction, feature analysis, and model construction. Patients were randomly allocated to training and test cohorts in an 8:2 ratio.

Flow chart of study inclusion

Study flowchart

Deep learning radiomics workflow

Publication 2023
Back Pain Bone Marrow Bone Marrow Examination Chest COF protocol Diagnosis Edema Foreign Bodies Fracture, Compression Infection Lumbar Region Muscle Tissue Neoplasms Osteoporotic Fractures Pathological Fracture Patients Physical Examination Physicians Skeleton Vertebra
From July 2016 to June 2021, a total of 80 patients with the first diagnosed AML were recruited in this research. The inclusion criteria were as follows: (i) first diagnosed with AML by morphology, immunology, cytogenetics, and molecular biology of bone marrow (MCIM); (ii) > 18 years old; (iii) willing to provide bone marrow (BM). Patients complicated with BM failure syndromes or other cancers were excluded. Besides, a total of 20 patients who were diagnosed with non‐myelodysplasia hematologic malignancies and needed BM examination were enrolled as disease controls (DCs). Furthermore, a total of 20 healthy donors (HDs) were enrolled during the same period when they were examined for eligibility for bone marrow transplantation. This study received the approval of the Ethics Committee. Written informed consent was obtained from all subjects or their guardians.
Publication 2023
Bone Marrow Bone Marrow Examination Bone Marrow Failure Disorders Bone Marrow Transplantation Donors Eligibility Determination Ethics Committees Hematologic Neoplasms Legal Guardians Malignant Neoplasms Patients Syndrome, Myelodysplastic
Travel history, family history, clinical history, serology, and vaccination were reviewed with a structured form at admission. The treatment of ITP was based on institutional protocols and physician preference. If a bone marrow examination showed no malignancy or megakaryocytic hypoplasia and patients did not have a severe infection, methylprednisolone was administered in doses of 30 mg/kg (maximum 1 g) for three consecutive days [25 (link),26 (link),27 (link)].
If patients had minor bleeding symptoms or had not been hospitalized, they did not routinely require treatment or were given oral prednisolone 2 mg/kg/day at the outpatient clinic, tapering off in 3–4 weeks [28 (link)]. If patients had severe bleeding or if bone marrow pathology had not yet been excluded, treatment with intravenous immunoglobulin (IVIG) 0.4 mg/kg/day for five consecutive days or 1 g/kg for two days was administered [25 (link),29 (link),30 (link)].
After initial management, patients were scheduled for a follow-up appointment. The institutional follow-up protocols suggest follow-up platelet counts weekly for 1 month after diagnosis, then monthly for 1–6 months, and finally every 3 months for 7–12 months after diagnosis. However, if patients’ platelet counts do not recover, they are continuously followed up according to the judgment of the physician, even up to 10 years after diagnosis.
Publication 2023
Bone Marrow Bone Marrow Examination Diagnosis hypoplasia Immunoglobulins Infection Intravenous Immunoglobulins Intravenous Infusion Malignant Neoplasms Megakaryocytes Methylprednisolone Patients Physicians Platelet Counts, Blood Prednisolone Vaccination
Cats were considered to be eligible for inclusion if they presented with a neutropenia (neutrophil concentration <2.5 × 109/L) or thrombocytopenia (<150 × 109/L), or both with or without anemia (hematocrit or packed cell volume <27%) between February 1st and December 11th 2021. Additionally, cats had to have had exposure to 1 of the recalled diets as well as undergone microscopic bone marrow examination of diagnostic quality.
Data collected included date of presentation, signalment, duration and type of clinical signs, indoor/outdoor status, laboratory and body cavity imaging findings, bone marrow examination results, feline immunodeficiency, feline leukemia and feline panleukopenia virus testing results, other diagnostics and dietary information for each cat affected.
Publication 2023
Anemia Bone Marrow Bone Marrow Examination Dental Caries Diagnosis Diet Dietary Exposure Felidae Immunologic Deficiency Syndromes Leukemia, Feline Leukopenia Microscopy Neutrophil Thrombocytopenia Virus, Feline Panleukopenia Volumes, Packed Erythrocyte
The primary outcomes of the study were survival, acute and chronic GVHD, cytomegalovirus (CMV) infection, Epstein–Barr virus (EBV) infection, and relapse. Acute and chronic GVHD was diagnosed and graded using the modified Glucksberg system and the 2014 National Institutes of Health Chronic GVHD Diagnosis and Staging Consensus Recommendations [21 (link),22 (link)]. CMV infection was defined by detecting viral protein or CMV DNA in plasma or serum [23 (link)]. EBV infection was defined when viral protein or EBV DNA was detected [24 (link)]. Relapse was defined via bone marrow examinations and short tandem repeat-based techniques. One-year survival, 5-year survival, and 10-year survival were calculated from the date of HSCT to the date of the last follow-up or death by any cause. The last follow-up of the survivors was censored at 365 days for 1-year survival, at 1825 days for 5-year survival, and at 3650 days for 10-year survival.
The second outcomes of the study were transfusion and engraftment. Transfusion was measured for the requirement of Hb and PLT transfusion. Neutrophil engraftment was defined as the first day when the absolute neutrophil count was more than 0.5 × 109/L for 3 consecutive days. PLT engraftment was defined as the first day when the PLT count was more than 20 × 109/L for 7 consecutive days without PLT transfusion.
Publication 2023
Blood Transfusion Bone Marrow Examination Cytomegalovirus Cytomegalovirus Infections Diagnosis Epstein-Barr Virus Epstein-Barr Virus Infections Neutrophil Plasma Relapse Serum Short Tandem Repeat Survivors Viral Proteins

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More about "Bone Marrow Examination"

Bone marrow examination, also known as bone marrow aspiration or biopsy, is a crucial diagnostic procedure that provides valuable insights into various hematological disorders, cancer metastasis, and other medical conditions.
This comprehensive evaluation assesses the cellular composition and function of the bone marrow, a critical component of the body's blood and immune system.
The process involves the extraction of a small sample of bone marrow, typically from the hip or breastbone, for analysis.
Clinicians and researchers may utilize a range of advanced techniques and tools to enhance the bone marrow examination process, such as flow cytometry (e.g., Navios), immunohistochemistry (e.g., Anti-CD68 antibody, Anti-CD138, Anti-MUM1), and statistical analysis software (e.g., SPSS version 22.0).
PubCompare.ai, an innovative AI-driven platform, can elevate the bone marrow examination process by helping researchers and clinicians locate the best protocols from literature, pre-prints, and patents.
This data-driven approach allows for the optimization of research and the identification of the most effective protocols and products for bone marrow examinations.
By leveraging the insights gained from the bone marrow examination, healthcare professionals can make more informed decisions, improve patient outcomes, and advance our understanding of various medical conditions, including leukemia, lymphoma, and metastatic cancers.
The combination of advanced techniques, cutting-edge tools, and data-driven platforms like PubCompare.ai can revolutionize the way bone marrow examinations are conducted and interpreted, leading to more precise diagnoses and more effective treatment strategies.