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1.
Physiol Meas ; 43(7)2022 07 18.
Article in English | MEDLINE | ID: mdl-35724646

ABSTRACT

Objective.Fetal heart rate (FHR) is an important parameter for assessing fetal well-being and is usually measured by doppler ultrasound. Fetal phonocardiography can provide non-invasive, easy-to-use and passive alternative for fetal monitoring method if reliable FHR measurements can be made even in noisy clinical environments. Therefore, this work presents an automatic algorithm to determine FHR from the fetal heart sound recordings in a noisy clinical environment.Approach.Using an electronic stethoscope fetal heart sounds were recorded from the expecting mother's abdomen, during weeks 30-40 of their pregnancy. Of these, 60 recordings were analyzed manually by two observers to obtain reference heart rate measurement. An algorithm was developed to determine FHR using envelope detection and autocorrelation of the signals. Algorithm performance was improved by implementing peak validation algorithm utilizing knowledge of valid FHR from prior windows and power spectral density function. The improvements in accuracy and reliability of algorithm were measured by mean absolute error (MAE) and positive percent agreement.Main results.By including the validation step, the MAE reduced from 11.50 to 7.54 beats per minute and positive percent agreement improved from 81% to 87%.Significance.We classified the recordings into good, moderate and poor quality to understand how the algorithm works in each of the case. The proposed algorithms provide good accuracy overall but are sensitive to the noises in recording environment that influence the quality of the signals.


Subject(s)
Fetal Monitoring , Heart Rate, Fetal , Algorithms , Female , Fetal Monitoring/methods , Heart Rate , Heart Rate, Fetal/physiology , Humans , Phonocardiography/methods , Pregnancy , Reproducibility of Results
2.
Blood Adv ; 4(16): 3943-3951, 2020 08 25.
Article in English | MEDLINE | ID: mdl-32822484

ABSTRACT

Neurotoxicity or immune effector cell-associated neurotoxicity syndrome (ICANS) is the second most common acute toxicity after chimeric antigen receptor (CAR) T-cell therapy. However, there are limited data on the clinical and radiologic correlates of ICANS. We conducted a cohort analysis of 100 consecutive patients with relapsed or refractory large B-cell lymphoma (LBCL) treated with standard of care axicabtagene ciloleucel (axi-cel). ICANS was graded according to an objective grading system. Neuroimaging studies and electroencephalograms (EEGs) were reviewed by an expert neuroradiologist and neurologist. Of 100 patients included in the study, 68 (68%) developed ICANS of any grade and 41 (41%) had grade ≥3. Median time to ICANS onset was 5 days, and median duration was 6 days. ICANS grade ≥3 was associated with high peak ferritin (P = .03) and C-reactive protein (P = .001) levels and a low peak monocyte count (P = .001) within the 30 days after axi-cel infusion. Magnetic resonance imaging was performed in 38 patients with ICANS and revealed 4 imaging patterns with features of encephalitis (n = 7), stroke (n = 3), leptomeningeal disease (n = 2), and posterior reversible encephalopathy syndrome (n = 2). Abnormalities noted on EEG included diffuse slowing (n = 49), epileptiform discharges (n = 6), and nonconvulsive status epilepticus (n = 8). Although reversible, grade ≥3 ICANS was associated with significantly shorter progression-free (P = .02) and overall survival (progression being the most common cause of death; P = .001). Our results suggest that imaging and EEG abnormalities are common in patients with ICANS, and high-grade ICANS is associated with worse outcome after CAR T-cell therapy in LBCL patients.


Subject(s)
Neurotoxicity Syndromes , Posterior Leukoencephalopathy Syndrome , Antigens, CD19/therapeutic use , Biological Products , Humans , Immunotherapy, Adoptive , Neurotoxicity Syndromes/diagnostic imaging , Neurotoxicity Syndromes/etiology
3.
Am J Clin Nutr ; 109(4): 1064-1070, 2019 04 01.
Article in English | MEDLINE | ID: mdl-30982859

ABSTRACT

BACKGROUND: The 2007 World Health Organization/Food and Agriculture Organization/United Nations University (WHO/FAO/UNU) recommendation for the Estimated Average Requirement (EAR) of additional protein during pregnancy for a gestational weight gain (GWG) of 12 kg (recalculated from a GWG of 13.8 kg) is 6.7 and 21.7 g/d in the second and the third trimester, respectively. This EAR is based on measurements of potassium accretion in high-income country (HIC) pregnant women. It is not known if low- to middle-income country, but well-nourished, pregnant women have comparable requirements. OBJECTIVE: We aimed to estimate total body potassium (TBK) accretion during pregnancy in Indian pregnant women, using a whole-body potassium counter (WBKC), to measure their additional protein EAR. METHODS: Well-nourished pregnant women (20-40 y, n = 38, middle socioeconomic stratum) were recruited in the first trimester of pregnancy. Anthropometric, dietary, and physical activity measurements, and measurements of TBK using a WBKC, were performed at each trimester and at birth. RESULTS: The mid-trimester weight gain was 2.7 kg and 8.0 kg in the second and the third trimester, respectively, for an average 37-wk GWG of 10.7 kg and a mean birth weight of 3.0 kg. Protein accretion was 2.7 and 5.7 g/d, for an EAR of 8.2 and 18.9 g/d in the second and the third trimester, respectively. The additional protein EAR, calculated for a GWG of 12 kg, was 9.1 and 21.2 g/d in the second and the third trimester, respectively. CONCLUSION: The additional protein requirements of well-nourished Indian pregnant women for a GWG of 12 kg in the second and third trimesters were similar to the recalculated 2007 WHO/FAO/UNU requirements for 12 kg.


Subject(s)
Dietary Proteins/metabolism , Potassium/metabolism , Pregnancy/metabolism , Adolescent , Adult , Body Mass Index , Diet , Dietary Proteins/analysis , Female , Gestational Weight Gain , Humans , India , Potassium/analysis , Pregnancy Trimesters/metabolism , Prenatal Nutritional Physiological Phenomena , Young Adult
4.
J Clin Oncol ; 24(36): 5672-9, 2006 Dec 20.
Article in English | MEDLINE | ID: mdl-17179102

ABSTRACT

PURPOSE: Raf kinase inhibitor protein (RKIP) inhibits the Raf and nuclear factor kappa B signaling pathways, and suppresses metastasis in animal models. We examined whether RKIP expression in primary colorectal cancers (CRCs) correlates with the risk of metastasis and overall survival. PATIENTS AND METHODS: RKIP expression was examined immunohistochemically in three separate cohorts: a tissue microarray containing 276 samples from human tumors and normal tissues, and retrospective studies of 268 CRC patients and 65 early-stage CRCs. Overall and metastasis-free survival rates were measured. RESULTS: RKIP was expressed in normal epithelia but was reduced in metastatic tumors. RKIP expression in primary CRC was an independent prognostic marker for survival using multivariate Cox regression analysis (hazard ratio, 2.808; 95% CI, 1.58 to 4.96; P = .0002), independent of Dukes' stage. Patients with Dukes' C RKIP-positive tumors had similar 5-year survival rates as early-stage patients if tumors had equivalent RKIP expression levels. An independent study of early-stage CRCs confirmed that reduced RKIP expression predicted metastatic recurrence and reduced disease-free survival (hazard ratio, 4.5; 95% CI, 1.7 to 12.3; P = .003). RKIP expression was independent of sex, age, mitotic index, lymphatic and vascular invasion, depth of invasion, and tumor site, but correlated positively with apoptotic index (P = .024). Weak or loss of RKIP expression was the most significant and independent prognostic marker using a multivariate regression equation (hazard ratio, 4.5; 95% CI, 1.7 to 12.3; P = .003). CONCLUSION: RKIP expression in primary CRCs correlates with overall and disease-free survival, and can be useful for identifying early-stage CRC patients at risk of relapse.


Subject(s)
Colorectal Neoplasms/metabolism , Colorectal Neoplasms/mortality , Phosphatidylethanolamine Binding Protein/metabolism , Adult , Aged , Aged, 80 and over , Cohort Studies , Colorectal Neoplasms/pathology , Disease-Free Survival , Female , Gene Expression Profiling , Humans , Immunohistochemistry , Male , Middle Aged , Neoplasm Metastasis , Neoplasm Recurrence, Local , Neoplasm Staging , Phosphatidylethanolamine Binding Protein/genetics , Retrospective Studies , Risk Assessment
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