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1.
Clin Exp Hypertens ; 42(6): 512-518, 2020 Aug 17.
Article in English | MEDLINE | ID: mdl-31941385

ABSTRACT

OBJECTIVE: In recent times, new methods of blood pressure measurements have been introduced, including cuffless blood pressure (BP) measurement device using pulse transit time (PTT) for calculation of BP values. However, it is still unknown how values obtained with a new cuffless device compare with standard ambulatory measurements in children. The main aim of the study was to investigate whether BP values measured by a cuffless PTT device are comparable with measurements by a standard upper arm cuff-based BP device. METHODS: Thirty children were prospectively included. Blood pressure measurements using the cuffless device (Somnotouch-NIBP) and cuff-based standard device (Omron 907) were performed simultaneously on the left and right arm. RESULTS: Mean systolic BP of the standard measurements was 123,47 ± 14,91 mmHg and 127,48 ± 15,98 mmHg (p < .001) measured by cuffless method. Mean diastolic BP of the standard ABPM measurements was 66,88 ± 11,86 mmHg and 68,52 ± 12,36 mmHg (p < .001). There were significant positive correlations between standard and cuffless measurements. CONCLUSION: The results show that the created PWV-BP function produces a significant correlation between BP derived from the PWV and the SBP measured by sphygmomanometry. When applying this device in clinical practice, one may keep in mind that the reported mean values over 24 hours, awake and asleep time are not directly interchangeable with cuff-based standard 24-hour BP values. The measured BP values were higher by the new technique. Although differences in SBP between both methods reached values up to 20 mmHg, we think that the development of a cuffless BP monitoring system will provide novel solutions in various medical situations.


Subject(s)
Blood Pressure Determination , Hypertension , Sphygmomanometers , Adolescent , Blood Pressure/physiology , Blood Pressure Determination/instrumentation , Blood Pressure Determination/methods , Blood Pressure Determination/standards , Child , Circadian Clocks/physiology , Electrocardiography/methods , Female , Humans , Hypertension/diagnosis , Hypertension/physiopathology , Male , Photoplethysmography/methods , Pulse Wave Analysis/methods , Sphygmomanometers/classification , Sphygmomanometers/standards
2.
Ther Apher Dial ; 20(6): 639-644, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27786420

ABSTRACT

Patients after a cardiac surgery in cardiopulmonary bypass often present an acute kidney failure. Continuous renal replacement therapy (CRRT) is often required. The aim of this study was to present effectiveness and safety of CRRT with regional citrate anticoagulation (RCA-CRRT) in small children after cardiac surgery. A retrospective analysis was conducted on 15 patients after cardiac surgery and who had RCA-CRRT performed in 2014. The established protocol was followed. Mean time on the RCA-CRRT was 192 h 40 min with the circuit mean lifetime of 43 h 33 min. Clotting was found to be a cause of shutdown in 29% of circuits. No severe electrolyte and metabolic disorders were observed. The RCA-CRRT is a safe procedure for critically ill children with contraindications to the CRRT with heparin anticoagulation. To avoid adverse effects related to metabolic disorders a proper procedure protocol has to be followed.


Subject(s)
Acute Kidney Injury/therapy , Anticoagulants/therapeutic use , Cardiac Surgical Procedures , Citrates/therapeutic use , Postoperative Complications/therapy , Renal Replacement Therapy/methods , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Retrospective Studies , Time , Treatment Outcome
3.
Blood Press ; 21(4): 233-9, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22424480

ABSTRACT

BACKGROUND/AIMS: The aim was to evaluate the level of neutrophil gelatinase-associated lipocalin (NGAL), interleukin 18 (IL-18) and retinol binding protein (RBP) in children with primary hypertension and no features of hypertensive nephropathy. METHODS: The study group consisted of 19 children (15 males) aged 14.8 ± 2.18 years with primary hypertension. Estimated glomerular filtration rate (eGFR) and albumin/creatinine ratio (ACR) were within the normal range. Mean blood pressure (BP) was 141/79 mmHg (mean systolic BP percentile was 98, mean diastolic BP percentile was 80). Ambulatory BP measurement (ABPM), blood and urine biochemical measurements and features of end organ damage were assessed. The control group consisted of 20 healthy children. RESULTS: Hypertensive children showed significantly increased serum and urine NGAL concentration vs controls. Urine RBP was significantly higher in the study group vs controls. A positive correlation was found between urine NGAL and the index of mean systolic BP measured in ABPM, between urine IL-18 and the index of office diastolic BP, between serum NGAL and ACR, and between urine NGAL concentration and serum HDL. CONCLUSION: In children with primary hypertension, increased serum and urine NGAL may reflect kidney injury earlier than typical markers of hypertensive nephropathy.


Subject(s)
Acute-Phase Proteins/metabolism , Hypertension/metabolism , Interleukin-18/metabolism , Kidney Diseases/diagnosis , Lipocalins/metabolism , Proto-Oncogene Proteins/metabolism , Retinol-Binding Proteins/metabolism , Adolescent , Biomarkers/metabolism , Child , Female , Humans , Hypertension/complications , Kidney Diseases/etiology , Lipocalin-2 , Male , Pilot Projects , Prognosis
4.
J Nephrol ; 25(6): 1060-6, 2012.
Article in English | MEDLINE | ID: mdl-22322817

ABSTRACT

BACKGROUND: The aim of our study was to analyze the efficacy and safety of rituximab, a chimeric monoclonal antibody against CD20 lymphocytes, as a nonstandard immunosuppressive therapy in children with different types of primary glomerulonephritis who were not eligible for routine treatment. METHODS: The study group was composed of 16 children with proteinuric glomerulopathies, not responding to standard immunosuppressive therapy. The indications included steroid-resistant nephrotic syndrome (n=14) and steroid-dependent nephrotic syndrome (n=2). The dose of rituximab was established as 375 mg/m2 of body surface area, administered by intravenous infusion once weekly for 1 to 4 weeks, depending on the CD19 lymphocyte count. We evaluated proteinuria and plasma concentration of CD19 lymphocytes at intervals of 1, 3 and 6 months, after which patients received a single repeat dose. RESULTS: Remission, defined as proteinuria less than 150 mg per 24 hours, was observed in 7 of the 16 children. There were no statistically significant differences in leukocyte counts between single and multiple rituximab doses. We also did not observe any clinical or biochemical side effects. CONCLUSIONS: In conclusion, we postulate that alternative rituximab therapy should be taken into consideration in nephrotic patients not responding to standard therapy.


Subject(s)
Antibodies, Monoclonal, Murine-Derived/therapeutic use , Glomerulonephritis/drug therapy , Immunosuppressive Agents/therapeutic use , Adolescent , Age Factors , Antibodies, Monoclonal, Murine-Derived/administration & dosage , Antibodies, Monoclonal, Murine-Derived/adverse effects , Antigens, CD19/blood , Biomarkers/blood , Child , Drug Administration Schedule , Drug Dosage Calculations , Drug Monitoring , Female , Glomerulonephritis/blood , Glomerulonephritis/immunology , Humans , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/adverse effects , Infusions, Intravenous , Lymphocyte Count , Lymphocytes/drug effects , Lymphocytes/immunology , Male , Nephrotic Syndrome/drug therapy , Proteinuria/drug therapy , Remission Induction , Rituximab , Time Factors , Treatment Outcome
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