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1.
Clin Chim Acta ; : 119848, 2024 Jul 06.
Article in English | MEDLINE | ID: mdl-38977168

ABSTRACT

The harmonization of laboratory biomarkers is pivotal in ensuring consistent and reliable diagnostic outcomes across different clinical settings. This systematic review examines the harmonization of C-Reactive Protein (CRP) and N-Terminal Prohormone of Brain Natriuretic Peptide (NT-proBNP) measurements, both of which are jointly utilized in the diagnosis and management of cardiovascular diseases. To identify relevant studies, we searched the PubMed electronic database using specific medical subject headings and keywords such as C-Reactive Protein, CRP, high sensitivity C-Reactive Protein (hs-CRP), N-terminal pro B-type natriuretic peptide, and NT-proBNP, focusing on publications from June 1 to September 26, 2021. The query filtered studies to include only those in English involving human subjects. From our search, 97 articles met the inclusion criteria and were included for in-depth analysis. Despite their widespread use, significant variability remains in the measurements of CRP and NT-proBNP due to a lack of standardized pre-analytical, analytical, and post-analytical practices. This review highlights the consequences of this variability on clinical decision-making and patient outcomes and emphasizes the need for international standards and guidelines to achieve better harmonization. Our findings advocate for the establishment of universal protocols to enhance the reliability of these biomarker measurements across different clinical environments, ensuring improved healthcare delivery.

2.
Trop Med Int Health ; 28(3): 226-231, 2023 03.
Article in English | MEDLINE | ID: mdl-36647788

ABSTRACT

OBJECTIVES: Parvovirus B19 (B19V) infection in pregnancy is generally asymptomatic, but in about 3% it can cause complications, including miscarriage, severe foetal anaemia and foetal hydrops. The seroprevalence in pregnancy ranges from 20% to 82% in Africa, but there are no data for Benin. We therefore retrospectively assessed the seroprevalence of B19V in pregnant women attending the Saint Jean de Dieu Hospital in Tanguiéta, a rural district of Atacora, in northern Benin. METHODS: We searched for anti-B19V immunoglobulin M (IgM) and immunoglobulin G (IgG) antibodies in 227 sequential sera from as many women (mean age 26.3 years, range: 16-41) of whom 30 were in the first trimester, 66 in the second and 131 in the third. Samples that tested positive for IgM were analysed with an immunoblot test and the viral genome (DNA-B19V) was searched for using a polymerase chain reaction. RESULTS: Of the 227 women, 153 (67.4%) were positive for IgG anti-B19V, 7 (3.1%) for IgM and 73 (32.2%) were non-immune. Six IgM-positive women were also IgG positive. The difference in IgG seroprevalence between trimesters or ages was not statistically significant. Of the seven IgM-positive samples, three were confirmed positive by immunoblot (of which two were DNA-B19V positive), three were indeterminate (DNA-B19V negative) and one was negative (DNA-B19V negative). Of the three women with confirmed positive IgM, two were in the third trimester and one in the second trimester of pregnancy. CONCLUSIONS: The seroprevalence of anti-B19V IgG among pregnant women in Benin is high and in line with those reported in some African countries. IgM seroprevalence is also similar to that described in some African countries in non-epidemic periods. The low viral load observed depicts non-acute infections, but it is difficult to establish the precise time of the infection, especially for women tested in the second or third trimester of pregnancy, when the observed viremia could be a sign of an acute infection that occurred in the previous trimester. Consequently, clinical follow-up and further investigations to highlight possible foetal consequences are indicated.


Subject(s)
Abortion, Spontaneous , Parvoviridae Infections , Parvovirus B19, Human , Female , Pregnancy , Humans , Adult , Pregnant Women , Parvovirus B19, Human/genetics , Benin , Prevalence , Seroepidemiologic Studies , Retrospective Studies , Parvoviridae Infections/complications , Parvoviridae Infections/diagnosis , Immunoglobulin G , Immunoglobulin M , Antibodies, Viral , DNA, Viral
3.
Blood Transfus ; 18(2): 106-116, 2020 03.
Article in English | MEDLINE | ID: mdl-31855149

ABSTRACT

BACKGROUND: Moderate to severe iron deficiency anaemia is a common finding in patients admitted to the Emergency Department (ED). According to Patient Blood Management principles, intravenous iron should be the therapy of choice instead of blood transfusion for selected cases affected by chronic iron deficiency anaemia. However, this option is only rarely taken into account by physicians in the ED. As a result, in many circumstances, treatment of iron deficiency anaemia in the ED can differ from that of the Anaemia Clinic. With the aim of reducing inappropriate transfusions, and to implement intravenous iron usage, we shared a specific protocol with the ED. MATERIAL AND METHODS: We reviewed the medical records of all subjects admitted to the ED (n=267, Post-protocol group) with hemoglobin ≤9.0 g/dL and mean corpuscular volume <80 fL in a 13-month period, except if the massive transfusion protocol was activated, and results were compared with an equivalent Pre-protocol historical cohort (n=226). RESULTS: In comparison with the Pre-protocol series, the number of patients transfused did not change, but the appropriateness in terms of transfusion and red blood cell volume transfused improved sharply (87.0 vs 13.3%; p<0.001) with a significant increase in intravenous iron administration (50.2 vs 4.4% of cases; p<0.001). As a positive consequence, both the time spent in the ED by patients who were then directly discharged and costs per subject treated dropped by 37.9% and 59.0%, respectively. Treatment with infusion only in comparison with transfusion only led to a statistically significant Relative Risk reduction in transfusion on the ward and post-discharge transfusion of 55.6% and 44.4%, respectively. DISCUSSION: The implementation of Patient Blood Management principles and early intravenous iron therapy in the Emergency Department have proved to be effective tools to optimise resources both in terms of units transfused and costs.


Subject(s)
Anemia, Iron-Deficiency/therapy , Erythrocyte Transfusion , Iron/therapeutic use , Administration, Intravenous/economics , Aged , Aged, 80 and over , Anemia, Iron-Deficiency/economics , Costs and Cost Analysis , Emergency Medical Services/economics , Emergency Service, Hospital/economics , Erythrocyte Transfusion/economics , Female , Health Care Costs , Hospitalization/economics , Humans , Iron/administration & dosage , Iron/economics , Length of Stay/economics , Male
4.
J Cardiovasc Med (Hagerstown) ; 11(5): 359-64, 2010 May.
Article in English | MEDLINE | ID: mdl-20051875

ABSTRACT

OBJECTIVES: The aim of this study was to describe the time course of NT pro-B-type natriuretic peptide (NT pro-BNP) levels in patients with large anterior ST-segment elevation myocardial infarction (STEMI) treated with primary angioplasty (PPCI) and to investigate the relationship between these values and both microvascular reperfusion and left ventricular (LV) function. BACKGROUND: The clinical efficacy of PPCI is largely dependent on the achievement of microvascular reperfusion. Myocardial blush is an angiographic method to evaluate the presence of effective reperfusion after PPCI. NT pro-BNP is a biomarker of LV stress whose levels are also related to clinical outcome in STEMI. METHODS: We studied 84 patients with large anterior STEMI treated with PPCI. NT pro-BNP was measured at baseline, after 2 days (day 2) and 7 days (day 7). Echocardiographic LV ejection fraction (LVEF) was measured at baseline, day 7 and after 6 months. Myocardial blush was graded immediately after PPCI. RESULTS: NT pro-BNP increased from admission to day 2 and decreased from day 2 to day 7 in patients with significant myocardial blush (grade 2-3) as well as in patients with 0-1 myocardial blush. However, in the latter group median NT pro-BNP levels globally increased from admission to day 7, whereas they decreased in patients with significant myocardial blush. Moreover, in such patients LVEF was higher at all time points than in patients with a grade 0-1 myocardial blush. CONCLUSION: This study shows that the time course of NT pro-BNP in the first week after an anterior STEMI is dependent on the effectiveness of microvascular reperfusion assessed after PPCI and reflects the evolution of LVEF over time.


Subject(s)
Angioplasty, Balloon, Coronary , Myocardial Infarction/blood , Myocardial Reperfusion , Natriuretic Peptide, Brain/blood , Peptide Fragments/blood , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Stroke Volume
5.
Chest ; 134(1): 101-8, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18403669

ABSTRACT

BACKGROUND: We investigated the role of the clinical pulmonary infection score (CPIS), serum levels of procalcitonin (PCT), C-reactive protein (CRP), and serum amyloid A (SAA) in the detection of patients with early ventilator-associated pneumonia (VAP). METHODS: Observational study in a university hospital. In 58 patients with severe brain injury receiving mechanical ventilation, CPIS, PCT, CRP and SAA were evaluated at ICU entry and at days 3 to 4 of hospital stay for VAP diagnosis (confirmed by endotracheal aspirate or BAL cultures). RESULTS: We found the following: (1) PCT at entry was increased in patients who later had early VAP develop (25 patients) compared to no VAP (median, 1.4 ng/mL; 25-75 percentiles, 0.14-0.78; vs median, 0.2 ng/mL; 25-75 percentiles, 0.76-2.4, p<0.001; sensitivity, 76%; and specificity, 75%); (2) CPIS increased at the day of VAP diagnosis, compared to entry (median, 6.6+/-1.1 vs 1.5+/-1.1, p<0.001; sensitivity, 97%; specificity, 100%), while other serum inflammatory markers did not change; and (3) deterioration in oxygenation and changes in tracheal secretions were the main determinants of CPIS changes. CONCLUSIONS: PCT may be a useful marker to predict which patients subsequently have early VAP. The CPIS could help as an early way to detect the patients with early VAP and who need further diagnostic testing.


Subject(s)
Brain Injuries/therapy , C-Reactive Protein/metabolism , Calcitonin/blood , Pneumonia, Ventilator-Associated/blood , Pneumonia, Ventilator-Associated/diagnosis , Protein Precursors/blood , Serum Amyloid A Protein/metabolism , Ventilators, Mechanical/adverse effects , Adult , Aged , Biomarkers/blood , Calcitonin Gene-Related Peptide , Early Diagnosis , Female , Humans , Male , Middle Aged , Pneumonia, Ventilator-Associated/microbiology , Prognosis , Retrospective Studies , Sensitivity and Specificity , Ventilators, Mechanical/microbiology
6.
Dig Dis Sci ; 53(1): 47-51, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17468955

ABSTRACT

CONTEXT: The usefulness of stool calprotectin determination in diagnosis of inflammatory disease of the colon has been reported; information about its usefulness for patients with polyposis are scarce, however. OBJECTIVE: To evaluate the significance of stool calprotectin concentrations for patients affected by colonic polyposis. PATIENTS: Sixty-three consecutive patients (35 males, 28 females, mean age 60.3 years, range 39-78 years) were enrolled: 26 patients (41.3%) with polyps, 17 patients (27.0%) with asymptomatic diverticular disease, and 20 subjects (31.7%) with normal endoscopic appearance of the colon. RESULTS: Stool calprotectin concentrations were 17.4 +/- 24.5 microg g(-1) for patients with colonic polyposis, significantly higher than concentrations for patients with diverticulosis (7.1 +/- 5.7 microg g(-1); P = 0.026) or for patients with normal appearance of the colon (calprotectin 6.0 +/- 5.8 microg g(-1); P = 0.003). For patients with a single polyp, stool calprotectin concentrations were similar to those for patients with multiple polyps. Calprotectin fecal concentrations for patients with sessile polyps and those with flat polyps were not significantly different. Calprotectin concentrations were not significantly related to the size of the polyps. CONCLUSION: Our data show that colonic polyposis may cause an increase in stool calprotectin values and that these colonic lesions should be suspected when elevated stool calprotectin concentrations are found.


Subject(s)
Colonic Polyps/metabolism , Feces/chemistry , Leukocyte L1 Antigen Complex/metabolism , Adult , Aged , Biomarkers/metabolism , Colonic Polyps/pathology , Colonoscopy , Diagnosis, Differential , Diverticulum, Colon/diagnosis , Enzyme-Linked Immunosorbent Assay , Female , Humans , Male , Middle Aged , Prognosis , Retrospective Studies , Severity of Illness Index
7.
J Gastroenterol ; 42(9): 754-60, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17876545

ABSTRACT

BACKGROUND: Fecal calprotectin determination has been demonstrated to be useful in diagnosing various inflammatory diseases of the gastrointestinal tract; however, data available for patients with pancreatic diseases are scarce. Our aim was to assess fecal calprotectin in order to evaluate the presence of intestinal inflammation in patients with pancreatic disease. METHODS: Eligible patients with suspected pancreatic illness were enrolled, and in all of them fecal calprotectin and elastase-1, as well as serum amylase and lipase activities, were assayed using commercially available kits. RESULTS: A total of 90 subjects (47 men, 43 women, mean age 58.6 +/- 14.9 years) were enrolled: 20 (22.2%) had chronic pancreatitis; 15 (16.7%) had pancreatic cancer; six (6.7%) had chronic nonpathological pancreatic hyperenzymemia; 16 (17.8%) had nonpancreatic diseases; and 23 (25.6%) had no detectable diseases. Diarrhea was present in 19 patients (21.1%). In univariate analyses, the presence of diarrhea and low fecal elastase-1 concentrations were significantly associated (P = 0.019 and P = 0.002, respectively) with abnormally high fecal calprotectin concentration, and the multivariate analysis demonstrated that low fecal elastase-1 concentration was the only variable independently associated with a high fecal calprotectin concentration. CONCLUSIONS: Pancreatic insufficiency may cause intestinal inflammation, probably because of a modification of the intestinal ecology.


Subject(s)
Exocrine Pancreatic Insufficiency/metabolism , Feces/chemistry , Gastritis/metabolism , Leukocyte L1 Antigen Complex/metabolism , Pancreatic Elastase/metabolism , Amylases/blood , Biomarkers/metabolism , Enzyme-Linked Immunosorbent Assay , Exocrine Pancreatic Insufficiency/complications , Female , Gastritis/etiology , Humans , Male , Middle Aged , Prognosis , Risk Factors
8.
Am J Gastroenterol ; 102(1): 168-73, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17100963

ABSTRACT

OBJECTIVES: The aim of this study was to estimate the prevalence of undiagnosed celiac disease (CD) in the parents of preterm and/or small for gestational age (SGA) infants. METHODS: A sample of 1,714 parents (868 women, 846 men) of 905 preterm (<37 wk of gestational age) and/or SGA (<10th percentile of birthweight) infants consecutively born in Lombardy, Northern Italy, and not diagnosed with CD prior to pregnancy, were tested for CD. Diagnosis was based on antitissue transglutaminase and anti-endomysial antibodies and confirmed by duodenal biopsy. RESULTS: The overall prevalence of undiagnosed CD was 0.64% (95% confidence interval [CI] 0.32-1.15%), 0.92% (0.40-1.81%) in women and 0.35% (0.07-1.03%) in men. In the mothers of preterm infants prevalence of CD was 0.39% (0.05-1.39%). In the mothers of SGA infants prevalence of CD was 1.60% (0.64-3.27%), and the observed number of mothers with CD was 2.25 times higher than the expected one in the Italian female population (P = 0.039). Undiagnosed CD in mothers was associated with an increased risk of SGA birth (odds ratio 6.97, 95% CI 1.11-43.55%). CONCLUSIONS: While additional powered studies are needed, the present results suggest that the prevalence of undiagnosed CD in the mothers of SGA infants is higher than in the general female population.


Subject(s)
Celiac Disease/epidemiology , Parents , Adult , Female , Humans , Infant, Newborn , Infant, Small for Gestational Age , Italy/epidemiology , Logistic Models , Male , Prevalence , Statistics, Nonparametric
9.
Blood Coagul Fibrinolysis ; 17(4): 303-6, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16651873

ABSTRACT

Recent evidence indicates a possible role of D-dimer in the early diagnosis of ischemic stroke subtypes. Whether D-dimer can also predict the long-term outcome following ischemic stroke is controversial. To define the prognostic role of D-dimer, patients hospitalized after an acute ischemic cerebrovascular event underwent D-dimer measurement (Liatest D-D; normal level < 0.50 microg/ml) on admission and were followed up for recurrent cerebrovascular events, occurrence of other cardiovascular events, and mortality. We enrolled 96 patients (mean age 74.9 years, 42 men). Mean follow-up was 61.5 months; 47 (48.5%) patients died, 23 (48.9%) because of a vascular event. There was no difference in mean D-dimer levels between dead patients and survivors (1.68 and 1.63 microg/ml, P = NS), but the mortality risk was higher with D-dimer of at least 0.50 microg/ml (odds ratio, 5.32; 95% confidence interval, 1.79-15.84). After adjustment for age and stroke subtype, the odds ratio was not significant. Mean D-dimer was similar between patients with and without a new vascular event (1.43 and 1.68 microg/ml, P = NS), and D-dimer of at least 0.50 microg/ml was not predictive of an increased risk of subsequent events. D-dimer levels measured in the acute phase after an acute cerebrovascular event probably do not predict the long-term clinical outcome.


Subject(s)
Biomarkers/blood , Brain Ischemia/diagnosis , Fibrin Fibrinogen Degradation Products/analysis , Acute Disease , Aged , Aged, 80 and over , Brain Ischemia/blood , Cohort Studies , Female , Follow-Up Studies , Humans , Male , Predictive Value of Tests , Prognosis , Regression Analysis , Survival Rate
11.
Clin Biochem ; 38(6): 504-8, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15885227

ABSTRACT

OBJECTIVES: To evaluate myocardial damage during coronary artery bypass grafting using three different intermittent cardioplegia and then measuring cTnI and CKMBm release. DESIGN AND METHODS: Forty-two patients belonging to the hypothermic crystalloid (n = 16), hypothermic (n = 13), and normothermic blood (n = 13) groups were collected when removing the aortic cross-clamp (t = 0) and after 4, 12, 24 and 48 h. For each patient, cumulative cTnI and CKMBm release was calculated as the five measurement mean. There were no significant preoperative and operative differences in the three groups. RESULTS: In the normothermic group, cTnI mean values at 4, 12, and 24 h were significantly lower than those in both hypothermic groups; moreover, CKMBm mean values were higher at 4, 12, and 24 h in the hypothermic crystalloid group and at 4 and 12 h in the hypothermic blood group than in the normothermic group. In the normothermic group, the area under the curve of the release of both markers was significantly lower than in the hypothermic groups. No significant difference was reported in the release of both markers in hypothermic groups. CONCLUSIONS: A strategy of normothermic cardioplegia seems to preserve myocardium better than hypothermic cardioplegia.


Subject(s)
Coronary Artery Bypass/methods , Heart Arrest, Induced/methods , Myocardial Reperfusion Injury/prevention & control , Aged , Area Under Curve , Biomarkers/blood , Cardioplegic Solutions/administration & dosage , Cold Temperature , Creatine Kinase/blood , Crystalloid Solutions , Female , Humans , Hypothermia, Induced , Isotonic Solutions , Kinetics , Male , Middle Aged , Myocardium/metabolism , Plasma Substitutes , Sensitivity and Specificity , Treatment Outcome , Troponin I/blood
12.
J Pediatr Gastroenterol Nutr ; 36(3): 392-6, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12604981

ABSTRACT

UNLABELLED: Fecal elastase is considered to be a highly sensitive and specific non-invasive exocrine pancreatic function test. However, enteropathy may theoretically cause decreased exocrine pancreatic enzyme secretion through alteration of enteric hormone release. OBJECTIVE: The aim of this study was to evaluate the possible influence of transient small bowel damage on pancreatic elastase secretion. METHODS: We studied 166 children (aged 4 months to 14 years, mean 2 years); 114 of these children had acute enteritis and 52 children were control subjects (with gastro-intestinal symptoms or extra-intestinal diseases). Feces were collected from each patient 3 days after the onset of diarrhea and then tested for fecal elastase, bacterial pathogens, Rotavirus, and Adenovirus. Liquid fecal samples were not considered eligible for elastase measurement. Pancreatic elastase was measured using an ELISA method (Sche.Bo.Tech, Germany). We classified the results, expressed in microg/g stool, as: severe pancreatic insufficiency (<100 microg/g), moderate pancreatic insufficiency (100 to 200 microg/g), and normal (>200 microg/g). RESULTS: In the acute enteritis group we found severe levels in 14 (12%) children, moderate levels in 18 children (16%), and normal levels in 82 children (72%). In contrast, 52 of 52 (100%) control subjects demonstrated normal results. Statistical analysis (Wilcoxon rank test) demonstrated a significant difference between the enteritis and control groups (P < 0.01). Serial measurement of fecal elastase performed in 10 patients with enteritis showed a progressive increase of levels in 6 patients and an early decline with subsequent increases in the other 4 patients. CONCLUSIONS: Transient exocrine pancreatic insufficiency may be present in transient small bowel disease, caused by both bacterial and viral infections, possibly related to reduced enteric CCK secretion.


Subject(s)
Enteritis/physiopathology , Exocrine Pancreatic Insufficiency/diagnosis , Feces/enzymology , Intestine, Small/pathology , Pancreas/physiology , Pancreatic Elastase/analysis , Pancreatic Function Tests , Acute Disease , Adolescent , Biomarkers/analysis , Child , Child, Preschool , Enteritis/microbiology , Enteritis/virology , Enzyme-Linked Immunosorbent Assay/methods , Exocrine Pancreatic Insufficiency/enzymology , Female , Humans , Infant , Male , Pancreas/enzymology , Pancreatic Function Tests/methods , Severity of Illness Index
13.
Arch Intern Med ; 162(22): 2589-93, 2002.
Article in English | MEDLINE | ID: mdl-12456231

ABSTRACT

BACKGROUND: Different coagulation abnormalities according to stroke subtypes have been reported. We have assessed the clinical utility of D-dimer, a product of fibrin degradation, in the early diagnosis of stroke subtypes. METHODS: Patients hospitalized after an acute ischemic cerebrovascular event underwent D-dimer assay (STA Liatest D-Dimer) (reference level, <0.50 micro g/mL) on days 1, 6 +/- 1, and 12 +/- 1 and were studied to identify stroke subtypes. RESULTS: We included 126 patients (mean age, 75.5 years) and 63 age-matched control subjects. Stroke subtypes were cardioembolic in 34 patients (27%), atherothrombotic in 34 (27%), lacunar in 31 (25%), and unknown in 27 (21%). At all 3 measurements, D-dimer levels were significantly higher in the cardioembolic group (mean +/- SEM, 2.96 +/- 0.51, 2.58 +/- 0.40, and 3.79 +/- 0.30 micro g/mL, respectively) than in the atherothrombotic (1.34 +/- 0.21, 1.53 +/- 0.26, and 2.91 +/- 0.23 micro g/mL, respectively) (P<.05) and lacunar (0.67 +/- 0.08, 0.72 +/- 0.15, and 0.64 +/- 0.06 micro g/mL, respectively) groups (P<.01). The difference was also significant between the latter 2 groups (P<.01). We found no difference between the lacunar group and controls (0.53 +/- 0.14 micro g/mL). According to day 1 measurements, the optimal cutoff point for predicting cardioembolic stroke was 2.00 micro g/mL, resulting in a specificity of 93.2% and in a sensitivity of 59.3%. For predicting lacunar stroke, the cutoff point was 0.54 micro g/mL, with a specificity of 96.2% and a sensitivity of 61.3%. CONCLUSION: The increasing use of the D-dimer assay in clinical practice could be extended to patients presenting with acute cerebrovascular ischemic events to help predict stroke subtype.


Subject(s)
Fibrin Fibrinogen Degradation Products/analysis , Stroke/diagnosis , Aged , Aged, 80 and over , Analysis of Variance , Biomarkers/blood , Brain Ischemia/blood , Brain Ischemia/diagnosis , Brain Ischemia/mortality , Case-Control Studies , Female , Humans , Male , Middle Aged , Predictive Value of Tests , Probability , Reference Values , Sensitivity and Specificity , Statistics, Nonparametric , Stroke/blood , Stroke/mortality , Survival Analysis
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