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Hb 201 analyzer

Manufactured by HemoCue
Sourced in Sweden, United States

The HemoCue Hb 201+ analyzer is a portable hemoglobin measurement device. It provides fast, reliable, and accurate hemoglobin measurements from a small blood sample.

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27 protocols using hb 201 analyzer

1

Hematological Profiling of Rat Samples

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Blood samples were collected from subsets of rats used in the metabolism (section 2.3) and pulse oximetry (section 2.4) experiments. Blood was sampled from the severed neck vessels immediately following decapitation. For hematocrit, blood was collected into heparinized hematocrit tubes (HematoClad; Drummond) and centrifuged for 5 min (RCF 3,900 × g; ZIPocrit; LW Scientific). The hematocrit was then estimated from the ratio of packed red cell volume to the total sample volume. Hematocrit was determined in the same manner for a small number of adult rats, except that adult rats were killed by CO2 inhalation prior to decapitation. For hemoglobin concentration, blood was analyzed with an Hb 201+ analyzer (HemoCue). For lactate concentration, blood was collected directly onto test strips and analyzed using a Lactate Pro analyzer (Arkray).
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2

Rat Pup Blood Collection and Analysis

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Shortly after the completion of the ventilation measurements in Experiment #2, some rat pups were euthanized with CO2 and decapitated for blood collection. Blood was sampled from the severed neck vessels. For hematocrit, blood was collected into heparinized hematocrit tubes (HematoClad; Drummond) in duplicate and centrifuged for 5 min (ZIPocrit; LW Scientific). The hematocrit was then estimated from the average ratio of packed red cell volume to the total sample volume. Hemoglobin concentration was determined from separate blood samples from the same individuals using an Hb 201+ analyzer (HemoCue).
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3

Plasma Extraction Efficiency Measurement

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We measured the plasma extraction efficiency of the target DNA through the Vivid membrane and into the underlying Fusion 5 during blood fractionation. To calculate the plasma extraction efficiency, we measured the mass of the underlying Fusion 5 membrane before and after blood fractionation. We define plasma extraction efficiency as plasma in the Fusion 5 membrane divided by the total plasma in the sample as, ηP.Extract = (mP.F5/ρP)/Vblood * (1 − HCT), where mP.F5 is the mass of plasma residing in the underlying Fusion 5 membrane after fractionation, ρP is the density of human plasma, Vblood is the volume of blood applied to the Vivid plasma separation membrane, and HCT is the blood hematocrit value. We measured the blood hematocrit value using a Hb 201+ analyzer (HemoCue, USA). We also qualitatively investigated cell fractionation as well as quantified hemolysis. We visualized cell fractionation using a hemocytometer (Bright Line Hemacytometer 1492, Hausser Scientific, USA) with a TMS Inverted Microscope (Nikon, JPN). Hemolysis was measured using the Harboe method [53 (link),54 (link)] with plasma filtered by the device and a spectrophotometer (NanoDrop 2000, ThermoFisher Scientific, USA) and compared against plasma that had been separated using a centrifuge.
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4

Infant Iron Status Screening Protocol

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Nonfasting capillary blood samples were taken from infants by a registered phlebotomist using a standard “heel prick” test as part of health screening at each visit (baseline, postintervention, and at 9 mo). Indicators of iron status were Hb, SF, and CRP. The phlebotomist assessed Hb using a HemoCue Hb 201+ Analyzer immediately as blood was drawn, and if outside the normal range, the mother was notified and given a referral letter to see their general practitioner (Hb below normal: baseline, n = 5; postintervention, n = 2; 9 mo, n = 4). Aliquots of serum were stored at –80°C until subsequent analysis of SF and CRP at LabTests (Auckland, New Zealand) by their biochemistry department via particle-enhanced immunoturbidimetric assay; this laboratory undergoes regular quality assurance testing by an external agency known as International Accreditation New Zealand. Established cutoffs of Hb <110 g/L and SF <10 µg/L to assess the presence of iron deficiency and iron-deficiency anemia were used (34–36 (link)); a cutoff of ≥10 mg/L CRP suggested the presence of infection or inflammation (37–40 ).
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5

Assessing Anemia and Nutritional Status

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Before praziquantel administration, finger-prick blood (100 µL) was collected to measure hemoglobin concentration (Hb conc) in g/dL using the HemoCue Hb 201+ analyzer (HemoCue AB Angelholm, Sweden) [40 (link)]. A child was defined as anemic if the Hb conc was less than 11.5 g/dL [41 ]. Anthropometric measurements were used to assess the nutritional status of the children. Bodyweight was measured in kilograms (kg), and height was measured in centimeter (cm). Body mass index (BMI) was calculated as a ratio of body weight (in kg) to height square (in meters). To assess for stunting and wasting, the anthropometry were converted to Z scores as height for age Z score (HAZ) and body mass index (BMI) for age Z score (BAZ) using the WHO Anthro-Plus software version 1.0.4 (Department of Nutrition, WHO, Avenue Appie, Geneva, Switzerland) [42 ]. All children with HAZ and BAZ scores less than two standard deviations were considered stunted and wasted, respectively.
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6

Hematological Measurements in REDS-RISE Trial

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In the REDS-RISE trial, hemoglobin was measured using the HemoCue Hb 201 analyzer (HemoCue, Lake Forest, CA), serum ferritin by a quantitative chemiluminescent immunoassay (ADVIA Centaur; Siemens Healthcare Diagnostics, Deerfield, IL), and sTfR by quantitative immunoturbidimetry (Tina-quant; Roche Diagnostics, Indianapolis, IN).8 (link)
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7

Maternal and Fetal Anemia Diagnosis

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Peripheral finger-prick blood was used to determine hemoglobin level by using HemoCue Hb 201+ analyzer (HemoCue AB Angelholm, Sweden). Anemia was defined when the maternal hemoglobin level was <11 g/dL. Mild, moderate, and severe anemia was defined when maternal Hb level was 10–10.9 g/dL, 7–9.9 g/dL and <7 g/dL, respectively [43 ]. Fetal anemia was defined when the cord blood Hb was <12.5 g/dL [44 (link)].
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8

Assessing Child Health Impacts of MNP Intervention

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Baseline (BL) and endline (EL) MNP intervention of the child’s health was assessed (including axillary temperature), and a capillary blood sample of 500µL from the finger or heel was taken into a 0.5 mL ethylene diamine tetra-acetic acid (EDTA) tube. A HemoCue Hb 201+ analyzer (HemoCue AB, Angelholm, Sweden) was used to measure haemoglobin levels, and children found to be severely anaemic (Hb < 70 g/L) were immediately referred. The Malaria Rapid Diagnostic Test (RDT) (Paracheck Pf Unit, Orchid Biomedical Systems Verna, Goa, India) was performed quickly in the field, and a 3-day course of treatment was given to those who tested positive for malaria. They were only enrolled later upon recovery if any other eligibility requirements had been met. The remaining sample was transferred to the haematological, malaria microscopy and immunogenetic testing laboratory.
During the MNP intervention period and at six-month follow-up, children found to be febrile (i.e., axillary temperature > 37.5 °C) or have had a fever in the past 48 h were, blood sampled of 100μL in 0.5 mL EDTA for haematological and malaria tests. Anthropometric, socioeconomic, demographic, adherence to MNP intervention, insecticide-treated bed net use and participants' morbidity data were collected during the study as previously described in details elsewhere [22 (link), 23 (link)].
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9

Assessing Anemia Prevalence in Indian Children

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For the ecological analysis, the primary outcomes were district-level anemia prevalence and average hemoglobin concentration by district, measured in g/dL. Anemia prevalence information by district for the ecological analysis was obtained from the India NFHS-4 survey. The primary outcomes of the individual-level analysis were the presence of anemia (“yes” if hemoglobin was <11 g/dL and “no” if it was above 11 g/dL) and hemoglobin level.
Blood specimens were collected from all children aged between 6 and 59 months who resided in the households selected for the survey. Consent was obtained from parent(s) or guardian(s). Blood samples were drawn using a finger or heel prick. Hemoglobin concentrations were measured on-site using the HemoCue Hb 201+ analyzer by trained medical personnel in each district.17 ,34 (link),35 Blood samples were dried overnight and packaged using a systematic protocol in air-tight plastic bags the following day. After all biomarker testing in each PSU was completed, samples were sent via. Speed Post to the designated laboratory for testing.
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10

Hemoglobin Level Determination and Anemia

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Hgb level was determined using a portable hemoglobin spectrophotometer (the HemoCue Hb 201 Analyzer (HemoCue, Angelholm, Sweden) and a specially designed microcuvette (the HemoCue Hb 201 Microcuvette, HemoCue, Angelholm, Sweden). Then, anemia was defined as Hgb level less than 11 g/dl [17 ].
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