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1.
Int J Lab Hematol ; 44(3): 673-678, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35029326

RESUMO

OBJECTIVE: To evaluate, using longitudinal laboratory data, potential care gaps, and the prevalence of anemia in pregnant women residing in New Mexico, USA. METHODS: A total of 985 pregnant women aged 13-60 were included from December 1, 2018 to December 1, 2019. Parameters included frequency of CBC, iron studies, reticulocyte panel, prevalence of anemia, iron deficiency anemia (IDA), iron deficiency (ID), anemia change throughout pregnancy, and ICD-10 codes utilization. RESULTS: CBC was completed in 896/985 (91%) of the sample population in the first trimester and 528/985 (53.6%) in the third trimester. Two hundred and fifty-two (25.6%) women had anemia at any given point during pregnancy. ID was prevalent in 1.3% of women in the first trimester and 1.0% in the third, while IDA was prevalent in 0.4% in their first trimester and 5.5% in the third. Data also show an overall worsening of anemia from first to third trimester (2.8% and 40.9%, respectively, p < .0001). A positive correlation was found between mean corpuscular volume (MCV) and reticulocyte hemoglobin (RET-He) (r = .8592, 95% CI 0.7475 to 0.9237). CONCLUSION: Test utilization for anemia screening during pregnancy can be improved to guide patient management to reduce anemia rate and potential anemia-associated complications.


Assuntos
Anemia Ferropriva , Anemia , Deficiências de Ferro , Anemia/diagnóstico , Anemia/epidemiologia , Anemia Ferropriva/diagnóstico , Anemia Ferropriva/epidemiologia , Feminino , Hemoglobinas/análise , Humanos , Ferro , Gravidez
2.
J Emerg Med ; 41(4): 362-5, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20656443

RESUMO

BACKGROUND: Lice infestation is a commonly encountered disorder in emergency medicine. The louse survives from a blood meal from its host; hence, iron deficiency anemia is a theoretic possibility. A limited number of reports of severe iron deficiency anemia have appeared in the veterinary literature, but a thorough review of the medical literature did not reveal a single instance in human beings. OBJECTIVE: We report a small case series of patients with heavy louse infestation and profound iron deficiency anemia. CASE REPORT: The index case along with two other cases discovered from an exhaustive search of 4 years of the institution's Emergency Department records all had heavy infestation with head and body lice. Laboratory evaluation revealed serum hemoglobin levels under 6 gm/dL, low serum ferritin levels, and microcytic red blood cell indices. All patients were admitted to the hospital, received transfusions, and had evaluation of their anemia. No patient had evidence of gastrointestinal blood loss or alternative explanation for their anemia. CONCLUSIONS: Although cause and effect cannot be established from this case series, to the best of our knowledge, this is the first published evidence of a provocative association of louse infestation and severe iron deficiency anemia in humans.


Assuntos
Anemia Ferropriva/parasitologia , Infestações por Piolhos/complicações , Pediculus , Animais , Pessoas Mal Alojadas , Humanos , Masculino , Pessoa de Meia-Idade
3.
Am J Manag Care ; 27(2): 60-65, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-33577153

RESUMO

OBJECTIVES: To assess the impact of providing laboratory-generated near-real-time clinical insights for pregnant Medicaid members to managed care organization (MCO) care coordinators. STUDY DESIGN: A prospective, nonrandomized feasibility study was conducted over 11 months to examine the benefits of laboratory-generated clinical insights on prenatal care quality metrics and clinical outcomes. Measures included early identification of pregnancy and births to facilitate care, care gaps with prenatal laboratory testing, emergency department (ED) visits, preterm births, and neonatal intensive care unit (NICU) admissions and length of stay. METHODS: Weekly MCO care coordinators were provided a laboratory-generated prenatal targeted intervention module (TIM) to supplement their existing systems in a longitudinal, patient-centric format. Care coordinators contacted patients for enrollment in prenatal or postpartum services based on the TIM, which identified concomitant health conditions, missing prenatal care, and risks. RESULTS: The prenatal TIM identified 1355 pregnant members, 77% (n = 1040) of whom were detected in the first trimester. A total of 488 births were identified within 24 hours of parturition. Sixty-four percent of women had at least 80% of prenatal care gaps associated with laboratory testing closed. Women with ongoing prenatal care had fewer ED visits (17% vs 23%) and NICU admissions (11% vs 18%) compared with those without prenatal care. After adjusting for confounders, ongoing prenatal care had a borderline effect at decreasing the probability of having an ED visit and a NICU admission. CONCLUSIONS: An innovative collaboration between an MCO and a clinical laboratory improved quality measures for prenatal members enrolled in Medicaid.


Assuntos
Nascimento Prematuro , Cuidado Pré-Natal , Feminino , Humanos , Recém-Nascido , Laboratórios , Medicaid , Gravidez , Estudos Prospectivos , Estados Unidos
4.
J Appl Lab Med ; 5(5): 978-986, 2020 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-32916713

RESUMO

BACKGROUND: The National Committee on Quality Assurance's Healthcare Effectiveness Data and Information Set on Comprehensive Diabetes Care requires patients with diabetes obtain a hemoglobin A1c (Hb A1c) and urine albumin-to-creatinine ratio (ACR) test every year. To improve these measures, managed care organizations (MCOs) rely on claim and prescription data to identify members for care management. TriCore Reference Laboratories collaborated with Blue Cross Blue Shield of New Mexico (BCBSNM) to determine if laboratory information would augment BCBSNM's diabetes care management services. METHOD: In January 2018, BCBSNM provided its Medicaid enrollment file to TriCore for identifying members and determining their diabetes status by evaluating their recent Hb A1c results. Of the 6,138 members with diabetes, a random sample of 600 was extracted, and half were provided to BCBSNM to perform care management from January 18 to May 1, 2018. Completion of Hb A1c and ACR were measured. RESULTS: Significantly more (P = 0.03) study group members (25%) than control group members (18%) received an Hb A1c test. The study group (14%) also received more ACR tests than the control group (9%; P = 0.07). We then calculated the monetary penalty to which New Mexico Medicaid MCOs are subject, leading to the identification of additional value ($3,693,000) that clinical laboratories provide beyond the cost per test. CONCLUSION: Clinical laboratories play a critical role in healthcare, and this article demonstrates an approach for laboratories to collaborate with MCOs in their care management efforts. In addition, we calculate the value of this novel collaboration, which may play an integral role in laboratories' pursuit of value-based care.


Assuntos
Diabetes Mellitus , Laboratórios , Diabetes Mellitus/diagnóstico , Diabetes Mellitus/terapia , Hemoglobinas Glicadas/análise , Humanos , Programas de Assistência Gerenciada , New Mexico , Estados Unidos
7.
Science ; 327(5961): 78-81, 2010 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-19892942

RESUMO

Genome sequencing of large numbers of individuals promises to advance the understanding, treatment, and prevention of human diseases, among other applications. We describe a genome sequencing platform that achieves efficient imaging and low reagent consumption with combinatorial probe anchor ligation chemistry to independently assay each base from patterned nanoarrays of self-assembling DNA nanoballs. We sequenced three human genomes with this platform, generating an average of 45- to 87-fold coverage per genome and identifying 3.2 to 4.5 million sequence variants per genome. Validation of one genome data set demonstrates a sequence accuracy of about 1 false variant per 100 kilobases. The high accuracy, affordable cost of $4400 for sequencing consumables, and scalability of this platform enable complete human genome sequencing for the detection of rare variants in large-scale genetic studies.


Assuntos
DNA/química , Genoma Humano , Análise em Microsséries , Análise de Sequência de DNA/métodos , Sequência de Bases , Biologia Computacional , Custos e Análise de Custo , DNA/genética , Bases de Dados de Ácidos Nucleicos , Biblioteca Genômica , Genótipo , Haplótipos , Projeto Genoma Humano , Humanos , Masculino , Nanoestruturas , Nanotecnologia , Técnicas de Amplificação de Ácido Nucleico , Polimorfismo de Nucleotídeo Único , Análise de Sequência de DNA/economia , Análise de Sequência de DNA/instrumentação , Análise de Sequência de DNA/normas , Software
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