Abnormal Laboratory Result

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Aurora Esperanza Arrevillaga-lopez - One of the best experts on this subject based on the ideXlab platform.

  • [Metabolic Abnormalities and relationship with cardiovascular risk factors in children].
    Riesgo cardiovascular y alteraciones metabolicas en ninos., 2012
    Co-Authors: Santiago Manuel Palacios-mancilla, Miguel Angel Rubio-lezama, Margarito De Jesus De La Torre-lopez, Aurora Esperanza Arrevillaga-lopez
    Abstract:

    OBJECTIVE: to describe cardiovascular risk factors in pediatric patients of the General Hospital Zone 58 and its relationship with metabolic Abnormalities., METHODS: we studied a population of 30 healthy; children randomized. We measured weight, height, body mass index, blood pressure, waist circumference, determination of blood glucose, total cholesterol, HDL, LDL, triglycerides and uric acid. We applied a structured questionnaire about: how many hours a day the child watch television, hours of sleeping, birth weight, consumption of junk food, plus additional questions to investigate family history of cardiovascular disease., ResultS: the group consisted of 17 girls (56 %) and 13 children (44 %), average age: 9.7 years. Patients who had at least one Abnormal Laboratory Result were 27 (90 %). Cardiovascular risk factors showed an arithmetic mean birth weight 3175 g, 3.6 h hours of watching TV, sleep diary 8.9, lots of junk food every day 2.9. 15 patients had normal BMI, 5 more than the 95 centile and 7 below the 10 centile., CONCLUSIONS: the main factor that determined metabolic disorders was family history of cardiovascular disease or lipid disorders.

  • Cardiovascular and metabolic risk in children.
    Riesgo cardiovascular y alteraciones metabolicas en ninos., 2012
    Co-Authors: Santiago Manuel Palacios-mancilla, Miguel Angel Rubio-lezama, M De J De La Torre-lopez, Aurora Esperanza Arrevillaga-lopez
    Abstract:

    Objective: To describe cardiovascular risk factors in pediatric patients of the General Hospital Zone 58 and its relationship with metabolic Abnormalities. Methods: We studied a population of 30 healthy; children randomized. We measured weight, height, body mass index, blood pressure, waist circumference, determination of blood glucose, total cholesterol, HDL, LDL, triglycerides and uric acid. We applied a structured questionnaire about: how many hours a day the child watch television, hours of sleeping, birth weight, consumption of junk food, plus additional questions to investigate family history of cardiovascular disease. Results: The group consisted of 17 girls (56%) and 13 boys (44%), average age: 9.7 years. Patients who had at least one Abnormal Laboratory Result were 27 (90%). Cardiovascular risk factors showed an arithmetic mean birth weight 3175 g, 3.6 h hours of watching TV, sleep diary 8.9, junk food every day 2.9. 15 patients had normal BMI, 5 more than the 95 centile and 7 below the 10 centile. Conclusions: The main factor that determined metabolic disorders was family history of cardiovascular disease or lipid disorders.

Santiago Manuel Palacios-mancilla - One of the best experts on this subject based on the ideXlab platform.

  • [Metabolic Abnormalities and relationship with cardiovascular risk factors in children].
    Riesgo cardiovascular y alteraciones metabolicas en ninos., 2012
    Co-Authors: Santiago Manuel Palacios-mancilla, Miguel Angel Rubio-lezama, Margarito De Jesus De La Torre-lopez, Aurora Esperanza Arrevillaga-lopez
    Abstract:

    OBJECTIVE: to describe cardiovascular risk factors in pediatric patients of the General Hospital Zone 58 and its relationship with metabolic Abnormalities., METHODS: we studied a population of 30 healthy; children randomized. We measured weight, height, body mass index, blood pressure, waist circumference, determination of blood glucose, total cholesterol, HDL, LDL, triglycerides and uric acid. We applied a structured questionnaire about: how many hours a day the child watch television, hours of sleeping, birth weight, consumption of junk food, plus additional questions to investigate family history of cardiovascular disease., ResultS: the group consisted of 17 girls (56 %) and 13 children (44 %), average age: 9.7 years. Patients who had at least one Abnormal Laboratory Result were 27 (90 %). Cardiovascular risk factors showed an arithmetic mean birth weight 3175 g, 3.6 h hours of watching TV, sleep diary 8.9, lots of junk food every day 2.9. 15 patients had normal BMI, 5 more than the 95 centile and 7 below the 10 centile., CONCLUSIONS: the main factor that determined metabolic disorders was family history of cardiovascular disease or lipid disorders.

  • Cardiovascular and metabolic risk in children.
    Riesgo cardiovascular y alteraciones metabolicas en ninos., 2012
    Co-Authors: Santiago Manuel Palacios-mancilla, Miguel Angel Rubio-lezama, M De J De La Torre-lopez, Aurora Esperanza Arrevillaga-lopez
    Abstract:

    Objective: To describe cardiovascular risk factors in pediatric patients of the General Hospital Zone 58 and its relationship with metabolic Abnormalities. Methods: We studied a population of 30 healthy; children randomized. We measured weight, height, body mass index, blood pressure, waist circumference, determination of blood glucose, total cholesterol, HDL, LDL, triglycerides and uric acid. We applied a structured questionnaire about: how many hours a day the child watch television, hours of sleeping, birth weight, consumption of junk food, plus additional questions to investigate family history of cardiovascular disease. Results: The group consisted of 17 girls (56%) and 13 boys (44%), average age: 9.7 years. Patients who had at least one Abnormal Laboratory Result were 27 (90%). Cardiovascular risk factors showed an arithmetic mean birth weight 3175 g, 3.6 h hours of watching TV, sleep diary 8.9, junk food every day 2.9. 15 patients had normal BMI, 5 more than the 95 centile and 7 below the 10 centile. Conclusions: The main factor that determined metabolic disorders was family history of cardiovascular disease or lipid disorders.

Miguel Angel Rubio-lezama - One of the best experts on this subject based on the ideXlab platform.

  • [Metabolic Abnormalities and relationship with cardiovascular risk factors in children].
    Riesgo cardiovascular y alteraciones metabolicas en ninos., 2012
    Co-Authors: Santiago Manuel Palacios-mancilla, Miguel Angel Rubio-lezama, Margarito De Jesus De La Torre-lopez, Aurora Esperanza Arrevillaga-lopez
    Abstract:

    OBJECTIVE: to describe cardiovascular risk factors in pediatric patients of the General Hospital Zone 58 and its relationship with metabolic Abnormalities., METHODS: we studied a population of 30 healthy; children randomized. We measured weight, height, body mass index, blood pressure, waist circumference, determination of blood glucose, total cholesterol, HDL, LDL, triglycerides and uric acid. We applied a structured questionnaire about: how many hours a day the child watch television, hours of sleeping, birth weight, consumption of junk food, plus additional questions to investigate family history of cardiovascular disease., ResultS: the group consisted of 17 girls (56 %) and 13 children (44 %), average age: 9.7 years. Patients who had at least one Abnormal Laboratory Result were 27 (90 %). Cardiovascular risk factors showed an arithmetic mean birth weight 3175 g, 3.6 h hours of watching TV, sleep diary 8.9, lots of junk food every day 2.9. 15 patients had normal BMI, 5 more than the 95 centile and 7 below the 10 centile., CONCLUSIONS: the main factor that determined metabolic disorders was family history of cardiovascular disease or lipid disorders.

  • Cardiovascular and metabolic risk in children.
    Riesgo cardiovascular y alteraciones metabolicas en ninos., 2012
    Co-Authors: Santiago Manuel Palacios-mancilla, Miguel Angel Rubio-lezama, M De J De La Torre-lopez, Aurora Esperanza Arrevillaga-lopez
    Abstract:

    Objective: To describe cardiovascular risk factors in pediatric patients of the General Hospital Zone 58 and its relationship with metabolic Abnormalities. Methods: We studied a population of 30 healthy; children randomized. We measured weight, height, body mass index, blood pressure, waist circumference, determination of blood glucose, total cholesterol, HDL, LDL, triglycerides and uric acid. We applied a structured questionnaire about: how many hours a day the child watch television, hours of sleeping, birth weight, consumption of junk food, plus additional questions to investigate family history of cardiovascular disease. Results: The group consisted of 17 girls (56%) and 13 boys (44%), average age: 9.7 years. Patients who had at least one Abnormal Laboratory Result were 27 (90%). Cardiovascular risk factors showed an arithmetic mean birth weight 3175 g, 3.6 h hours of watching TV, sleep diary 8.9, junk food every day 2.9. 15 patients had normal BMI, 5 more than the 95 centile and 7 below the 10 centile. Conclusions: The main factor that determined metabolic disorders was family history of cardiovascular disease or lipid disorders.

Milan Remko - One of the best experts on this subject based on the ideXlab platform.

  • Are we to pay attention to factor XII deficiency?
    Vnitrni lekarstvi, 2020
    Co-Authors: Anna Remková, Milan Remko
    Abstract:

    Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious and not well known inherited condition. Unlike other coagulation factor deficiencies, it is totally asymptomatic. Surprisingly, it does not lead to Abnormal bleeding, even with major surgical procedures. The explanation for the lack of bleeding manifestations is unknown. It is suggested, but unproven, that patients are not sufficiently protected from thrombosis. FXII deficiency is usually discovered by accident through a routine coagulation testing done prior to surgery. Since FXII plays an important role in clot formation during in vitro measurements, its deficiency causes a marked prolongation of the activated partial thromboplastin time in the Laboratory examination. The main concern related to FXII deficiency is the unnecessary testing, delay in health care and worry of surgical interventions that may be prompted by the Abnormal Laboratory Result.

  • Are we to pay attention to factor XII deficiency?
    Vnitrni lekarstvi, 2020
    Co-Authors: Anna Remková, Milan Remko
    Abstract:

    Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious and not well known inherited condition. Unlike other coagulation factor deficiencies, it is totally asymptomatic. Surprisingly, it does not lead to Abnormal bleeding, even with major surgical procedures. The explanation for the lack of bleeding manifestations is unknown. It is suggested, but unproven, that patients are not sufficiently protected from thrombosis. FXII deficiency is usually discovered by accident through a routine coagulation testing done prior to surgery. Since FXII plays an important role in clot formation during in vitro measurements, its deficiency causes a marked prolongation of the activated partial thromboplastin time in the Laboratory examination. The main concern related to FXII deficiency is the unnecessary testing, delay in health care and worry of surgical interventions that may be prompted by the Abnormal Laboratory Result. activated partial thromboplastin time - bleeding - blood coagulation - factor XII.

Anna Remková - One of the best experts on this subject based on the ideXlab platform.

  • Are we to pay attention to factor XII deficiency?
    Vnitrni lekarstvi, 2020
    Co-Authors: Anna Remková, Milan Remko
    Abstract:

    Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious and not well known inherited condition. Unlike other coagulation factor deficiencies, it is totally asymptomatic. Surprisingly, it does not lead to Abnormal bleeding, even with major surgical procedures. The explanation for the lack of bleeding manifestations is unknown. It is suggested, but unproven, that patients are not sufficiently protected from thrombosis. FXII deficiency is usually discovered by accident through a routine coagulation testing done prior to surgery. Since FXII plays an important role in clot formation during in vitro measurements, its deficiency causes a marked prolongation of the activated partial thromboplastin time in the Laboratory examination. The main concern related to FXII deficiency is the unnecessary testing, delay in health care and worry of surgical interventions that may be prompted by the Abnormal Laboratory Result.

  • Are we to pay attention to factor XII deficiency?
    Vnitrni lekarstvi, 2020
    Co-Authors: Anna Remková, Milan Remko
    Abstract:

    Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious and not well known inherited condition. Unlike other coagulation factor deficiencies, it is totally asymptomatic. Surprisingly, it does not lead to Abnormal bleeding, even with major surgical procedures. The explanation for the lack of bleeding manifestations is unknown. It is suggested, but unproven, that patients are not sufficiently protected from thrombosis. FXII deficiency is usually discovered by accident through a routine coagulation testing done prior to surgery. Since FXII plays an important role in clot formation during in vitro measurements, its deficiency causes a marked prolongation of the activated partial thromboplastin time in the Laboratory examination. The main concern related to FXII deficiency is the unnecessary testing, delay in health care and worry of surgical interventions that may be prompted by the Abnormal Laboratory Result. activated partial thromboplastin time - bleeding - blood coagulation - factor XII.