Literature DB >> 21083357

Effect of hydroxyurea on physical fitness indices in children with sickle cell anemia.

Yasser A Wali1, Hisham Moheeb.   

Abstract

The current studies aimed at determining physical fitness indices and anthropometrics profiles of children with sickle cell anemia (SCA) after the use of hydroxyurea (HU). Ninety-three male schoolchildren--who participated previously in a similar study before the introduction of HU--comprising 2 groups participated in the studies. Group 1 was 41 children who were suffering from sickle cell disease (SCD) and were on HU for a minimum of 2 years, whereas group 2 was 50 normal healthy controls. Anthropometrics measurement and parameters of physical fitness were assessed in all subjects. All children were also subjected to a minimum of 6-minute running exercise test on a flat motorized treadmill at speed corresponding to 5 km/h. Throughout the test heart rate was monitored and recorded during exercise and for 10 minutes during recovery. Blood hemoglobin (Hb) and HbF% were measured after the use of HU. The mean values of weight, height, and lean body mass were still lower in the SCD children (P < .05) compared with the healthy subjects. However, they had significant decrease in the mean heart rate values and they spent longer time on the treadmill before they got tired compared to their previous performance and were just below the normal controls. Hydroxyurea treatment improved the aerobic exercise tolerance and most of the physical fitness parameters in children with SCD.

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Year:  2010        PMID: 21083357     DOI: 10.3109/08880018.2010.524278

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  7 in total

1.  Hydroxyurea and growth in young children with sickle cell disease.

Authors:  Sohail Rana; Patricia E Houston; Winfred C Wang; Rathi V Iyer; Jonathan Goldsmith; James F Casella; Caroline K Reed; Zora R Rogers; Myron A Waclawiw; Bruce Thompson
Journal:  Pediatrics       Date:  2014-09       Impact factor: 7.124

Review 2.  Update on the use of hydroxyurea therapy in sickle cell disease.

Authors:  Trisha E Wong; Amanda M Brandow; Wendy Lim; Richard Lottenberg
Journal:  Blood       Date:  2014-10-06       Impact factor: 22.113

3.  Exercise Testing of Adolescents and Young Adults With Sickle Cell Disease: Perceptual Responses and the Gas Exchange Threshold.

Authors:  Suzanne Ameringer; R K Elswick; India Sisler; Wally Smith; Thokozeni Lipato; Edmund O Acevedo
Journal:  J Pediatr Oncol Nurs       Date:  2019-04-26       Impact factor: 1.636

4.  Effects of Hydroxyurea on Skeletal Muscle Energetics and Function in a Mildly Anemic Mouse Model.

Authors:  Constance P Michel; Laurent A Messonnier; Benoit Giannesini; Benjamin Chatel; Christophe Vilmen; Yann Le Fur; David Bendahan
Journal:  Front Physiol       Date:  2022-06-15       Impact factor: 4.755

Review 5.  Summer Camps for Children with Sickle Cell Disease.

Authors:  Lauren Narcisse; Edward A Walton; Lewis L Hsu
Journal:  Ochsner J       Date:  2018

Review 6.  Motivators and Barriers to Physical Activity among Youth with Sickle Cell Disease: Brief Review.

Authors:  Olalekan Olatokunbo Olorunyomi; Robert Ie Liem; Lewis Li-Yen Hsu
Journal:  Children (Basel)       Date:  2022-04-17

7.  SOCIOECONOMIC AND NUTRITIONAL CHARACTERISTICS OF CHILDREN AND ADOLESCENTS WITH SICKLE CELL ANEMIA: A SYSTEMATIC REVIEW.

Authors:  Amanda Cristina da Silva de Jesus; Tulio Konstantyner; Ianna Karolina Véras Lôbo; Josefina Aparecida Pellegrini Braga
Journal:  Rev Paul Pediatr       Date:  2018 Oct-Dec
  7 in total

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