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Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members.
Yawn BP, Buchanan GR, Afenyi-Annan AN, Ballas SK, Hassell KL, James AH, Jordan L, Lanzkron SM, Lottenberg R, Savage WJ, Tanabe PJ, Ware RE, Murad MH, Goldsmith JC, Ortiz E, Fulwood R, Horton A, John-Sowah J. Yawn BP, et al. JAMA. 2014 Sep 10;312(10):1033-48. doi: 10.1001/jama.2014.10517. JAMA. 2014. PMID: 25203083 Review.
IMPORTANCE: Sickle cell disease (SCD) is a life-threatening genetic disorder affecting nearly 100,000 individuals in the United States and is associated with many acute and chronic complications requiring immediate medical attention. ...A recommendatio …
IMPORTANCE: Sickle cell disease (SCD) is a life-threatening genetic disorder affecting nearly 100,000 individuals in the Un
Syphilis during pregnancy: a preventable threat to maternal-fetal health.
Rac MW, Revell PA, Eppes CS. Rac MW, et al. Am J Obstet Gynecol. 2017 Apr;216(4):352-363. doi: 10.1016/j.ajog.2016.11.1052. Epub 2016 Dec 9. Am J Obstet Gynecol. 2017. PMID: 27956203 Review.
We recommend all viable pregnancies receive the first dose of benzathine penicillin G in a labor and delivery department under continuous fetal monitoring for at least 24 hours. Thereafter, the remaining benzathine penicillin G doses can be given in an …
We recommend all viable pregnancies receive the first dose of benzathine penicillin G in a labor and delivery department under …
Sickle Cell Disease.
Bender MA. Bender MA. 2003 Sep 15 [updated 2021 Jan 28]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. 2003 Sep 15 [updated 2021 Jan 28]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. PMID: 20301551 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Sickle cell disease (SCD) is characterized by intermittent vaso-occlusive events and chronic hemolytic anemia. ...Hb S/S (homozygous p.Glu6Val in HBB) accounts for 60%-70% of SCD in the United States. Other forms of SCD result …
CLINICAL CHARACTERISTICS: Sickle cell disease (SCD) is characterized by intermittent vaso-occlusive events and chronic hemolyt …
Management of Sickle Cell Disease: Recommendations from the 2014 Expert Panel Report.
Yawn BP, John-Sowah J. Yawn BP, et al. Am Fam Physician. 2015 Dec 15;92(12):1069-76. Am Fam Physician. 2015. PMID: 26760593 Free article.
This overview highlights some of the most important clinical activities that can and should be carried out in the community care setting. Children with sickle cell anemia should receive prophylactic penicillin from birth through at least five years of age, an …
This overview highlights some of the most important clinical activities that can and should be carried out in the community care setting. Ch …
Bone Marrow Transplantation In Sickle Cell Disease.
Ashorobi D, Bhatt R. Ashorobi D, et al. 2021 Jul 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan–. 2021 Jul 12. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan–. PMID: 30860750 Free Books & Documents. Review.
Sickle cell disease is the most common hemoglobinopathy affecting about 100,000 Americans,, mostly of African descent and 20 million worldwide. ...For instance, in most parts of the United States, sickle cell screening is done befo
Sickle cell disease is the most common hemoglobinopathy affecting about 100,000 Americans,, mostly of African descent a
Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.
Ashley-Koch A, Yang Q, Olney RS. Ashley-Koch A, et al. Am J Epidemiol. 2000 May 1;151(9):839-45. doi: 10.1093/oxfordjournals.aje.a010288. Am J Epidemiol. 2000. PMID: 10791557 Review.
Sickle cell disease is caused by a variant of the beta-globin gene called sickle hemoglobin (Hb S). ...Hb S carriers are protected from malaria infection, and this protection probably led to the high frequency of Hb S in individuals of African and Mediterrane
Sickle cell disease is caused by a variant of the beta-globin gene called sickle hemoglobin (Hb S). ...Hb S carriers ar
Pediatric sickle cell disease: past successes and future challenges.
Meier ER, Rampersad A. Meier ER, et al. Pediatr Res. 2017 Jan;81(1-2):249-258. doi: 10.1038/pr.2016.204. Epub 2016 Oct 5. Pediatr Res. 2017. PMID: 27706129 Review.
Once a fatal disease of childhood, more than 95% of patients born today with sickle cell disease (SCD) in developed countries are expected to survive into adulthood, largely because of improvements in supportive and preventive care (newborn screening, penicillin
Once a fatal disease of childhood, more than 95% of patients born today with sickle cell disease (SCD) in developed countries …
Antibiotic Prophylaxis for Children With Sickle Cell Anemia.
Reeves SL, Tribble AC, Madden B, Freed GL, Dombkowski KJ. Reeves SL, et al. Pediatrics. 2018 Mar;141(3):e20172182. doi: 10.1542/peds.2017-2182. Epub 2018 Feb 5. Pediatrics. 2018. PMID: 29437860 Free PMC article.
BACKGROUND: Children with sickle cell anemia (SCA) are at increased risk for invasive pneumococcal disease; antibiotic prophylaxis significantly reduces this risk. ...Overall, only 18% of children received 300 days of antibiotics. Each additional sickle ce
BACKGROUND: Children with sickle cell anemia (SCA) are at increased risk for invasive pneumococcal disease; antibiotic prophyl …
Sickle cell disease and perioperative considerations: review and retrospective report.
Stanley AC, Christian JM. Stanley AC, et al. J Oral Maxillofac Surg. 2013 Jun;71(6):1027-33. doi: 10.1016/j.joms.2012.12.004. Epub 2013 Feb 20. J Oral Maxillofac Surg. 2013. PMID: 23434171 Review.
PURPOSE: To review the current literature on sickle cell disease (SCD) and patient management in the perioperative setting and to retrospectively evaluate the treatment and complications of oral and maxillofacial surgical patients with SCD treated in the Regional Me …
PURPOSE: To review the current literature on sickle cell disease (SCD) and patient management in the perioperative setting and …
How we prevent and manage infection in sickle cell disease.
Sobota A, Sabharwal V, Fonebi G, Steinberg M. Sobota A, et al. Br J Haematol. 2015 Sep;170(6):757-67. doi: 10.1111/bjh.13526. Epub 2015 May 27. Br J Haematol. 2015. PMID: 26018640 Review.
Sickle cell disease (SCD) affects approximately 100,000 people in the US, 12,500 in the UK, and millions worldwide. ...A secondary complication is infection, which can be bacterial, fungal or viral. Universal newborn screening, routine use of penicillin proph
Sickle cell disease (SCD) affects approximately 100,000 people in the US, 12,500 in the UK, and millions worldwide. ...A secon
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