Literature DB >> 10767192

A prospective study of soft-tissue ultrasonography in sickle cell disease patients with suspected osteomyelitis.

R R William1, S S Hussein, W D Jeans, Y A Wali, Z A Lamki.   

Abstract

AIM: A prospective study was done to assess the accuracy of soft tissue ultrasonography in patients with sickle cell disease (SCD) presenting with suspected osteomyelitis.
MATERIALS AND METHODS: Thirty-one SCD patients had soft tissue ultrasonography on 38 occasions (18 men, 13 women; mean age 8.2 years). The initial ultrasonographic signs and diagnosis were compared with the final clinical diagnosis, which was based on clinical progress and scintigraphy. RESULT: The overall sensitivity of ultrasound in diagnosing osteomyelitis was 74% with a specificity of 63%. The principal ultrasonographic finding of subperiosteal fluid was present in 14 (74%) patients with osteomyelitis and seven (37%) patients without infection. A finding of a subperiosteal fluid depth of 4 mm or more was significantly associated with osteomyelitis (P < 0.01).
CONCLUSION: Ultrasonography should be the initial investigation in SCD patients if osteomyelitis is suspected clinically. In such a clinical setting, a finding of 4 mm depth or more of subperiosteal fluid appears to be diagnostic. Previous statements that the presence of any subperiosteal fluid indicates infection are shown to be inaccurate. Patients with less than 4 mm of subperiosteal fluid require further imaging or aspiration to establish the diagnosis of osteomyelitis.

Entities:  

Mesh:

Year:  2000        PMID: 10767192     DOI: 10.1053/crad.1999.0377

Source DB:  PubMed          Journal:  Clin Radiol        ISSN: 0009-9260            Impact factor:   2.350


  8 in total

Review 1.  Sonography of musculoskeletal infection in children.

Authors:  Monique Shahid; Colin Holton; Sean O'Riordan; Jeannette K Kraft
Journal:  Ultrasound       Date:  2020-01-27

2.  Utility of unenhanced fat-suppressed T1-weighted MRI in children with sickle cell disease -- can it differentiate bone infarcts from acute osteomyelitis?

Authors:  Jorge Delgado; Maria A Bedoya; Abby M Green; Diego Jaramillo; Victor Ho-Fung
Journal:  Pediatr Radiol       Date:  2015-07-25

Review 3.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

4.  [Scintigraphic findings in a patient with sickle-cell thalassemia and recurrent pain attacks].

Authors:  Peter Mikosch; Barbara Jauk; Wilhelm Kaulfersch; Hans-Jürgen Gallowitsch; Peter Lind
Journal:  Wien Med Wochenschr       Date:  2003

Review 5.  Rheumatic Manifestations of Haemoglobinopathies.

Authors:  Michael Hughes
Journal:  Curr Rheumatol Rep       Date:  2018-08-14       Impact factor: 4.592

6.  Dilemma in differentiating between acute osteomyelitis and bone infarction in children with sickle cell disease: the role of ultrasound.

Authors:  Baba P D Inusa; Adeola Oyewo; Felicity Brokke; Gayathriy Santhikumaran; K Haran Jogeesvaran
Journal:  PLoS One       Date:  2013-06-06       Impact factor: 3.240

7.  Guidelines on neonatal screening and painful vaso-occlusive crisis in sickle cell disease: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular: Project guidelines: Associação Médica Brasileira - 2016.

Authors:  Josefina Aparecida Pellegrini Braga; Mônica Pinheiro de Almeida Veríssimo; Sara Teresinha Olalla Saad; Rodolfo Delfini Cançado; Sandra Regina Loggetto
Journal:  Rev Bras Hematol Hemoter       Date:  2016-04-08

Review 8.  Management of Osteomyelitis in Sickle Cell Disease: Review Article.

Authors:  Humaid Al Farii; Sarah Zhou; Anthony Albers
Journal:  J Am Acad Orthop Surg Glob Res Rev       Date:  2020-09
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.