Color duplex ultrasonography of temporal arteries: role in diagnosis and follow-up of suspected cases of temporal arteritis

被引:62
作者
Habib, Hisham M. [1 ,2 ]
Essa, Ashraf A. [3 ,4 ]
Hassan, Ayman A. [5 ,6 ]
机构
[1] Al Ahsa Hosp, Dept Rheumatol, Al Hasa, Saudi Arabia
[2] Mansoura Univ, Dept Rheumatol & Rehabil, Mansoura, Egypt
[3] Beni Suef Univ, Dept Radiol, Bani Suwayf, Egypt
[4] Al Ahsa Hosp, Dept Radiol, Al Hasa, Saudi Arabia
[5] Ain Shams Univ, Dept Vasc Surg, Cairo, Egypt
[6] Al Ahsa Hosp, Dept Vasc Surg, Al Hasa, Saudi Arabia
关键词
Color duplex ultrasonography; Temporal arteries; Temporal artery biopsy; GIANT-CELL ARTERITIS; POLYMYALGIA-RHEUMATICA; DOPPLER ULTRASONOGRAPHY; SONOGRAPHY; EFFICACY; BIOPSY;
D O I
10.1007/s10067-011-1808-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objectives of this study are to study the diagnostic value of color duplex ultrasonography (CDU) compared with the clinical results and temporal artery biopsy (TAB) in patients with suspected temporal arteritis (TA) and evaluate the prognostic value of CDU in follow-up of patients of sure diagnosis of TA under treatment in correlation to clinical response. The study included 32 consecutive patients of clinically suspected TA, and 30 age- and gender-matched control subjects. Baseline clinical characteristics and bilateral CDU of temporal arteries were performed to all subjects. CDU aimed to assess presence of a dark halo around the arterial lumen (a halo sign) or presence of stenoses and occlusions of temporal arteries. Unilateral TAB was performed then in all patients but not in control subjects. Subsequent CDU examinations were performed at 2, 4, 8, and 12 weeks after onset of treatment in patients with abnormal CDU. A halo sign at baseline CDU was evident in 13 TA patients (81%) and in 2 non-TA patients (12%) but none in control subjects. The presence of a halo sign in total yielded 81% sensitivity and 88% specificity whereas the presence of bilateral halo sign yielded 37% sensitivity and 100% specificity. Subsequent CDU examinations of TA patients showed disappearance of a halo sign in nine patients at 2 weeks and in four patients at 4 weeks with a mean of disappearance of 21 days after initiation of treatment. CDU is non-invasive, easy, and inexpensive method for diagnosis of TA. It is of higher sensitivity and specificity. It can be used in combination with clinical and laboratory tools for diagnosis of TA. It can effectively predict which patient will need TAB. In patients with bilateral halo sign, TAB is not necessary.
引用
收藏
页码:231 / 237
页数:7
相关论文
共 23 条
  • [1] The diagnostic value of ultrasonography-derived edema of the temporal artery wall in giant cell arteritis: a second meta-analysis
    Arida, Aikaterini
    Kyprianou, Miltiades
    Kanakis, Meletios
    Sfikakis, Petros P.
    [J]. BMC MUSCULOSKELETAL DISORDERS, 2010, 11
  • [2] Ball EL, 2010, BRJ SURG, V97, P1965
  • [3] Giant cell arteritis: diagnosis and management
    Bhatti, M. Tariq
    Tabandeh, Homayoun
    [J]. CURRENT OPINION IN OPHTHALMOLOGY, 2001, 12 (06) : 394 - 400
  • [4] Efficacy of unilateral versus bilateral temporal artery biopsies for the diagnosis of giant cell arteritis
    Boyev, LR
    Miller, NR
    Green, WR
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1999, 128 (02) : 211 - 215
  • [5] Hall JK, 2003, OPHTHALMOLOGY, V110
  • [6] Hellmann DB, 2004, CURRENT RHEUMATOLOGY, P235
  • [7] The early history of giant cell arteritis and polymyalgia rheumatica: First descriptions to 1970
    Hunder, Gene G.
    [J]. MAYO CLINIC PROCEEDINGS, 2006, 81 (08) : 1071 - 1083
  • [8] HUNDER GG, 1990, ARTHRITIS RHEUM, V33, P1122
  • [9] CLINICAL EFFICACY OF TEMPORAL ARTERY BIOPSY IN NASHVILLE, TENNESSEE
    IKARD, RW
    [J]. SOUTHERN MEDICAL JOURNAL, 1988, 81 (10) : 1222 - 1224
  • [10] Colour duplex sonography of temporal arteries before decision for biopsy: a prospective study in 55 patients with suspected giant cell arteritis
    Karahaliou, Maria
    Vaiopoulos, George
    Papaspyrou, Spiros
    Kanakis, Meletios A.
    Revenas, Konstantinos
    Sfikakis, Petros P.
    [J]. ARTHRITIS RESEARCH & THERAPY, 2006, 8 (04)