Lower ocular pulse amplitude with dynamic contour tonometry is associated with biopsy-proven giant cell arteritis

被引:6
作者
Ing, Edsel [1 ]
Pagnoux, Christian [2 ]
Tyndel, Felix [3 ]
Sundaram, Arun [3 ]
Hershenfeld, Seymour [1 ]
Ranalli, Paul [3 ]
Chow, Shirley [2 ]
Le, Tran [1 ]
Lutchman, Carla [1 ]
Rutherford, Susan [1 ]
Lam, Kay [1 ]
Bedi, Harleen [1 ]
Torun, Nurhan [4 ]
机构
[1] Univ Toronto, Med Sch, Dept Ophthalmol & Vis Sci, Toronto, ON, Canada
[2] Univ Toronto, Med Sch, Dept Med Rheumatol, Toronto, ON, Canada
[3] Univ Toronto, Med Sch, Dept Med Neurol, Toronto, ON, Canada
[4] Harvard Med Sch, Beth Israel Deaconess Hosp, Boston Dept Ophthalmol, Boston, MA USA
来源
CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE | 2018年 / 53卷 / 03期
关键词
TEMPORAL ARTERITIS; DIAGNOSTIC YIELD; SPECIMEN LENGTH; MANAGEMENT; MANIFESTATIONS; PNEUMOPLETHYSMOGRAPHY; RECOMMENDATIONS; CLASSIFICATION; CRITERIA; RULE;
D O I
10.1016/j.jcjo.2017.10.027
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objectives: To determine the role of the ocular pulse amplitude (OPA) from Pascal dynamic contour tonometry in predicting the temporal artery biopsy (TABx) result in patients with suspected giant cell arteritis (GCA). Design: Prospective validation study. Participants: Adults aged 50 years or older who underwent TABx from March 2015 to April 2017. Methods: Subjects on high-dose glucocorticoids more than 14 days or without serology before glucocorticoid initiation were excluded. The OPA from both eyes was obtained and averaged just before TABx of the predominantly symptomatic side. The variables chosen for the a priori prediction model were age, average OPA, and C-reactive protein (CRP). Erythrocyte sedimentation rate (ESR), platelets, jaw claudication, and eye findings were also recorded. In this study, subjects with a negative biopsy were considered not to have GCA, and contralateral biopsy was performed if the clinical suspicion for GCA remained high. An external validation set (XVAL) was obtained. Results: Of 109 TABx, 19 were positive and 90 were negative. On univariate logistic regression, the average OPA had 0.60 odds for positive TABx (p = 0.03), with no statistically significant difference in age, sex, CRP, ESR, or jaw claudication. In suspected GCA, an OPA of 1 mm Hg had positive likelihood ratio 4.74 and negative likelihood ratio 0.87 for positive TABx. Multivariate regression of the prediction model using optimal mathematical transforms (inverse OPA, log CRP, age >65 years) had area under the receiver operating characteristic curve (AUROC) = 0.85 and AUROC(xvAL) = 0.81. Conclusions: OPA is lower in subjects with biopsy -proven GCA and is a statistically significant predictor of GCA.
引用
收藏
页码:215 / 221
页数:7
相关论文
共 56 条
  • [41] Management of the patient with suspected temporal arteritis - A decision-analytic approach
    Niederkohr, RD
    Levin, LA
    [J]. OPHTHALMOLOGY, 2005, 112 (05) : 744 - 756
  • [42] Oh LJ, 2016, ANZ J SURG
  • [43] How to develop a more accurate risk prediction model when there are few events
    Pavlou, Menelaos
    Ambler, Gareth
    Seaman, Shaun R.
    Guttmann, Oliver
    Elliott, Perry
    King, Michael
    Omar, Rumana Z.
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2015, 351
  • [44] Concordance of bilateral temporal artery biopsy in giant cell arteritis
    Pless, M
    Rizzo, JF
    Lamkin, JC
    Lessell, S
    [J]. JOURNAL OF NEURO-OPHTHALMOLOGY, 2000, 20 (03) : 216 - 218
  • [45] Temporal Artery Biopsy is not Required in all Cases of Suspected Giant Cell Arteritis
    Quinn, Edel Marie
    Kearney, David E.
    Kelly, Justin
    Keohane, Catherine
    Redmond, Henry Paul
    [J]. ANNALS OF VASCULAR SURGERY, 2012, 26 (05) : 649 - 654
  • [46] Fatal giant cell arteritis of small to medium-sized visceral arteries: atypical manifestation or new entity?
    Sciotto, Francesco
    Seebach, Joerg D.
    Lobrinus, Johannes A.
    Kannuna, Hala
    Carballo, David
    Perrier, Arnaud
    Stirnemann, Jerome
    [J]. VASA-EUROPEAN JOURNAL OF VASCULAR MEDICINE, 2015, 44 (03) : 229 - 232
  • [47] FLUORESCEIN ANGIOGRAPHY IN THE DIAGNOSIS OF GIANT-CELL ARTERITIS
    SIATKOWSKI, RM
    GASS, JDM
    GLASER, JS
    SMITH, JL
    SCHATZ, NJ
    SCHIFFMAN, J
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1993, 115 (01) : 57 - 63
  • [48] Different Scoring Methods of FDG PET/CT in Giant Cell Arteritis
    Stellingwerff, Menno D.
    Brouwer, Elisabeth
    Lensen, Karel-Jan D. F.
    Rutgers, Abraham
    Arends, Suzanne
    van der Geest, Kornelis S. M.
    Glaudemans, Andor W. J. M.
    Slart, Riemer H. J. A.
    [J]. MEDICINE, 2015, 94 (37)
  • [49] Sutton-Brown M, 2015, EVIDENCE-BASED NEUROLOGY: MANAGEMENT OF NEUROLOGICAL DISORDERS, 2ND EDITION, P291
  • [50] Thomassen I, 2012, AM SURGEON, V78, P1362