Using calculated globulin fraction to reduce diagnostic delay in primary and secondary hypogammaglobulinaemias: results of a demonstration project

被引:32
作者
Holding, Stephen [1 ,2 ]
Khan, Sujoy [3 ]
Sewell, William A. C. [4 ,5 ]
Jolles, Stephen [6 ]
Dore, Philip C. [1 ,5 ]
机构
[1] Hull Royal Infirm, Dept Immunol, Kingston Upon Hull HU3 2JZ, N Humberside, England
[2] Univ Hull, Postgrad Med Inst, Kingston Upon Hull HU6 7RX, N Humberside, England
[3] Apollo Gleneagles Hosp, Kolkata, W Bengal, India
[4] PathLinks Immunol, Scunthorpe, North Lincolnsh, England
[5] Hull York Med Sch, Kingston Upon Hull, N Humberside, England
[6] Univ Wales Hosp, Cardiff CF4 4XW, S Glam, Wales
关键词
Sensitivity and specificity; common variable immunodeficiency; hypogammaglobulinaemia; screening; globulins; primary immunodeficiency; lymphoproliferative disease; diagnostic delay; COMMON VARIABLE IMMUNODEFICIENCY; PRIMARY ANTIBODY DEFICIENCY; NON-IMMUNOLOGISTS; PATIENT;
D O I
10.1177/0004563214545791
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background Median diagnostic delay of five to six years seen in primary hypogammaglobulinaemia results in morbidity including bronchiectasis. Patients typically have multiple health care encounters and blood tests before the diagnosis is considered. We report outcomes from using the difference between total protein and albumin (globulin fraction) to reduce diagnostic delay in unsuspected hypogammaglobulinaemia. Methods A prospective >5 year programme in the setting of a National Health Services Hospital Blood Sciences pathology service processing serum samples from primary and secondary care. Patients with globulin fraction below the first percentile were reviewed in the context of supplied clinical details. Immunoglobulin measurements were performed in selected patients. Results Of 2,910,850 globulin fractions 27,304 (0.9%) were below the 1st percentile globulin fraction (<18g/L). After exclusions, 933 (3% of these) had immunoglobulins measured. Of these, 292 had IgG<5g/L, 186<4g/L and 80<3g/L, giving respective positive predictive values of 31%, 20% and 8.6%. Positive predictive value for common variable immunodeficiency was 1.3%. We identified 12 new cases of common variable immunodeficiency, 10 new haematological disorders and 20 hypogammaglobulinaemias secondary to medication. Locally derived cut-offs are required as small differences between analysers have a significant effect on screen-positive rates. Conclusions Use of a 1st percentile globulin fraction improved early detection of hypogammaglobulinaemia. This is a useful adjunct to alert clinicians to unsuspected hypogammaglobulinaemia but should not replace immunoglobulin measurement. Patients with globulin fraction below the first percentile should be reviewed for possible hypogammaglobulinaemia.
引用
收藏
页码:319 / 326
页数:8
相关论文
共 14 条
[1]   Autoimmunity in common variable immunodeficiency [J].
Agarwal, Shradha ;
Cunningham-Rundles, Charlotte .
CURRENT ALLERGY AND ASTHMA REPORTS, 2009, 9 (05) :347-352
[2]   Granulomatous disease: Distinguishing primary antibody disease from sarcoidosis [J].
Arnold, D. F. ;
Wiggins, J. ;
Cunningham-Rundles, C. ;
Misbah, S. A. ;
Chapel, H. M. .
CLINICAL IMMUNOLOGY, 2008, 128 (01) :18-22
[3]   Sarcoid-like granulomas in common variable immunodeficiency [J].
Artac, Hasibe ;
Bozkurt, Banu ;
Talim, Beril ;
Reisli, Ismail .
RHEUMATOLOGY INTERNATIONAL, 2009, 30 (01) :109-112
[4]   PRIMARY ANTIBODY DEFICIENCY AND DIAGNOSTIC DELAY [J].
BLORE, J ;
HAENEY, MR .
BRITISH MEDICAL JOURNAL, 1989, 298 (6672) :516-517
[5]   Common variable immunodeficiency: Clinical and immunological features of 248 patients [J].
Cunningham-Rundles, C ;
Bodian, C .
CLINICAL IMMUNOLOGY, 1999, 92 (01) :34-48
[6]   Identifying undiagnosed primary immunodeficiency diseases in minority subjects by using computer sorting of diagnosis codes [J].
Cunningham-Rundles, C ;
Sidi, P ;
Estrella, L ;
Doucette, J .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2004, 113 (04) :747-755
[7]   Patient-centred screening for primary immunodeficiency: a multi-stage diagnostic protocol designed for non-immunologists [J].
de Vries, E. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2006, 145 (02) :204-214
[8]   Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update [J].
de Vries, E. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2012, 167 (01) :108-119
[9]  
*EUR SOC IMM, 2006, DIAGN CRIT PRIM IMM
[10]   The German national registry for primary immunodeficiencies (PID) [J].
Gathmann, B. ;
Goldacker, S. ;
Klima, M. ;
Belohradsky, B. H. ;
Notheis, G. ;
Ehl, S. ;
Ritterbusch, H. ;
Baumann, U. ;
Meyer-Bahlburg, A. ;
Witte, T. ;
Schmidt, R. ;
Borte, M. ;
Borte, S. ;
Linde, R. ;
Schubert, R. ;
Bienemann, K. ;
Laws, H. -J. ;
Dueckers, G. ;
Roesler, J. ;
Rothoeft, T. ;
Krueger, R. ;
Scharbatke, E. C. ;
Masjosthusmann, K. ;
Wasmuth, J. -C. ;
Moser, O. ;
Kaiser, P. ;
Gross-Wieltsch, U. ;
Classen, C. F. ;
Horneff, G. ;
Reiser, V. ;
Binder, N. ;
El-Helou, S. M. ;
Klein, C. ;
Grimbacher, B. ;
Kindle, G. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2013, 173 (02) :372-380