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Published in: Journal of Clinical Immunology 2/2013

01-02-2013 | Original Research

Primary Immunodeficiency Diseases in Children: 15 Year Experience in a Tertiary Care Medical Center in Qatar

Authors: Mohammad S. Ehlayel, Abdulbari Bener, Mohammad Abu Laban

Published in: Journal of Clinical Immunology | Issue 2/2013

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Abstract

Background

Primary immunodeficiency diseases (PID) are a group of heterogeneous, rare, genetic, mainly childhood disorders that affect specific components of immune system leading to serious complications.

Objectives

This study is aimed at describing the prevalence and the categories of PID, the ages of onset and the diagnosis, the clinical presentations, the treatment modalities and the overall outcome of affected patients.

Materials and Methods

A retrospective study was conducted on 131 pediatric patients (aged 0–14 years) diagnosed with PID at Hamad General Hospital during a 15-year period (1998–2012).

Results

Data of 131 patients (75 males & 56 females) was analyzed with an estimated prevalence of 4.7 PID patients per 100,000 children younger than 14 years of age. The most common type of PID was predominantly antibody deficiency (23.7 %), followed by other well-defined immunodeficiency syndromes (22.9 %), 19.1 % combined T and B cell immunodeficiency, but rare CVID, and no cases of complement deficiency. The mean onset age was 24.01 months and diagnosis age was 42.2 months. Recurrent infections, particularly pneumonia (48.9 %), failure to thrive (34.4 %), otitis media (26 %), sepsis (23.7 %), and chronic diarrhoea (21.4 %) were commonest presenting conditions. P. aeruginosa (15.7 %), Salmonella species (13.2 %), and Non-TB mycobacteria (13.2 %) were the most common bacterial isolates. The overall mortality rate was 21.4 % with combined immunodeficiency’s accounting for 53.4 % of deaths.

Conclusions

This study reveals that PIDs are not rare in children in Qatar; and like other studies predominantly antibody deficiencies are the most common. Strategies that reinforce awareness and education of practicing physicians, bone marrow transplantation, and establishing PID national registry should be adopted to reduce mortality and morbidity of PID patients in Qatar.
Literature
1.
go back to reference Rezaei N, Bonilla FA, Sullivan KE, et al. Chapter 1. An introduction to primary immunodeficiency diseases. In: Nima R, Asghar A, Notarangelo LD, editors. Primary immunodeficiency diseases, definition diagnosis and management. Berlin: Springer; 2008. p. 1–38.CrossRef Rezaei N, Bonilla FA, Sullivan KE, et al. Chapter 1. An introduction to primary immunodeficiency diseases. In: Nima R, Asghar A, Notarangelo LD, editors. Primary immunodeficiency diseases, definition diagnosis and management. Berlin: Springer; 2008. p. 1–38.CrossRef
2.
go back to reference Rezaei N, Hedayat M, Aghamohammadi A, Nichols KE. Primary immunodeficiency diseases associated with increased susceptibility to viral infections and malignancies. J Allergy Clin Immunol. 2011;127:1329–41.e2; quiz 1342–3. Rezaei N, Hedayat M, Aghamohammadi A, Nichols KE. Primary immunodeficiency diseases associated with increased susceptibility to viral infections and malignancies. J Allergy Clin Immunol. 2011;127:1329–41.e2; quiz 1342–3.
3.
go back to reference Leechawengwongs E, Shearer WT. Lymphoma complicating primary immunodeficiency syndromes. Curr Opin Hematol. 2012;19:305–12.PubMedCrossRef Leechawengwongs E, Shearer WT. Lymphoma complicating primary immunodeficiency syndromes. Curr Opin Hematol. 2012;19:305–12.PubMedCrossRef
4.
go back to reference Goyal R, Bulua A, Nikolov N, et al. Rheumatologic and autoimmune manifestations of primary immunodeficiency disorders. Curr Opin Rheumatol. 2009;21:78–84.PubMedCrossRef Goyal R, Bulua A, Nikolov N, et al. Rheumatologic and autoimmune manifestations of primary immunodeficiency disorders. Curr Opin Rheumatol. 2009;21:78–84.PubMedCrossRef
5.
go back to reference Joshi AY VV, Hagan JB, St Sauver JL, Boyce TG. Incidence and temporal trends of primary immunodeficiency: a population-based cohort study. Mayo Clin Proc. 2009;84:16–22.PubMedCrossRef Joshi AY VV, Hagan JB, St Sauver JL, Boyce TG. Incidence and temporal trends of primary immunodeficiency: a population-based cohort study. Mayo Clin Proc. 2009;84:16–22.PubMedCrossRef
6.
go back to reference Nourijelyani K, Aghamohammadi A, Sadaghiani MS, et al. Physicians awareness on primary immunodeficiency disorders in Iran. Iran J Allergy Asthma Immunol. 2012;11:57–64.PubMed Nourijelyani K, Aghamohammadi A, Sadaghiani MS, et al. Physicians awareness on primary immunodeficiency disorders in Iran. Iran J Allergy Asthma Immunol. 2012;11:57–64.PubMed
7.
go back to reference de Vries E, European Society for Immunodeficiencies (ESID) members. Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update. Clin Exp Immunol. 2012;167:108–19.PubMedCrossRef de Vries E, European Society for Immunodeficiencies (ESID) members. Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update. Clin Exp Immunol. 2012;167:108–19.PubMedCrossRef
8.
go back to reference Modell V, Gee B, Lewis DB et al. Global study of primary immunodeficiency diseases (PI)-diagnosis, treatment, and economic impact: an updated report from the Jeffrey Modell Foundation. Immunol Res 2011; 61–70. Modell V, Gee B, Lewis DB et al. Global study of primary immunodeficiency diseases (PI)-diagnosis, treatment, and economic impact: an updated report from the Jeffrey Modell Foundation. Immunol Res 2011; 61–70.
9.
go back to reference Yüksek M, Ikincioğullari A, Doğu F, et al. Primary immune deficiency disease awareness among a group of Turkish physicians. Turk J Pediatr. 2010;52:372–7.PubMed Yüksek M, Ikincioğullari A, Doğu F, et al. Primary immune deficiency disease awareness among a group of Turkish physicians. Turk J Pediatr. 2010;52:372–7.PubMed
10.
go back to reference Reda SM, Afifi HM, Amine MM. Primary immunodeficiency diseases in Egyptian children: a single-center study. J Clin Immunol. 2008;29:343–51.PubMedCrossRef Reda SM, Afifi HM, Amine MM. Primary immunodeficiency diseases in Egyptian children: a single-center study. J Clin Immunol. 2008;29:343–51.PubMedCrossRef
11.
go back to reference Barbouche MR, Galal N, Ben-Mustapha I, et al. Primary immunodeficiencies in highly consanguineous North African populations. Ann N Y Acad Sci. 2011;1238:42–52.PubMedCrossRef Barbouche MR, Galal N, Ben-Mustapha I, et al. Primary immunodeficiencies in highly consanguineous North African populations. Ann N Y Acad Sci. 2011;1238:42–52.PubMedCrossRef
12.
go back to reference Aghamohammadi A, Moin M, Rezaei N. History of primary immunodeficiency diseases in Iran. Iran J Pediatr. 2010;20:16–34.PubMed Aghamohammadi A, Moin M, Rezaei N. History of primary immunodeficiency diseases in Iran. Iran J Pediatr. 2010;20:16–34.PubMed
13.
go back to reference Rezaei N, Aghamohammadi A, Moin M, et al. Frequency and clinical manifestations of patients with primary immunodeficiency disorders in Iran: update from the Iranian Primary Immunodeficiency Registry. J Clin Immunol. 2006;26:519–32.PubMedCrossRef Rezaei N, Aghamohammadi A, Moin M, et al. Frequency and clinical manifestations of patients with primary immunodeficiency disorders in Iran: update from the Iranian Primary Immunodeficiency Registry. J Clin Immunol. 2006;26:519–32.PubMedCrossRef
14.
go back to reference Dar-Odeh NS, Hayajneh WA, Abu-Hammad OA, et al. Orofacial findings in chronic granulomatous disease: report of twelve patients and review of the literature. BMC Res Notes. 2010;17:37.CrossRef Dar-Odeh NS, Hayajneh WA, Abu-Hammad OA, et al. Orofacial findings in chronic granulomatous disease: report of twelve patients and review of the literature. BMC Res Notes. 2010;17:37.CrossRef
15.
go back to reference Al-Herz W. Primary immunodeficiency disorders in Kuwait: first report from Kuwait National Primary Immunodeficiency Registry (2004–2006). J Clin Immunol. 2008;28:186–93.PubMedCrossRef Al-Herz W. Primary immunodeficiency disorders in Kuwait: first report from Kuwait National Primary Immunodeficiency Registry (2004–2006). J Clin Immunol. 2008;28:186–93.PubMedCrossRef
16.
go back to reference Al-Herz W, Zainal M, Salama M, et al. Primary immunodeficiency disorders: survey of pediatricians in Kuwait. J Clin Immunol. 2008;28:379–83.PubMedCrossRef Al-Herz W, Zainal M, Salama M, et al. Primary immunodeficiency disorders: survey of pediatricians in Kuwait. J Clin Immunol. 2008;28:379–83.PubMedCrossRef
17.
go back to reference Al-Herz W, Bousfiha A, Casanova JL, et al. Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency. Front Immunol. 2011;2:54. Epub 2011 Nov 2018.PubMed Al-Herz W, Bousfiha A, Casanova JL, et al. Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency. Front Immunol. 2011;2:54. Epub 2011 Nov 2018.PubMed
19.
go back to reference Ehlayel M, de Beaucoudrey L, Fike F, et al. Simultaneous presentation of 2 rare hereditary immunodeficiencies: IL-12 receptor beta1 deficiency and ataxia-telangiectasia. J Allergy Clin Immunol. 2008;122:1217–9.PubMedCrossRef Ehlayel M, de Beaucoudrey L, Fike F, et al. Simultaneous presentation of 2 rare hereditary immunodeficiencies: IL-12 receptor beta1 deficiency and ataxia-telangiectasia. J Allergy Clin Immunol. 2008;122:1217–9.PubMedCrossRef
20.
go back to reference Meller J, Malinin NL, Panigrahi S, et al. Novel aspects of Kindlin-3 function in humans based on a new case of leukocyte adhesion deficiency III (LAD-III). J Thromb Haemost. 2012;10:1397–408.PubMedCrossRef Meller J, Malinin NL, Panigrahi S, et al. Novel aspects of Kindlin-3 function in humans based on a new case of leukocyte adhesion deficiency III (LAD-III). J Thromb Haemost. 2012;10:1397–408.PubMedCrossRef
23.
go back to reference Naidoo R, Ungerer L, Cooper M, et al. Primary immunodeficiencies: a 27-year review at a tertiary paediatric hospital in Cape Town, South Africa. J Clin Immunol. 2011;31:99–105.PubMedCrossRef Naidoo R, Ungerer L, Cooper M, et al. Primary immunodeficiencies: a 27-year review at a tertiary paediatric hospital in Cape Town, South Africa. J Clin Immunol. 2011;31:99–105.PubMedCrossRef
24.
go back to reference Gupta S, Madkaikar M, Singh S, Sehgal S. Primary immunodeficiencies in India: a perspective. Ann N Y Acad Sci. 2012;1250:73–9.PubMedCrossRef Gupta S, Madkaikar M, Singh S, Sehgal S. Primary immunodeficiencies in India: a perspective. Ann N Y Acad Sci. 2012;1250:73–9.PubMedCrossRef
26.
go back to reference Leiva LE, Zelazco M, Oleastro M, et al. Primary immunodeficiency diseases in Latin America: the second report of the LAGID registry. J Clin Immunol. 2007;27:101–8.PubMedCrossRef Leiva LE, Zelazco M, Oleastro M, et al. Primary immunodeficiency diseases in Latin America: the second report of the LAGID registry. J Clin Immunol. 2007;27:101–8.PubMedCrossRef
27.
go back to reference Golan H, Dalal I, Garty BZ, et. al. The incidence of primary immunodeficiency syndromes in Israel. Isr Med Assoc J 2002; 868–871. Golan H, Dalal I, Garty BZ, et. al. The incidence of primary immunodeficiency syndromes in Israel. Isr Med Assoc J 2002; 868–871.
28.
go back to reference Sanal O, Tezcan I. Thirty years of primary immunodeficiencies in Turkey. Ann N Y Acad Sci. 2011;1238:15–23.PubMedCrossRef Sanal O, Tezcan I. Thirty years of primary immunodeficiencies in Turkey. Ann N Y Acad Sci. 2011;1238:15–23.PubMedCrossRef
29.
go back to reference Al-Tamemi S, Ibtisam E, Dennison D. Primary immunodeficiency diseases in Oman: five years’ experience at Sultan Qaboos University Hospital. World Allergy Organ J. 2012;5:52–6.PubMedCrossRef Al-Tamemi S, Ibtisam E, Dennison D. Primary immunodeficiency diseases in Oman: five years’ experience at Sultan Qaboos University Hospital. World Allergy Organ J. 2012;5:52–6.PubMedCrossRef
30.
go back to reference Al-Muhsen S, Casanova JL. The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases. J Allergy Clin Immunol. 2008;122:1043–51.PubMedCrossRef Al-Muhsen S, Casanova JL. The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases. J Allergy Clin Immunol. 2008;122:1043–51.PubMedCrossRef
31.
go back to reference Fieschi C, Dupuis S, Catherinot E, et al. Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications. J Exp Med. 2003;197:527–35.PubMedCrossRef Fieschi C, Dupuis S, Catherinot E, et al. Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications. J Exp Med. 2003;197:527–35.PubMedCrossRef
32.
go back to reference Lee WI, Kuo ML, Huang JL, et al. Distribution and clinical aspects of primary immunodeficiencies in a Taiwan pediatric tertiary hospital during a 20-year period. J Clin Immunol. 2005;25:162–73.PubMedCrossRef Lee WI, Kuo ML, Huang JL, et al. Distribution and clinical aspects of primary immunodeficiencies in a Taiwan pediatric tertiary hospital during a 20-year period. J Clin Immunol. 2005;25:162–73.PubMedCrossRef
Metadata
Title
Primary Immunodeficiency Diseases in Children: 15 Year Experience in a Tertiary Care Medical Center in Qatar
Authors
Mohammad S. Ehlayel
Abdulbari Bener
Mohammad Abu Laban
Publication date
01-02-2013
Publisher
Springer US
Published in
Journal of Clinical Immunology / Issue 2/2013
Print ISSN: 0271-9142
Electronic ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-012-9812-y

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