eISSN: 2391-6052
ISSN: 2353-3854
Alergologia Polska - Polish Journal of Allergology
Current issue Archive Manuscripts accepted About the journal Supplements Special issues Editorial board Abstracting and indexing Subscription Contact Instructions for authors Publication charge Ethical standards and procedures
Editorial System
Submit your Manuscript
Share:
Share:
Original paper

Evaluation of primary immunodeficiency awareness of physicians in Türkiye

Mehmet Kılınç
1
,
Fatih Çölkesen
1
,
Filiz Sadi Aykan
1
,
Recep Evcen
1
,
Eray Yıldız
2
,
Şevket Arslan
1

  1. Department of Clinical Immunology and Allergy, Necmettin Erbakan University, Faculty of Medicine, Konya, Türkiye
  2. Department of Clinical Immunology and Allergy, Necip Fazıl City Hospital, Kahramanmaraş, Türkiye
Alergologia Polska – Polish Journal of Allergology 2024; 11, 1:
Online publish date: 2024/02/19
Article files
Get citation
 
PlumX metrics:
 

Introduction

Primary immunodeficiency (PID) is a rare, heterogeneous and broad group of diseases that includes over 400 innate immune defects that affect the development and function of the immune system [1]. PID has a prevalence reported between 1 : 16 000 and 1 : 50 000 [2]. The International Union of Immunology Societies (IUIS) updated in 2022, bringing the total number of PIDs to 485 [3]. PID is characterized by predisposition to severe recurrent infections, malignancies, atopy and autoimmune conditions [4]. The resulting complications lead to decreased quality of life and increased mortality in PID [5]. Over the last decade, studies have led to a better understanding of the pathophysiology of PID, enabling the development of more diagnostic and therapeutic strategies [6]. In many countries, lack of awareness of physicians about PIDs is one of the biggest problems that play a role in delayed diagnosis [7]. Published data on physicians’ awareness of PID are limited. In a study conducted in the United States of America and Iran, PID awareness was found in 32% of physicians [8, 9].

Aim

The aim of this study was to evaluate PID awareness in internal medicine, infectious disease and family physicians who are likely to encounter PID and to contribute to early diagnosis and timely treatment of patients.

Material and methods

Study design and population
This cross-sectional study included internists, infectious disease physicians and family physicians working in university hospitals, private hospitals, public hospitals and family health centers in Türkiye between May 2023 and October 2023. The study was approved by the local ethics committee of the Necmettin Erbakan University Faculty of Medicine (Decision no. 2023/4417).
An electronic questionnaire was created using the Google Forms platform (Google Inc., San Francisco, USA). The survey was distributed through WhatsApp (WhatsApp Inc., Mountain View, CA, USA) and email. Physicians answered the questions using the forms sent to them, but the doctor’s name was not disclosed in the forms. Electronic informed consent was obtained from each participant in accordance with the Helsinki Declaration. Survey questions presented to participants. The survey consisted of 15 questions developed by the authors and was conducted in Turkish. The English version of the questionnaire is provided in Supplementary material. Physicians were asked to complete the questionnaire only once.
The first part of the questionnaire identified the participating doctors by age, gender, academic degrees, years of work experience, specialty type and type of hospital (public hospital, university hospital, private hospital, family health center). The second part presented 8 questions about PID training and knowledge (clinical findings, auxiliary tests for diagnosis, treatment agents and follow-up etc.).
All participants evaluated the ‘PID 10 warning signs’ developed by the Jeffrey Modell Foundation (JMF) to assess the level of PID suspicion. Each correct answer was given 1 point, and the total was scored from 0 to 10. A comparison was made between specialties [10].
Statistical analysis
Categorical and ordinal variables were presented using frequency distribution, and proportions were compared using the χ2 test. Continuous variables were presented as median with interquartile range (IQR). The analysis of variance (ANOVA) presupposes the data normality. Due to lack of normality in the data, which was checked by the Kolmogorov-Smirnov test, the nonparametric Kruskal-Wallis test was used to compare the medians among more than two groups. All analyses were conducted using the SPSS statistical package (ver. 22.0; IBM Corp., Armonk, NY, USA). For all data analyses, differences were considered statistically significant when p < 0.05.

Results

Demographic characteristics of physicians
A total of 320 physicians were included in the study and 44.7% of them were male. The median age of participants was 32 years (IQR: 25–68 years) and the median years of practicing medicine was 7 (IQR: 1–42). Most of the participants (46.3%) worked in the university hospitals. Internal medicine was the most common specialty, and research assistant was the most common academic degree (45% and 57.2%, respectively) (Table 1).
PID training
Most participants (67.8%) had previously received training about PID, and 22% had followed a patient diagnosed with PID throughout their career.
Distribution of physicians’ answers to questions
Among the questions regarding the clinical presentation of PID, the most common response was ‘recurrent opportunistic infections’ (77.8%), and only 6.9% of physicians answered all of them correctly. Among the questions regarding the warning signs of PID, the most common response rate was ‘two or more new otitis media within 1 year’ (75%), and only 6.6% of physicians answered all of them correctly. The most common response to questions regarding the clue findings of PID was ‘lymphoid hyperplasia’ (81.9%), and only 4% of physicians answered all of them correctly. The most common response to questions regarding tests helpful in diagnosing PID was ‘immunoglobulins’ (98.1%), and 11.6% of physicians answered all of them correctly. In PID, the rate of those who answered the questions about vaccination incorrectly was 40%, and those who gave all the correct answers were 25%. The most common response to questions regarding treatment in PID was ‘immunoglobulin replacement therapy’ (98.8%), and 14.6% of physicians answered all of them correctly (Table 2).
PID 10 warning signs comparison between specialties
6.6% of participants were familiar with all PID warning signs. According to specialties, the most frequently familiar group was infectious disease and internal medicine physicians (14.6% and 6.9%, respectively). However,there was no statistically significant difference between groups (p = 0.058). ‘One pneumonia per year for more than 2 years’ was the most frequently observed warning sign by internal medicine physicians (90.2%). ‘Need for intravenous antibiotics to clear infections’ was the most frequently observed warning sign by infectious diseases physicians (85%). ‘Two or more new otitis media within 1 year’ was the most frequently observed warning sign by family medicine physicians (87.6%). However, there was no statistically significant difference (p = 0.4, p = 0.28, p = 0.68, respectively) (Table 3). There were no significant differences in other warning signs between the groups.
According to the JMF 10 warning signs, the total median score of internal medicine physicians was 7 points (IQR: 2–10), the total median score of infectious disease physicians was 7 points (IQR: 3–10), and the total median score of family physicians was 6 points (IQR: 2–10). However, no significant difference was observed between groups (p = 0.45) (Table 3).

Discussion

In this study, physician awareness and physician practices regarding the diagnosis and treatment of PID were evaluated. Early diagnosis and treatment of PID offers the best opportunity to reduce mortality and morbidity. It is estimated that the presence of PID is more common than expected and 70% to 90% of PIDs go undiagnosed [1]. In this study, internal medicine, infectious disease, and family physicians who are likely to encounter PID were included. It has been observed that approximately one third of the physicians have never received any training on PID and only 20% of them have followed a patient diagnosed with PID. Physicians most frequently chose recurrent opportunistic infections as the symptom of PID, while non-infectious findings (such as autoimmunity, malignancy) were less preferred. According to another important finding, only 6.6% of physicians were familiar with all of the JMF PID warning signs, which play an important role in the early diagnosis of PID. The rate of physicians who correctly answered all questions related to the diagnosis and management of PID was very low (4–14.6%). Complications of PID are usually detected after complications have occurred. It has been reported that the average delay in the diagnosis of common variable immunodeficiency (CVID), the most common symptomatic PID, is 6–7 years [11]. In developed countries, delay in diagnosis is an important problem regardless of the socioeconomic level, and a 5–10-year delay in the diagnosis of CVID has been found [12]. Furthermore, it was found that the delay in diagnosis decreased with the implementation of an educational program for early diagnosis of PID [13]. According to the JMF, physician education plays an important role in the early diagnosis of PIDs [14]. About 70% of physicians had received PID training in specialty training or medical school, but 45% were not familiar with PID warning signs [15]. Similarly, in this study, approximately one third of the physicians had never received any PID training before. Insufficient education of physicians about PID and difficulties in accessing training programs are among the main problems associated with delay in diagnosis or misdiagnosis [16]. The correct response rate of physicians to the questions in previous survey studies on PID awareness was very low (11.4% and 26%) and it was emphasized that there was a deficiency in PID knowledge [17, 18]. In this study, similarly, the correct response rate of physicians to questions related to the diagnosis and management of PID was very low (4–14.6%). The range of immune defects and clinical presentations may have reduced the awareness of PID. Nevertheless, the omission of PID-related presentations such as autoimmunity, autoinflammation and malignancy is a concern in the 10 warning signs proposed by the JMF [19]. It is therefore recommended that autoimmunity be included in the list of 10 warning signs of PID [20]. Majority of physicians associate infectious conditions due to opportunistic or unusual organisms with immunodeficiencies. More typical infectious findings enable physicians to better recognize PID [21]. Similarly, in this study, it was found that the highest level of awareness among the clinical presentations of PID was in the direction of recurrent infections, while awareness of non-infectious symptoms such as autoimmunity and malignancy was lower. In many studies, the 10 warning signs scale determined by the JMF has been reported to be useful in screening and early diagnosis of PID [14, 22]. In a similar previous study, the three most common clinical conditions recognized among the 10 warning signs of PID were pneumonia once a year for more than 2 years, two or more new otitis media within 1 year, and the need for recurrent intravenous antibiotics, respectively [23]. In a previous study, the most common warning signs of PID reported by physicians were recurrent otitis media and two or more pneumonias within one year [24]. In similar previous studies, it was observed that more than half of the physicians were not familiar with the JMF warning signs [23, 24]. In this study, similarly, familiarity with JMF warning signs was not found in the majority of physicians. PID 10 warning sign is frequently used in the comparison of PID awareness among physicians [23, 24]. In a comparison of PID awareness in hematology, general internal medicine physicians and pediatricians, familiarity with the PID 10 warning signs was higher in pediatricians than in other specialties. These differences were due to the experience of the doctors. Nevertheless, familiarity was similar between hematology and general internal medicine physicians, which are specialties related to adult patients [23]. Likewise, no significant difference was found between specialties in terms of familiarity with the ‘10 warning signs of PID’ in this study. For early and accurate diagnosis of PID, consideration of medical history and immunological evaluation is essential. The JMF’s ‘4 Stages of PID Test’ is useful for immunological evaluation in the diagnosis of PID. In accordance with the ‘4 Stages of PID Test’, 1st stage is general medical examination, differential complete blood count, serum immunoglobulin G (IgG), IgA, IgM, IgM, IgE and C-reactive protein (CRP) analysis, 2nd stage is serum IgG2 analysis, 3rd stage is lymphocyte subtype analysis, 4th stage is genetic tests [23]. Nevertheless, difficulty in access to laboratory tests and physicians and high test costs constitute an obstacle in the diagnosis of PID [17]. In a former study, most physicians responded in favor of evaluation of serum immunoglobulin levels after CRP and differential complete blood count tests [23]. Another study indicated that differential complete blood count and serum immunoglobulin levels were the most frequently requested tests, followed by IgG subgroup determination and chest X-ray [25]. In this study, the most frequently ordered test was serum immunoglobulins, followed by complete blood count. It is thought that genetic tests are necessary for the differential and definitive diagnosis of PID [26]. In recent 10 years, the discovery of monogenic causes of PID has been accelerating with next-generation sequencing (NGS) and has become the first-line diagnostic tool for most patients with suspected PID [27]. Genetic diagnosis, however, remains limited due to difficult access to NGS tests, high cost, and lack of information on the use of whole exome sequencing (WES) and targeted panels [28]. Similar to this study, in a previous study, genetic tests were among the least requested tests by physicians at the first stage in suspected PID [23]. New advances in the pathogenesis of PIDs have led to targeted therapies, hematopoietic stem cell transplantation (HSCT) and gene therapy in addition to symptomatic and maintenance therapy (immunoglobulin replacement therapy, antimicrobial, anti-inflammatory and immunosuppressive therapies) [28]. As to the awareness of PID treatment, the majority of physicians prefer immunoglobulin replacement therapy [9]. In the present study, immunoglobulin replacement therapy was the most preferred PID treatment option. However, as in a previous study, the majority of physicians in this study were not familiar with all treatment options [23]. Inactivated vaccines can be administered in the routine vaccination program in patients with PID. Live-attenuated vaccines (e.g., Bacillus Calmette-Guerin (BCG), oral polio virus, varicella) are generally contraindicated in PID due to the risk of side effects [29]. In case a child has a family history of immunodeficiency, clinicians should postpone BCG vaccination until immunodeficiency is excluded [30]. The majority of physicians in a previous study marked BCG vaccination as no in suspected PID. In this study, the majority of physicians predicted that live vaccines were contraindicated in PID. There are several limitations of this study. The first one is that this study was limited to physicians working in the departments of general internal medicine, infectious diseases, and family physicians, so the distribution of physicians may not be homogeneous. Secondly, as participation in the study was not compulsory, not all physicians to whom the questionnaire was sent could be included in the study, which may have reduced the participation rate. Despite the limitations, this study is one of the important studies that draws attention to PID awareness among physicians who are likely to encounter PID.

Conclusions

We demonstrate the lack of awareness about PID among general internal medicine, infectious disease, and family physicians. Despite recent rapid advances in the pathophysiology of PID, the delay in diagnosis of these diseases is still a major problem within the healthcare system. In PID, prompt diagnosis and treatment can be life-saving, and improve the quality of life of patients. An understanding of the causes of lack of awareness about PID will help in the correct management of these patients. According to this information, revising PID warning signs and organizing comprehensive training programs and courses on PID seem to be important factors in increasing physicians’ awareness of PID.

Conflict of interest

The authors declare no conflict of interest.
References
1. Bousfiha AA, Jeddane L, Ailal F, et al. Primary immunodeficiency diseases worldwide: more common than generally thought. J Clin Immunol 2013; 33: 1-7.
2. Grimbacher B. The European society for immunodeficiencies (ESID) registry 2014. Clin Exp Immunol 2014; 178 (Suppl 1): 18.
3. Tangye SG, Al-Herz W, Bousfiha A, et al. Human inborn errors of immunity: 2022 update on the classification from the international union of immunological societies expert committee. J Clin Immunol 2022; 42: 1473-507.
4. Quinn J, Orange JS, Modell V, et al. The case for severe combined immunodeficiency (SCID) and T cell lymphopenia newborn screening: saving lives… one at a time. Immunol Res 2020; 68: 48-53.
5. Sigstad HMH, Stray-Pedersen A, Frøland SS. Coping, quality of life, and hope in adults with primary antibody deficiencies. Health Quality Life Outcomes 2005; 3: 31.
6. Parvaneh N, Casanova JL, Notarangelo LD, et al. Primary immunodeficiencies: a rapidly evolving story. J Allergy Clin Immunol 2013; 131: 314-23.
7. 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.
8. Waltenburg R, Kobrynski L, Reyes M, et al. Primary immunodeficiency diseases: practice among primary care providers and awareness among the general public, United States, 2008. Genet Med 2010; 12: 792-800.
9. 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.
10. Quinn J, Modell V, Holle J, et al. Jeffrey’s insights: Jeffrey Modell Foundation’s global genetic sequencing pilot program to identify specific primary immunodeficiency defects to optimize disease management and treatment. Immunol Res 2020; 68: 126-34.
11. Costa-Carvalho BT, Wandalsen GF, Pulici G, et al. Pulmonary complications in patients with antibody deficiency. Allergol Immunopathol 2011; 39: 128-32.
12. Kainulainen L, Nikoskelainen J, Ruuskanen O. Diagnostic findings in 95 Finnish patients with common variable immunodeficiency. J Clin Immunol 2001; 21: 145-9.
13. Seymour B, Miles J, Haeney M. Primary antibody deficiency and diagnostic delay. J Clin Pathol 2005; 58: 546-7.
14. Modell V. The impact of physician education and public awareness on early diagnosis of primary immunodeficiencies: Robert A. Good Immunology Symposium. Immunol Res 2007; 38: 43-7.
15. de Vries E. Patient-centred screening for primary immunodeficiency: a multi-stage diagnostic protocol designed for non-immunologists. Clin Exp Immunol 2006; 145: 204-14.
16. Errante PR, Franco JL, Espinosa‐Rosales FJ, et al. Advances in primary immunodeficiency diseases in Latin America: epidemiology, research, and perspectives. Ann N Y Acad Sci 2012; 1250: 62-72.
17. Dantas EO, Aranda CS, Silva AR, et al. Doctors’ awareness concerning primary immunodeficiencies in Brazil. Allergol Immunopathol 2015; 43: 272-8.
18. 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.
19. Arkwright PD, Gennery AR. Ten warning signs of primary immunodeficiency: a new paradigm is needed for the 21st century. Ann NY Acad Sci 2011; 1238: 7-14.
20. Bjelac JA, Yonkof JR, Fernandez J. Differing performance of the warning signs for immunodeficiency in the diagnosis of pediatric versus adult patients in a two-center tertiary referral population. J Clin Immunol 2019; 39: 90-8.
21. Mazzucchelli J, Bonfim C, Castro G, et al. Severe combined immunodeficiency in Brazil: management, prognosis, and BCG-associated complications. J Investig Allergol Clin Immunol 2014; 24: 184-91.
22. Reda SM, Afifi HM, Amine MM. Primary immunodeficiency diseases in Egyptian children: a single-center study. J Clin Immunol 2009; 29: 343-51.
23. Imai K, Oh A, Morishita A, et al. Physician awareness and understanding of primary immunodeficiency disorders: a web-based study in Japan. Immunol Med 2023; 46: 45-57.
24. Veramendi-Espinoza LE, Zafra-Tanaka JH, Toribio-Dionicio C, et al. Awareness of primary immunodeficiency diseases at a national pediatric reference center in Peru. Einstein (São Paulo) 2021; 19: eAO6289.
25. Al-Hammadi S, Al-Reyami E, Al-Remeithi S, et al. Attentiveness of pediatricians to primary immunodeficiency disorders. BMC Res Notes 2012; 5: 393.
26. Bousfiha A, Moundir A, Tangye SG, et al. The 2022 update of IUIS phenotypical classification for human inborn errors of immunity. J Clin Immunol 2022; 42: 1508-20.
27. Heimall J. Now is the time to use molecular gene testing for the diagnosis of primary immune deficiencies. J Allergy Clin Immunol Pract 2019; 7: 833-8.
28. Delmonte OM, Notarangelo LD. Targeted therapy with biologicals and small molecules in primary immunodeficiencies. Med Princ Pract 2020; 29: 101-12.
29. Bonilla FA, Khan DA, Ballas ZK, et al. Practice parameter for the diagnosis and management of primary immunodeficiency. J Allergy Clin Immunol 2015; 136: 1186-205. e1178.
30. Santos A, Dias A, Cordeiro A, et al. Severe axillary lymphadenitis after BCG vaccination: alert for primary immunodeficiencies. J Microbiol Immunol Infect 2010; 43: 530-7.
Copyright: © Polish Society of Allergology This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivatives 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.


Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.