Skip to content

Advertisement

  • Poster presentation
  • Open Access

The spectrum of paediatric rheumatic diseases in two tertiary centres in Cape Town, South Africa

  • 1 and
  • 1
Pediatric Rheumatology201412 (Suppl 1) :P155

https://doi.org/10.1186/1546-0096-12-S1-P155

  • Published:

Keywords

  • Scleroderma
  • Connective Tissue Disease
  • Paediatric Rheumatology
  • Neutrophillic Dermatosis
  • Periodic Fever Syndrome

Introduction

Access to paediatric rheumatology services in sub-Saharan Africa is currently very limited with major challenges such as lack of trained personnel, diagnostic and therapeutic resources. Knowledge of the spectrum and incidence of paediatric rheumatologic diseases is important to aid in the advocacy for making paediatric rheumatology more visible and to improve access to the services in areas such as sub-Saharan Africa where the greatest unmet needs exist. However, data on the occurrence and incidence of paediatric rheumatologic diseases in Africa is scant. Single centre registry studies studies may help bridge this gap and guide planning interventions to address the diagnostic, therapeutic and human resource needs.

Objectives

To determine the spectrum and frequency of diseases seen in the paediatric rheumatology service of two tertiary health care facilities in Cape Town, South Africa.

Methods

We reviewed patient folders and the electronic data base of the department of paediatric rheumatology at the Red Cross children’s and Groote Schuur hospitals in Cape Town. The demographic features and diagnosis for patients seen between 2010 and May 2014 was extracted, analyzed and descriptive statistics presented using StataIC 11 software.

Results

A total of 462 patients were in the data base; 264 (57.8%) female. The median age at first presentation at our centre was 10 (IQR 6-12.8) years. One hundred and fifty four (33.3%) were diagnosed with JIA. Other notable diagnoses included HIV associated arthritis 15 (3.3%), neutrophillic dermatoses 4 and periodic fever syndromes 6 cases. Less common conditions seen included fibrodysplasia ossificans progressiva 3, aicardi guttierrez syndrome 2 and poncet’s disease 4 cases. The findings are summarized in the table below.
Table 1

Frequency table of category of diseases seen

Diagnosis

Frequency

Percent

Cumulative

JIA

154

33.3

33.3

Systemic CTDs

48

10.4

43.7

Uveitis

15

3.25

46.97

Vasculitis

22

4.8

51.77

Arthritis, HIV

15

3.25

55.02

Arthralgia other arthritis

81

17.5

72.52

Pain, CRPS and other

49

10.6

83.12

Other

78

16.9

100

Total

462

100

 

CTD=Connective tissue disease

Conclusion

A wide spectrum of paediatric rheumatologic diseases was seen in this study setting. JIA was the most frequent diagnosis at 33.3% of cases. Connective tissue diseases e.g SLE, JDM and scleroderma for which scant reports exist from Africa comprised a significant part of the work load (10.4%). Vasculitis 22 (4.8%) of the cases may have been underestimated as most cases of henoch schonlein and kawasaki’s disease were followed up in the general paediatrics department. Cross sectional studies such as this could aid in understanding the scope of the problem of paediatric rheumatologic diseases, and in guiding the planning and identification of resource needs as well as preparation of practice guidelines.

Disclosure of interest

None declared.

Authors’ Affiliations

(1)
Paediatric Rheumatology, Red Cross Children's Hospital, University Of Cape Town, Cape Town, South Africa

Copyright

Advertisement