Incidence of anxiety and depression in a predominantly HIV-infected population with severe adverse drug reactions

  • Eddy Zitha
  • Bonga Chiliza
  • Rudzani Muloiwa
  • Rannakoe Lehloenya
Open Access
Poster presentation


Depressive Symptom Drug Reaction Adverse Drug Reaction Eosinophilia Tertiary Hospital 
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Little is known on the short-term or medium-term psychological and psychiatric sequelae following Stevens Johnson syndrome (SJS), toxic epidermal necrolysis (TEN) and drug reaction with eosinophilia and systemic symptoms (DRESS). Based on this we did a prospective study designed to assess anxiety and depression in patients with severe cutaneous adverse drug reactions by indicating higher Hospital anxiety and depression scale (HADS).


We prospectively assessed 46 consecutive admissions with SJS, TEN and DRESS at a tertiary hospital in South Africa at 6 weeks and 6 months post discharge from hospital. We used a validated scoring system Hospital anxiety and depression scale (HADS) to assess anxiety and depressive in this cohort.


Forty-six patients were seen at six weeks and (n=38) 83% were reviewed at 6 months. Seventy-six percent of the participants were females and 82% were HIV-infected. Anxiety and depression were diagnosed in 37% and 30% respectively with six weeks with 8.6% exhibiting mixed anxiety and depressive symptoms. In comparison, at six months 13% had anxiety, 55% were depressed and 18.4% showed mixed anxiety and depressive symptoms. Nine and eight percent respectively at six weeks and six months warranted referral to a psychiatrist. Twenty-five percent of patients had anxiety and 40% had depression throughout the whole six months. The incidence of anxiety and depression was significantly associated with severity of the drug reaction.


SJS/TEN and DRESS are associated with anxiety and depression for at least 6 months. SJS/TEN showed higher degree of anxiety and depression compares to DRESS. Our findings should help to improve awareness of psychological impact of severe adverse skin reactions as these may impact on treatment compliance

Copyright information

© Zitha et al; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Authors and Affiliations

  • Eddy Zitha
    • 1
  • Bonga Chiliza
    • 2
  • Rudzani Muloiwa
    • 3
  • Rannakoe Lehloenya
    • 4
  1. 1.Division of Dermatology Department of MedicineUniversity of Cape Town and Groote Schuur HospitalSouth Africa
  2. 2.Department of PsychiatryUniversity of Stellenbosch and Tygerberg HospitalSouth Africa
  3. 3.Department of Paediatrics and Child HealthUniversity of Cape Town and Red Cross Children's HospitalSouth Africa
  4. 4.TBCIndia

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