Abstract
Stevens-Johnson Syndrome (SJS) is a severe and rare adverse drug reaction associated with significant morbidity and mortality. Although SJS is commonly triggered by multiple drugs, non-steroidal anti-inflammatory drugs (NSAIDs), including diclofenac, have been frequently implicated. A middle-aged woman, who is 50 years old, has a prior medical record of high blood pressure, type 2 diabetes, and has recently suffered from a pulmonary embolism. She was later admitted to the intensive care unit (ICU), where she was ultimately diagnosed with Steven Johnson syndrome. Careful drug selection, close monitoring of patients with predisposing factors, and prompt identification of adverse events are crucial to prevent severe drug reactions.
Keywords: Stevens-Johnson Syndrome, Anti-Inflammatory Agents, Adverse drug reaction, Diclofenac, Case report
Graphical Abstract
Highlights
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Stevens-Johnson Syndrome (SJS) is a rare but serious reaction of the skin and mucous membranes
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Drug-associated SJS is considered the most severe type of drug hypersensitivity reaction and can be life-threatening
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One medication that has been linked to the development of SJS is Diclofenac
1. Introduction
Stevens-Johnson Syndrome (SJS) is a rare but serious reaction of the skin and mucous membranes that can be caused by certain medications, infections, or autoimmune diseases [1]. It is estimated that the annual incidence rate of SJS in the US is around 3.4–6.1 per million population [2]. SJS is characterized by flu-like symptoms and a painful rash that spreads and blisters [3]. It can lead to severe complications, including skin infections, changes in skin color, scarring, and problems with organs such as the lungs, liver, and kidneys [4]. It can also cause long-term inflammation or vision problems in the eyes [5]. Drug-associated SJS is considered the most severe type of drug hypersensitivity reaction and can be life-threatening, with a mortality rate of up to 50% [6].
One medication that has been linked to the development of SJS is Diclofenac, which belongs to the nonsteroidal anti-inflammatory drug (NSAID) group [7]. Diclofenac is commonly used for its anti-inflammatory properties to reduce swelling, pain, or fever [8]. However, it should be avoided by individuals who have had allergic reactions to diclofenac or other NSAIDs, experienced side effects from taking NSAIDs, or have certain medical conditions such as lupus, hypertension, blood clotting disorders, Crohn's disease or ulcerative colitis, heart failure, severe liver or kidney disease, stomach ulcers, bleeding in the stomach or intestines, or are pregnant, planning to get pregnant, or breastfeeding [9].
Given the potential for serious morbidity and mortality associated with SJS, it is crucial to promptly identify and discontinue the causative medication. By understanding the risk factors and potential drug interactions, healthcare professionals can minimize the likelihood of developing SJS and improve patient outcomes. In particular, individuals with lupus should be cautious when considering the use of diclofenac, as it may exacerbate their existing skin problems and increase the risk of developing SJS. The work has been reported in line with the SCARE 2020 Criteria [10].
2. Presentation of case
A 50-year-old woman with a medical history of hypertension, type 2 diabetes, and recent development of pulmonary embolism was admitted to the ICU. The patient's condition required aggressive treatment, including heparin at a dose of 1000 units per hour. Additionally, a course of antibiotics, including meropenem and metronidazole, was initiated to target potential infections.
To manage the patient's pain, the physician prescribed diclofenac suppositories. Two days after the initiation of diclofenac treatment, the patient's general status began deteriorating, presenting respiratory distress and inadequate ventilation. Consequently, she required intubation and initiation of mechanical ventilation.
Following intubation, the patient's skin started peeling and erythematous lesions were observed throughout her body. Dermatology consultation was requested, and the patient was diagnosed with SJS triggered by diclofenac usage (Fig. 1.).
Fig. 1.
Stevens-Johnson Syndrome.
Upon the diagnosis of SJS, diclofenac was immediately discontinued. Supportive measures were initiated, including meticulous wound care, strict infection control, fluid resuscitation, nutritional support, and pain management. The patient was also started on systemic corticosteroids to modulate the immune response.
The patient's condition gradually stabilized and showed signs of improvement. Widespread skin detachment was managed, and replacement of damaged tissues occurred. Supportive therapy lasted for several weeks, emphasizing strict monitoring of vital signs, fluid and electrolyte balance, prevention of secondary infections, and pain control. Despite all efforts, the patient succumbed to respiratory failure and severe infection.
3. Discussion
SJS is a severe and potentially life-threatening hypersensitivity reaction that can be triggered by various medications [7]. In this case study, we present a 50-year-old woman who developed SJS after using a diclofenac suppository. The aim of this discussion is to explore the possible underlying mechanisms, highlight the importance of prompt recognition and management, and discuss the implications of this case.
The development of SJS in our patient following diclofenac suppository use raises concerns about the potential for this medication to induce severe adverse reactions [8]. Diclofenac is a NSAID commonly used for its analgesic and anti-inflammatory properties [9]. Although SJS is a rare adverse event associated with diclofenac use, previous reports have suggested a potential link between the drug and the syndrome.
It is important to note that SJS is a multifactorial condition that can be triggered by various factors, including genetic predisposition, viral infections, and medication use [11]. In our case, the temporal relationship between the initiation of diclofenac and the development of SJS suggests a possible drug-induced reaction. However, further investigations, such as patch testing or genetic studies, would be necessary to confirm the causal relationship.
The pathogenesis of SJS involves a complex interplay between the immune system and the drug or its metabolites [12]. It is hypothesized that certain drugs, including diclofenac binding to endogenous proteins and triggering an immune response. This immune response leads to the destruction of epidermal cells, resulting in the characteristic skin manifestations seen in SJS [13]. The severity of the reaction can vary, with SJS being the milder form and toxic epidermal necrolysis (TEN) representing the more severe end of the spectrum [14].
Prompt recognition and management of SJS are crucial to prevent further complications and improve patient outcomes [15]. In our case, the patient presented with fever, mucosal involvement, and a characteristic skin rash, which prompted the diagnosis of SJS. Immediate discontinuation of diclofenac, supportive care, and consultation with a dermatologist were essential in managing the patient's condition. Early recognition and appropriate management can help reduce morbidity and mortality associated with SJS [16].
The implications of this case study highlight the need for healthcare professionals to be aware of the potential risk of SJS associated with diclofenac use. Patient education regarding the signs and symptoms of SJS and the importance of seeking medical attention in case of any adverse reactions is crucial. Furthermore, healthcare providers should consider alternative treatment options or exercise caution when prescribing diclofenac to patients with a history of hypersensitivity reactions.
Educating patients about COVID-19 and potential drug reactions is crucial for nurses in ensuring the well-being of those under their care [17], [18], [19], [20], [21], [22], [23]. By providing clear and concise information, nurses empower patients to make informed decisions about their health. In the context of COVID-19, this education can include guidance on preventive measures, symptom recognition, and vaccination information [24], [25], [26], [27], [28], [29]. Additionally, informing patients about potential drug reactions helps in managing their medications effectively and reduces the risk of adverse effects [3], [4], [5], [6], [7], [8], [9], [10], [11], [12], [13], [14], [15], [16], [17], [18], [19], [20], [21], [22], [23], [24], [25], [26], [27], [28], [29], [30], [31]. Through education, nurses play a pivotal role in promoting patient safety, enabling individuals to actively participate in their own healthcare, and fostering a sense of trust and confidence in the healthcare system [32].
4. Conclusion
This case highlights the importance of vigilance when prescribing medications, especially in patients with multiple comorbidities. Diclofenac, although widely used for its analgesic effects, carries the risk of severe adverse effects such as Stevens-Johnson syndrome. It is crucial that healthcare professionals recognize these potential complications and exercise caution when prescribing diclofenac.
By understanding and identifying the risks associated with diclofenac, healthcare providers can minimize adverse outcomes and ensure patient safety. Promoting awareness about medication side effects, particularly in vulnerable populations, is vital for optimizing patient care and reducing preventable morbidity and mortality.
Ethical approval
The ethics committee of Urmia University of Medical Sciences approved the study (Ethical code: IR.UMSU.REC.1402.348).
Sources of funding
None.
Consent
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal on request.
CRediT authorship contribution statement
Pariya Mohsennezhad: Formal analysis, Data curation. Raheleh Pourbahram: Writing – review & editing. Elaheh Salamat: Supervision. Naser Parizad: Formal analysis, Supervision, Validation, Visualization. Yousef Mohammadpour: Project administration. Samaneh Bazbandi: Funding acquisition. Navid Faraji: Writing – original draft, Validation. Rasoul Goli: Data curation.
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Handling Editor: Dr. L.H. Lash
Contributor Information
Rasoul Goli, Email: goli.r@umsu.ac.ir.
Samaneh Bazbandi, Email: samanehbazbandy1397@gmail.com.
Data Availability
No data was used for the research described in the article.
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Associated Data
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Data Availability Statement
No data was used for the research described in the article.


