Abstract
Recurrent pericarditis is one of the most frequent pericardial diseases, affecting up to 30% of the patients who have experienced acute pericarditis. While the diagnosis of acute pericarditis is sometime straight forward, its etiology and therapeutic management are still a challenge for physicians. In developed countries, the idiopathic form is the most frequent, and the search for an infectious etiology is almost invariably negative. Nevertheless, since standard treatment with nonsteroidal anti-inflammatory drugs and colchicine is not always able to neutralize pericardial inflammation in recurrent pericarditis, anakinra, an IL-1 receptor antagonist, has been proposed as a possible therapeutic alternative for refractory forms. IL-1 is a cytokine that exerts a pivotal role in innate immunity and in the pathogenesis of some autoimmune diseases, such as rheumatoid arthritis, and in autoinflammatory disorders, as familial Mediterranean fever and cryopyrin-associated periodic syndromes. The successful management of patients with acute idiopathic recurrent pericarditis (IRP) needs a teamwork approach, where cardiologists, rheumatologists, clinical immunologists and internists are involved. In this review, we will discuss the clinical and therapeutical challenges of IRP both in adults and children from a clinical practice standpoint. We will also briefly illustrate the main pathogenic mechanisms of IRP to provide internists and cardiologists with the rationale for approaching the use of anakinra in selected clinical cases.
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Introduction
Acute pericarditis, particularly in its recurrent form, often requires the input of other specialists, such as rheumatologists and clinical immunologists in addition to cardiologists and internists. Not only can pericarditis be a clinical feature of a generalised autoimmune disorder, such as systemic lupus erythematosus (SLE), or of an autoinflammatory disease, such as familial Mediterranean fever (FMF), but it can also be secondary to an infectious or a malignant disease [1]. In developed countries, the idiopathic forms are the more frequently encountered in Emergency and Internal Medicine Units, and internists, together with cardiologists, often initially deal with these conditions [2]. Despite its diagnosis sometimes being straight forward, recurrent pericarditis challenges the physicians with therapeutic management [1]. Indeed, it is not infrequent in clinical practice to observe patients with recurrences due to an inappropriate therapeutic approach. In particular, corticosteroids sometimes are also used for the first acute episode, are known to favor relapses and chronicity [3], as well as an extreme rapid tapering of appropriate treatment [1]. In selected cases, when neither NSAIDs nor colchicine are able to induce a stable remission of pericardial inflammation, the use of anakinra, an IL-1 receptor antagonist (IL-1Ra), seems to offer a valuable therapeutic option [4, 5].
In this review, we will outline the main aetiopathogenic, diagnostic and clinical aspects of idiopathic recurrent pericarditis (IRP), with particular attention to the new therapeutic options, such as anakinra, with the aim to help teamwork and interaction between the different specialists involved in the clinical management of these patients.
Search strategy and selection criteria for review
We searched PubMed mainly matching the key search terms “idiopathic recurrent pericarditis”, “anakinra and pericarditis”, “interleukin-1 and pericarditis”, “recurrent pericarditis and treatment”. Full texts, as well as abstracts of 98 published original articles were reviewed. We also include some review papers. We considered 66 articles for the final literature revision. The search was limited to papers published in English language, and was conducted without any date limits through December 2017.
Epidemiology
Pericarditis has an important socio-economic impact, since it accounts for about 0.1% of hospitalisation for all causes. Moreover, it is responsible for 0.2% of all cardiovascular admissions, and about 5% of emergency department admissions for chest pain are due to pericarditis [6, 7]. Men, especially in the very young and adult age, have a higher risk of pericarditis than women, and mortality for acute pericarditis during hospitalisation is estimated to be about 1.1%, increasing with age and co-infections [8, 9].
In developed countries, acute pericarditis is a quite frequent disease. According to available studies, its incidence varies on the basis of the studies, ranging from 27.7 to 168/100,000 people/year [10, 11]. Data from Finland show an incidence of hospitalisations for acute pericarditis of about 3.3/100,000 people/year, but these data probably underestimate the problem, since it accounts for only hospitalized patients [9]. Additionally, IRP is not a rare event, considering that up to 30% of patients within 18 months after the first episode of acute pericarditis have a relapse [12]. Moreover, patients with a previous recurrence of pericarditis, have a new relapse in up to 50% of cases [13].
Aetiopathogenesis
In developed countries, about 80% of pericarditis cases are defined as “idiopathic” [12,13,14,15]. This term probably reflects our current incapacity to reveal the intimate mechanisms of the disease both for acute as for recurrent episodes [16]. The more accepted pathogenetic scenario is represented by the interaction between infectious agents (mostly viral), and the immune system via different pathways [17, 18]. For years, a derangement of adaptive immunity has been considered the main explanation for the recurrence of pericarditis. The most important direct and indirect clues supporting this hypothesis are: (1) the occurrence of pericardial involvement in autoimmune diseases, especially SLE [19], (2) the positive response to glucocorticoids [17], immunosuppressants interfering with cell mediated immunity (azathioprine) [20] or immunomodulatory treatments (intravenous immunoglobulins, IVIg) [21], and (3) the frequent presence of antinuclear antibodies (ANA) and the demonstration of auto-antibodies directed towards specific cardiac antigens [22].
However, more recently, innate immunity has emerged as pivotal in the pathogenesis of recurrent pericarditis [23, 24]. There is much evidence, including clinical, genetic and therapeutic that allows to assignment of several cases with recurrent pericarditis to autoinflammatory disorders. Many of the idiopathic forms, especially in the pediatric age, have a phenotype characterised by abrupt episodes of fever, dramatic elevation of inflammatory markers (erythrocyte sedimentation rate, ESR and C-reactive protein, CRP) and sometimes along with pleuropulmonary involvement, polyserositis and arthralgias [21]. Similarly, episodes are often followed by interval-free symptoms with complete wellness and full normalization of ESR and CRP [24]. In addition, this clinical course of IRP surprisingly resembles the clinical features of some autoinflammatory disorders, such as familial Mediterranean fever (FMF) or periodic syndrome associated with the tumor necrosis factor receptor (TRAPS) [25].
Autoinflammatory syndromes are a heterogeneous group of monogenic and polygenic disorders characterised by inflammation due to apparently unprovoked activation of the innate immune system [24, 26]. Genetic mutations mainly involve cryopyrin, a major component of a complex intracellular platform, known as inflammasome [27]. The latter is an enzymatic complex activated by cellular sensors like pathogen associated molecular patterns (PAMPs) or damage associated molecular patterns (DAMPs) through specific membrane (toll-like receptors, TLRs) or intracellular (NOD-like receptors, NLRs) receptors. This mechanism leads to the production of large amounts of IL-1, which in turn is able to recruit effector cells such as monocytes, macrophages and neutrophils [27]. The great production of IL-1 explains the remarkable therapeutic response to IL-1 receptor antagonist anakinra [24, 26] (Fig. 1).
FMF mutations are generally absent in IRP [28], while those associated with TRAPS have been observed in about 6–7% of patients with recurrences [29, 30]. Most of TRAPS-positive patients have a family history for pericarditis or recurrent fever syndromes, and usually are resistant to colchicine [24]. On the other hand, recurrent pericarditis can be one of the clinical manifestations of an autoinflammatory disorder, such as TRAPS [31] and FMF [32], and of note, a familial predisposition is present in up to 10% of the cases.
Diagnostic criteria and definitions
Acute, recurrent and refractory disease
Acute pericarditis
Acute pericarditis is defined as an inflammatory condition involving the pericardium, with a sudden onset, and characterised by at least two of the four following clinical features:
-
(a)
typical chest pain (almost in 100% of cases in adults);
(b)pericardial rubs (33% of cases);
(c)typical electrocardiographic changes (e.g., new widespread ST-elevation or PR segment depression) in about 50–60% of cases;
(d)pericardial effusion (new or worsening) in 60% of cases, and usually mild, less than 10 mm.
Acute pericarditis can be accompanied by other systemic manifestations, depending on the underlying causes (e.g., fever, arthralgias, pleural involvement, etc), elevation of ESR and CRP and leukocytosis are common (80% of cases) [1, 33]. Pleural effusions and pleuropulmonary involvement occur in approximately one-third of cases, particularly during the first and often more severe attacks, often associated with fever and elevated CRP [3].
Recurrent pericarditis
Pericarditis is defined as recurrent when a symptom-free interval of 4–6 weeks or longer occurs between a first acute episode and a relapse [1]. Clinical and ECG criteria of a recurrence are the same as in the first acute episode, the elevation of CRP being the most reliable biomarker, which is raised in approximately 80% of cases [1, 33]. As mentioned above, recurrences are relatively frequent (ranging from 15 to 50% of cases), and often occur due to inappropriate treatment of a first episode [1]. In doubtful or atypical cases, imaging can help to reach the diagnosis by the demonstration of pericardial inflammation by CT or cardiac magnetic resonance imaging (pericardial edema on T2-weighted imaging or pericardial late gadolinium enhancement) [1].
Refractory pericarditis
“Refractory pericarditis” is a pericarditis that recurs despite optimal medical therapy including colchicine and corticosteroids. In general, refractory cases (approximately 5% of the recurrent forms) are those that need to be controlled with: (a) doses of prednisone chronically higher than 10–15 mg/day, (b) alternative treatment (e.g., azathioprine, intravenous immunoglobulin) despite adequate treatment with aspirin or NSAIDs at high dosages plus colchicine [33].
Clinical course and management
When should I have to test for secondary forms of pericarditis?
In clinical practice, during the first episode of acute pericarditis, it is not mandatory to test for secondary forms [1]. Indeed, at least in industrialized countries, idiopathic (and probably viral) forms are the most common, and to find a specific viral diagnosis is often irrelevant for the management and treatment. Clinical features at presentation associated with a non-viral or non-idiopathic etiology are: (a) fever > 38 °C, (b) subacute course (symptoms developing over several days or weeks), (c) large pericardial effusion (diastolic echo-free space > 20 mm in width) or cardiac tamponade, and (d) inadequate response within 7 days to NSAIDs [34]. When one or more of these factors are present, a detailed diagnostic work-up is recommended based on the pre-test probability of a specific condition, such as neoplasms or tuberculosis or a defined rheumatic autoimmune disease (e.g., chest CT scan to assess possible neoplasms) [1].
Examples may be patients with: (1) refractory/recurrent courses despite adequate treatment, (2) familial or personal history for periodic fevers, (3) associated systemic symptoms (e.g., weight loss, arthralgias, pleural involvement, proteinuria, etc), and (4) coming from geographic area at high prevalence of tuberculosis.
Due to the risk of procedural complications (4–10% of cases) and the low diagnostic yield (the sensitivity of cytology for neoplasms is approximately 50%, as well as the sensitivity of Mycobacterium culture for tuberculosis), pericardiocentesis is generally indicated for symptomatic huge pericardial effusions not responsive to medical therapy or when high suspicion of infectious or neoplastic etiology is present [1].
How should I manage a patient with pericarditis? Poor prognostic factors, needs for hospital admission and biomarkers
Commonly, pericarditis has a good clinical course and prognosis in both adults and children [1, 35]. However, some risk factors (major and minor) are associated with a worse prognosis. Major risk factors, according to multivariate analysis [34], are the same described above as associated with a non-viral and non-idiopathic etiology (high-fever, subacute course, large pericardial effusion, and inadequate response to NSAIDs). Minor prognostic risk factors are less clearly defined, but the following are considered: (i) the presence of associated myocarditis, (ii) immune depression (determined from the presence of underlying inflammatory disease or due to the use of immunosuppressants), (iii) trauma, and (iv) oral anticoagulant treatment [1].
In clinical practice, every patient with a risk factor (either major or minor) should be hospitalized for a safer management, and the search carried out for secondary causes of pericarditis [1]. On the contrary, when risk factors are absent, patients can be safely managed and treated in the outpatient clinic. In this case, the use of empirical therapy with aspirin or NSAIDs plus colchicine is suggested, together with a short term follow-up (usually 1 week), to look for early complications [1] (Fig. 2).
The most reliable biomarker for monitoring pericarditis is CRP [1]. The normalisation of CRP, together with the disappearance of symptoms is used in clinical practice to follow patients, and to adjust and taper treatment. In particular, every tapering or discontinuation of the treatment (aspirin/NSAIDs, colchicine or corticosteroids), should be done according to CRP levels [1, 7, 33]. Among others, IL-8 (also known as CXCL8, a serum chemochine able to recruit neutrophils) has been related with a more frequent transition from acute pericarditis to IRP [36]. Nevertheless, its usage is currently limited to the research area.
Treatments
General overview
The first line treatment of acute and recurrent pericarditis is essentially the same, and consists of the use of aspirin or NSAIDs in combination with colchicine [1, 37] (Table 1). In selected cases (e.g., patients intolerant or in whom first line drugs have failed), low-doses of corticosteroids are allowed, but when possible, they should always be avoided as first line treatment, since they favor recurrences [38]. The treatment should be tailored to the patients’ features, co-morbidity and co-treatments, to increase the therapeutic compliance and reduce recurrences [1, 37]. As previously reported, the treatment duration, adjustment or discontinuation, need to be adequate according to clinical course and CRP levels [1] (Table 1).
Important practical tips to reaching a good control of the disease are the following: (a) use of NSAIDs at higher tolerated dosages, (b) aspirin, ibuprofen, and indomethacin should be administered every 8 h, (c) intravenous preparations are preferred in hospitalized patients, (d) add analgesics at fixed intervals (not on demand) such as codeine, tramadol, opioids for better pain control instead of increasing the dose of corticosteroids, (e) add paracetamol at fixed intervals for a better control of hyperpyrexia, (f) aspirin is preferred in patients who need antiplatelet therapy.
With regard to colchicine, avoid loading dosage or a daily dose higher than 1 mg (0.5 mg twice daily in patients with a body weight > 70 kg, and 0.5/day if under 70 kg or in patients over 70 kg who do not tolerate the standard daily dose). The dose is usually reduced in elderly patients and for renal insufficiency, considering that colchicine interacts with chlarytromicin, statins and diltiazem.
When combined with NSAIDs and colchicine, low doses of prednisone, starting with 7.5–10 mg/daily, usually allows control of pericarditis. Furthermore, the tapering of prednisone must be very slow since recurrences are typically expected when corticosteroid is reduced or discontinued. In case of relapse, NSAIDs should be increased instead of prednisone. Even though it is well known that corticosteroids should be avoided in the absence of a specific indication, they are often used in clinical practice, and also are sometimes also the first line treatment in pericarditis. Corticosteroids work very well in pericarditis, but unfortunately they have several drawbacks in this condition. Indeed, corticosteroids can (a) favor the recurrences of pericarditis, especially when used at high dose, (b) promote steroid-dependence, (c) reduce the efficacy of colchicine, and finally (d) cause severe side effects, especially in children, like growth retardation and disfiguring striae rubrae [1, 21]. However, corticosteroids can have a role in specific conditions, and in particular, to treat pericarditis secondary to autoimmune diseases (e.g., SLE) and in patients who are intolerant of aspirin or NSAIDs [1].
Therapy of refractory cases
The first therapeutic choice for refractory pericarditis is represented by the association of aspirin or NSAIDs at full dosage, intravenously in hospitalized patients combined with colchicine at the maximum dosage of 1 mg/daily plus low dose corticosteroids [33]. During drug tapering, it is not unusual for relapses to occur. Indeed, about 5% of the patients do not respond to this combined treatment. These patients, corticosteroid-dependent or colchicine-resistant, are the true refractory cases, and need a more intensive treatment, sometimes with immunosuppressive therapies [1].
In these cases, the treatments available are azathioprine (at a dosage of 2–3 mg/kg/day) [20], and IVIg [39] as on top treatment. More recently, the IL-1Ra anakinra has been successfully used [4, 40, 41] both in adults and children. Other systemic immunosuppressive treatments as cyclophosphamide [42], methotrexate and cyclosporine [43] have been anecdotally reported (Table 1). Finally, in selected patients with refractory recurrent pericarditis, pericardiectomy can be considered as an alternative to medical treatments [44].
Role of anakinra
Anakinra has emerged as a useful drug, beyond its indication in rheumatoid arthritis (RA) and cryopyrin-associated periodic syndromes (CAPS) [45]. Indeed, anakinra is currently used in several inflammatory immune-mediated conditions, most of them considered as polygenic autoinflammatory disorders [46,47,48,49].
Evidences supporting the use of anakinra for acute idiopathic recurrent pericarditis
Several previous data (mainly derived by case reports, case series and retrospective studies) and one recent randomised controlled trial, have demonstrated in the past few years, the valuable role of anakinra for the treatment of acute IRP [50].
Case reports and case series
Picco et al. described the first small series of patients treated with anakinra in 2009 [51]. Anakinra was prescribed to three pediatric subjects with corticosteroid-dependent IRP with an immediate clinical and laboratory response. This proof-of-concept observation points out three important conclusions: (1) all the patients were able to reduce/withdraw corticosteroids, (2) all the patients experienced a relapse during the follow-up after treatment was stopped, (3) for the first time the autoinflammatory nature of IRP was suggested. After a few years, Vassilopoulos and colleagues described the efficacy of anakinra in three adult patients with IRP [52], while two following case reports also reported a good clinical response in two pediatric subjects [53, 54].
Reports of particular cases
Some additional interesting cases were published in 2014. Massardier reported the efficacy of anakinra in two female patients over 60-years-old, with pericardial constriction refractory to conventional treatments. Interestingly, both the patients were steroid free at the time of starting anakinra because of comorbidities (diabetes in one and RA in the other one). The clinical message of interest for clinicians is that anakinra can be prescribed to patients with contraindications to corticosteroids, or with other systemic conditions that respond to anti-IL1ra [55]. In recent years, some papers have reported the efficacy of anakinra in refractory, truly autoinflammatory pericarditis, related to TNF-receptor mutations [30, 56, 57].
A minority (about 1%) of patients with acute IRP can develop in a few weeks/months subacute constrictive forms [1]. In such cases, the first line treatment consists of NSAIDs and colchicine, eventually followed by corticosteroids. However, these drugs can also worsen the haemodynamic of these patients, inducing further retention of water and sodium [16, 58]. In these cases, anakinra, at least in isolated case reports, seems to represent an effective alternative to pericardiectomy [41, 58, 59].
Retrospective studies
Two retrospective studies support the efficacy of anakinra in recurrent/refractory forms of pericarditis. The first one was a retrospective multicentric national evaluation of the long-term efficacy of anakinra both in children (n = 12) and adults (n = 3) with recurrent steroid-dependent pericarditis. All patients experienced a clinical and laboratory response, and were able to withdraw treatments (including corticosteroids). During the attempt to taper the treatment with anakinra, about half of the patients experienced a flare of disease, promptly controlled by the reintroduction of anakinra. Interestingly, during the whole follow-up (median 39 months, range 6–57 months), a reduction of about 95% of relapses was observed in respect to the pre-treatment period, thus demonstrating the long-term efficacy of anakinra monotherapy [60]. In one other retrospective study, Jain and colleagues evaluate the efficacy of anakinra in 13 patients with recurrent pericarditis, refractory to conventional treatments. All the patients experienced a response (complete or partial) in a few days. At the last follow-up (about 2 years), 85% of the patients had discontinued other treatments (including corticosteroids), and two of them had also discontinued anakinra [61]. More recently, in a multicentre cohort study comprising 110 pediatric cases of recurrent pericarditis collected in dedicated centres in Italy, anakinra was prescribed in 12 patients, with a significant reduction of recurrences [21].
Prospective studies
Lazaros [62] published a prospective open label study with anakinra as rescue treatment in ten refractory adult patients with IRP non-responder or intolerant to first line treatments (aspirin and NSAIDs), colchicine, steroids and azathioprine. The anti-IL-1ra was rapidly effective in all the patients, allowing a discontinuation of corticosteroids and colchicine. Following the discontinuation of anakinra, about 70% of the patients experience a relapse, well managed by reintroducing the drug.
Randomised controlled trial
Brucato et al. published the AnakInRa-Treatment of Recurrent Idiopathic Pericarditis trial (AIR-TRIP), the first randomised controlled trial on the efficacy of anakinra in patients with IRP colchicine-resistant or corticosteroid-dependent [4]. All patients included in the study (20 adults and 1 child 15-years-old) had a history of at least three recurrences and high levels of CRP.
The study clearly shows that anakinra, compared to placebo, was able to significantly reduce the risk of recurrence for a median period of 14 months, thus allowing the discontinuation of treatment with corticosteroids. Pericarditis flares were are markedly reduced in patients receiving anakinra, occurring in only 2 out of 11 (18%) patients randomised to anakinra, compared to nine out of ten (90%) patients randomised to placebo during the double-blind period [4]. Two out of 11 patients have flares of pericarditis during anakinra treatment, giving a rate of failure or of incomplete response to the standard dose of approximately 10–20%. This is in agreement with our current real world experience in which few patients need higher dosages of anakinra, or a combined therapy with colchicine or NSAIDs or low-dose corticosteroids to maintain complete control of the disease.
For a complete list of the studies on the use of anakinra in IRP see Table 2.
Anakinra in refractory pericarditis in the clinical practice: a brief guide
When to start anakinra and in which patient
In adults, anakinra should be reserved to adult patients with refractory corticosteroid-dependent and colchicine-resistant IRP and, importantly, elevated CRP. In children, anakinra should probably be considered instead of corticosteroids as a second line treatment after the failure of truly high doses of NSAIDs (i.e., full dosage every 8 h or intravenously) in combination with colchicine. This difference is due to the side effects of corticosteroids that heavily affect children more than adults. Moreover, children have a more overt autoinflammatory “phenotype” with fever, arthralgias and pleural involvement [21].
Dosage and duration of the treatment: suggestions from the studies and the clinical practice
In adults, the standard dose of anakinra is 100 mg/day subcutaneously, while in children, the suggested dose is 1–2 mg/kg/day. All studies have recorded high percentages of recurrences after anakinra discontinuation, so it should be cautiously tapered, only after a complete resolution of the symptoms and normalisation of serum inflammatory markers (especially CRP).
In Fig. 3 we propose a practical scheme based on expert-opinion, to gradually taper anakinra after a 3–6 months symptom-free-period and CRP normalisation.
Safety profile, adverse effects and management of the injection-site reactions
Among biological treatments, anakinra has demonstrated a good safety profile, particularly considering the very low risk of tuberculosis reactivation observed. However, whenever is possible, a serological screening is recommended before starting the treatment [46, 63, 64].
Severe reactions to anakinra have rarely been reported, but mild to moderate cutaneous adverse manifestations (mainly erythematous) at the injections site are frequent. In the AIR-TRIP trial they occurred in 20/21 patients (95%) during the first month of therapy, and then disappeared; three patients temporarily discontinued anakinra but resumed it after topical treatment and systemic antihistamines, and no patients discontinued the study for this adverse events.
In particular, warming the syringe to room temperature before use is advisable, along with application of a cold pack to the injection site approximately 2–3 min before and immediately after the injection. Patients should be informed in advance about the potential for such reactions to prevent unjustified drug discontinuation.
In selected cases, when anakinra has been poorly tolerated, desensitization to anakinra-related acute and delayed reactions have been proposed [65, 66].
Selection of the patients to treat with anakinra
Strict selection of patients is important: only patients with a clear inflammatory phenotype are good candidates for this therapy. Such patients usually have a history of high-fever, strikingly elevated levels of CRP, and pleural effusion, particularly in the pediatric age indicating a pivotal pathogenic role of IL-1. Conversely, patients with mild or doubtful symptoms or normal or near normal levels of CRP are not good candidates for anti-IL-1 therapy. Similarly, anakinra seems less suitable for patients with idiopathic large pericardial effusion and normal CRP.
On the other hand, anakinra might be considered in selected IRP patients with raised CRP, in whom conventional therapy with NSAIDs and corticosteroids might be risky, such as: (1) anticoagulated patients, (2) patients with kidney or heart failure, at risk of sodium and water retention, (3) patients with gastrointestinal hemorrhages, and (4) patients with recent cardiac surgery.
Cost of therapy with anakinra
At present, one dose of 100 mg of anakinra costs 26.3 € (US$ 32.3) to the health system in Italy. One year of therapy for each patient costs about 6000–8000 €, considering progressive tapering and dose reduction. The economic balance should consider that these unfortunate patients have a long history of hospital admissions and school or work absenteeism that are generally reduced after starting anakinra.
Importance of a multidisciplinary care for refractory patients
Cardiologists are usually the first physicians dealing with IRP, and are usually in charge of the instrumental follow-up (ECG, echocardiography). Similarly, internists working in Emergency Units or emergency physicians often initially care for these patients. However, due to the immune-mediated pathogenesis of IRP, and its refractoriness to conventional drugs, other specialists are also usually involved. Indeed, rheumatologists and clinical immunologists should be considered for a multidisciplinary approach, especially when secondary forms are suspected or the use of immunosuppressants or anakinra is planned.
Conclusions and perspectives
The IL-1 pathway has emerged as pivotal in the pathogenesis of IRP [18], and a recent randomised controlled trial demonstrates that the IL1ra anakinra is a valuable therapeutic option to treat this condition in clinical practice [4, 5]. Anakinra has demonstrated its efficacy both in adults and in children, with a good safety profile [4, 41]. However, some points need to be clarified in the near future: (1) what kind of patients really needs treatment with anakinra? (2) Might this drug be considered as first line therapy in selected patients? (3) How long should this therapy be prolonged, and how and when should it be tapered or discontinued?
Despite these unanswered questions, anakinra is now gaining a more established role in the treatment of refractory forms of IRP. A multidisciplinary approach is warranted in most complicated cases, and cardiologists and internists must be confident with the use of anakinra in clinical practice.
References
Adler Y, Charron P, Imazio M, Badano L, Barón-Esquivias G, Bogaert J et al (2015) ESC Guidelines for the diagnosis and management of pericardial diseases: the Task Force for the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology (ESC) endorsed by: the European Association for Cardio-Thoracic Surgery (EACTS). Eur Heart J 36:2921–2964. https://doi.org/10.1093/eurheartj/ehv318
Imazio M, Gaita F, LeWinter M (2015) Evaluation and treatment of pericarditis: a systematic review. JAMA 314:1498–1506. https://doi.org/10.1001/jama.2015.12763
Brucato A, Brambilla G, Moreo A, Alberti A, Munforti C, Ghirardello A et al (2006) Long-term outcomes in difficult-to-treat patients with recurrent pericarditis. Am J Cardiol 98:267–271
Brucato A, Imazio M, Gattorno M, Lazaros G, Maestroni S, Carraro M et al (2016) Effect of anakinra on recurrent pericarditis among patients with colchicine resistance and corticosteroid dependence: the AIRTRIP randomized clinical trial. JAMA 316:1906–1912. https://doi.org/10.1001/jama.2016.15826
Buckley L, Viscusi MM, Van Tassell B, Abbate A (2017) Interleukin-1 blockade for the treatment of pericarditis. Eur Heart J Cardiovasc Pharmacother. https://doi.org/10.1093/ehjcvp/pvx018
LeWinter MM (2014) Clinical practice. Acute pericarditis. N Engl J Med 371:2410–2416. https://doi.org/10.1093/ehjcvp/pvx018
Imazio M, Gaita F (2015) Diagnosis and treatment of pericarditis. Heart 2101:1159–1168. https://doi.org/10.1136/heartjnl-2014-306362
Shakti D, Hehn R, Gauvreau K, Sundel RP, Newburger JW (2014) Idiopathic pericarditis and pericardial effusion in children: contemporary epidemiology and management. J Am Heart Assoc 7 3(6):e001483. https://doi.org/10.1161/jaha.114.001483
Kytö V, Sipilä J, Rautava P (2014) Clinical profile and influences on outcomes in patients hospitalized for acute pericarditis. Circulation 130:1601–1606. https://doi.org/10.1161/CIRCULATIONAHA114.010376
Imazio M, Cecchi E, Demichelis B, Chinaglia A, Ierna S, Demarie D et al (2008) Myopericarditis versus viral or idiopathic acute pericarditis. Heart Br Card Soc 94:498–501. https://doi.org/10.1136/hrt.2006.104067
Søgaard KK, Farkas DK, Ehrenstein V, Bhaskaran K, Bøtker HE, Sørensen HT (2017) Pericarditis as a marker of occult cancer and a prognostic factor for cancer mortality. Circulation 12(136):996–1006. https://doi.org/10.1161/CIRCULATIONAHA.116.024041
Imazio M, Brucato A, Cemin R, Ferrua S, Maggiolini S, Beqaraj F et al (2013) A randomized trial of colchicine for acute pericarditis. N Engl J Med 17(369):1522–1528. https://doi.org/10.1056/NEJMoa1208536
Imazio M, Brucato A, Cemin R, Ferrua S, Belli R, Maestroni S et al (2011) Colchicine for recurrent pericarditis (CORP): a randomized trial. Ann Intern Med 155:409–414. https://doi.org/10.7326/0003-4819-155-7-201110040-00359
Imazio M, Bobbio M, Cecchi E, Demarie D, Pomari F, Moratti M et al (2005) Colchicine as first-choice therapy for recurrent pericarditis: results of the CORE (COlchicine for REcurrent pericarditis) trial. Arch Intern Med 165:1987–1991. https://doi.org/10.1001/archinte.165.17.1987
Imazio M, Belli R, Brucato A, Cemin R, Ferrua S, Beqaraj F et al (2014) Efficacy and safety of colchicine for treatment of multiple recurrences of pericarditis (CORP-2): a multicentre, double-blind, placebo-controlled, randomised trial. Lancet Lond Engl 383:2232–2237. https://doi.org/10.1016/S0140-6736(13)62709-9
Brucato A, Valenti A, Maisch B (2017) Acute and recurrent pericarditis: still idiopathic? J Am Coll Cardiol 69:2775. https://doi.org/10.1016/j.jacc.2017.02.072
Cremer PC, Kumar A, Kontzias A, Tan CD, Rodriguez ER, Imazio M et al (2016) Complicated pericarditis: understanding risk factors and pathophysiology to inform imaging and treatment. J Am Coll Cardiol 29(68):2311–2328. https://doi.org/10.1016/j.jacc.2016.07.785
Imazio M (2014) Idiopathic recurrent pericarditis as an immune-mediated disease: current insights into pathogenesis and emerging treatment options. Expert Rev Clin Immunol 10:1487–1492. https://doi.org/10.1586/1744666X.2014.965150
Urowitz MB, Tselios K (2017) Cardiovascular and pulmonary manifestations of systemic lupus erythematosus. Curr Rheumatol Rev. https://doi.org/10.2174/1573397113666170704102444
Vianello F, Cinetto F, Cavraro M, Battisti A, Castelli M, Imbergamo S et al (2011) Azathioprine in isolated recurrent pericarditis: a single centre experience. Int J Cardiol 147:477–478. https://doi.org/10.1016/j.ijcard.2011.01.027
Imazio M, Brucato A, Pluymaekers N, Breda L, Calabri G, Cantarini L et al (2016) Recurrent pericarditis in children and adolescents: a multicentre cohort study. J Cardiovasc Med Hagerstown Md 17:707–712. https://doi.org/10.2459/JCM.0000000000000300
Caforio ALP, Brucato A, Doria A, Brambilla G, Angelini A, Ghirardello A et al (2010) Anti-heart and anti-intercalated disk autoantibodies: evidence for autoimmunity in idiopathic recurrent acute pericarditis. Heart Br Card Soc 96:779–784. https://doi.org/10.1136/hrt.2009.187138
Maestroni S, Di Corato PR, Cumetti D, Chiara DBLC, Ghidoni S, Prisacaru L et al (2012) Recurrent pericarditis: autoimmune or autoinflammatory? Autoimmun Rev 12:60–65. https://doi.org/10.1016/j.autrev.2012.07.023
Cantarini L, Vitale A, Lucherini OM, De Clemente C, Caso F, Costa L et al (2015) The labyrinth of autoinflammatory disorders: a snapshot on the activity of a third-level center in Italy. Clin Rheumatol 34:17–28. https://doi.org/10.1007/s10067-014-2721-0
Rigante D, Vitale A, Lucherini OM, Cantarini L (2014) The hereditary autoinflammatory disorders uncovered. Autoimmun Rev 13:892–900. https://doi.org/10.1016/j.autrev.2014.08.001
Cattalini M, Soliani M, Lopalco G, Rigante D, Cantarini L (2016) Systemic and organ involvement in monogenic autoinflammatory disorders: a global review filtered through internists’ lens. Intern Emerg Med 11:781–791. https://doi.org/10.1007/s11739-016-1466-y
de Torre-Minguela C, Mesa Del Castillo P, Pelegrín P (2017) The NLRP3 and pyrin inflammasomes: implications in the pathophysiology of autoinflammatory diseases. Front Immunol 8:43. https://doi.org/10.3389/fimmu.2017.00043
Brucato A, Shinar Y, Brambilla G, Robbiolo L, Ferrioli G, Patrosso MC et al (2005) Idiopathic recurrent acute pericarditis: familial Mediterranean fever mutations and disease evolution in a large cohort of Caucasian patients. Lupus 14:670–674. https://doi.org/10.1191/0961203305lu2197oa
Cantarini L, Lucherini OM, Brucato A, Barone L, Cumetti D, Iacoponi F et al (2012) Clues to detect tumor necrosis factor receptor-associated periodic syndrome (TRAPS) among patients with idiopathic recurrent acute pericarditis: results of a multicentre study. Clin Res Cardiol Off J Ger Card Soc 101:525–531. https://doi.org/10.1007/s00392-012-0422-8
Emmi G, Barnini T, Silvestri E, Milco D’Elios M, Emmi L, Prisco D (2014) A new case of idiopathic recurrent acute pericarditis due to R104Q mutation in TNFRSF1A successfully treated with anakinra: expanding the questions. Clin Exp Rheumatol 32:297 Epub 2013 Dec 2
Dodé C, André M, Bienvenu T, Hausfater P, Pêcheux C, Bienvenu J et al (2002) The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome. Arthritis Rheum 46:2181–2188. https://doi.org/10.1002/art.10429
Lachmann HJ, Papa R, Gerhold K, Obici L, Touitou I, Cantarini L et al (2014) The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry. Ann Rheum Dis 73:2160–2167. https://doi.org/10.1136/annrheumdis-2013-204184
Imazio M, Spodick DH, Brucato A, Trinchero R, Adler Y (2010) Controversial issues in the management of pericardial diseases. Circulation 121:916–928. https://doi.org/10.1161/CIRCULATIONAHA.108.844753
Imazio M, Cecchi E, Demichelis B, Ierna S, Demarie D, Ghisio A et al (2007) Indicators of poor prognosis of acute pericarditis. Circulation 115:2739–2744. https://doi.org/10.1161/CIRCULATIONAHA.106.662114
Imazio M, Brucato A, Badano L, Charron P, Adler Y (2016) What’s new in 2015 ESC guidelines on pericardial diseases? J Cardiovasc Med Hagerstown Md 17:315–322. https://doi.org/10.2459/JCM.0000000000000358
Vasileiou P, Tsioufis C, Lazaros G, Hadziyannis E, Kasiakogias A, Stefanadis C et al (2014) Interleukin-8 as a predictor of acute idiopathic pericarditis recurrences. A pilot study. Int J Cardiol 1 172(3):e463–e464. https://doi.org/10.1016/j.ijcard.2014.01.029
Imazio M, Brucato A, Trinchero R, Spodick D, Adler Y (2009) Individualized therapy for pericarditis. Expert Rev Cardiovasc Ther 7:965–975. https://doi.org/10.1586/erc.09.82
Imazio M, Brucato A, Cumetti D, Brambilla G, Demichelis B, Ferro S et al (2008) Corticosteroids for recurrent pericarditis: high versus low doses: a nonrandomized observation. Circulation 118:667–671. https://doi.org/10.1161/CIRCULATIONAHA.107.761064
Moretti M, Buiatti A, Merlo M, Massa L, Fabris E, Pinamonti B et al (2013) Usefulness of high-dose intravenous human immunoglobulins treatment for refractory recurrent pericarditis. Am J Cardiol 1(112):1493–1498. https://doi.org/10.1016/j.amjcard.2013.06.036
Gaspari S, Marsili M, Imazio M, Brucato A, Di Blasi Lo Cuccio C, Chiarelli F et al (2013) New insights in the pathogenesis and therapy of idiopathic recurrent pericarditis in children. Clin Exp Rheumatol 31:788–794 (epub 2 Aug 2013)
Lazaros G, Vasileiou P, Danias P, Koutsianas C, Vlachopoulos C, Tousoulis D et al (2015) Effusive-constrictive pericarditis successfully treated with anakinra. Clin Exp Rheumatol 33:945 Epub 2015 Oct 30
Marcolongo R, Russo R, Laveder F, Noventa F, Agostini C (1995) Immunosuppressive therapy prevents recurrent pericarditis. J Am Coll Cardiol 26:1276–1279. https://doi.org/10.1016/0735-1097(95)00302-9
Raatikka M, Pelkonen PM, Karjalainen J, Jokinen EV (2003) Recurrent pericarditis in children and adolescents: report of 15 cases. J Am Coll Cardiol 42:759–764
Khandaker MH, Espinosa RE, Nishimura RA, Sinak LJ, Hayes SN, Melduni RM et al (2010) Pericardial disease: diagnosis and management. Mayo Clin Proc 85:572–593. https://doi.org/10.4065/mcp.2010.0046
Cantarini L, Lopalco G, Cattalini M, Vitale A, Galeazzi M, Rigante D (2015) Interleukin-1: Ariadne’s thread in autoinflammatory and autoimmune disorders. Isr Med Assoc J IMAJ 17:93–97
Emmi G, Talarico R, Lopalco G, Cimaz R, Cantini F, Viapiana O et al (2016) Efficacy and safety profile of anti-interleukin-1 treatment in Behçet’s disease: a multicenter retrospective study. Clin Rheumatol 35:1281–1286. https://doi.org/10.1007/s10067-015-3004-0
Vitale A, Insalaco A, Sfriso P, Lopalco G, Emmi G, Cattalini M et al (2016) A snapshot on the on-label and off-label use of the interleukin-1 inhibitors in Italy among rheumatologists and pediatric rheumatologists: a Nationwide Multi-Center Retrospective Observational Study. Front Pharmacol 7:380. https://doi.org/10.3389/fphar.2016.00380
Colafrancesco S, Priori R, Valesini G, Argolini L, Baldissera E, Bartoloni E et al (2017) Response to interleukin-1 inhibitors in 140 Italian patients with adult-onset Still’s disease: a Multicentre Retrospective Observational Study. Front Pharmacol 8:369. https://doi.org/10.3389/fphar.2017.00369
Fabiani C, Vitale A, Emmi G, Lopalco G, Vannozzi L, Guerriero S et al (2017) Interleukin (IL)-1 inhibition with anakinra and canakinumab in Behçet’s disease-related uveitis: a multicenter retrospective observational study. Clin Rheumatol 36:191–197. https://doi.org/10.1007/s10067-016-3506-4
Lazaros G, Antonatou K, Vassilopoulos D (2017) The therapeutic role of interleukin-1 inhibition in idiopathic recurrent pericarditis: current evidence and future challenges. Front Med 4:78. https://doi.org/10.3389/fmed.2017.00078
Picco P, Brisca G, Traverso F, Loy A, Gattorno M, Martini A (2009) Successful treatment of idiopathic recurrent pericarditis in children with interleukin-1beta receptor antagonist (anakinra): an unrecognized autoinflammatory disease? Arthritis Rheum 60:264–268. https://doi.org/10.1002/art.24174
Vassilopoulos D, Lazaros G, Tsioufis C, Vasileiou P, Stefanadis C, Pectasides D (2012) Successful treatment of adult patients with idiopathic recurrent pericarditis with an interleukin-1 receptor antagonist (anakinra). Int J Cardiol 160:66–68. https://doi.org/10.1016/j.ijcard.2012.05.086
Camacho-Lovillo M, Méndez-Santos A (2013) Successful treatment of idiopathic recurrent pericarditis with interleukin-1 receptor antagonist (anakinra). Pediatr Cardiol 34:1293–1294. https://doi.org/10.1007/s00246-013-0663-y
Scardapane A, Brucato A, Chiarelli F, Breda L (2013) Efficacy of an interleukin-1β receptor antagonist (anakinra) in idiopathic recurrent pericarditis. Pediatr Cardiol 34:1989–1991. https://doi.org/10.1007/s00246-012-0532-0
Massardier C, Dauphin C, Eschalier R, Lusson JR, Soubrier M (2014) Resistant or recurrent acute pericarditis: a new therapeutic opportunity? Int J Cardiol 177(2):e75–e77. https://doi.org/10.1016/j.ijcard.2014.09.192
Cantarini L, Lucherini OM, Cimaz R, Galeazzi M (2010) Recurrent pericarditis caused by a rare mutation in the TNFRSF1A gene and with excellent response to anakinra treatment. Clin Exp Rheumatol 28:802 Epub 2010 Oct 22
Camprubí D, Mitjavila F, Arostegui JI, Corbella X (2017) Efficacy of anakinra in an adult patient with recurrent pericarditis and cardiac tamponade as initial manifestations of tumor necrosis factor receptor-associated periodic syndrome due to the R92Q TNFRSF1A variant. Int J Rheum Dis 20:510–514. https://doi.org/10.1111/1756-185X.13029
D’Elia E, Brucato A, Pedrotti P, Valenti A, De Amici M, Fiocca L et al (2015) Successful treatment of subacute constrictive pericarditis with interleukin-1β receptor antagonist (anakinra). Clin Exp Rheumatol 33:294–295 Epub 2015 Jan 29
Schatz A, Trankle C, Yassen A, Chipko C, Rajab M, Abouzaki N et al (2016) Resolution of pericardial constriction with anakinra in a patient with effusive-constrictive pericarditis secondary to rheumatoid arthritis. Int J Cardiol 223:215–216. https://doi.org/10.1016/j.ijcard.2016.08.131
Finetti M, Insalaco A, Cantarini L, Meini A, Breda L, Alessio M et al (2014) Long-term efficacy of interleukin-1 receptor antagonist (anakinra) in corticosteroid-dependent and colchicine-resistant recurrent pericarditis. J Pediatr 164(1425–1431):e1. https://doi.org/10.1016/j.jpeds.2014.01.065
Jain S, Thongprayoon C, Espinosa RE, Hayes SN, Klarich KW, Cooper LT et al (2015) Effectiveness and safety of anakinra for management of refractory pericarditis. Am J Cardiol 116:1277–1279. https://doi.org/10.1016/j.amjcard.2015.07.047
Lazaros G, Vasileiou P, Koutsianas C, Antonatou K, Stefanadis C, Pectasides D et al (2014) Anakinra for the management of resistant idiopathic recurrent pericarditis. Initial experience in 10 adult cases. Ann Rheum Dis 73:2215–2217. https://doi.org/10.1136/annrheumdis-2014-205990
Lopalco G, Rigante D, Giannini M, Galeazzi M, Lapadula G, Iannone F et al (2016) Safety profile of anakinra in the management of rheumatologic, metabolic and autoinflammatory disorders. Clin Exp Rheumatol 34:531–538 (epub 26 Feb 2016)
Emmi G, Silvestri E, Squatrito D, Vitale A, Bacherini D, Vannozzi L et al (2017) Long-term efficacy and safety of anakinra in a patient with Behçet’s disease and concomitant tuberculosis infection. Int J Dermatol 56:218–220. https://doi.org/10.1111/ijd.13337
Şoyyiğit S, Kendirlinan R, Aydın O, Çelik GE (2014) Successful desensitization with anakinra in a case with immediate hypersensitivity reaction. Ann Allergy Asthma Immunol Off Publ Am Coll Allergy Asthma Immunol 113:325–326. https://doi.org/10.1016/j.anai.2014.06.017
Emmi G, Silvestri E, Cantarini L, Lopalco G, Cecchi L, Chiarini F et al (2017) Rapid desensitization to anakinra-related delayed reaction: need for a standardized protocol. J Dermatol 44:981–982. https://doi.org/10.1111/1346-8138.13619
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The authors would like to thank Maria L. Urban, Alessandra Bettiol, Stefano Salvati, Chiara Marvisi and Valerio Maniscalco for their help in preparing tables and figures.
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Brucato, A., Emmi, G., Cantarini, L. et al. Management of idiopathic recurrent pericarditis in adults and in children: a role for IL-1 receptor antagonism. Intern Emerg Med 13, 475–489 (2018). https://doi.org/10.1007/s11739-018-1842-x
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DOI: https://doi.org/10.1007/s11739-018-1842-x