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EULAR recommendations for the management of antiphospholipid syndrome in adults
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  1. Maria G Tektonidou1,
  2. Laura Andreoli2,
  3. Marteen Limper3,
  4. Zahir Amoura4,
  5. Ricard Cervera5,
  6. Nathalie Costedoat-Chalumeau6,
  7. Maria Jose Cuadrado7,
  8. Thomas Dörner8,
  9. Raquel Ferrer-Oliveras9,
  10. Karen Hambly10,
  11. Munther A Khamashta11,
  12. Judith King12,
  13. Francesca Marchiori13,
  14. Pier Luigi Meroni14,
  15. Marta Mosca15,
  16. Vittorio Pengo16,
  17. Luigi Raio17,
  18. Guillermo Ruiz-Irastorza18,
  19. Yehuda Shoenfeld19,
  20. Ljudmila Stojanovich20,
  21. Elisabet Svenungsson21,
  22. Denis Wahl22,
  23. Angela Tincani2,
  24. Michael M Ward23
  1. 1 First Department of Propaedeutic Internal Medicine, Joint Rheumatology program, National and Kapodistrian University of Athens, Athens, Greece
  2. 2 Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
  3. 3 Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, The Netherlands
  4. 4 Sorbonne University, French National Center for SLE and Aps, Service de Medecine Interne 2, InstitutE3M, Pitié Salpétrière, Paris, France
  5. 5 Autoimmune Diseases, Hospital Clinic, IDIBAPS, University of Barcelona, Barcelona, Spain
  6. 6 Centre de référence maladies auto-immunes et systémiques rares de l'île deFrance, Cochin Hospital, Université Paris Descartes-Sorbonne Paris Cité;INSERM U 1153, CRESS, Paris, France
  7. 7 Rheumatology Department, Clinica Universidad de Navarra, Madrid, Spain
  8. 8 Department of Med/Rheumatology and Clinical Immunology, Charite University Hospital, Berlin, Germany
  9. 9 Obstetrics and Gynecology Department and Systemic Diseases Research Unit, Vall ďHebron Research Institute-VHIR, Barcelona, Spain
  10. 10 School of Sport and Exercise Sciences, University of Kent, Chatham, UK
  11. 11 Rheumatology Department, Dubai Hospital, Dubai, United Arab Emirates
  12. 12 EULAR PARE Patient Research Partner, London, UK
  13. 13 EULAR PARE Patient Research Partner, Rome, Italy
  14. 14 MaACR, Immunorheumatology Research Laboratory, Istituto Auxologico Italiano, Milan, Italy
  15. 15 Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy
  16. 16 Department of Cardiac Thoracic and Vascular Sciences and Public Health, University of Padova, Padua, Italy
  17. 17 Department of Obstetrics and Gynaecology, University Hospital of Bern, Inselspital, Bern, Switzerland
  18. 18 Autoimmune Diseases Unit, Hospital Universitario Cruces, Barakaldo, Spain
  19. 19 Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel-Aviv University, Israel
  20. 20 Bezhanijska Kosa, Belgrade University, Belgrade, Serbia
  21. 21 Department of Medicine, Solna, Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden
  22. 22 Vascular Medicine Division and Regional Competence Center for Rare Vascular and Systemic Autoimmune Diseases and Vascular Medicine Division, Nancy University Hospital, INSERM UMR-S 1116 University of Lorraine, Nancy, France
  23. 23 Intramural Research Program, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland, USA
  1. Correspondence to Prof Maria G Tektonidou, First Department of Propaedeutic Internal Medicine, University of Athens, Athens 11527, Greece; mtektonidou{at}gmail.com

Abstract

The objective was to develop evidence-based recommendations for the management of antiphospholipid syndrome (APS) in adults. Based on evidence from a systematic literature review and expert opinion, overarching principles and recommendations were formulated and voted. High-risk antiphospholipid antibody (aPL) profile is associated with greater risk for thrombotic and obstetric APS. Risk modification includes screening for and management of cardiovascular and venous thrombosis risk factors, patient education about treatment adherence, and lifestyle counselling. Low-dose aspirin (LDA) is recommended for asymptomatic aPL carriers, patients with systemic lupus erythematosus without prior thrombotic or obstetric APS, and non-pregnant women with a history of obstetric APS only, all with high-risk aPL profiles. Patients with APS and first unprovoked venous thrombosis should receive long-term treatment with vitamin K antagonists (VKA) with a target international normalised ratio (INR) of 2–3. In patients with APS with first arterial thrombosis, treatment with VKA with INR 2–3 or INR 3–4 is recommended, considering the individual’s bleeding/thrombosis risk. Rivaroxaban should not be used in patients with APS with triple aPL positivity. For patients with recurrent arterial or venous thrombosis despite adequate treatment, addition of LDA, increase of INR target to 3–4 or switch to low molecular weight heparin may be considered. In women with prior obstetric APS, combination treatment with LDA and prophylactic dosage heparin during pregnancy is recommended. In patients with recurrent pregnancy complications, increase of heparin to therapeutic dose, addition of hydroxychloroquine or addition of low-dose prednisolone in the first trimester may be considered. These recommendations aim to guide treatment in adults with APS. High-quality evidence is limited, indicating a need for more research.

  • antiphospholipid antibodies
  • antiphospholipid syndrome
  • systemic lupus erythematosus
  • thrombosis
  • pregnancy morbidity
  • management
  • recommendations

https://doi.org/10.1136/annrheumdis-2019-215213

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    Introduction

    Antiphospholipid syndrome (APS) is a systemic autoimmune disorder with a wide range of vascular and obstetric manifestations associated with thrombotic and inflammatory mechanisms orchestrated by antiphospholipid (aPL) antibodies. Common APS clinical features include venous thromboembolism, stroke, recurrent early miscarriages and late pregnancy losses.1 According to current laboratory criteria for APS, aPL antibodies can be one of three types: lupus anticoagulant, anticardiolipin antibodies or antibeta2 glycoprotein I antibodies. Definite APS, fulfilling at least one clinical and one laboratory criteria of the updated Sapporo classification criteria, can occur in association with other autoimmune diseases, mainly systemic lupus erythematosus (SLE), or in its primary form (primary APS).1 2 Rarely, a life-threatening form of multiorgan thrombosis, known as catastrophic APS (CAPS), can occur. The presence of aPL in asymptomatic individuals or patients with SLE does not confirm the diagnosis of APS but can be associated with increased risk of thrombosis or pregnancy morbidity, depending on aPL characteristics and coexistence of other risk factors.3 4 The aPL type, the presence of multiple (double or triple) versus single aPL type, their titre (moderate-high titre vs low) and the persistence of aPL positivity in repeated measurements are defined as the ‘aPL profile’. The aPL profile is an important factor determining the risk of thrombotic and obstetric events, and consequently the intensity of treatment.3 4

    Clinical practice in APS is highly variable, in part because it is a rare disorder, and because knowledge about its diagnosis/classification, clinical spectrum and management is continuously advancing. There is a great heterogeneity among studies on the laboratory and clinical criteria used to define APS and the treatment approaches used over the past four decades. These factors make it often difficult to know the best approach to apply in daily practice. In addition, there is a paucity of high-quality randomised controlled trials (RCTs) in APS because of the difficulties in conducting adequately sized trials in an uncommon disease and using randomised designs among patients with often devastating clinical presentations. The objective of this project was to develop evidence-based recommendations for the prevention and management of adult APS that will help guide practice and improve quality of care and patient outcomes.

    Methods

    We followed the updated European League Against Rheumatism (EULAR) standardised operating procedure5 and used the Appraisal of Guidelines for Research & Evaluation II tool.6 The steering committee included the convenor (MGT), co-convenor (AT), methodologist (MMW) and two physicians (LA, ML) responsible for the systematic literature reviews (SLRs) (both were members of the Emerging EULAR Network -(EMEUNET)). The task force included members from 11 European countries: 12 specialists in rheumatology or internal medicine, 2 obstetricians (RF-O, LR), 2 physicians from vascular medicine/thrombosis centres (VP, DW), 1 healthcare professional (KH), and 2 patient representatives (FM, JK).

    The convenor prepared the first task force meeting and the first set of research questions on four major topics: risk stratification and risk modification in asymptomatic aPL-positive patients, primary and secondary thromboprophylaxis in APS, management of obstetric APS, and management of CAPS. The research questions were discussed among the task force members, and a set of 31 research questions was formulated using the PICO format (P, population; I, intervention; C, comparator; O, outcomes) and voted according to the Delphi method at a meeting in December 2017.

    The data sources for the SLR were PubMed, Embase and the Cochrane Library, which were searched for relevant English-language published articles from their inceptions through 31 January 2018. We included one RCT published after this date because of the importance of its reported safety results (Trial on Rivaroxaban in Antiphospholipid Syndrome (TRAPS) trial).7 Search terms were developed with the aid of an experienced librarian, who performed the searches. All titles and abstracts of retrieved articles were first reviewed independently by the two literature reviewers. The full-text articles were then reviewed independently by three persons: one literature reviewer, convenor and methodologist. The data abstraction was performed by the two literature reviewers according to a written protocol and supervised by the methodologist. Data abstraction was then independently double-checked by the convenor and methodologist. Each included article was graded for its methodological quality and assigned to the relevant PICO question by the convenor and methodologist. Data were tabulated and summarised by the methodologist in an evidence report that included summary of findings tables with pooled estimates of effect sizes for studies that directly addressed the population, intervention and comparator of PICO questions. Based on this evidence, a first draft of recommendations on 12 topics was prepared by the convenor and co-convenor. The draft recommendations and evidence report were sent to all task force members for review prior to the second task force meeting.

    The second task force meeting, held on 3 September 2018, included the presentation of SLR results, discussions of the first draft of recommendations in four working groups, working group presentations of the edited draft for each topic, and discussion and voting of the text. Incorporating additional discussions on wording changes, the final set of overarching principles and recommendations, including the level of evidence (LoE) and grade of recommendations (GoR) according to the Oxford Centre for Evidence-Based Medicine standards8 prepared by the methodologist in collaboration with convenors, was sent by the convenor to all task force members, who voted anonymously on the level of agreement (LoA). A rating scale of 0–10 (0: do not agree; 10: fully agree) was used for each recommendation. The manuscript was reviewed and approved by all task force members and the EULAR Executive Committee before submission.

    Results

    The SLR yielded 7534 articles and 15 hand-searched articles. After the titles and abstracts review, 670 articles were selected for full-text review. The full-text review yielded 249 articles for data abstraction; 61 were excluded and 188 articles were finally considered to be relevant. A detailed presentation of the results of the SLRs that informed the task force recommendations is published separately and should be reviewed together with this report.9 Based on the SLR results and expert opinion, 3 overarching principles and 12 recommendations were developed.

    Overarching principles

    1. Identifying the presence of factors associated with high risk for thrombotic and obstetric events is critical in patient management. A major risk factor is the high-risk aPL profile, including any of the following: the presence of lupus anticoagulant as the aPL subtype most closely related to thrombosis, the presence of double (any combination of lupus anticoagulant, anticardiolipin antibodies or antibeta2 glycoprotein I antibodies) or triple (all three subtypes) aPL positivity, or the presence of persistently high aPL titres,4 10 as also shown by the aPL score11 and Global Anti-Phospholipid Syndrome (GAPSS) Score.12 Definitions of medium-high aPL titres and of high-risk and low-risk aPL profiles are included in box 1. Additional risk factors for clinical events are coexistence of other systemic autoimmune diseases, especially SLE, a history of thrombotic and/or obstetric APS, and the presence of traditional cardiovascular risk factors.3 4 10

    2. The guidelines for cardiovascular disease (CVD) prevention in the general population should be followed. Screening for and management of venous thrombosis risk factors are also recommended. Heparin at prophylactic dosage, preferably low molecular weight heparin (LMWH), should be used in high-risk situations such as surgery, prolonged immobilisation and the puerperium.

    3. All patients treated with vitamin K antagonists (VKA) should receive counselling about treatment adherence, the need for close international normalised ratio (INR) monitoring especially in the setting of newly initiated treatment or bridging with heparin, the protocol of perioperative bridging therapy with heparin, and drug and food interactions. Counselling should be provided on the use of contraceptives, pregnancy planning and postmenopausal hormone therapy for all women with APS.13 Patients should also receive dietary counselling for CVD prevention. Physical activity is encouraged in patients with APS including those on oral anticoagulants.

    Box 1

    Definitions of medium-high antiphospholipid antibody (aPL) titres, and of high-risk and low-risk aPL profile

    Medium-high aPL titres.

    • Anticardiolipin (aCL) antibody of IgG and/or IgM isotype in serum or plasma present in titres >40 IgG phospholipid (GPL) units or >40 IgM phospholipid (MPL) units, or >the 99th percentile, measured by a standardised ELISA. Antibeta2 glycoprotein I antibody of IgG and/or IgM isotype in serum or plasma in titre >the 99th percentile, measured by a standardised ELISA.1

    High-risk aPL profile.

    • The presence (in 2 or more occasions at least 12 weeks apart) of lupus anticoagulant (measured according to ISTH guidelines), or of double (any combination of lupus anticoagulant, aCL antibodies or antibeta2 glycoprotein I antibodies) or triple (all three subtypes) aPL positivity, or the presence of persistently high aPL titres.

    Low-risk aPL profile.

    • Isolated aCL or antibeta2 glycoprotein I antibodies at low-medium titres, particularly if transiently positive.3

    Recommendations

    Table 1 presents the LoE, GoR and LoA for each recommendation. For recommendations with B GoR, we used the statement ‘is recommended’. For C and D grades, we mostly used the terms ‘may be considered’ or ‘could be considered’, with some exceptions according to experts’ judgement about the importance of the intervention. Recommendations that are phrased as ‘is recommended’ are those that the task force meant, based on the evidence and their experience, should be followed in almost all cases.

    View this table:
    Table 1

    EULAR recommendations for the prevention and management of APS in adults

    Primary thromboprophylaxis in aPL-positive subjects

    1. In asymptomatic aPL carriers (not fulfilling any vascular or obstetric APS classification criteria) with a high-risk aPL profile with or without traditional risk factors, prophylactic treatment with low - dose aspirin ( LDA ) (75 – 100 mg daily) is recommended.

    Use of LDA for primary prophylaxis is supported by results of a meta-analysis of seven observational studies of 460 asymptomatic aPL carriers that found the risk of first thrombosis to be reduced by half in those who used LDA versus those who did not use LDA.14 Most patients had high-risk aPL profiles, but few had traditional CVD risk factors. An association of similar magnitude was present in a smaller individual patient meta-analysis derived from these studies.15 Neither meta-analyses display worrisome variations as the directions were clear. Although evidence was largely from observational studies, the panel recommended the use of LDA for primary prophylaxis in asymptomatic aPL individuals with high-risk profile given the likelihood of benefit and low risk of adverse events of this intervention.

    2. In patients with SLE and no history of thrombosis or pregnancy complications:

    A. W ith high-risk aPL profile, prophylactic treatment with LDA is recommended .

    B. W ith low-risk aPL profile, prophylactic treatment with LDA may be considered.

    Treatment with LDA for patients with SLE and high-risk aPL profile is supported by a subanalysis of eight studies, mostly observational, in a meta-analysis.14 In this analysis, risk of first thrombosis was reduced by almost half among patients treated with LDA versus patients not treated, without major bleeding events. In an individual patient analysis, this association was independent of the use of hydroxychloroquine (HCQ), suggesting that LDA offers additional benefit in this patient group.15 Patients with high-risk aPL profile comprised the majority (but not all) of patients in these studies. Although there was heterogeneity between the studies, the direction of effect was clear. Less evidence is available on the use of LDA in patients with SLE and low-risk aPL profile, but pooled data from two cohort studies indicate that the use of LDA was also associated with a lower risk of thrombosis in this group.16 17

    3. In non-pregnant women with a history of obstetric APS only (with or without SLE), prophylactic treatment with LDA after adequate risk/benefit evaluation is recommended.

    The primary prevention of thrombosis with LDA in women with a history of obstetric APS without SLE was addressed in a meta-analysis including five observational studies.14 The pooled OR for first thrombosis associated with use of LDA was 0.25 (95% CI 0.10 to 0.62). Studies of women with SLE and prior obstetric APS are scarce, but the protective effect of LDA was supported by three retrospective studies that included a minority of patients with SLE.18–20 The panel recommended the use of LDA in women with a history of obstetric APS only, according to their thrombosis/bleeding risk (aPL profile, coexistent traditional cardiovascular risk factors, intolerance/contraindication to aspirin).

    Secondary thromboprophylaxis in APS

    4. In patients with definite APS and first venous thrombosis:

    A. Treatment with VKA with a target INR 2 – 3 is recommended.

    In patients with APS and first venous thrombosis, after an initial therapy with unfractionated heparin (UFH) or LMWH and bridging therapy of heparin plus VKA, treatment with VKA with a target INR of 2–3 is recommended. Data from an RCT21 reporting exclusively on patients with venous events and pooled data from five studies that included a majority with venous events21–25 showed no additional benefit of a target INR of 3–4 vs INR of 2–3. However, evidence is limited by the frequent failure to achieve the target INR in the high-intensity groups in the RCTs. Data on bleeding were not reported for patients with venous thrombosis specifically. However, although not based on data from these studies, higher level of anticoagulation would be anticipated to also have a higher risk of bleeding.

    B. Rivaroxaban should not be used in patients with triple aPL positivity due to the high risk of recurrent events. Direct oral anticoagulant s ( DOACs ) could be considered in patients not able to achieve a target INR despite good adherence to VKA or those with contraindications to VKA ( eg, allergy or intolerance to VKA).

    Despite the broadening use of DOACs in secondary thrombosis prevention in the general population, there is limited evidence about their effectiveness and safety in APS. In a post-hoc analysis of patients with APS included in three RCTs of dabigatran versus warfarin,26 and in one RCT of rivaroxaban versus warfarin in patients with venous thrombotic APS,27 there were no differences in outcomes between treatment with DOACs and VKA for venous thrombosis, but the evidence is limited by small samples, under-representation of high-risk patients with APS and short follow-up. A recent RCT of rivaroxaban versus warfarin in patients with APS with triple aPL positivity was prematurely terminated due to an excess of thromboembolic events (mostly arterial) in the rivaroxaban arm.7 Accordingly, rivaroxaban should not be used in patients with triple aPL positivity. The panel agreed that DOACs may be considered in patients with difficulty achieving a target INR of 2–3 despite compliance with VKA or who have contraindications to VKA. Switching from treatment with VKA to DOACs due to low adherence to VKA or INR monitoring should be avoided.

    C. In patients with unprovoked first venous thrombosis, anticoagulation should be continued long term.

    Use of long-term anticoagulation in patients with APS is supported by two small direct comparison studies (one RCT, one retrospective cohort)28 29 that showed a lower risk of recurrent venous thrombosis among patients with APS on long-term vs 3–6 months of oral anticoagulation. However, studies did not specify the proportion of patients with unprovoked thrombosis, making this evidence indirect.

    D. In patients with provoked first venous thrombosis, therapy should be continued for a duration recommended for patients without APS according to international guidelines. Longer anticoagulation could be considered in patients with high-risk aPL profile in repeated measurements or other risk factors for recurrence.

    This recommendation was based on expert opinion because we did not identify any studies that directly addressed the question of treatment duration after the initial provoked venous thrombosis. The panel recommended a duration of anticoagulation according to international guidelines for patients without APS30 because the benefit of long-term anticoagulation in this population is unclear. In patients with repeatedly high-risk aPL profile or those with additional risk factors for thrombosis recurrence, longer anticoagulation may be considered.

    5. In patients with definite APS and recurrent venous thrombosis despite treatment with VKA with a target INR of 2 – 3:

    A. I nvestigation of, and education on, adherence to VKA treatment, along with frequent INR testing, should be considered.

    B . If the target INR of 2 – 3 had been achieved, addition of LDA, increase of INR target to 3 – 4 or change to LMWH may be considered.

    There is limited evidence, mainly from case series, about therapeutic strategies for patients who have recurrent venous thrombosis despite a target INR of 2–3. Evaluation of the intensity of anticoagulation and adherence to treatment, patient counselling, frequent INR monitoring or a self-monitoring programme are important in optimising anticoagulation management. For adherent patients who have a recurrent thrombotic event, the addition of LDA, increase of INR target to 3–4 or switch to LMWH can be considered based on the individual’s characteristics and preferences (aspirin intolerance/contraindication, cost and side effects of continuous LMWH use). There is insufficient evidence to determine the relative efficacy and safety of these options in this patient group.

    6. In patients with definite APS and first arterial thrombosis:

    A . Treatment with VKA is recommended over treatment with LDA only.

    The use of VKA over LDA is supported by data from observational studies that showed a lower likelihood of recurrent thrombosis among patients with APS and prior arterial thrombosis (mainly stroke) treated with VKA versus LDA alone.31 32 An early study in older patients with strokes reported no difference in event recurrences between LDA and warfarin, but aPL was tested only once and was mainly of low titre in this study.33 These issues make it difficult to apply the latter results to patients of any age who fulfil the laboratory criteria for APS.

    B . Treatment with VKA with INR 2 – 3 or INR 3 – 4 is recommended, considering the individual’s risk of bleeding and recurrent thrombosis. Treatment with VKA with INR 2 – 3 plus LDA may also be considered.

    Patients with APS with arterial thrombosis have a higher risk of recurrence compared with those with venous thrombosis, and a tendency for recurrences in the same vascular (arterial) bed.34 An earlier SLR including mainly observational studies reported that recurrent events occurred more often in patients with APS treated with VKA with a target INR of 2–3 compared with an INR of 3–4, but outcomes among patients with first arterial thrombosis were not analysed specifically.35 This review did not compare the target INR 2–3 and INR 3–4 arms within the same study, but disaggregated the arms. Pooled data from two retrospective studies and two RCTs21–24 showed that there was no statistically significant difference in thrombosis recurrences between treatment with VKA with a target INR of 3–4 and treatment with INR of 2–3 (relative risk (RR) 0.46 (0.06–3.52)). However, these studies included a mixture of patients with either venous or arterial thrombosis, and a minority had arterial events. In one trial that provided data specifically on patients with arterial thrombosis, there was no difference in recurrences between those treated to a target INR of 2–3 or INR of 3–4 but without statistical significance (HR 3.1 (0.3–30.0)), although the sample was small and the achievement of a target INR of 3–4 was low.21 Because of these limitations, the higher intensity INR approach is preferred by some centres. In decision-making, physicians should take into account the individual’s risk of recurrent thrombosis and major bleeding, as well as the patient’s preferences after discussion. Alternatively, treatment with VKA with a target INR of 2–3 plus LDA is used by some experts, supported by limited data from one retrospective cohort study and one small RCT.36 37

    C. Rivaroxaban should not be used in patients with triple aPL positivity and arterial events. Based on the current evidence, we do not recommend use of DOACs in patients with definite APS and arterial events due to the high risk of recurrent thrombosis.

    According to the results of the TRAPS trial,7 rivaroxaban should not be used in triple aPL-positive patients with APS. In addition, an ongoing trial of apixaban in APS (Apixaban for the Secondary Prevention of Thromboembolism among patients with the AntiphosPholipid Syndrome ((ASTRO-APS)) (ClinicalTrials.gov identifier: NCT02295475) was recently modified after evaluation of their initial data to exclude patients with arterial thrombosis. Based on these data and those from case series reporting arterial thrombosis recurrences in patients with APS treated with DOACs, use of DOACs is not currently recommended in patients with definite APS and arterial events.38 Ongoing clinical trials will help to better define the role of DOACs in APS.

    7. In patients with recurrent arterial thrombosis despite adequate treatment with VKA, after evaluating for other potential causes, an increase of INR target to 3 – 4 , addition of LDA or switch to LMWH can be considered.

    Evidence on the management of recurrent arterial thrombosis despite VKA treatment is limited. The panel agreed that after evaluating other risk factors for thrombosis (eg, traditional cardiovascular risk factors, cancer, other thrombophilic states) and investigating the adherence to VKA treatment, increase of target INR to 3–4, or INR 2–3 with the addition of LDA, or switching to LMWH may be considered. Adjunctive therapy with antimalarials or statins could also be considered.4 10 39–41

    Obstetric APS

    8. In women with a high-risk aPL profile but no history of thrombosis or pregnancy complications (with or without SLE), treatment with LDA (75 – 100 mg/day ) during pregnancy should be considered.

    Data from one placebo-controlled RCT of LDA in six women with SLE42 and data from three low-quality studies (two RCTs, one retrospective cohort)43–45 of women without SLE found no difference in the prevalence of live births with use of LDA. However, these studies did not specifically include women with a high-risk aPL profile. The panel agreed that use of LDA should be considered in pregnant women with high-risk aPL profile due to the risk of obstetric and thrombotic complications during pregnancy associated with high-risk aPL profile.

    9. In women with a history of obstetric APS only (no prior thrombotic events), with or without SLE:

    A. W ith a history of ≥ 3 recurrent spontaneous miscarriages < 10 th week of gestation and in those with a history of fetal loss ( ≥ 10 th week of gestation), combination treatment with LDA and heparin at prophylactic dosage during pregnancy is recommended.

    Pooled data from one RCT including only patients with a history of first trimester losses46 and eight supporting observational studies47–54 that did not exclusively study women with early pregnancy losses indicated a higher likelihood of live births with combination treatment with LDA and heparin at prophylactic dosage versus LDA alone. Some experts believe that LDA alone can be also effective. For women with a history of fetal loss, combination treatment with LDA and heparin was associated with a higher likelihood of live birth compared with treatment with LDA alone. However, these studies included women with histories of both early and mid-pregnancy losses.48–52 LDA should be preferably started prior to conception, and heparin (LMWH or UFH) should be added as soon as pregnancy is confirmed. LMWH is preferred for practical reasons.

    B . W ith a history of delivery < 34 th week of gestation due to eclampsia or severe pre-eclampsia or due to recognised features of placental insufficiency, treatment with LDA or LDA and heparin at prophylactic dosage is recommended considering the individual’s risk profile.

    Data from two studies (one RCT, one retrospective cohort)48 55 showed that the likelihood of live births did not differ between women treated with LDA plus heparin and those treated with LDA alone. Physicians should tailor their treatment approach to the individual’s risk assessment including aPL profile and other risk situations (eg, presence of other cardiovascular risk factors or immobility).

    C. W ith clinical ‘ non-criteria ’ obstetric APS, treatment with LDA alone or in combination with heparin might be considered based on the individual’s risk profile.

    The ‘non-criteria’ obstetric APS manifestations included in our search were the presence of two recurrent spontaneous miscarriages <10th week of gestation or delivery ≥34 weeks of gestation due to severe pre-eclampsia or eclampsia. Because studies combined several types of pregnancy losses without specifying on the proportion of ‘non-criteria’ APS and due to very limited evidence, this recommendation is mainly based on expert opinion. Because of a potential higher risk for obstetric and/or thrombotic complications during pregnancy in women with a history of clinical ‘non-criteria’ obstetric APS, the panel agreed that treatment with LDA alone or in combination with heparin might be considered, based on an individual’s risk profile (aPL profile, concomitant SLE, prior live births, and additional risk factors for pregnancy loss or thrombosis).

    D. W ith obstetric APS treated with prophylactic dose heparin during pregnancy, continuation of heparin at prophylactic dose for 6 weeks after delivery should be considered to reduce the risk of maternal thrombosis.

    No studies directly tested the efficacy of extending treatment with prophylactic heparin after delivery. The panel suggested that in women receiving prophylactic dose heparin during pregnancy, the same dosage of heparin should be continued for 6 weeks after delivery due to an increased risk of thrombosis at puerperium.

    10 . In women with ‘ criteria ’ obstetric APS with recurrent pregnancy complications despite combination treatment with LDA and heparin at prophylactic dosage, increas ing heparin dose to therapeutic dose or addition of HCQ or low - dose prednisolone in the first trimester may be considered. Use of intravenous immunoglobulin (IVIG) might be considered in highly selected cases.

    The most common practice if the combination of LDA and prophylactic dose heparin fails is to increase the dose of heparin to therapeutic dose, although no supporting evidence exists. Other treatment strategies may include the addition of HCQ or low prednisolone doses in the first trimester. Evidence directly supporting these treatment options is based on two small observational studies with limited representativeness.56 57 Use of IVIG was not associated with a higher proportion of live births compared with conventional treatment in three small observational studies58–60 that directly addressed this question, although confounding by indication may have occurred. Although the expectation of benefit is small, the panel agreed that IVIG might be considered in highly selected cases when other treatments have failed.

    11 . In women with a history of thrombotic APS, combination treatment of LDA and heparin at therapeutic dosage during pregnancy is recommended.

    In observational studies, treatment with LDA and therapeutic dose heparin was associated with live births in 79% of pregnancies on average.52 61–64 Because a history of thrombotic APS is associated with increased risk for future thrombotic or obstetric events,65 treatment with LDA and heparin at therapeutic dosage during pregnancy is recommended. Switching treatment from VKA to therapeutic dose LMWH or UFH is recommended as soon as pregnancy is confirmed, ideally before the sixth week of gestation due to the teratogenic effects of warfarin.66

    Catastrophic APS

    12. The most common precipitating factors for the development of CAPS are anticoagulation discontinuation among patients with prior diagnosis of APS, infections and surgical procedures.67 Early diagnosis and management of infections and minimisation of discontinuation or low-intensity anticoagulation, especially perioperatively, are recommended.68 Based on the recently published clinical practice guidelines for CAPS management, combination therapy with glucocorticoids, heparin and plasma exchange or IVIG is recommended over single agents as first-line treatment of patients with CAPS.69 Concurrent treatment of precipitating factors is also recommended (eg, infections, gangrene or malignancy). For refractory CAPS, B cell depletion (eg, rituximab) or complement inhibition (eg, eculizumab) therapies may be considered based on data from case reports.69

    Discussion

    APS is a complex disorder and its management often involves collaboration among several medical specialties. The aim of these recommendations is to provide guidance to all health professionals involved in patient care, inform patients and support their engagement in shared decision-making, and provide evidence to researchers, funders and policy makers. The task force included members from several professional groups covering different perspectives and also involved two patients who participated actively in both meetings.

    The main challenge in developing recommendations for the management of adult APS was the low certainty of evidence. Many studies included patients with a mix of different clinical features and did not provide stratified data for arterial or venous thrombosis separately or for each of various types of obstetric APS. This resulted in only indirect evidence for many of the treatment decisions that were examined. Several meta-analyses also pooled studies of heterogeneous patient groups. A high risk of bias and low power, mostly due to the rarity of the syndrome, were also common in RCTs. Therefore, a significant number of recommendations necessarily relied more, or only, on low-quality evidence or expert opinion. An important consideration for future research would be well-designed observational studies and RCTs of homogeneous patient populations. These studies will hopefully increase the quality of evidence for the currently used treatments and answer questions about controversial issues and new potential therapies (box 2).

    Box 2

    Research agenda

    Risk stratification.

    • Better definition of high-risk and low-risk aPL profile. Better delineation of the risk associated with different aPL profiles to allow improved classification of patients in research studies.

    Primary thrombosis prevention.

    • Impact on thrombosis risk of intensive management of traditional risk factors such as smoking cessation, control of hypertension, dyslipidaemia and sedentary behaviour.

    • Evaluation of the role of HCQ for primary thrombosis prevention in subjects with high-risk aPL profile: (1) asymptomatic aPL carriers, (2) patients with a history of obstetric APS without SLE and (3) non-criteria APS manifestations (eg, thrombocytopaenia, heart valve disease and aPL-associated nephropathy).

    • Evaluation of the role of statins or coenzyme Q10 for primary thrombosis prevention.

    Secondary thrombosis prevention.

    • Controlled studies of the efficacy and safety of treatment with VKA with target INR of 3–4 versus combination treatment of VKA with target INR of 2–3 and LDA for patients with a history of first arterial thrombosis.

    • Duration of VKA in provoked first venous thrombosis.

    • Controlled studies of the efficacy of therapy of VKA alone versus VKA plus HCQ for patients with a history of first arterial thrombosis.

    • Controlled studies of the efficacy and safety of targeted therapies (eg, B cell depletion therapy, complement inhibitors, or mammalian target of rapamycin (mTOR) inhibitors) in recurrent arterial thrombotic events despite treatment with VKA with a target INR of 3–4.

    • Adjunctive treatment for recurrent arterial thrombosis: HCQ, statins or vitamin D. Evaluation of the role of platelet inhibitors (other than LDA), for example, ADP receptor inhibitors, adenosine reuptake inhibitors and others.

    • Discontinuation of VKA treatment in patients who became negative for aPL in repeated measurements.

    Obstetric APS.

    • Controlled studies of the efficacy and safety of treatment with LDA and heparin versus treatment with LDA, heparin and HCQ in women with a history of recurrent obstetric complications.

    • Efficacy of 150 mg daily versus 100 mg daily of aspirin.

    • Safety and efficacy of statins in pregnant women with APS who develop pre-eclampsia despite treatment with LDA and heparin.

    • aPL, antiphospholipid antibody; APS, antiphospholipid syndrome; HCQ, hydroxychloroquine; INR, international normalised ratio; LDA, low-dose aspirin; SLE, systemic lupus erythematosus; VKA, vitamin K antagonist.

    The cost and availability of suggested treatments are not a barrier to implementation of these recommendations, with the exception of IVIG and plasmapheresis. However, both treatments were recommended as first-line treatment only in CAPS which occurs in less than 1% of patients, while B cell depletion and complement inhibitors may be considered in refractory cases of CAPS. Implementation into clinical practice can be facilitated by the dissemination of the recommendations using online media, by presentations in national and international congresses, development of workshops in meetings of different specialties involved in APS management, or educational lectures for healthcare providers in referral hospitals.

    Better understanding of the pathophysiological mechanisms of APS will help to identify new therapeutic targets, and a balance between anticoagulation and immunomodulatory drugs for different APS manifestations. In addition, studies that examine homogeneous patient groups can better evaluate the efficacy and safety of the currently available and new treatments. When sufficient new information will be available, an update of the current recommendations will take place. The task force members believe that these recommendations will help to improve the quality of care in patients with APS and foster future research by highlighting evidence gaps.

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    Footnotes

    • Handling editor Josef S Smolen

    • AT and MMW contributed equally.

    • Correction notice This article has been corrected since it published Online First. The discussion section has been amended and the title in table one.

    • Contributors Full-text review, data abstraction and risk of bias assessments were performed by LA and ML, and independently double-checked by MGT and MMW. MMW supervised the methodology of the SLR and prepared the evidence report. MGT and AT prepared the first draft of recommendations, and all authors have participated in the discussion and formulation of recommendations. MGT supervised the project and drafted the manuscript. All authors reviewed the manuscript and approved its final version.

    • Funding This project was funded by the European League Against Rheumatism. MMW was funded by the Intramural Research Program, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH.

    • Competing interests None declared.

    • Patient consent for publication Not required.

    • Provenance and peer review Not commissioned; externally peer reviewed.