Abstract
Our objective was to evaluate whether IV immunoglobulin (IVIg) increases the risk of thromboembolic events in neurology outpatients with inflammatory neuropathies, as there is conflicting evidence supporting this hypothesis, mainly from non-neurologic cohorts. We investigated this question over 30 months in our cohort of patients with inflammatory neuropathies receiving regular IVIg and found a greater incidence of arterial and venous thromboembolic events than population-based rates determined by hospital admissions data. Vascular risk factors were more common in the event group but there were no IVIg administration factors that contributed to the risk. This study suggests that IVIg may have a small but contributory role in determining thromboembolic risk in the inflammatory neuropathy cohort and more evidence is required before it is clear whether the current primary prevention guidelines are appropriate in this group of patients.
Glossary
- CIDP=
- chronic inflammatory demyelinating polyneuropathy;
- CVD=
- cardiovascular disease;
- IVIg=
- IV immunoglobulin;
- MI=
- myocardial infarct;
- MMN=
- multifocal motor neuropathy;
- NHS=
- National Health Service;
- TEE=
- thromboembolic event
Introduction
Immune-mediated neuropathies are commonly managed with long-term IV immunoglobulin (IVIg). Adverse events associated with IVIg are usually mild and transient and include changes in blood pressure, tachycardia, mild flu-like symptoms, and headache. More serious adverse events are rare and include acute renal failure, aseptic meningitis, acute anaphylactic reactions, and hemolytic anaemia.1 An association between IVIg and either arterial or venous thromboembolic events (TEE) was suggested as long ago as 1986.2 Since then, studies looking at the incidence of IVIg-associated TEE have provided a wide range of rates from 3% to 11.2%.3,4
There are a number of pathogenic changes that occur following IVIg administration that could theoretically predispose to an increased TEE risk including an increase in serum viscosity, vasospasm, the release of vasoactive cytokines and clotting factors, sudden intravascular compartment expansion, and changes in venous compliance resulting in reduced capillary blood flow.1 However, the underlying characteristics of the individual and the disease being treated are likely to contribute and might explain some of the variation in observed rates.
A study looking specifically at inflammatory neuropathy patients receiving IVIg found that 11.3% of patients had a thromboembolic event over a 2-year period.4 Those who had an event were more likely to have a history of coronary artery disease, poor mobility, and cardiovascular risk factors than those who had no events. A dose of greater than 35 g/d was also associated with an increased risk of an event, although the total dose of IVIg per course was not. Clinically based studies tend to suggest an increased TEE risk but are limited by small numbers. The larger, prescription database studies are potentially biased by underreporting and are difficult to validate. Analysis of such data from the US health insurance records suggests a lower rate of thromboembolic events in otherwise high vascular risk individuals receiving IVIg and that IVIg may be protective due to its anti-inflammatory effects.3
Given this discrepancy, the risk of TEE events in patients on long-term IVIg remains uncertain and there are no guidelines about how the risk can be mitigated. In 2013, the Food and Drug Administration issued a black box warning for thrombosis related to human immunoglobulin products.5 They also suggest care should be taken in patients deemed to be at high risk of TEE to ensure adequate hydration and suggest monitoring baseline viscosity in patients at risk of hyperviscosity. There are inadequate epidemiologic and scientific data to support this advice.
Aim
The National Hospital for Neurology and Neurosurgery (NHNN) has a large cohort of well-characterized and closely monitored patients with inflammatory neuropathies (predominantly chronic inflammatory demyelinating polyneuropathy [CIDP] and multifocal motor neuropathy [MMN] with conduction block) managed with regular, long-term IVIg. Our aim was to ascertain the frequency of TEE in our patients and to investigate patient and treatment factors that potentially increase risk.
Methods
All patients with inflammatory neuropathy on regular IVIg between January 1, 2014, and July 31, 2016, were identified from our IVIg database and a retrospective chart review was performed. Patients treated acutely for Guillain-Barré syndrome (acute inflammatory demyelinating polyneuropathy) were excluded. Diagnosis, IVIg dose, frequency, vascular risk factors, pre- and post-treatment IgG levels, and plasma viscosity were recorded. Patients who had a TEE were identified from case note review and direct communication with the clinicians involved. Population-based TEE rates were obtained from contemporaneous hospital admissions data provided by National Health Service (NHS) Digital. NHS Digital is responsible for collecting and publishing data from the health and social care system in England and the hospital admission data are derived from the Hospital Episodes Statistics data warehouse where all admissions, appointments, and attendances for patients at NHS hospitals in England are recorded.6,7
QRISK2 is an assessment tool used in primary care to assess the 10-year risk of developing cardiovascular disease (CVD). A CVD risk score of 10% or more is a cutoff for considering statin treatment for primary prevention of CVD.8
Standard protocol approvals, registrations, and patient consents
This study was approved by the University College London Hospital Trust (UCLH) clinical governance ethics and consent framework.
Patient consent was waived for this retrospective audit.
Data availability
The neurology cohort data that support the findings of this study are available from the corresponding author upon reasonable request. Hospital admissions data on NHS Digital are freely available at digital.nhs.uk.
Results
A total of 112 patients were included. CIDP (61 patients) and MMN with conduction block (41) were the commonest indications; others included chronic immune sensory polyradiculopathy,6 dorsal root ganglionopathy,2 CANOMAD (chronic ataxic neuropathy ophthalmoplegia M-protein agglutination disialosyl antibodies),1 and small fiber neuropathy.1 Patients received a mean (SD) dose of 1.6 (1.2) g/kg/mo at a mean interval of 4.4 (3.0), range 1–18 weeks.
Thromboembolic events
Twelve TEEs were documented during the study period: 6 myocardial infarcts (MI), 2 strokes, and individual occurrences of deep vein thrombosis, pulmonary embolus, and superior vena cava obstruction secondary to thrombosis. None of the events occurred during or after the first course of IVIg. The incidence rates for any TEE, and arterial events or venous events considered separately, were markedly higher in our IVIg cohort compared to the general population (table). In the cohort, 85 (76%) patients mobilized independently, 13 (12%) used a single-point stick, 4 (3%) used 2 sticks, and 7 (6%) used a wheelchair; in the 11 patients with TEEs, 7 (64%) mobilized independently, 2 (18%) used 2 sticks, 2 (18%) used a wheelchair, and mobility status was unknown in 2 (18%) patients at time of event.
Incidence rates of thromboembolic events
Cardiovascular risk factors
Vascular risk factors were more common in the event group, including age, hypertension, diabetes, and hypercholesterolemia (p < 0.05). Smoking status was not different between the 2 groups (p = 0.67); of note, smoking rates were low in both groups (>75% nonsmokers).
In our group, the QRISK2 score was higher in those who had events (p < 0.05) (figure). However, 1 individual had an event despite a score of less than 10%. This patient had commenced on strontium and hormone replacement therapy for bone protection after having a pathologic fracture during an unsuccessful trial of corticosteroids for her neuropathy; she had a right-sided lacunar infarct within 2 weeks of her second IVIg treatment. The hematology opinion was that the cumulative procoagulant effect of these 3 treatments was the cause of her stroke. Another patient had a complex, multifactorial cause for TEE. This patient had an MI secondary to an unusual left circumflex artery occlusion with otherwise patent coronary vasculature. Extensive cardiologic investigation concluded that this embolic event was related to the combination of the procoagulant effect of IVIg, an indwelling central venous access device to facilitate home IVIg treatment, and a patent foramen ovale identified on bubble contrast echocardiography.
IVIg-related factors
There was no difference in the average monthly IVIg dose (p = 0.69) or daily dose in g/d (p = 0.28). There was a smaller treatment-related change in plasma IgG level (p < 0.05) and lower post-treatment plasma viscosity in those who had an event (p < 0.05).
Discussion
We did not identify a relationship between TEE and factors directly related to IVIg administration but there was a higher rate of vascular risk factors in the event group. This suggests that IVIg confers a small but contributory thromboembolic risk in the inflammatory neuropathy cohort and that we should screen for vascular risk factors prior to IVIg commencement and treat them assertively, perhaps with a lower threshold for primary prevention than in the general population. In those without obvious, modifiable vascular risk factors, other procoagulant risks should be considered. Recording of suspected adverse events is essential for detecting unrecognized trends and hazards. Interestingly, the National Immunoglobulin Database, which records all clinical and administration data regarding the use of immunoglobulin by the NHS, only has 4 TEEs recorded as adverse events since its inception in 2010 (email correspondence).
These data support the concern that incidence of TEE is higher in patients receiving long-term IVIg compared to population-based estimates and that large database studies are likely to underestimate this risk due to underreporting.
Author contributions
Jennifer Spillane: drafting/revising the manuscript, data acquisition, study concept or design, analysis or interpretation of data, accepts responsibility for conduct of research and final approval, acquisition of data, statistical analysis, study supervision. Christina Englezou: data acquisition, study concept or design, accepts responsibility for conduct of research and final approval, acquisition of data, study supervision. Scherezade Sarri-Gonzalez: analysis or interpretation of data, accepts responsibility for conduct of research and final approval, acquisition of data. Mahima Kapoor: drafting/revising the manuscript, accepts responsibility for conduct of research and final approval, statistical analysis. Robert Bell: drafting/revising the manuscript, accepts responsibility for conduct of research and final approval, study supervision. Alexander Rossor: drafting/revising the manuscript, accepts responsibility for conduct of research and final approval, acquisition of data. Hadi Manji: drafting/revising the manuscript, accepts responsibility for conduct of research and final approval, acquisition of data. Mary M. Reilly: drafting/revising the manuscript, study concept or design, accepts responsibility for conduct of research and final approval, study supervision, obtaining funding. Michael P. Lunn: drafting/revising the manuscript, data acquisition, study concept or design, analysis or interpretation of data, accepts responsibility for conduct of research and final approval, study supervision. Aisling Carr: drafting/revising the manuscript, study concept or design, analysis or interpretation of data, accepts responsibility for conduct of research and final approval, statistical analysis, study supervision.
Study funding
This research was supported by the National Institute for Health Research University College London Hospitals Biomedical Research Centre.
Disclosure
J. Spillane, C. Englezou, S. Sarri-Gonzalez, M. Kapoor, and R. Bell report no disclosures relevant to the manuscript. A. Rossor is funded by a Wellcome Trust Postdoctoral Fellowship for Clinicians (110043/Z/15/Z). H. Manji reports no disclosures relevant to the manuscript. M. Reilly received a Medical Research Council Centre grant (G0601943) and support from the National Institutes of Neurologic Diseases and Stroke and Office of Rare Diseases (U54NS065712). M. Lunn was a Primary Investigator in studies for CSL Behring, UCB Pharma, Novartis, and Octapharma, and has received ad hoc consulting fees from CSL Behring, UCB, and an honorarium from Terumo BCT. A. Carr reports Grifols sponsorship for attendance at meeting and honorarium from CSL and Lupin for an advisory role. Go to Neurology.org/N for full disclosures.
Footnotes
Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
The Article Processing Charge was funded by Wellcome Trust and UKRI.
- Received January 10, 2019.
- Accepted in final form August 15, 2019.
- Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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