Pain management strategies for neuropathic pain in Fabry disease - a systematic review

PubMed and Embase were searched from 1947 until September 2014 for relevant studies and reports on pain management strategies for neuropathic pain in FD. Key terms used were ‘Fabry disease’ and ‘pain’, including alternative notations. Also, ClinicalTrials.gov was searched to identify additional published or unpublished data. Additional reports were identified by hand searching the reference lists in the retrieved papers.

We included clinical trials, case series and case reports on the effect of pain medication in children as well as adults with FD and neuropathic pain. Studies on the effect of ERT on pain and reviews were not included in this review. Furthermore, studies lacking data on outcome were excluded. Articles reporting only on analgesics (acetaminophen and NSAIDs) were excluded, because these are known to be ineffective in the treatment of neuropathic pain in FD and the renal involvement due to FD makes NSAIDs unsuitable for chronic use in these patients. Title and abstract of all identified studies were read. If considered relevant, full text was read and analyzed. Data on pain severity and number of patients treated, drug and dosing regimen, study design, study duration and follow up, outcome measures and results, withdrawals and adverse events were extracted by one author (YS). As primary outcome we recorded chronic pain reduction after any treatment period as assessed in each study. Pain reduction was classified as complete relief of pain, partial relief of pain and no effect on the scale used in each study. As secondary outcome measures we recorded i) reduction of the frequency of pain attacks as reported by the patient, ii) any pain related outcome indicating improvement or worsening, iii) treatment withdrawals due to lack of effect, and iv) any (serious) adverse event while on treatment.

The search provided 728 articles (Fig. 1, study flow diagram). Three additional articles were found by searching the reference lists [17, 21, 22]. We excluded 629 articles after screening of title and abstract. One hundred and two articles were read in full text, of which 76 were subsequently excluded. Forty-eight of these 76 articles were considered to be less relevant, because referrals to other studies were made, no information was provided about analgesic treatment, or only conservative pain management (e.g., rest, holding ice packs) was described [11, 18, 20, 23‐38]. Twenty-seven articles provided information on pain management, but details on outcome were lacking. One case report describing a male patient using carbamazepine was excluded [39]. This 34-year old male carried a GLA variant (A143T) which is generally considered a polymorphism based on normal biopsy results and normal lysoGb3 levels in individuals carrying this variant [40‐42]. He had a 5-year history of activity-induced foot and leg cramps and fasciculations with pain, which is not a typical presentation of FD neuropathic pain, while the intraepidermal nerve fiber density, kidney biopsy and cardiac and brain investigations were all normal. Taking the controversial mutation and his clinical picture together, we considered his symptoms not to be caused by FD.

Twenty-six studies were included in the final analysis and these reported on 55 patients in total [21, 43‐67]. Patients were 3-45 years old, and at least 15 patients were below 18 years of age. An exact number could not be calculated due to the lack of data in the majority of included studies. Case-reports predominated; only 7/26 reports included more than 1 patient. None of the studies were randomized controlled trials. Three studies were performed with the specific aim to evaluate the effectiveness of a treatment for neuropathic pain in FD [43, 49, 53]. Treatment group sizes were small, ranging from 1 to 8 patients per report. A variety of different pain assessment tools was reported, including visual analogue scales (VAS) (4 %), the brief pain inventory (BPI) (4 %), pain relief scores (8 %), or other subjective pain scoring tools (84 %). The majority of studies (84 %) did not specify study duration. Where mentioned, most studies were of relatively short duration: individual treatment periods ranged from several days (case reports) to up to 5 years (observational studies). Details of included studies are reported in Table 1.

The following analgesics were used: carbamazepine, gabapentin, phenytoin, neurotropin and opioids Results of all pain strategies are summarized in Table 1.

Carbamazepine was used in 27/55 patients (49 %, reported in 18 studies), most often as mono-therapy (25 patients, 44 %, reported in 17 studies). Patients used carbamazepine dosages of 100-600 mg/day, or 0.8-15.9 mg/kg/day. Complete relief of pain was described in 5 of the 25 patients on mono-therapy [43, 58, 61, 67], partial relief in 16 patients [43, 46‐48, 52, 54, 55, 57, 59, 60, 62, 63, 65] and no effect in 3 [43, 67]. Additionally, 1 patient reported a reduced frequency and duration of crises. Four of the 25 patients were treated simultaneously with enzyme replacement therapy (ERT) and all showed partial pain relief. The effect of carbamazepine was confirmed by a double-blind cross-over design in one patient [54]. It was started with a daily dosage of 200 mg, which was enough to suppress the pain. Substitution by placebo was followed by a reappearance of the excruciating pain within 48 h, and readministration of the drug relieved the pain completely. In the same patient, the effect appeared faster and lasted longer than in the case of phenytoin [54]. Oral administration of carbamazepine was only partially helpful in alleviating the shooting pain in one patient (reported in two studies), but after treatment with neurotropin orally in addition to carbamazepine, the constant paresthesia and episodic shooting pain disappeared almost completely [45, 46]. Other combination strategies resulted in complete pain relief with gabapentin and carbamazepine in 1 patient [45]. Gabapentin alone was ineffective in a study by Park et al., but it should be noted that it was discontinued after just 2 days. Subsequently, a combination of phenytoin and carbamazepine was administered, which caused partial pain relief [51]. Gabapentin monotherapy has been described in one other study in which 6 patients were included. All of these patients showed a partial relief of pain on an average daily dose of 917 mg [53].

In a study by Filling-Katz, 5 of 7 patients on carbamazepine therapy had a history of phenytoin use [43]. Phenytoin at therapeutic dosages provided inadequate pain control by patient report in all 5 subjects. The effect of phenytoin was reported in an additional 22 patients (in 7 studies), with a dose range of 100-400 mg/day. Complete pain relief was achieved in 1 patient, and partial pain relief in 12 patients. Phenytoin was ineffective in 6 patients, even though treatment duration ranged from 6 months to 5 years [43]. In 8 patients a significant reduction in the frequency of pain attacks was described [56].

One study published in 1962 described the use of pethidine in 2 male patients, in whom partial pain relief was achieved with 500-700 mg/day IM [21]. Another study reports beneficial effect on pain during a crisis with intravenous lidocaine [67].

Three out of 20 studies including 4 patients reported on adverse effects of carbamazepine. Dose-related autonomic complications were reported in 2 patients, and necessitated dose reduction in 1 patient and discontinuation in the other [43]. Carbamazepine was discontinued because of drowsiness in 1 patient [62]. One patient had no adverse effects of carbamazepine [54]. Vertigo and blurred speech were reported in 1 patient treated with gabapentin, which disappeared upon dose reduction [53]. In the same study, it was stated that gabapentin was tolerated generally well in the other patients. The other study on patients using gabapentin did not report on adverse effects. Only 1 out of 8 studies in which phenytoin was used (n = 27 patients) reported on adverse effects. In this study 1 patient suffered from dizziness, drowsiness and headache [49]. Furthermore, discontinuation was reported for phenytoin because of poor compliance in 1 patient [44]. Few adverse effects (not further specified) were reported on the combination of neurotropin with carbamazepine in 1 patient [45].

As is evident from this review, the literature does not provide an answer to the important pragmatic question which drug should be prescribed for the treatment of neuropathic pain in FD. In addition, there is no sound evidence in which order drugs should be evaluated. Clinical practice has shown that most patients may achieve good results with carbamazepine or phenytoin. Phenytoin, however, is known to be associated with a number of potentially troublesome adverse events, including neurologic and hematologic effects [69]. In addition, there is an increased risk of teratogenicity for both carbamazepine and phenytoin. The teratogenic potential of the newer antiepileptic drugs and antidepressants in still unclear; small sample sizes and exposure to multiple drugs have precluded a definite conclusion so far. It is therefore important to discuss carefully and tailored to each patient, the benefit and risks of each drug for mother and fetus [70‐72]. Both carbamazepine and phenytoin are known to be broad-spectrum enzyme inducers by stimulating the activity of many cytochrome P450 (CYP) enzymes (CYP2B6, CYP2C9, CYP3A4 and CYP1A2) [73]. They can therefore reduce the effectiveness of several co-administered medications, such as statins (simvastatine, atorvastatine), SSNRI’s (duloxetine, venlafaxine), (dihydropyridine) calcium antagonists (e.g., amlodipine, nifedipine), angiotensin receptor blockers (ARBs) (losartan, candesartan, irbesartan), anticoagulants (warfarin) and steroids [74]. Taking into account that the incidence of kidney- and heart-related comorbidities is high in FD patients, interaction with calcium antagonists and ARBs is inconvenient.

Vice versa, other commonly prescribed drugs in patients with FD (fluoxetine, verapamil, amiodarone) may increase the serum concentration of phenytoin and carbamazepine by inducing CYP enzymes [75]. In women with neuropathic pain, it is important to note that carbamazepine, as well as phenytoin, increase the clearance of contraceptive hormones, which may lead to contraceptive failure. The use of carbamazepine and phenytoin is further limited by their potential to cause undesirable side-effects, such as gastrointestinal complaints and cytopenia. In addition, the need for laboratory monitoring (sodium, leukocytes, transaminases) in patients on carbamazepine resulted in preference for newer antiepileptic drugs, such as gabapentin and pregabalin. These are excreted unchanged through the kidneys with no reliance on liver metabolism. Therefore they do not lead to stimulation of the CYP enzymes and lower concentrations of other drugs as carbamazepine does [76]. On the other hand, the excretion by the kidneys results in the need for a dose reduction in renal insufficiency, one of the features of FD [77]. Since pharmacokinetics of gabapentin are nonlinear, dosing requires careful titration [76]. Pregabalin has pharmacokinetic advantages to gabapentin as it has linear pharmacokinetics. Consequently, dosing is more straightforward and requires only a twice daily administration [78]. The effectiveness and tolerability of pregabalin seem to be similar to those of gabapentin. Both drugs are fairly well tolerated. Dose-dependent dizziness and sedation can easily be reduced by starting with lower dosages and dose titration. However, although pregabalin and gabapentin are widely prescribed and effective for neuropathic pain in general, little is known about their effect in FD neuropathy [79].

Little has been reported about the use of dual serotonin and norepinephrine reuptake inhibitors such as venlafaxine and duloxetine in treating neuropathic pain due to FD. Duloxetine has shown consistent effectiveness in painful diabetic peripheral neuropathy, with effectiveness sustained for 1 year in an open-label trial [80]. Unfortunately, duloxetine has not been studied in other types of neuropathic pain, and so its effectiveness in such conditions is unknown. Besides, both duloxetine and venlafaxine have potential concomitant and undesirable adverse-effects in patients with FD because of their anti-cholinergic effect (e.g., constipation, anhydrosis, palpitations) [68]. Finally, opioids are shown to be effective in the treatment of painful crises [44], but it should be noted that the chronic use of opioids may cause obstipation, dependence, drowsiness and involves the risk of substance abuse.

Most of the medications we have discussed provide only partial pain relief, and adverse effects may limit dose escalation. Hence, in clinical practice, it would make sense to use 2 or more medications in combination in order to achieve either an additive beneficial effect or a reduction in the adverse effects associated with the use of a high dose of a single drug. However, little evidence is available to support the use of such combinations. Recently, combination therapy is advised if at least two monotherapies failed to relieve pain in FD [37]. A treatment algorithm is proposed, which advises second generation antiepileptics (pregabalin, gabapentin) to be used as medicines of first choice. Drugs of second and third choice were phenytoin, carbamazepine, and duloxetine. On the contrary, a report of an expert panel on the treatment of neuropathic pain in FD recommends carbamazepine as the drug of first choice. Anticonvulsants and antidepressants are also considered viable options [68]. Due to the limited amount of evidence with respect to the effectiveness of pain medication in FD, clinicians are often forced to rely on general neuropathic pain protocols. In a recently published meta-analysis about pharmacotherapy for neuropathic pain in adults, which included 229 studies, a strong recommendation was given for tricyclic antidepressants (amitriptyline), serotonin-noradrenaline reuptake inhibitors (duloxetine, venlafaxine), pregabalin, and gabapentin as first line treatment for neuropathic pain. Recommendations about carbamazepine were inconclusive [81]. Another guideline for the pharmacological management of neuropathic pain recommends duloxetine, venlafaxine, gabapentin, pregabalin and topical lidocaine as drugs of first choice. Opioids are recommended as drugs of second choice, and carbamazepine as drug of third choice [76].

Since conditions that cause neuropathic pain in children are relatively uncommon, data on general neuropathic pain treatment in children are limited by small numbers and few randomized controlled trials, leaving clinicians with many unanswered questions regarding clinical practice [82]. It is unclear if generalization of interventions used for neuropathic pain in adults may be appropriate. Therefore, trials are needed on both the safety and efficacy of drugs for the treatment of neuropathic pain in children [82, 83]. Despite the paucity of evidence, a treatment algorithm for the treatment of neuropathic pain in children with FD was published. It discusses the use of carbamazepine, antidepressants and anticonvulsants and includes dosing and titration schemes [84].

Although evidence exists suggesting that some diseases causing neuropathic pain respond differently to the same medications [85], we can conclude that it seems inevitable to base a treatment algorithm for FD patients for the greater part on experiences with neuropathic pain in general.

Taking all these findings and considerations into account we developed a treatment algorithm for pain management in patients (adults as well as children) with FD at our hospital (Academic Medical Center, Amsterdam, The Netherlands). In line with the expert panel report [68], the included studies in this review and our own clinical experiences, carbamazepine is considered the drug of first choice. In case of treatment failure or contraindications, we consider second generation anti-epileptics to be proper drugs of second choice. Drugs of third choice include SSNRI’s such as duloxetine and venlafaxine. In Appendix 1, an overview of all agents is presented.

Studies on the effect of ERT on neuropathic pain have shown conflicting results. Agalsidase alfa reduced the severity of neuropathic pain in a randomized controlled trial (RCT), but an imbalance in baseline pain scores hampers the interpretation of the results [86]. A RCT on the effect of agalsidase beta showed a significant reduction in pain in both the treatment and the placebo group [87]. Several observational studies showed no reduction of pain severity with ERT [87‐90], while there is some evidence that ERT has a positive effect on pain in children [31, 91]. Altogether, it remains unclear whether ERT has an effect on the neuropathic pain in patients with FD. Recently published European recommendations for initiation and cessation of ERT in FD indicate that ERT should be considered in patients with neuropathic pain, and may even be considered if the pain is completely controlled with pain medication [2]. The formulation of this recommendation implies that the decision to start ERT should be made on an individual basis taking into account FD features and personal preferences. In clinical practice, physicians will often start with pain management, for which the current algorithm can be of help to try to achieve maximum response. However, for future research, it would be interesting to conduct a properly designed study to clearly evaluate the effectiveness of ERT with or without concurrent use of pain medication on neuropathic pain.

The predominance of case-reports in this review has to be considered as a source of bias and therefore caution is needed in interpreting the data. Meaningful comparison of effectiveness with other interventions is not possible. In addition, this review suffers greatly from the lack of details provided in the case reports and case series.