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Oral versus intramuscular administration of vitamin B12 for vitamin B12 deficiency in primary care: a pragmatic, randomised, non-inferiority clinical trial (OB12)

Published in The British Medical Journal -

Introduction

Vitamin B12 (VB12) is an essential nutrient for the synthesis of cellular DNA. It is generally accepted that daily needs in adults range from 1 to 2 µg/day,1 but other standards recently recommend 3–4 µg/day.2 The Western diet is estimated to contain 7–30 µg/day of cobalamin, of which 1–5 µg is absorbed and stored (estimated reserves of 2–5 mg); therefore, symptoms resulting from a VB12 deficit would not appear until 3–5 years after establishing a low-ingestion or poor-absorption regimen.1 VB12 deficiency can lead to haematological and neuropsychiatric disorders,3 as well as cardiovascular risk factors.4 The prevalence of VB12 deficiency in the elderly is highly variable across studies, which report values of 1.5%–15%.5–8

In primary care, the most commonly observed causes of VB12 deficiency are related to abnormalities in digestion (atrophic gastritis, achlorhydria) or absorption (autoimmune pernicious anaemia, chronic pancreatitis, Crohn’s disease, the effect of medications that alter the mucosa of the ileum such as metformin, antacids -proton-pump inhibitors and H2-receptor antagonists, antibiotics and colchicine)9 or the consequences of surgical resection.10 A deficiency stemming solely from dietary habits is rare and usually affects strict vegans.11 In the elderly, different alterations in the processes involved in VB12 absorption increase the prevalence of this deficit, which can appear in the absence of specific symptoms, thereby hindering its diagnosis.12

The traditional treatment for VB12 deficiency consists of intramuscular (IM) injection of cyanocobalamin, generally 1 mg/day for 1 week, followed by 1 mg/week for 1 month and then 1 mg every 1 or 2 months ad perpetuum.10 13 14 The vitamin may, however, be administered orally. Several studies have shown serum VB12 concentrations to normalise after taking large oral doses.15 16 Studies taking into consideration the patients’ preferences have found differences in favour of the oral route.17 18 Furthermore, oral treatment could avoid injection nuisances, reduce unnecessary travel for the patients or nurses and minimise treatment costs.19

Some authors have questioned the use of oral administration while others favour it, although no firm conclusions can be drawn due to the methodological limitations of the evidence the authors provide.10 20–22 The 2018 Cochrane Review5 includes three randomised clinical trials comparing the effectiveness of oral and IM administration. There are differences among the trials in terms of treatment regimens and follow-up duration, ranging from 3 to 4 months, and average age of the patients, as well as the frequency and VB12 daily dose for both routes. In terms of outcomes, adverse events and cost, the overall quality of the evidence was low due to the small number of studies and limited sample sizes.23–25 In their conclusions, the authors state the need for trials with improved methods for random allocation and masking, larger sample sizes and information on other relevant outcome variables that are preferably conducted in the primary care setting.

The aim of this study was to compare the effectiveness of oral-administered and IM-administered VB12 in the normalisation of serum VB12 concentrations at 8, 26 and 52 weeks in patients aged ≥65 years with VB12 deficiency treated at primary healthcare centres (PHC). Secondary outcomes included safety (adverse events), quality of life and adherence to treatment. Additional aims were to describe patient preferences and satisfaction with treatment and to explore the immediate response (8 weeks) as a normalisation predictor of 1 year outcomes to propose clinical recommendations.

Methods

Study design and participants

A pragmatic, randomised, multicentre, non-inferiority clinical trial with a duration of 12 months was conducted in a PHC. On ethical grounds, a placebo-controlled trial was not appropriate.26 Methodological issues of this trial have been published elsewhere (online supplementary 1).27

Supplemental material

Competitive recruitment was performed in 22 PHC in Madrid (Spain) from July 2014 to November 2016. Eligible patients were 65 years of age or older and had been attending a PHC for consultation on any medical matter. Patients were assessed for eligibility and invited to participate consecutively by their general practitioners. Written informed consent was obtained from all participants. A blood test was performed, and in patients with a serum concentration of VB12 of <211 pg/mL, the remaining inclusion and exclusion criteria were evaluated. The cut-off value selected in the trial register/trial protocol was <179 pg/mL; this value was modified by the laboratory following the recommendations of the provider. This change took place prior to the beginning of the recruitment. Patient recruitment was always performed using the same methodology and cut-off point. The procedures for measurement of the biomarkers were ADVIA Centaur XP (Siemens Diagnostics, Tarrytown, NY, USA).

Randomisation and masking

Patients were allocated by simple randomisation at a 1:1 ratio to oral or IM administration of VB12. The randomisation system was incorporated into the electronic data collection system to assure allocation concealment. Because of the nature of the intervention, patients and general practitioners were aware of their treatment allocation. Analysis was performed by the trial statistician, who was blinded to allocation.

Intervention

The pharmaceutical formulations used in the study are commercially available in Spain (Optovite vials). Its pharmaceutical presentation is in silk-screen-printed clear glass ampoules that are presented in blister support. The treatment regimen was : (a) IM route: 1 mg of cyanocobalamin on alternate days during weeks 1–2, 1 mg/week during weeks 3–8 and 1 mg/month during weeks 9–52; (b) oral route: 1 mg/day of cyanocobalamin for 8 weeks and 1 mg/week during weeks 9–52. The period between 1 and 8 weeks was considered the charging period.

In the oral route, the medication was provided to the patient at the health centre, along with instructions for self-administration at home. The information sheet explained to the patient the procedure for oral administration, that is, how to open the ampoule and dilute its contents in a glass, then drink it.

In the IM route, the medication was administered by the nurse at the health centre.

Outcomes

The main outcome was the normalisation of serum VB12 concentrations (≥211 pg/mL) at 8, 26 and 52 weeks. The secondary outcomes were the serum VB12 concentrations (pg/mL), adverse events, adherence to treatment (number of vials for the oral arm and the number of injections for the IM arm during each visit; good adherence was considered greater than 80%), quality of life (EQ-5D-5L)28 and patient preferences and satisfaction were assessed. Anamnesis, demographic and lifestyle information, clinical variables, analytical variables and concomitant treatment were recorded.27

Procedures

After signing the consent form, those who agreed to participate had serum VB12 concentrations determined. If the VB12 value was <211 pg/mL, a haemogram, biochemical analysis and anti-intrinsic factor antibody levels were assessed.27 The patients also received a medication diary to be filled out daily. Baseline data were collected by the family physician and/or a nurse. IM treatments were administered by nurses in the health centres. The follow-up visits were conducted during weeks 8, 26 and 52.27

Statistical analysis

Sample size

Assuming that 70% of patients reach a serum VB12 concentration of ≥211 pg/mL in both groups, for a threshold of non-inferiority of 10%, statistical power of 60% with significance set at p<0.05 and a 5% loss to follow-up, the final sample size was word 320 (160 in each arm).

As recommended for non-inferiority studies, both per-protocol (PPT) and intention-to-treat (ITT) analyses were performed, with the null hypothesis being that there were differences between treatments at the three monitoring points. Comparing both arms, we calculated the difference between the percentage of patients in each treatment arm whose serum VB12 concentrations became normalised at 8, 26 and 52 weeks, with their 95% CI. If the CIs do not fall outside the non-inferiority limit (10%), it can be concluded that the oral treatment is not inferior to the IM treatment.29 30 In ITT analyses, missing values for the main outcome variable were added using the ‘last observation carried forward’ method.31

To explore factors affecting the normalisation of serum VB12 concentration at 52 weeks, serum VB12 levels were studied at 8 weeks. A receiver operating characteristic curve was built to determine the likelihood ratios of each cutpoint after the charging period to ‘predict’ the normalisation of levels at the end of the study. After this, a generalised linear model was built (function logit).32 33 The normalisation of serum VB12 levels at 52 weeks was the dependent variable, and the treatment group was the independent variable. Variables considered significant by the researchers from a clinical perspective were included in the model. To test the non-inferiority hypothesis, adding the information contained in these data to previous knowledge, additional statistical analyses were performed using a Bayesian approach. Secondary outcome variables were analysed using the appropriate statistical tests, and their means or proportions were used to estimate differences between groups. All analyses were performed using STATA V.14 and EPIDAT V.4.2 software.

Patient involvement

Patients were not involved in the development of plans for recruitment, design, outcome measures or implementation of the study conduct. No patients were asked to advise on the interpretation or writing of the results. Patients explained the experience of participating in the study on the occasion of International Clinical Trial’s day in Radio Nacional de España. We will pursue patient and public involvement in the development of an appropriate method for further dissemination.

Results

Characteristics of the study participants

A total of 2342 patients were offered participation, and 2152 provided informed consent. A total of 307 patients showed a VB12 deficit (14.3%), 283 of whom were allocated to receive VB12 treatment via the IM route (n=143) or orally (n=140). The follow-up period (52 weeks) was completed by 229 patients (80.9%). Losses to follow-up were similar in both regimens, 28 out of 140 and 26 out of 143 losses in the oral and IM arms, respectively (p=0.697) (figure 1).

Figure 1

Trial profile.

The average age was 75.2 (6.34), and 58.3% of the patients were women. Table 1 describes the baseline characteristics of the patients included in the trial. No relevant differences were found between groups at baseline for demographic and medical characteristics or for the study endpoints.

Table 1

Baseline characteristics at baseline by group

Primary outcomes

At week 8, the difference in the success rate between the oral and IM routes was −0.7% (95% CI: −3.2% to 1.8%; p=0.0999) and 4.8% (95% CI: −1.3% to 10.9%; p=0.124) with the PPT and ITT analyses, respectively. At week 26, these differences were −12.9% (95% CI: −17.9% to −6.1%; p<0.001) and −3.2% (95% CI: −11.8% to 5.4%; p=0.470), respectively. At week 52, these differences were −6.3% (95% CI: −11.9% to −0.07%; p=0.025) and −6.8% (95% CI: −16.6% to 2.9%; p=0.171), respectively (figure 2).

Figure 2

Difference between the oral and intramuscular routes in the proportion of patients whose VB12 levels returned to normal (≥211 pg/mL). IM, intramuscular; ITT, intention-to-treat; PPT, per-protocol.

In the PPT analysis under a Bayesian approach, the probabilities of differences in the treatment effectiveness being >10% between the oral and IM groups were 0.001, 0.201 and 0.036 at weeks 8, 26 and 52, respectively. In the ITT analysis, these values were 0.000, 0.015 and 0.060 at weeks 8, 26 and 52, respectively (online supplementary 2). The result of the likelihood ratio for the cutpoints at the main percentiles of the distribution of VB12 serum levels at week 8 to predict normalisation at the end of the study is shown in online supplementary 3. The level at the fifth percentile of the distribution was selected as the most useful value because it showed the best classification ability. When patients did not reach this level at week 8, they were almost 12 times more likely to not reach suitable VB12 levels at the end of the study than if they had reached levels over 281 pg/mL (12~1/negative likelihood ratio).

Supplemental material

Supplemental material

In the ITT analysis, the factors affecting the success rate at week 52 were age, for each year of increase in age, the success rate decreased by 5%, and having attained VB12 levels of ≥281 pg/mL at week 8, which yielded a success rate 8.1 times higher (table 2).

Table 2

Factors associated with VB12 concentrations ≥211 pg/mL at week 52

The mean levels of VB12 for each follow-up visit were above the normalisation threshold in both groups, although these values were much greater in the IM group (online supplementary 4). In 51 patients (46 IM and 5 oral), the levels of VB12 in week 8 were above the normal range limit of the laboratory (≥911 pg/mL), so the treatment regimen was changed from the initial planned pattern.

Supplemental material

Secondary outcomes

In terms of quality of life and the presence of signs related to VB12 deficiency, no significant differences were found between treatment arms at any of the follow-up visits (table 3).

Table 3

Secondary outcomes (quality of life and exploratory findings) at weeks 8, 26 and 52

Eleven adverse events were reported and none of them were severe; five (3.57%) occurred with patients in the oral arm and six (4.20%) with patients in the IM arm, yielding a difference of −0.63% (95% CI: −5.12% to 3.87%, p=0.786). Three patients withdrew from the study: one patient in the oral group due to urticaria, and two in the IM group due to reddening and pruritic facial erythema and generalised itching (mainly in the cheeks with scarce urticariform lesions). In three other cases, treatment for the adverse events was prescribed (constipation and erythema), and in five cases, it was not necessary to take further measures (table 4).

Table 4

Description of adverse events by patient and route of administration

At week 8, adherence to treatment was evaluated in 265 patients, of whom 95.5% were adherent (97.8% oral and 93.8% IM); the difference between the groups was 4% (95% CI: −0. 1% to 8.7%; p=0.109). At week 52, adherence was evaluated in 229 patients, of whom 220 (96.1%) were adherent (98.2% oral and 94.0% IM); the difference was 4.2% (95%CI: −0.7% to 9.1%; p=0.172).

Overall, 89.5% of the patients reported being satisfied or very satisfied with the treatment via the oral route (91.3%) and the IM route (87.6%). The difference was 3.7% (95% CI: −4.0% to 11.3%; p=0.348).

A total of 83.4% of patients preferred the oral route (97.6% among the patients receiving VB12 orally vs 68.6% of the patients in the IM group); the difference was 29.0% (95% CI: 20.3 to 37.7; p<0.001). The preferences expressed by the patients referred to their potential choice regardless of the arm to which they were assigned.

Discussion

Main findings of the study

Supplementing VB12 in patients with VB12 deficiency, whether orally or intramuscularly, achieves the normalisation of VB12 levels in most cases. The oral route was not inferior to the IM route during the charging period. Formally, the pre-established conditions for determining the non-inferiority of oral administration were not met for the complete follow-up period, but these results merit a deeper analysis.

Differences between the administration routes were found at 26 and 52 weeks. The IM maintenance treatment of 1 mg/month was effective in maintaining VB12 levels, while oral administration of 1 mg/week had a probability of being inferior (by more than 10%) to the IM route by 20% in the most unfavourable scenario (PPT). However, given that no strategy was superior in the charging period, and in view of the model results showing that when VB12 levels reached ≥281 pg/mL during the charging period, the success rate at 12 months was eight times higher, the probability that the differences between groups would exceed Δ was very low, independent of the administration route. The most plausible explanation for the observed difference between routes might be that in patients below this threshold, the maintenance oral dose should be higher than the dose used in the present study. Some authors have recommended that an oral dose of 2 mg/week be administered as a maintenance dose.34

The incidence of adverse events was very low and similar for oral and IM administration, and non-serious adverse events were found. These findings were similar to other studies.5 Patients’ preferences can be a decisive factor for determining the administration route. In this trial, similar to previous studies,17 there was a clear preference for the oral route, especially among the patients assigned to this group.

The effect of VB12 supplements on quality of life remains unclear,35 36 but the present results show that the treatment route does not improve patients’ perception of their health-related quality of life or related symptoms.

We did not find significant differences in adherence. Adherence to the treatment via the IM route was lower than expected. Although drug administration was assured once the patient attended the consultation, the patient could choose not to attend appointments for various reasons. However, in usual practice, adherence with the oral route could be more compromised than with the IM route, and this factor should be taken into consideration to personalise prescription.

Comparison with other studies

The comparison with other studies is difficult, due to the treatment different doses used, but especially because of the follow-up length had been inferior to 4 months and the number of patients included was small.

As far as we know, the present trial is the largest clinical trial with the longest follow-up period, and it is the first to evaluate, in addition to VB12 levels, clinical signs and symptoms, health-related quality of life and patient preferences. The three clinical trials23–25 described in the 2018 Cochrane Systematic Review5 had a duration between 3 and 4 months and included a total of 153 patients. In the Saraswathy trial, patients in the oral route at 3 months normalised levels 20/30 (66.7%) versus 27/30 (90%) of the patients in the IM route.25 In Kuzminski’s trial, patients in the oral route at 4 months normalised levels 18/18 (100%) versus 10/14 (71.4%) of the patients in the IM route.23 These differences were statistically non-significant in both studies.

Two studies have recently been published and add evidence in favour of oral and sublingual administration of VB12.37 38 The follow-up of Moleiro’s study reached 24 months versus 12 months in our study. However, Moleiro et al performed a prospective uncontrolled study that included 26 patients submitted to total gastrectomy. All patients received oral VB12 supplementation (1 mg/day), and all of them maintained normalisation V12 at 6, 12, 18 and 24 months. There was a progressive increase in serum V12 levels within the first 12 months, which remained stable thereafter.37 The long-term effectiveness of the oral route in absorption-deficient people such as gastrectomised patients would support the results of our study.

Bensky et al compared the efficacy of sublingual versus IM administration of VB12 in a retrospective observational study from the computerised pharmacy records of Maccabi Health Service. Among 4281 patients treated with VB12 supplements (830 (19.3%) with IM and 3451 (80.7%) with sublingual tablets), the IM group achieved a significant increase in VB12 levels compared with the sublingual group, OR 1.85, CI 95% 1.5 to 2.3.38 Although this study has a large sample size, the important methodological limitations on its effectiveness (retrospective design; reliance on clinical records; absence of epidemiological information such as patient age and sex or the aetiology of the deficit) should be considered in the interpretation of their results.

Strengths and limitations

Our study was pragmatic39 in both the inclusion and diagnostic methods criteria. The majority of the patients with deficits included in this study presented no symptomatology or very low-level symptoms, with no anaemia, which is the common profile of most patients who present with VB12 deficits in primary care. The study design did not allow for masking the patients to the received treatment. However, these limitations were compensated for by the objective measurement of the main outcome variable.

As occurs in all pragmatic clinical trials, patient recruitment was complicated, and the sample size reached only 88.4% of the calculated necessary size, which implies that the power of the study was limited. Hence, the analysis was complemented using Bayesian methods that allow for studying a posteriori the likelihood of a difference between two outcomes to exceed a certain limit.40 Under this approach, the a posteriori probability for differences to exceed the proposed Δ=−10% was not significant during the charging period, and the probabilities were low but not negligible in the PPT analysis and low in the ITT analysis over the complete follow-up period.

Loss to follow-up was low at 8 and 26 weeks and higher at 52 weeks. This effect has been observed in pragmatic clinical trials with long follow-up periods. Missing data were greater in the IM arm, during the interval between randomisation and initiation of treatment (6% IM vs 1% oral), over 8 weeks (9% IM vs 4% oral) and over 26 weeks (15% IM vs 6% oral). These differences could represent a lower acceptability of the IM route by patients, since the missing data were mostly due to patient dropout. At 52 weeks, the numbers of losses in the two arms were similar (20% oral and 18% IM), and in the case of oral treatment, several of those losses were withdrawals occasioned by not achieving particular levels of VB12.

Implications of the study findings

On the basis of our results and the available evidence, we propose the oral administration of VB12 at 1 mg/day during the charging period. Subsequently, the recommended dose would vary as a function of the VB12 levels reached during the charging period. For VB12 concentrations between the normal levels of 211 pg/mL (in our laboratory) and 281 pg/mL (the fifth percentile of the distribution in this trial), a dose of 2 mg/week is suggested. When the levels reached in the charging period are between 281 and 380 pg/mL (the 20th percentile of the distribution), it may be appropriate to perform an analysis between 8 and 26 weeks to confirm that normal levels are maintained. All patients who reach a level of 380 pg/mL by week 8 could be maintained at the initial dosage (1 mg/week) without subsequent analyses during the year of follow-up.

If the IM route is chosen, the proposed dose for this route during the first few weeks may be excessive for patients with VB12 deficiency. The scheduled IM dose should be reconsidered in the first 2 weeks based on VB12 levels, and the scheduled dose could be limited to 1 mg/week if warranted by the outcome. Nevertheless, these recommendations must be assessed in further research.

Oral administration of VB12 in patients older than 65 years is probably as effective as IM administration, and it also lacks adverse effects and is preferred by patients. We must also highlight the potential benefit of the oral route in terms of safety for patients with coagulation problems, for whom IM-administered medication is often contraindicated. A small number of patients may require additional follow-up after 8 weeks if a certain concentration of VB12 in blood is not reached.

Acknowledgments

To Margarita Blázquez Herranz, Instituto de Salud Carlos III, for making the impossible possible. To Juan Carlos Abánades Herranz for trusting us and his contribution to facilitate our work. To Antonio Jesús Alemany López and Marta Sánchez-Celaya, Managing Director of Primary Healthcare for accepting to sponsor this research after the dissolution of CAIBER. To the Fundación para la Investigación e Innovación Biomédica de Atención Primaria (FIIBAP) for the grant awarded for the publishing of the research. To Fernando Cava Valencia and Raquel Guillén Santos from the Clinical Laboratory BRSALUD. To Elena Tolosa Oropesa from the Pharmacy Department, Gerencia Asistencial de Atención Primaria de Madrid. To our colleagues from the Research Unit, including the assistants Marcial Caboblanco Muñoz, Juan Carlos Gil and Isabel Morales Ropero for their unconditional support; project manager Pilar Pamplona-Gardeta, researchers Juan A. López Rodríguez, Jaime Barrio Cortes, Cristina Lozano Hernandez and Medical Residents Daniel Toledo Bartolomé, Irene Wijers and Palmira Jurado Macías for their technical advice in finalising this paper. To Javier Zamora Romero, head of the Unit of Biostatistics, Hospital Ramón y Cajal of Madrid, for revising the manuscript. To all the professionals from the participating healthcare centres. To all patients who contributed to this research.

Published in The British Medical Journal -
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