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      Oral vitamin B12 versus intramuscular vitamin B12 for vitamin B12 deficiency

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          Abstract

          Vitamin B 12 deficiency is common, and the incidence increases with age. Most people with vitamin B 12 deficiency are treated in primary care with intramuscular (IM) vitamin B 12 . Doctors may not be prescribing oral vitamin B 12 formulations because they may be unaware of this option or have concerns regarding its effectiveness. To assess the effects of oral vitamin B 12 versus intramuscular vitamin B 12 for vitamin B 12 deficiency. We searched CENTRAL, MEDLINE, Embase, and LILACS, as well as the WHO ICTRP and ClinicalTrials.gov. The latest search date was 17 July 2017. We applied no language restrictions. We also contacted authors of relevant trials to enquire about other published or unpublished studies and ongoing trials. Randomised controlled trials (RCTs) comparing the effect of oral versus IM vitamin B 12 for vitamin B 12 deficiency. We used standard methodological procedures expected by Cochrane. Our primary outcomes were serum vitamin B 12 levels, clinical signs and symptoms of vitamin B 12 deficiency, and adverse events. Secondary outcomes were health‐related quality of life, acceptability to patients, haemoglobin and mean corpuscular volume, total homocysteine and serum methylmalonic acid levels, and socioeconomic effects. We used GRADE to assess the quality of the evidence for important outcomes. We did not perform meta‐analyses due to the small number of included trials and substantial clinical heterogeneity. Three RCTs met our inclusion criteria. The trials randomised 153 participants (74 participants to oral vitamin B 12 and 79 participants to IM vitamin B 12 ). Treatment duration and follow‐up ranged between three and four months. The mean age of participants ranged from 38.6 to 72 years. The treatment frequency and daily dose of vitamin B 12 in the oral and IM groups varied among trials. Only one trial had low or unclear risk of bias across all domains and outcome measures. Two trials reported data for serum vitamin B 12 levels. The overall quality of evidence for this outcome was low due to serious imprecision (low number of trials and participants). In two trials employing 1000 μg/day oral vitamin B 12 , there was no clinically relevant difference in vitamin B 12 levels when compared with IM vitamin B 12 . One trial used 2000 μg/day vitamin B 12 and demonstrated a mean difference of 680 pg/mL (95% confidence interval 392.7 to 967.3) in favour of oral vitamin B 12 . Two trials reported data on adverse events (very low‐quality evidence due to risk of performance bias, detection bias, and serious imprecision). One trial stated that no treatment‐related adverse events were seen in both the oral and IM vitamin B 12 groups. One trial reported that 2 of 30 participants (6.7%) in the oral vitamin B 12 group left the trial early due to adverse events. Orally taken vitamin B 12 showed lower treatment‐associated costs than IM vitamin B 12 in one trial (low‐quality evidence due to serious imprecision). No trial reported on clinical signs and symptoms of vitamin B 12 deficiency, health‐related quality of life, or acceptability of the treatment scheme. Low quality evidence shows oral and IM vitamin B 12 having similar effects in terms of normalising serum vitamin B 12 levels, but oral treatment costs less. We found very low‐quality evidence that oral vitamin B 12 appears as safe as IM vitamin B 12 . Further trials should conduct better randomisation and blinding procedures, recruit more participants, and provide adequate reporting. Future trials should also measure important outcomes such as the clinical signs and symptoms of vitamin B 12 deficiency, health related‐quality of life, socioeconomic effects, and report adverse events adequately, preferably in a primary care setting. Oral vitamin B 12 compared with intramuscular vitamin B 12 for vitamin B 12 deficiency Review question Does oral vitamin B 12 have similar effects as intramuscular injections of vitamin B 12 for people with vitamin B 12 deficiency? Background Vitamin B 12 (cobalamin) is necessary for basic body functions, such as the growth and development of red blood cells and the nervous system. Vitamin B 12 deficiency (a lack of vitamin B 12 ) is very common. Many factors contribute to vitamin B 12 deficiency, such as age, blood disease, vegetarian diet, indigestion, use of drugs, as well as poor nutrition. Doctors are more likely to give vitamin B 12 using injections into the muscle (intramuscular injection) because they may be unaware of the option to use oral vitamin B 12 or uncertain about how well it works. Study characteristics We found three randomised controlled studies (clinical studies where people are randomly put into one of two or more treatment groups). The studies randomised 153 participants (74 participants to oral vitamin B 12 and 79 participants to intramuscular vitamin B 12 ). Treatment duration and follow‐up ranged between three and four months. The mean age of participants ranged from 39 to 72 years. Key results Two studies used 1000 μg/day oral vitamin B 12 and showed no relevant difference to intramuscularly applied vitamin B 12 with regard to vitamin B 12 blood levels. One trial used 2000 μg/day vitamin B 12 and showed higher vitamin B 12 blood levels in favour of oral vitamin B 12 . Two studies reported side effects. One study stated that no treatment‐related side effects were seen in both the oral and intramuscular vitamin B 12 groups. One study reported that 2 of 30 participants in the oral vitamin B 12 group left the trial early due to side effects. Orally taken vitamin B 12 showed lower treatment‐associated costs than intramuscular vitamin B 12 in one trial. No study reported on clinical signs and symptoms of vitamin B 12 deficiency (e.g. fatigue, depression, neurological complications), health‐related quality of life, or acceptability of the treatment scheme. Quality of the evidence The overall quality of the evidence was low or very low, mainly due to the small number of included studies and the low numbers of participants in these studies.

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          Most cited references47

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          The impact of outcome reporting bias in randomised controlled trials on a cohort of systematic reviews

          To examine the prevalence of outcome reporting bias-the selection for publication of a subset of the original recorded outcome variables on the basis of the results-and its impact on Cochrane reviews.
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            Comparison of registered and published primary outcomes in randomized controlled trials.

            As of 2005, the International Committee of Medical Journal Editors required investigators to register their trials prior to participant enrollment as a precondition for publishing the trial's findings in member journals. To assess the proportion of registered trials with results recently published in journals with high impact factors; to compare the primary outcomes specified in trial registries with those reported in the published articles; and to determine whether primary outcome reporting bias favored significant outcomes. MEDLINE via PubMed was searched for reports of randomized controlled trials (RCTs) in 3 medical areas (cardiology, rheumatology, and gastroenterology) indexed in 2008 in the 10 general medical journals and specialty journals with the highest impact factors. For each included article, we obtained the trial registration information using a standardized data extraction form. Of the 323 included trials, 147 (45.5%) were adequately registered (ie, registered before the end of the trial, with the primary outcome clearly specified). Trial registration was lacking for 89 published reports (27.6%), 45 trials (13.9%) were registered after the completion of the study, 39 (12%) were registered with no or an unclear description of the primary outcome, and 3 (0.9%) were registered after the completion of the study and had an unclear description of the primary outcome. Among articles with trials adequately registered, 31% (46 of 147) showed some evidence of discrepancies between the outcomes registered and the outcomes published. The influence of these discrepancies could be assessed in only half of them and in these statistically significant results were favored in 82.6% (19 of 23). Comparison of the primary outcomes of RCTs registered with their subsequent publication indicated that selective outcome reporting is prevalent.
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              Is Open Access

              A checklist designed to aid consistency and reproducibility of GRADE assessments: development and pilot validation

              Background The grading of recommendation, assessment, development and evaluation (GRADE) approach is widely implemented in health technology assessment and guideline development organisations throughout the world. GRADE provides a transparent approach to reaching judgements about the quality of evidence on the effects of a health care intervention, but is complex and therefore challenging to apply in a consistent manner. Methods We developed a checklist to guide the researcher to extract the data required to make a GRADE assessment. We applied the checklist to 29 meta-analyses of randomised controlled trials on the effectiveness of health care interventions. Two reviewers used the checklist for each paper and used these data to rate the quality of evidence for a particular outcome. Results For most (70%) checklist items, there was good agreement between reviewers. The main problems were for items relating to indirectness where considerable judgement is required. Conclusions There was consistent agreement between reviewers on most items in the checklist. The use of this checklist may be an aid to improving the consistency and reproducibility of GRADE assessments, particularly for inexperienced users or in rapid reviews without the resources to conduct assessments by two researchers independently.
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                Author and article information

                Journal
                Cochrane Database of Systematic Reviews
                Wiley-Blackwell
                14651858
                March 15 2018
                :
                :
                Affiliations
                [1 ]Cochrane Metabolic and Endocrine Disorders Group
                Article
                10.1002/14651858.CD004655.pub3
                6494183
                29543316
                d175930c-9aa2-42f7-b1d9-d75b9faf95b2
                © 2018
                History

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