- Research article
- Open Access
- Open Peer Review
Assessing differential attrition in clinical trials: self-monitoring of oral anticoagulation and type II diabetes
BMC Medical Research Methodology volume 7, Article number: 18 (2007)
Analyzing drop out rates and when they occur may give important information about the patient characteristics and trial characteristics that affect the overall uptake of an intervention.
We searched Medline and the Cochrane library from the beginning of the databases to May 2006 for published systematic reviews that compared the effects of self-monitoring (self-testing) or self-management (self-testing and self-dosage) of oral anticoagulation or self-monitored blood glucose in type 2 diabetics who were not using insulin. We assessed all study withdrawals pre-randomization and post randomization and sought information on the reasons for discontinuation of all participants.
To measure the differential between groups in attrition we used the relative attrition (RA), which is equivalent to relative risk but uses attrition as the outcome (i.e. attrition in intervention group/attrition in control group). We determined the percentage drop outs for control and intervention groups and used DerSimonian and Laird random effects models to estimate a pooled relative attrition. L'abbe type plots created in R (version 2.0.2) were used to represent the difference in the relative attrition among the trials with 95% confidence areas and weights derived from the random effects model.
With self-monitoring of blood glucose in type 2 diabetes, attrition ranged from 2.3% to 50.0% in the intervention groups and 0% to 40.4% in the control groups. There was no significant difference between the intervention and control, with an overall RA of 1.18 [95% CI, 0.70–2.01]. With self-monitoring of oral anticoagulation attrition ranged from 0% to 43.2% in the intervention groups and 0% to 21.4% in the control group. The RA was significantly greater in the intervention group, combined RA, 6.05 [95% CI, 2.53–14.49].
This paper demonstrates the use of relative attrition as a new tool in systematic review methodology which has the potential to identify patient, intervention and trial characteristics which influences attrition in trials.
Loss to follow up after recruitment and attrition in randomized controlled trials affects the generalisability of the conclusions. [1, 2] Loss to follow up occurs when participants' information cannot be obtained for one reason or another, whereas attrition is the exclusion or drop-out of individuals for a particular reason after randomization to the intervention or control group.  Attrition forms one of the four predominant biases in clinical trials: selection, performance, attrition and detection bias. Investigators frequently exclude patients from trial analyses, most commonly because of ineligibility or protocol violations. Trials that exclude more patients tend to be larger and published earlier than those that do not. 
Analyzing drop out rates and when they occur may give important information about the patient characteristics and trial characteristics that affect the overall uptake of an intervention. It is equally important to assess the inclusion and exclusion criteria's impact on subsequent drop out rates and perhaps the most significant effect is observed by the assessment of the comparative losses between the control and intervention groups. 
To analyse the impact of relative attrition on results of systematic reviews we considered self-monitoring of oral anticoagulation and oral diabetes as the rates of attrition in these published systematic reviews vary considerably. On average 22% of patients assigned to self-monitoring of oral anticoagulation were unable to complete the intervention, range of 9 – 43%.  For type 2 diabetics receiving oral therapy, self-monitoring, withdrawals have been reported as high as 50%. [4, 5] We aimed to analyse the drop out rates from randomized controlled trials of self monitoring of oral anticoagulation and oral diabetes, to examine the patient and trial characteristics that effect attrition. In addition we aimed to analyse the relative difference between the intervention and control groups using a measure of relative attrition.
We searched Medline and the Cochrane library from the beginning of the databases to May 2006 for published systematic reviews that compared the effects of self-monitoring (self-testing) or self-management (self-testing and self-dosage) of oral anticoagulation or self-monitored blood glucose in type 2 diabetics who were not using insulin. MeSH terms used were "anticoagulants", "vitamin-K" OR "coumarins" AND "consumer-participation" OR "self-care" OR "self-administration". For diabetes terms used were "diabetes mellitus adult-onset" OR "diabetes mellitus" OR "non insulin dependent" OR "diabetes mellitus type II" OR "NIDDM" AND "self-care" OR "self-administration" OR "blood glucose self monitoring". In addition we used the systematic review filter "systematic". From these reviews we obtained the full-text papers of the included randomized controlled trials. We also repeated the search strategies of the systematic reviews to search for recently published randomized controlled trials in both areas.
We assessed all studies for inclusion and exclusion criteria and for study withdrawals before randomization and post randomization. We extracted information on disease characteristics and the training undertaken in the intervention and control groups. We extracted descriptors on the population studied, including the number of participants who refused or were excluded from entering the trial. We sought information on the reasons for discontinuation of all participants allocated to the intervention and the control. Where data was insufficient we wrote to authors for clarification.
To measure the differential between groups in attrition we used the relative attrition (RA), which is equivalent to relative risk but uses attrition as the outcome (i.e. attrition in intervention group/attrition in control group). A relative attrition of one means the attrition in both the intervention and control were equivalent; less than one, attrition is less in the intervention than the control arm, and greater than one, attrition in the intervention group was higher. With this measure we can estimate an average RA and detect trials with lower or higher than average RA, and look for trial characteristics that account for this effect.
We determined the percentage drop outs for control and intervention groups. Due to the heterogeneity in drop out rates between trials we used the DerSimonian and Laird random effects models to estimate a pooled relative attrition for all trials using STATA (version 8.2). Data was entered by two reviewers independently and checked. L'abbe type plots and Forest plots created in R (version 2.0.2) were used to represent the difference in the relative attrition among the trials with 95% confidence areas and weights derived from the random effects model. Heterogeneity was examined using chi-squared and I-squared statistics and where possible we used meta-regression to test for the effect of trial characteristics on attrition.
For self-monitoring of blood glucose in patients with type two diabetes, we identified five [6–10] reviews, and included eleven randomized trials (table 1), [4, 5, 11–19] comprising 1,689 participants. For oral anticoagulation we identified four reviews [3, 20–22] and included 16 randomized trials (table 2), [23–38] comprising 3,788 participants.
With self-monitoring of blood glucose in type 2 diabetes (table 1), attrition ranged from 2.3%  to 50.0%  in the intervention groups and 0%  to 40.4%  in the control groups. There was no significant difference between the intervention and control, with an overall RA of 1.18 (95% CI, 0.70 -2.01), heterogeoneity chi squared 24.87 (p value = 0.006), I-squared 59.8%. (figure 1)
Two of the included studies were considered to be of high quality [11, 12] in the Welschen systematic review and two studies [4, 18] had a significant effect of SMBG on HbA1c results. Attrition was not significantly related to study duration. Seven trials had less than 100 participants, [11–13, 15–17, 19] and one trial of 689 participants  accounted for 41% of the patients studied. Study size as well as the year of the study revealed no significant trends in terms of attrition. Table 3 gives the reasons for drop outs stated by the trial author.
Two studies report a RA smaller than the lower limit of the 95% CI, equivalent to a higher than expected attrition in the control group (figure 2). Of these two, the Estey trial  control group received a standard 3-day educational session. A comparison between those who dropped out and those who remained in the study did not indicate any significant differences with respect to baseline demographics. The second (Miles) study  invited all newly diagnosed diabetics attending a patient education programme, participants were randomly allocated to blood glucose or urinary glucose.
Three studies report a RA higher than the upper limit of the 95% CI, equivalent to higher than expected attrition in the intervention group. In the Gallichan study  most patients preferred urine testing (71%), and 33.3% dropped out of the intervention group. The Davidson trial  recruited patients in a community clinic on entering a diabetes managed care program. Only one patient did not return to see the nurse or dietician after randomization. In the Rutten trial  set in eight general practices, only 50% of the treatment group proved able to carry out accurate self-monitoring. Patients under 40 and older than 75 years of age were excluded, as were patients with co-morbid diseases under the care of a hospital.
In the largest trial of 689 participants,  the attrition was high at 47.5% relative to 40.4% in the control group RA, 1.18 (95% CI, 0.99–1.39). This is the only trial where participants received training in SMBG by the general practitioner. Of note 299 patients were not able to provide two HbA1c measurements in a two month run in period post randomization, and were removed from the study. The remaining 689 patients were asked to perform at least 6 capillary assays per week (3 different days per week including weekends). A further 303 patients dropped out of the study, of these 240 had a reason reported for discontinuation: adverse event (n = 6), patient non-compliance (n = 33), consent withdrawal (n = 15), patient lost to follow up (N = 19), death (n = 4), protocol violation (n = 21), lack of information on patients (n = 92), and other reasons as stated in the paper (n = 110).
Self-monitoring of oral anticoagulation
With self-monitoring of oral anticoagulation (table 2) attrition ranged from 0%  to 43.2%  in the intervention groups and 0% [23–25, 27, 29, 30, 36, 37] to 21.4%  in the control group. The RA was significantly greater in the intervention group, combined RA 6.05 (95% CI, 2.53–14.49), heterogeneity chi squared 120.91 (p value < 0.001), I-squared 88.4%.(figure 3)
Four of the included studies were judged to be of low quality [28, 31, 32, 38] in the Heneghan systematic review. Study duration ranged from two months  to two years, [32, 35] four trials had less than 100 participants [25, 28, 31, 38] and three trials [26, 32, 33] accounted for 51% of the patients studied. Study size as well as the year of the study revealed no trend in terms of attrition. In addition attrition was not significantly related to study duration. Furthermore analysis of self-management versus self-testing only, showed no significant difference in relative attrition (meta-regression p = 0.214). Table 4 gives the reasons for drop outs stated by the trial author.
Five trials report a RA higher than the upper limit of the 95% CI, equal to a higher than expected attrition in the intervention group, (figure 4); in comparison, only one (Kortke)  reported a RA below than the lower limit of the 95% CI. In this trial patients were assigned to the intervention directly after mechanical heart valve surgery. 90 patients were excluded from the analysis due to either post operative mortality or dropped out in the follow-up phase.
Of these five trials with higher RA one studied less than a 100 individuals: the Fitzmaurice trial  set in six general practices gave patients two training sessions and assessed competency for self-testing. Common reasons in this trial for exclusions pre-randomization were manual dexterity (13%), anxiety (12%), too elderly (12%), physically unwell (8%) and lack of cognitive ability (8%). During the study failure to attend training was the most frequent reason for withdrawal. Three trials [23, 27, 37] had similar drop outs in the intervention groups (range 19.2%–22.1%) and no drop outs in the control group. Beyth  recruited and trained hospitalized patients 65 years of age or older, 31 patients refused the intervention post randomization. Of 720 patients approached in the Gaddiseur trial  – set in anticoagulation clinics – 536 refused or were ineligible or unavailable. Of these 33% preferred existing system, 25% were too old, nervous or uncertain and 30% had no time or were not interested. Common reasons for drop outs were failing the training, problems with self dosing and differences greater than 20% between laboratory measures and the self testing device. The Voller trial  was discontinued due to poor recruitment, and the group comparisons were confined to an analysis of the INR measurements. Sunderji  recruited patients from a tertiary care institution or by referral as an outpatient. Clinical pharmacists and physicians selected patients on their assessment of competence, compliance and willingness to manage their own therapy. Despite this selection process 29% of the intervention group discontinued self testing compared to no drop outs in the control group: drop out reasons included difficulty with the monitor and a preference for physician management.
Three trials had very low drop out rates overall. [24, 29, 30] Katz unpublished trial  was set in anticoagulation clinics in a large integrated health system – mean age 63 years. Pre randomization patients had to prove they could schedule and attend anticoagulation clinics. A number found attending the anticoagulation clinics was geographically inaccessible. Patients phoned in results and were regularly contacted for telephone interviews. Horstkotte  recruited 150 consecutive patients directly following mechanical heart valve surgery. Cromheecke  study was a randomized crossover between self-adjusted treatment and anticoagulation clinic care.
Of the two largest trials [26, 33] Menendez  had fewer drop outs (21.5% vs. 41.5%). Patients received three months of anticoagulation pre-randomization and did not have severe medical or physical illness. Of the 368 patients randomized to self management 58 declined before training, mostly because of a lack of confidence. Of those who received training ten could not pass and 11 dropped out post training. The Fitzmaurice trial  recruited unselected patients from general practice. Patients had to have a long term indication for anticoagulation and had at least six month of therapy. Of the 337 allocated to the intervention 95 did not receive it; mainly withdrawing at the training stage. A further 45 discontinued the intervention post training, the main reason being the patients' decision. The Fitzmaurice trial was the only paper to report the mean age of those who dropped out. The mean age of those invited to participate was 69 years (range 18–95) compared with a mean of 65 years for those recruited to the study. In the intervention group the mean age of those completing training was significantly lower than that of those initially randomized 61 yrs v 64 yrs (p = 0.012).
Pre-randomization drop-outs affect the external validity of a study while post-randomization drop-out affects internal validity, resulting in study bias. The presence of statistical heterogeneity in the analysis of relative attrition identifies interventions that are potentially less generalisable than others.
Therefore, analysis of attrition rates provides a wealth of information over and above that of the assessment of biasing the outcomes. For instance, RA was greater for self monitoring of oral anticoagulation than for diabetes. Potential reason for the increased RA for self-monitoring oral anticoagulation include: trials being larger and of greater duration; also many patients who self-monitored already had experience of an alternative management strategy and potentially preferred this system or to stay with it in the first place. In one trial where patients went straight on to self-monitor  and had no experience of usual management drop out rates were relatively low. In diabetes no alternative comparable testing strategy exists apart from comparison to urine testing, when one trial assessed patient preference, 71% preferred urine testing over SMBG.  In addition control group care was not always comparable to intervention care, for instance, control groups were often not provided training and therefore could not fail to attend a session that the intervention group could drop out of. Therefore additional elements of the intervention can act to increase relative attrition. Patients recruited to managed care programmes  or integrated health systems  may reduce drop outs. Individual training used in trials of anticoagulation  may not fair as well as group training; peer support may offer improved benefits over and above individual training. Possible reasons include the extra support for individuals within these systems of health care. It is worth noting for diabetes that training by general practitioners may result in excessive drop outs.  In addition the requirement to perform many dose adjustments; may increase anxiety and the possibility that self-testing in this area is difficult to perform.
Reported reasons for individuals not undertaking or completing self-monitoring were poor dexterity, anxiety, too elderly, concurrent illness and lack of cognitive ability. We consider that age should not be a restriction to self-monitoring, however in the one trial  that used an unselected population and reported the mean age of the population attrition, drop out rates were higher, the age of participants who successfully self-monitored was younger than those who initially entered the trial. Whether the major factor here was physician reluctance to continue with self-monitoring or the patient decision cannot be clarified by the current paper. However, where age affects conditions such as frailty, dexterity or visual impairment then as a co-factor it becomes a restriction to self-monitoring.
Of interest some trials excluded those unable to attend the training or set distance limits due to the control group treatment and trial monitoring required.  Thus these trials potentially excluded those most likely to benefit from self-monitoring.
Finally, despite attempts by clinical pharmacists and physicians attempts to assess patients' competence, compliance and willingness to manage their own therapy attrition remained high  therefore further research should focus on effective assessment and targeting of self-testing.
There are limitations to the data we have presented. These are mainly due to under reporting of the reasons for dropping out of the trial from both arms. Thus we could not test for the interaction effects. However to further this area of research we are planning an individual patient data meta-analysis and collecting further drop out data, in addition to clinical outcomes.
In conclusion this paper demonstrates the use of relative attrition as a new tool in systematic review methodology which has the potential to identify patient, intervention and trial characteristics which may influence attrition in trials of self-monitoring of oral anticoagulation and diabetes. The method of relative attrition we present has the potential to be applied to other systematic reviews besides self-monitoring. It can be applied to both non-drug and drug interventions to elicit the reasons for attrition. The main limitation will be effective reporting of drop-outs in randomized trials.
Schulz KF, Grimes DA: Sample size slippages in randomised trials: exclusions and the lost and wayward. Lancet. 2002, 359: 781-785. 10.1016/S0140-6736(02)07882-0.
Tierney JF, Stewart LA: Investigating patient exclusion bias in meta-analysis. Int J Epidemiol. 2005, 34: 79-87. 10.1093/ije/dyh300.
Heneghan C, Alonso-Coello P, Garcia-Alamino JM, Perera R, Meats E, Glasziou P: Self-monitoring of oral anticoagulation: a systematic review and meta-analysis. Lancet. 2006, 367: 404-411. 10.1016/S0140-6736(06)68139-7.
Guerci B, Drouin P, Grange V, Bougneres P, Fontaine P, Kerlan V, Passa P, Thivolet C, Vialettes B, Charbonnel B: Self-monitoring of blood glucose significantly improves metabolic control in patients with type 2 diabetes mellitus: the Auto-Surveillance Intervention Active (ASIA) study. Diabetes Metab. 2003, 29: 587-594. 10.1016/S1262-3636(07)70073-3.
Rutten G, van Eijk J, de Nobel E, Beek M, van : Feasibility and effects of a diabetes type II protocol with blood glucose self-monitoring in general practice. Fam Pract. 1990, 7: 273-278. 10.1093/fampra/7.4.273.
Coster S, Gulliford MC, Seed PT, Powrie JK, Swaminathan R: Monitoring blood glucose control in diabetes mellitus: a systematic review. Health Technol Assess. 2000, 4: i-93.
Coster S, Gulliford MC, Seed PT, Powrie JK, Swaminathan R: Self-monitoring in Type 2 diabetes mellitus: a meta-analysis. Diabet Med. 2000, 17: 755-761. 10.1046/j.1464-5491.2000.00390.x.
Sarol JN, Nicodemus NA, Tan KM, Grava MB: Self-monitoring of blood glucose as part of a multi-component therapy among non-insulin requiring type 2 diabetes patients: a meta-analysis (1966-2004). Curr Med Res Opin. 2005, 21: 173-184. 10.1185/030079904X20286.
Welschen LM, Bloemendal E, Nijpels G, Dekker JM, Heine RJ, Stalman WA, Bouter LM: Self-monitoring of blood glucose in patients with type 2 diabetes who are not using insulin: a systematic review. Diabetes Care. 2005, 28: 1510-1517. 10.2337/diacare.28.6.1510.
Welschen LM, Bloemendal E, Nijpels G, Dekker JM, Heine RJ, Stalman WA, Bouter LM: Self-monitoring of blood glucose in patients with type 2 diabetes who are not using insulin. Cochrane Database Syst Rev. 2005, CD005060-
Allen BT, DeLong ER, Feussner JR: Impact of glucose self-monitoring on non-insulin-treated patients with type II diabetes mellitus. Randomized controlled trial comparing blood and urine testing. Diabetes Care. 1990, 13: 1044-1050. 10.2337/diacare.13.10.1044.
Davidson MB, Castellanos M, Kain D, Duran P: The effect of self monitoring of blood glucose concentrations on glycated hemoglobin levels in diabetic patients not taking insulin: a blinded, randomized trial. Am J Med. 2005, 118: 422-425. 10.1016/j.amjmed.2004.12.006.
Estey AL, Tan MH, Mann K: Follow-up intervention: its effect on compliance behavior to a diabetes regimen. Diabetes Educ. 1990, 16: 291-295. 10.1177/014572179001600408.
Fontbonne A, Billault B, Acosta M, Percheron C, Varenne P, Besse A, Eschwege E, Monnier L, Slama G, Passa P: Is glucose self-monitoring beneficial in non-insulin-treated diabetic patients? Results of a randomized comparative trial. Diabete Metab. 1989, 15: 255-260.
Gallichan M: Self-monitoring by patients receiving oral hypoglycaemic agents: a survey and a comparative trial. Practical Diabetes. 2002, 11: 28-30. 10.1002/pdi.1960110109.
Miles P, Everett J, Murphy J, Kerr D: Comparison of blood or urine testing by patients with newly diagnosed non-insulin dependent diabetes: patient survey after randomised crossover trial. BMJ. 1997, 315: 348-349.
Muchmore DB, Springer J, Miller M: Self-monitoring of blood glucose in overweight type 2 diabetic patients. Acta Diabetol. 1994, 31: 215-219. 10.1007/BF00571954.
Schwedes U, Siebolds M, Mertes G: Meal-related structured self-monitoring of blood glucose: effect on diabetes control in non-insulin-treated type 2 diabetic patients. Diabetes Care. 2002, 25: 1928-1932. 10.2337/diacare.25.11.1928.
Wing RR, Epstein LH, Nowalk MP, Scott N, Koeske R, Hagg S: Does self-monitoring of blood glucose levels improve dietary compliance for obese patients with type II diabetes?. Am J Med. 1986, 81: 830-836. 10.1016/0002-9343(86)90354-2.
Odegaard KJ: [Self-management in anticoagulation--a meta-analysis]. Tidsskr Nor Laegeforen. 2004, 124: 2900-2903.
Siebenhofer A, Berghold A, Sawicki PT: Systematic review of studies of self-management of oral anticoagulation. Thromb Haemost. 2004, 91: 225-232.
Sola-Morales SO, Elorza Ricart JM: [Portable coagulometers: a systematic review of the evidence on self-management of oral anticoagulant treatment]. Med Clin (Barc ). 2005, 124: 321-325. 10.1157/13072418.
Beyth RJ, Quinn L, Landefeld CS: A multicomponent intervention to prevent major bleeding complications in older patients receiving warfarin. A randomized, controlled trial. Ann Intern Med. 2000, 133: 687-695.
Cromheecke ME, Levi M, Colly LP, de Mol BJ, Prins MH, Hutten BA, Mak R, Keyzers KC, Buller HR: Oral anticoagulation self-management and management by a specialist anticoagulation clinic: a randomised cross-over comparison. Lancet. 2000, 356: 97-102. 10.1016/S0140-6736(00)02470-3.
Fitzmaurice DA, Hobbs FD, Murray ET, Holder RL, Allan TF, Rose PE: Oral anticoagulation management in primary care with the use of computerized decision support and near-patient testing: a randomized, controlled trial. Arch Intern Med. 2000, 160: 2343-2348. 10.1001/archinte.160.15.2343.
Fitzmaurice DA, Murray ET, McCahon D, Holder R, Raftery JP, Hussain S, Sandhar H, Hobbs FD: Self management of oral anticoagulation: randomised trial. BMJ. 2005, 331: 1057-10.1136/bmj.38618.580903.AE.
Gadisseur AP, Breukink-Engbers WG, van der Meer FJ, van den Besselaar AM, Sturk A, Rosendaal FR: Comparison of the quality of oral anticoagulant therapy through patient self-management and management by specialized anticoagulation clinics in the Netherlands: a randomized clinical trial. Arch Intern Med. 2003, 163: 2639-2646. 10.1001/archinte.163.21.2639.
Gardiner C, Williams K, Mackie IJ, Machin SJ, Cohen H: Patient self-testing is a reliable and acceptable alternative to laboratory INR monitoring. Br J Haematol. 2005, 128: 242-247. 10.1111/j.1365-2141.2004.05300.x.
Horstkotte D, Piper C, Wiemer M: Optimal Frequency of Patient Monitoring and Intensity of Oral Anticoagulation Therapy in Valvular Heart Disease. J Thromb Thrombolysis. 1998, 5 Suppl 1: 19-24. 10.1023/A:1013228718768.
Katz S, Lafata JE, Gooldy S, Peterson E: A clinical trial to evaluate Point of Care and Patient Self Testing Approaches to International Normalized Ratio of Prothrombin Time Monitoring in an Anticoagulation Clinic. 2006
Khan TI, Kamali F, Kesteven P, Avery P, Wynne H: The value of education and self-monitoring in the management of warfarin therapy in older patients with unstable control of anticoagulation. Br J Haematol. 2004, 126: 557-564. 10.1111/j.1365-2141.2004.05074.x.
Kortke H, Korfer R: International normalized ratio self-management after mechanical heart valve replacement: is an early start advantageous?. Ann Thorac Surg. 2001, 72: 44-48. 10.1016/S0003-4975(01)02656-X.
Menendez-Jandula B, Souto JC, Oliver A, Montserrat I, Quintana M, Gich I, Bonfill X, Fontcuberta J: Comparing self-management of oral anticoagulant therapy with clinic management: a randomized trial. Ann Intern Med. 2005, 142: 1-10.
Sawicki PT: A structured teaching and self-management program for patients receiving oral anticoagulation: a randomized controlled trial. Working Group for the Study of Patient Self-Management of Oral Anticoagulation. JAMA. 1999, 281: 145-150. 10.1001/jama.281.2.145.
Sidhu P, O'Kane HO: Self-managed anticoagulation: results from a two-year prospective randomized trial with heart valve patients. Ann Thorac Surg. 2001, 72: 1523-1527. 10.1016/S0003-4975(01)03049-1.
Sunderji R, Gin K, Shalansky K, Carter C, Chambers K, Davies C, Schwartz L, Fung A: A randomized trial of patient self-managed versus physician-managed oral anticoagulation. Can J Cardiol. 2004, 20: 1117-1123.
Voller H, Glatz J, Taborski U, Bernardo A, Dovifat C, Burkard G, Heidinger K: [Background and evaluation plan of a study on self-management of anticoagulation in patients with non-valvular atrial fibrillation (SMAAF Study)]. Z Kardiol. 2000, 89: 284-288. 10.1007/s003920050486.
White RH, McCurdy SA, von Marensdorff H, Woodruff DE, Leftgoff L: Home prothrombin time monitoring after the initiation of warfarin therapy. A randomized, prospective study. Ann Intern Med. 1989, 111: 730-737.
The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2288/7/18/prepub
Carl Heneghan is funded by a Department of Health Research Development Award.
The author(s) declare that they have no competing interests.
CH and RP conceived of the study. RP, CH, and PG had input to the statistical analyses. AW and EM contributed to the data extraction. DM had intellectual to the initial drafts of the manuscript. All authors contributed to the draft of the manuscript, approved the analyses and read and approved the final manuscript.
About this article
Cite this article
Heneghan, C., Perera, R., Ward A, A. et al. Assessing differential attrition in clinical trials: self-monitoring of oral anticoagulation and type II diabetes. BMC Med Res Methodol 7, 18 (2007). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2288-7-18
- Oral Anticoagulation
- Clinical Pharmacist
- Anticoagulation Clinic
- Trial Characteristic
- Manage Care Program