Table 1.
Reporting category | MD reporting criterion | Proportion of trials reporting criteria |
---|---|---|
Proportion of MD | Account for all participants who enter the studya | 69% (75/108) |
Report number of participants not included in the primary outcome analysisa | 94% (101/108) | |
Report number of participants with MD in each arm in the primary outcome analysisab | 87% (85/98)b | |
Report amount of item-levelc MD in the primary outcome analysis | 10% (5/50)d | |
Report MD trend over time for primary outcomes measured repeatedly | All time points: 7% (5/69) Some time points: 48% (33/69) |
|
Report amount of MD for secondary outcomes | For all: 9% (9/99)e For some: 18% (18/99) |
|
Reasons for MD | Report reason for MDa | 71% (66/93)f |
Report amount of MD because of death | 65% (60/93)f | |
Report amount of MD because of illness or disease progression | 46% (43/93)f | |
Minimizing MD | Report plans to minimize MD | 27% (29/108) |
Risk of bias posed by MD | Report comparison of baseline characteristics of those with observed data | 6% (6/93)f |
Report comparison of baseline characteristics of those with MD | 0% | |
Justification of MD analytical approach | Report assumed mechanism of MDg | 3% (3/108) |
Report criteria for MNAR (informative MD) | 1% (1/108) | |
Report pattern of missingness | 0% | |
Compare baseline characteristics of those with and without MD | 13% (12/93)e | |
Statistical methods to handle MD | Report methods used to handle MD | 48% (45/93)e |
Report methods used to handle truncated data because of death | 5% (3/60)h | |
Report MD sensitivity analyses | 16% (15/93)f | |
Report any changes to the planned MD analysis | 0% | |
Impact of MD on the trial findings | Discuss impact of MD on the interpretation of findings | 46% (43/93)f |
Abbreviations: MD, missing data; MNAR, missing not at random.
The Consolidated Standards of Reporting Trials 2010 statement recommendation.
In non–crossover trials only.
For example, missing individual questions from a questionnaire, survey, or scale.
In 50 trials, the primary outcome was a scale summary.
In trials that measured secondary outcomes only.
About 15 trials reported no MD and therefore were excluded.
For example, missing completely at random, missing at random, or MNAR.
In trials that reported data was truncated due to death.