1.1 Characteristics Table
Characteristics Table output by the QRP Reporting Tool is highly customizable. Using parameters in Baseline File, users can specify what will be included and the way in which it will be displayed in the final output file.
Characteristics Tables include patient and demographic characteristics, with options to add health characteristics, previous medical product use, laboratory tests and results, as well as health care and drug utilization metrics. Means and standard deviations are output for continuous variables while numbers and percentages of patients/episodes are output for categorical variables.
If the Query Request Program contains more than one monitoring period, then there will be one characteristics table produced per monitoring period. Additionally, users can specify whether to stratify characteristics tables by Data Partner (DP) using Create Report File.
When Characteristics Tables are stratified by DP, there is no need for aggregation of descriptive statistics. However, when multiple data sources are aggregated into one Characteristics Table, aggregated descriptive statistics are calculated as described below.
1.1.1 Calculation of Unweighted Aggregated Descriptive Statistics
Suppose there are two groups, \(t\) and \(c\), and \(k=1,2,\ldots,K\) DPs. Then, we let \(n_{t,k}\) denote the DPspecific sample size for group \(t\), \(\overline{x}_{t,k}\) denote the DPspecific means for group \(t\), \(s_{t,k}\) denote the DPspecific standard deviations for group \(t\), \(\hat{p}_{t,k}=\overline{x}_t\), and \(k\) denote the proportion of the group \(t\) with a given characteristic.
The aggregated sample mean, \(\overline{x}_t\), is calculated as:
\[\begin{equation} \tag{1.1} \end{equation}\]The aggregated standard deviation, \(s_t\), is calculated as a weighted average of the DPspecific standard deviations:
\[\begin{equation} s_t=\frac{\sum_{k=1}^{K}{\left(n_{t,k}1\right)s_{t,k}}}{\sum_{k=1}^{K}n_{t,k}K} \tag{1.2} \end{equation}\]The aggregated proportion of patients with a given characteristic, \({\hat{p}}_t\), is calculated as:
\[\begin{equation} {\hat{p}}_t=\overline{x}_t=\frac{\sum_{k=1}^{K}{n_{t,k}{\hat{p}}_{t,k}}}{\sum_{k=1}^{K}n_{t,k}} \tag{1.3} \end{equation}\]\(\overline{x}_c\), \(s_c\), \(\hat{p}_c\) will be calculated similarly.
The aggregated standardized difference for continuous variables between groups, \(d_{cont}\), is calculated as:
\[\begin{equation} d_{cont}=\frac{(\overline{x}_{t,k}\overline{x}_{c,k})}{\sqrt{\frac{s_{t,k}^2+s_{c,k}^2}{2}}} \tag{1.4} \end{equation}\]The aggregated standardized difference for categorical variables between groups, \(d_{cat}\), is calculated as:
\[\begin{equation} d_{cat}=\frac{({\hat{p}}_{t,k}{\hat{p}}_{c,k})}{\sqrt{\frac{{\hat{p}}_{t,k}\left(1{\hat{p}}_{t,k}\right)+{\hat{p}}_{c,k}\left(1{\hat{p}}_{c,k}\right)}{2}}} \tag{1.5} \end{equation}\]1.1.2 Calculation of Weighted Aggregated Descriptive Statistics
When analyses have weights applied, the weighted aggregated standardized difference is calculated analogously to the unweighted aggregated standardized difference, except that instead of using the DPspecific means, DPspecific weighted means are used, and instead of DPspecific variances, DPspecific weighted variances are used. In addition to the notation used above, let \(w_i\) denote the weight for each individual observation in \(i=1,2,\ldots,n\).
Thus, the weighted means, \(\overline{x}_t^w\) and \(\overline{x}_c^w\), are calculated as:
\[\begin{equation} \overline{x}_t^w=\frac{\sum_{k=1}^{K}{\left(\sum_{i=1}^{n_{t,k}}w_{i,k}\right)\overline{x}_{t,k}^w}}{\sum_{k=1}^{K}\left(\sum_{i=1}^{n_{t,k}}w_{i,k}\right)} \tag{1.6} \end{equation}\] \[\begin{equation} \overline{x}_c^w=\frac{\sum_{k=1}^{K}{\left(\sum_{j=1}^{n_{c,k}}w_{j,k}\right)\overline{x}_{t,k}^w}}{\sum_{k=1}^{K}\left(\sum_{j=1}^{n_{c,k}}w_{j,k}\right)} \tag{1.7} \end{equation}\]DPspecific weighted variances, \(\left(s_t^w\right)^2\) and \(\left(s_c^w\right)^2\), are calculated as:
\[\begin{equation} \left(s_t^w\right)^2= \frac{\sum_{k=1}^{K}v_k\left(s_{t,k}^w\right)^2}{\sum_{k=1}^{K}v_k} \text{ where } v_k= \frac{\left(\sum_{i=1}^{n_{t,k}}w_{i,k}\right)^2\left(\sum_{i=1}^{n_{t,k}}w_{i,k}^2\right)}{\left(\sum_{i=1}^{n_{t,k}}w_{i,k}\right)} \tag{1.8} \end{equation}\] \[\begin{equation} \left(s_c^w\right)^2=\frac{\sum_{k=1}^{K}u_k\left(s_{c,k}^w\right)^2}{\sum_{k=1}^{K}u_k} \text{ where } u_k=\frac{\left(\sum_{j=1}^{n_{c,k}}w_{j,k}\right)^2\left(\sum_{j=1}^{n_{c,k}}w_{j,k}^2\right)}{\left(\sum_{j=1}^{n_{c,k}}w_{j,k}\right)} \tag{1.9} \end{equation}\]The aggregated weighted standardized difference differs from the unweighted aggregated standardized differences in that sitespecific sums of weights and sums of weights squared among treatment and control groups are also required. The aggregated weighted standardized difference for continuous variables is calculated as follows:
\[\begin{equation} d_{cont} = \frac{\sum_{k=1}^{K} \left( \sum_{i=1}^{n_{t,k}} w_{i,k} \right) \overline{x}_{t,k}^{w}  \sum_{k=1}^{K} \left( \sum_{j=1}^{n_{c,k}} w_{j,k} \right) \overline{x}_{t,k}^{w}}{ \sqrt{\frac{ \frac{\sum_{k=1}^{K}v_k \left( s_{t,k}^{w} \right)^2 }{\sum_{k=1}^{K}v_k} + \frac{\sum_{k=1}^{K}u_k \left( s_{c,k}^{w} \right)^2 }{\sum_{k=1}^{K}u_k} }{2}} } \tag{1.10} \end{equation}\]The aggregated weighted standardized difference for categorical variables between groups is calculated as follows:
\[\begin{equation} d_{cat} = \frac{ \frac{\sum_{k=1}^{K} \left( \sum_{i=1}^{n_{t,k}} w_{i,k} \right) \overline{x}_{t,k}^{w}}{\sum_{k=1}^{K} \left( \sum_{i=1}^{n_{t,k}} w_{i,k} \right)}  \frac{\sum_{k=1}^{K} \left( \sum_{j=1}^{n_{c,k}} w_{j,k} \right) \overline{x}_{t,k}^{w}}{\sum_{k=1}^{K} \left( \sum_{j=1}^{n_{c,k}} w_{j,k} \right)} }{ \sqrt{\frac{ \frac{\sum_{k=1}^{K}v_k \left( s_{t,k}^{w} \right)^2 }{\sum_{k=1}^{K}v_k} + \frac{\sum_{k=1}^{K}u_k \left( s_{c,k}^{w} \right)^2 }{\sum_{k=1}^{K}u_k} }{2}} } \tag{1.11} \end{equation}\]\(v_k\) and \(u_k\) are as defined for DPspecific weighted variances.
1.1.3 Output
Users can specify how many Characteristics Tables to output using Baseline File. By default, all Characteristics Tables are “Table 1”, and increment alphabetically from “a” through “z”.
1.1.3.1 Groups Output
Users are required to specify which cohorts, analytical groups, or motherinfant linkage groups to output in Characteristics Tables by setting the Baseline File GROUP
parameter. Groups correspond to columns in Characteristics Tables.
By default, unadjusted tables in Propensity Score (PS) analyses and unweighted tables in Inverse Probability of Treatment Weighting (IPTW) analyses are deduplicated. In other words, if users specify multiple analytical groups from the same Propensity Score Estimate Group (via qrp.PSEstimationFile
), only 1 unadjusted or unweighted table will be output per PS Estimate Group.
In medical product use in pregnancy (Type 4) analyses, users can output separate baseline tables for livebirth and nonlive birth pregnancy outcomes via the Baseline File GROUP
parameter. Additionally, if a non pregnant cohort is created in QRP, it can be output to the Characteristics table by setting the Baseline File INCLUDENONPREGNANT parameter.
In all descriptive analyses except switching analyses, users can also specify that up to two cohorts, analytical groups, or motherinfant linkage groups appear in the same table using Baseline File BASELINEGROUPNUM parameter. By default, only one group will appear in each Characteristics Table, with the exception of Type 6 analyses which will have the initial cohort, patients with a first switch, and patients with a second switch (if applicable) output in separate columns in the same table by default. By specifying to include a second switch group, users can include up to three groups in Type 6 Characteristics Tables (i.e., the initial cohort, the “first switch” group, and the “second switch” group). All inferential analyses will output the exposed and referent analytic groups together by default.
When two groups are included in a single Characteristics Table, users can choose to compare them using absolute and standardized differences. When users request this option in Baseline File, QRP Report will output “Absolute Difference” and “Standardized Difference” columns in Characteristics Tables headed under “Characteristic Balance” in Descriptive (Level 1) analyses and under “Covariate Balance” in Inferential (Level 2) analyses. Groups cannot be compared in Type 6 “Switching” analyses. In inferential analyses, groups are compared by default.
Users can set a standardized difference threshold above which groups are considered to be meaningfully different using the appropriate parameter in Baseline File, and QRP Report will output values above this threshold in blue text.
1.1.3.2 Sections Output
As described above, there are numerous sections output in Characteristics Tables.
By default, the first section in the Characteristics Tables contains “Patient Characteristics.” The first row in this section for patientlevel analyses—i.e., analyses that do not allow cohort reentry—will contain the number of unique patients that were included. Analyses that allow cohort reentry and are thus constructed on the episodelevel will output the number of episodes included in the analysis. Inferential analyses with weights will additionally output the weighted number of patients. In Type 4 analyses, this section is labeled “Mother Characteristics” by default.
The next section output in Characteristics Tables is labeled “Demographic Characteristics” and contains rows describing mean patient age, age distribution based on userspecified categorical age groups, sex, calendar year of exposure, race, and ethnicity groups. Categories and units of demographic characteristics are specified using the appropriate parameters in qrp.CohortFile
. In Type 4, mean patient age is estimated at pregnancy outcome date except in inferential analysis which allows mean age to be estimated at index date specified (estimated pregnancy start, exposure date, or pregnancy outcome date).
In addition to the default sections, users can specify that Characteristics Tables also include the sections described below. For each section described below, if no values are specified, those sections will not be output.
 Health Characteristics, Medical Product Use, Laboratory, and Health Service Utilization Intensity Metrics
 The QRP Reporting Tool can output separate sections that contain individual userspecified comorbidities, medical product use, health service utilization metrics, and/or risk score.
 While any characteristic can be output under the “Health Characteristics,” “Medical Product Use,” and “Health Service Utilization” headers , only laboratory characteristics can be output under the “Laboratory Characteristics” header. If a lab is listed under any other header, only the number of episodes with that lab – but not the lab results – is displayed.
 Predefined risk scores can include the Combined Comorbidity Score,^{1,2}HASBLED score for major bleeding risk,^{2} CHA2DS2VASc score for atrial fibrillation stroke risk,^{3} obstetric comorbidity index,^{4} claimsbased frailty index,^{5}Adapted Diabetes Complications Severity Index (ADCSI),^{2} and the pediatric comorbidity index^{6}.Users can also choose to define a custom risk score in addition to those that are predefined. The scores are calculated based on diagnosis, procedure, and drug codes observed during a userdefined window with an anchor based on the choices made for covariate assessment, as well as demographic criteria (e.g., sex and age).
 The Laboratory Characteristics section reports the number of patients or episodes with evidence of the specified laboratory test during the evaluation window just as other characteristics (such as health and medical product) do. However, in addition to reporting the number with evidence of a laboratory test, laboratory characteristics also return the number of patients or episodes without evidence of the test in the evaluation window. When the laboratory test result is quantitative, the counts are returned by result unit. These counts are reported alongside the proportion of the entire cohort. In addition to overall counts of patients or episodes with and without a test record, laboratory characteristics also return a distribution of test results: 1. Laboratory tests with quantitative results additionally return the mean and standard deviation of the result value by result unit among patients or episodes with evidence of that test record in the evaluation window. Descriptive statistics for test records with missing or invalid units are reported separately. 2. Laboratory tests with qualitative results additionally return the number of patients or episodes with each unique qualitative result value alongside the proportion of all test records. Test results outside of acceptable values per the Sentinel Common Data Model guidance are reported together as “Invalid.”
 Available health service utilization metrics include: mean number of inpatient stays, institutional stays, emergency department visits,outpatient visits, ambulatory encounters, dispensings, unique generics dispensed, and unique drug classes dispensed.
 Using parameters in Baseline File, users specify which characteristics should be output under each section.
 The section headers are output as “Health Characteristics,” “Medical Product Use,” “Laboratory Characteristics”, and “Health Service Utilization Intensity Metrics,” respectively.
 The QRP Reporting Tool can output separate sections that contain individual userspecified comorbidities, medical product use, health service utilization metrics, and/or risk score.
 Sections Unique to Type 4 Analyses
 Pregnancy Characteristics
 Users may specify that certain pregnancyrelated characteristics be output in a separate section of Characteristics Tables after the “Demographics Characteristics” section using the Baseline File
PREGNANCYCHAR
parameter.  Optional rows include:
 preterm (less than 37 weeks), b) early term (37 0/7 weeks through 38 6/7 weeks), c) full term (39 0/7 weeks through 40 6/7 weeks), d) lateterm (41 0/7 weeks through 41 6/7 weeks), e) postterm (42 0/7 weeks and beyond), f) unknown term, and g) N/A
 Mean estimated gestational age at pregnancy outcome (in weeks)
 Rows for each pregnancy outcome (including stillbirth, spontaneous abortion, elective abortion, ectopic pregnancy, and trophoblastic disease)
 Users may specify that certain pregnancyrelated characteristics be output in a separate section of Characteristics Tables after the “Demographics Characteristics” section using the Baseline File
 Exposure Characteristics
 Users can choose to output characteristics of the pregnancyrelated exposure after the Pregnancy Characteristics section by specifying Baseline File
EXPOSURECHAR
.  Exposure characteristics can include:
 Mean gestational age of first exposure in weeks
 Mean number of dispensings in a) userspecified prepregnancy period, b) first trimester, c) second trimester, and d) third trimester
 Exposure status during the a) userspecified prepregnancy period, b) first trimester, c) second trimester, and d) third trimester
 Users can choose to output characteristics of the pregnancyrelated exposure after the Pregnancy Characteristics section by specifying Baseline File
 Infant Characteristics
 Users can choose to additionally include a section headed “Infant Characteristics,” which is output below the last row of “Mother Characteristics.”
 This section includes any userspecified infant characteristics preceded by rows for “Mean enrollment time after birth (days)” and “Mean difference between date of birth and date of enrollment (days).”
 Pregnancy Characteristics
1.1.3.3 Rows Output
Users have three options for specifying the order in which characteristic rows are output in Characteristics Tables. Using the Baseline File COVARSORT
parameter, rows within sections can be sorted in:
 Alphabetical order, based on the characteristic’s label
 Numerical order, based on the characteristic’s assignment in
qrp.CovariateCodes
 Userspecified order, based on the order specified in Baseline File.
In inferential propensity score analyses, users can additionally specify that a footnote be added to characteristics included in the propensity score logistic regression model using the appropriate parameter in Baseline File parameter.
Users may wish to additionally output a “profile” table that describes the number of patients and episodes that qualify for combinations of characteristics by setting the appropriate parameter in Baseline File.
1.1.3.4 Table Titles
The QRP Reporting Tool outputs default titles for Characteristics Tables based on the analysis Type and whether it is an inferential or descriptive analysis. The default titles use information from QRP to determine the minimum and maximum query period to output, and can be further customized by specifying values for GROUPLABEL
and BASELINELINELABEL
in the Label File LABELTYPE
parameter.
Additionally, the database name in Characteristics Tables will default to “Sentinel Distributed Database” unless otherwise specified in DP Info File. For data partnerspecific Characteristics Tables, the word “Aggregated” will be replaced with the masked ID requested in DP Info File.
The last phrase in all Characteristics Table titles will be “from Month Day, Year to Month Day, Year” where the start date is taken from qrp.MonitoringFile
and the end date is the maximum date of all the included data partner end dates (unless an explicit followup end date is specified in qrp.MonitoringFile
and is earlier than the maximum data partner end date, in which case the end date is the followup end date).
Table 1.1 describes default titles and placement of userspecified labels for each type of analysis.
Analysis Type  Inferential?  Default Title  Notes 

Background rates  No  Aggregated Characteristics of [Group Label], [Baseline Label], in the [Database] from [Start Date] to [End date] 

Exposures and FollowUp Time  No  Aggregated Characteristics of [Group Label], [Baseline Label], in the [Database] from [Start Date] to [End date]  
Medical Product Utilization  No  Aggregated Characteristics of [Group Label], [Baseline Label], in the [Database] from [Start Date] to [End date]  
Medical Product Switching Patterns  No  Aggregated Characteristics of [Group Label], [Baseline Label], in the [Database] from [Start Date] to [End date]  
Medical Product Use During Pregnancy  No  Aggregated Characteristics of [Group Label/MIL Group Label], [Baseline Label], in [Database] from [Start Date] to [End date] 

Exposures and FollowUp Time  Yes  Unadjusted: Unadjusted Aggregated Characteristics of [PS Estimate Group Label] in the [Database] from [Start Date] to [End Date] 

Yes  Adjusted: Adjusted Aggregated Characteristics of [Analysis Group Label] (Propensity Score Matched, [Fixed/Variable] Ratio [1:N], Caliper: [value]) in the [Database] from [Start Date] to [End Date] 


Yes  Unweighted: Unweighted Aggregated Characteristics of [Analysis Group Label] (Unweighted, Trimmed) in the [Database] from [Start Date] to [End Date] 


Yes 
Weighted:


Medical Product Use During Pregnancy  Yes  Unadjusted: Unadjusted Aggregated Characteristics of [PS Estimate Group Label] in the [Database] from [Start Date] to [End Date]  
Yes  Adjusted: Adjusted Aggregated Characteristics of [Analysis Group Label] (Propensity Score Matched, [Fixed/Variable] Ratio [1:N], Caliper: [value]) in the [Database] from [Start Date] to [End Date]  
Yes  Unweighted: Unweighted Aggregated Characteristics of [Analysis Group Label] (Unweighted, Trimmed) in the [Database] from [Start Date] to [End Date]  
Yes 
Weighted:

1.1.3.4.1 Customized Value Derivation
 Group Label: value specified in Label File
LABEL
whenLABELTYPE = GroupLabel
 Analysis Group Label: value specified in Label File
LABEL
whenGROUP = AnalysisGroup
andLABELTYPE = GroupLabel
 Baseline Label: value specified in Label File
LABEL
whenLABELTYPE = BaselineLabel
 Database: value specified in [DPInfo File]
DATABASE
 Start Date: value specified in
qrp.MonitoringFile.STARTDATE
 End Date: maximum date of all the included data partner end dates (unless
qrp.MonitoringFile.FUPENDDATE
is specified and is earlier than the maximum data partner end date, in which case the end date is the followup end date)  PS Estimate Group Label: value specified in Label File
LABEL
whenLABELTYPE = GroupLabel
andGROUP
is as specified inqrp.PSEstimationFile.PSESTIMATEGRP
 Standard Subgroup Label: value specified in
qrp.PSCSSubgroup.SUBGROUP
 Subgroup Category: value specified in
qrp.PSCSSubgroup.SUBGROUPCAT
 Fixed/Variable: value specified in
qrp.PSMatchFile.RATIO
 Ratio 1:N: value specified in
qrp.PSMatchFile.CEILING
 Caliper: value: value specified in
qrp.PSMatchFile.CALIPER
 Percentile: value: value specified in
qrp.StratificationFile.PERCENTILES
 Weight: weighting scheme: value specified in
qrp.IPTWFile.IPWEIGHT
1.1.3.5 Default Footnotes
The footnotes described in Table 1.2 are output to the Characteristics tables by default. If users desire additional footnotes, they will need to be manually entered.
Placement  Default Use  Footnote 

After table title  When a nonpregnant cohort is requested  Pregnancy is defined as a pregnancy that resulted in a live or nonlive birth identified using the method specified in the overview section of this report. 
After NonPregnant Cohort column header 
When a nonpregnant cohort is requested 
The nonpregnant cohort includes episodes with neither live nor nonlive birth outcomes (including livebirth delivery, stillbirth, ectopic pregnancy, spontaneous abortion, elective abortion, or trophoblastic disease) during the pregnancy episode of the matched pregnant patient, met all inclusion/exclusion criteria and were the same integer age on the last date of the matched pregnant patient’s pregnancy episode. 
After “Percent/Standard Deviation” column header(s)  Always  Value represents the standard deviation where no % symbol follows. 
After “Race categories” header  When race data included  Race data may not be completely populated at all Data Partners; therefore, data about race may be incomplete. 
After “Unknown” race category label  When race data collapsed  Includes members classified as having an unknown race by the Data Partner and patients in race categories where the total member count is between one and ten. 
After comorbidity score label  When combined comorbidity scores are output  The Combined Comorbidity Score is calculated based on comorbidities observed during a requesterdefined window around the exposure episode start date.^{1,2} 
After “Laboratory Characteristics” header  When Laboratory Characteristics are output  Only the laboratory result closest to the index date in the userdefined evaluation window is described. The number of [patients/episodes] with a given categorical result value, or the mean numerical result value among those reported inwith a given unit, is shown indented and italicized below the Romanized number of unique [patients/episodes] with or without a test record. 
After first switch group label  Medical product switching pattern analyses  Value represents the proportion of episodes with a first switch. 
After second switch group label  Medical product switching pattern analyses  Value represents the proportion of first switch episodes with a second switch. 
Within “Mean gestational age at pregnancy outcome” and “Mean gestational age of first exposure, weeks” covariates  Medical product use during pregnancy analyses  The length of the pregnancy episode was estimated using a hierarchy of pregnancy markers. If overlapping pregnancy episodes were constructed in the same patient due to observation of multiple pregnancy markers, then the markers providing more reliable estimation of pregnancy start was selected for estimation of pregnancy start date. If no pregnancy markers were observed, then a fixed pregnancy duration was assigned by pregnancy outcome type, as described in the overview section of this report. 
After each specified covariate  Inferential analyses when userspecified in COVINPS found in the QRP Report Baseline File  Covariate included in the propensity score logistic regression model. 
Medical product use during pregnancy analyses, when covariates are evaluated in mother and infant claims  Characteristics were evaluated in mother and infant claims  
Medical product use during pregnancy analyses, when covariates are evaluated only in infant claims  Characteristics were evaluated only in infant claims  
Medical product use during pregnancy analyses, for a nonpregnant cohort with covariates that were evaluated only in infant claims.  In nonpregnant patients, characteristics evaluated using only infant claims are not output  
After “Patient Characteristics” or “Mother Characteristics” header  Analyses where cohort reentry is allowed  All metrics are based on the total number of episodes per group except for sex, race, and Hispanic origin, which are based on total number of unique patients. 
When standardized differences are output  Characteristics in blue font have a betweengroup standardized difference greater than the value specified for SDTHRESHOLD in the Baseline File.  
In inferential propensity score stratum weighting analyses when patients are weighted using an “average treatment effect” weight  This table is meant to facilitate the assessment of covariate balance after inverse probability weighting and should not be interpreted as a description of the unweighted population. Patients were weighted by the proportion of the total patient population included in their propensity score (PS) stratum divided by the proportion of the total treated/comparator patient population included in their PS stratum.  
In inferential propensity score stratum weighting analyses when patients are weighted using an “average treatment effect in the treated” weight  This table is meant to facilitate the assessment of covariate balance after inverse probability weighting and should not be interpreted as a description of the unweighted population. Treated patients were assigned a weight of 1, and control patients were weighted by the proportion of the total treated patient population included in their propensity score (PS) stratum divided by the proportion of the total control patient population included in their PS stratum.  
In inferential IPTW analyses when patients are weighted using an “average treatment effect” weight  This table is meant to facilitate the assessment of covariate balance after inverse probability weighting and should not be interpreted as a description of the unweighted population. Treated patients were weighted by the inverse of their propensity score (PS), while comparator patients were weighted by the inverse of 1 minus their PS.  
In inferential IPTW analyses when patients are weighted using an “average treatment effect with stabilization” weight  This table is meant to facilitate the assessment of covariate balance after inverse probability weighting and should not be interpreted as a description of the unweighted population. Treated patients were weighted by the proportion of treated patients in the trimmed population divided by the inverse of their propensity score (PS). Comparator patients were weighted by 1 minus the proportion of treated patients in the trimmed population divided by 1 minus their PS.  
In inferential IPTW analyses when patients are weighted using an “average treatment effect in the treated” weight  This table is meant to facilitate the assessment of covariate balance after inverse probability weighting and should not be interpreted as a description of the unweighted population. Treated patients were assigned a weight of 1. Comparator patients were weighted by their propensity score (PS) divided by 1 minus their PS.  
In inferential weighted analyses with variable ratio matching  Each treated patient was matched to a variable number of comparators. Treated patients were assigned a weight of 1. Comparator patients were weighted by the inverse of the matching ratio for that specific matched set.  
After “Mother Characteristics” header  Medical product use during pregnancy analyses  Baseline period is in reference to the user defined index date (start of first valid exposed pregnancy, exposure date, or pregnancy outcome date). 
After “Laboratory Characteristics” header  When laboratory results are used as characteristics  Only the laboratory result closest to the index date in the userdefined evaluation window is described. The number of [patients/episodes] with a given categorical result value, or the mean numerical result value among those reported in given unit, is shown indented and italicized below the Romanized number of unique [patients/episodes] with or without a test record. 
Medical product use during pregnancy analyses when laboratory results are used as characteristics  Only the laboratory result closest to the anchor date for the end of the covariate evaluation window (either pregnancy start, pregnancy end date, or exposure date) is described. The number of [patients/episodes] with a given categorical result value, or the mean numerical result value among those reported in given unit, is shown indented and italicized below the Romanized number of unique [patients/episodes] with or without a test record. 
1.1.3.6 Missing Data
Missing data will be represented by .
in all fields where there are zero patients in the cohort, except patient and episode counts. In DPspecific tables, if the DP does not report race or Hispanic ethnicity data, then all categories for race and Hispanic ethnicity except “Unknown” will be displayed as missing. The “Unknown” category will be displayed as the actual numeric value. In aggregated tables, if at least one DP populates race or Hispanic ethnicity, the actual numeric value will be displayed.
1.1.4 Sample Characteristics Table
Figure 1.1 below is provided as an example of how Characteristics tables are output. No footnotes are included in the sample table for brevity. Not all rows and/or columns presented in the sample table may be output in the final report, based on userdefined specifications discussed above. For example, the “Pregnant patients” row would not be output unless a medical product use during pregnancy analysis is conducted, and a “Weighted patients” row would not be output unless a weighted inferential analysis is conducted.