Extraction form for project: Treatment of Hepatitis C in Chronic Kidney Disease. KDIGO 2022 update

Design Details

1. Reject Reason
Skip if not rejecting. Don't fill out rest if you are rejecting
Reason
Confirmed by CG
2. Secondary to other article?
List PMID(s) or other identifier for related article
3. Study or registry name
Skip if no identifying name available.
4. CKD stage
5. Treatment(s) investigated
6. KQ/Topic
7. KQ/Topic
8. Study design
Design
Direction
Protocol
9. Study design
Design
Direction
10. Sample size
Answer in one row only (but ok to leave data in both rows 1 and 2). Row 1 refers to N who meet all CKD criteria. Row 2 refers to total N when data for row 1 unclear (ie, in abstract). Similarly, row 3 is applicable only to abstract mapping phase. Across all arms. Ensure that each counted arm has N>=10.
N eligible (Specific Population)
N total (Broad population)
NR
11. Country/ies
Check citation title
12. Note/Comment

Arms

N/A

Arm Details

1. Regimen
For each drug: Drug name dose frequency. Split up specific drugs, even if they are given in a combination pill. Include duration only if the specific drug is used for a different duration than the whole regimen. (If duration varied by gt, note in next question.) Std abbreviations: qD, BID, TID, QID, qOD, qW, BIW; gt = genotype (put in parentheses if drug used only a specific gt). Eg: Ombitasvir 25 mg qD Paritaprevir 150 mg qD Dasabuvir 250 mg BID (gt 1) Ritonavir 100 mg qD (gt 1a, 4, cirrhosis)
2. Duration of treatment
If mean or median (with SD, IQR, etc.), specify explicitly. If duration (of whole regimen) varies by genotype or other factor, note it in parentheses. (If duration of one drug is different, note that in the prior question for that drug. Put the full duration of the regimen here.) Abbreviations: d, wk, mo (but try to convert to weeks). Eg, 12 wk 12 wk (gt 1b) 24 wk (gt 1a, 4, cirrhosis)
3. (GL 4) Time to start of DAA (relative to Txp)
4. Comment/Note

Sample Characteristics

1. Population characteristics
Enter as per template in row headers
2. Population
Should sum to 100% for each arm. We will treat groups >=90% as if they were 100%, but do note the <10% groups.
3. Note/Comment

Outcomes

TypeDomainSpecific measurement (i.e., tool/definition/specific outcome)PopulationsTimepoints
CategoricalSVR12
  • All Participants
  • 12 (wk post-Tx)
CategoricalSVR24
  • All Participants
  • 24 (wk)
CategoricalPatient death(prioritize 1 year)
  • All Participants
  • 1 (year)
CategoricalAE due to treatmentSerious AE
  • All Participants
  • Baseline
CategoricalDiscontinuation due to AE
  • All Participants
  • Baseline

Outcome Details

1. Comment/Note
SVR12
SVR24
Patient death
AE due to treatment
Discontinuation due to AE

Risk of Bias Assessment

1. RCT only_Random sequence generation
Rating
Notes/Comments (add for high/unclear):
2. RCT only_Allocation concealment
Rating
Notes/Comments (add for high/unclear):
3. RCT only_Blinding of participants
Rating
Notes/Comments:
4. ALL_Blinding of outcome assessors
There is low risk of detection bias if the blinding of the outcome assessment was ensured and it was unlikely that the blinding could have been broken; or if there was no blinding or incomplete blinding, but the review authors judge that the outcome is not likely to be influenced by lack of blinding. WE SHOULD DISCUSS WHICH OUTCOMES (MAYBE ALL) THIS IS RELEVANT FOR.
Rating
Notes/Comments:
5. ALL_Incomplete outcome data (dropouts, missing data)
20% threshold (or imbalance between groups)
Rating
Notes/Comments (add for high/unclear):
6. ALL_Selective Reporting (reporting bias)
There is LOW risk of reporting bias ONLY if the study protocol is available and all of the study’s pre-specified (primary and secondary) outcomes that are of interest in the review have been reported in the pre-specified way. There is a HIGH risk of reporting bias if not all of the study’s pre-specified primary outcomes have been reported (pre-specified either in protocol or in methods section). Also HIGH risk of bias if one or more outcomes of interest in the review are reported incompletely so that they cannot be entered in a meta-analysis. Usually UNCLEAR risk of bias.
Rating
Notes/Comments:
7. ALL_Intention-to-treat-analysis
If self-describe ITT, confirm actually is ITT. If 100% reporting, then equivalent to ITT. Provide info about meaning of ITT or reason not ITT
Rating
Notes/Comments (add for high/unclear):
8. ALL_Was selection of participants into the study based on participant characteristics observed AFTER the start of intervention?
If yes, consider whether should reject. Try your best to select Y or N
Rating
Notes/Comments (add for Yes or Probably Yes):
9. COMPARATIVE only_Cohorts comparable?
E.g., based off of "Table 1". No statistically significant (or large) differences of a clinically important factor.
Rating
Notes/Comments (add for No):
10. COMPARATIVE only_Were potential confounders properly accounted for?
Comparative studies only (where we evaluate the analysis of the comparison)
Rating
Notes/Comments (add for unclear):
11. ALL_Clear reporting with no discrepancies
Rating
Notes/Comments (add for no):
12. ALL_Were eligibility criteria clear?
Rating
Notes/Comments (add for no):
13. ALL_Were interventions adequately described?
Rating
Notes/Comments (add for no):
14. ALL_Were the outcomes adequately defined?
Rating
Notes/Comments (add for no):
15. ALL_Were the harms PRE-DEFINED using standardized or precise definitions
Rating
Notes/Comments (add for no):
16. Other Bias:
Rating
Notes/Comments:

Results

Categorical


SVR12

All Participants
Descriptive StatisticsBetween Arm Comparisons
12 (wk post-Tx)
Total (N analyzed)Odds Ratio (OR)
Events95% CI low (OR)
Percentage95% CI high (OR)
p value
Within Arm ComparisonsNet Comparisons

SVR24

All Participants
Descriptive StatisticsBetween Arm Comparisons
24 (wk)
Total (N analyzed)Odds Ratio (OR)
Events95% CI low (OR)
Percentage95% CI high (OR)
p value
Within Arm ComparisonsNet Comparisons

Patient death ((prioritize 1 year))

All Participants
Descriptive StatisticsBetween Arm Comparisons
1 (year)
Total (N analyzed)Odds Ratio (OR)
Events95% CI low (OR)
Percentage95% CI high (OR)
p value
Within Arm ComparisonsNet Comparisons

AE due to treatment (Serious AE)

All Participants
Descriptive StatisticsBetween Arm Comparisons
Baseline
Total (N analyzed)Odds Ratio (OR)
Events95% CI low (OR)
Percentage95% CI high (OR)
p value
Within Arm ComparisonsNet Comparisons

Discontinuation due to AE

All Participants
Descriptive StatisticsBetween Arm Comparisons
Baseline
Total (N analyzed)Odds Ratio (OR)
Events95% CI low (OR)
Percentage95% CI high (OR)
p value
Within Arm ComparisonsNet Comparisons