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Search review questions

Each row is one question a systematic review asked: who, what, compared with what, and which outcome, with the effect it found and how certain that is. Words match anywhere in the field.

Limit to evidence status or GRADE (optional)

2,434 questions in 139 reviews · Kidney and Transplant

current versions
No studies 504 · 20.7%Ungraded 40 · 1.6%Very low 611 · 25.1%Low 790 · 32.5%Moderate 414 · 17%High 75 · 3.1%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

QuestionEffectEvidenceStatus / GRADE
CERA vs other ESA
Transfusions: CERA every 2 weeks versus rHuEPO · patients with the anaemia of end‐stage kidney disease undergoing dialysis
Frequency of administration of erythropoiesis‐stimulating agents for the anaemia of end‐stage kidney disease… (2014) · Cochrane
RR 0.92 [0.64, 1.32]4 studies · 1341 participantsModerate
CERA vs other ESA
Numbers of adverse events due to hypertension: CERA every 2 weeks versus rHuEPO · patients with the anaemia of end‐stage kidney disease undergoing dialysis
Frequency of administration of erythropoiesis‐stimulating agents for the anaemia of end‐stage kidney disease… (2014) · Cochrane
RR 0.93 [0.69, 1.26]4 studies · 1341 participantsHigh
CERA vs other ESA
Numbers of adverse events due to access thrombosis: CERA every 2 weeks versus rHuEPO · patients with the anaemia of end‐stage kidney disease undergoing dialysis
Frequency of administration of erythropoiesis‐stimulating agents for the anaemia of end‐stage kidney disease… (2014) · Cochrane
RR 0.96 [0.56, 1.65]4 studies · 1341 participantsModerate
Intervention NR
Final Hb (g/dL) · patients with the anaemia of end‐stage kidney disease undergoing dialysis
Frequency of administration of erythropoiesis‐stimulating agents for the anaemia of end‐stage kidney disease… (2014) · Cochrane
no estimate extracted2 studies · 675 participantsModerate
Intervention NR
All‐cause mortality · patients with the anaemia of end‐stage kidney disease undergoing dialysis
Frequency of administration of erythropoiesis‐stimulating agents for the anaemia of end‐stage kidney disease… (2014) · Cochrane
RR 1.03 [0.6, 1.78]2 studies · 822 participantsHigh
Intervention NR
Major cardiovascular events · adults with chronic kidney disease
HMG CoA reductase inhibitors (statins) for kidney transplant recipients (2014) · Cochrane
RR 0.84 [0.66, 1.06]1 study · 2102 participantsLow
Intervention NR
All‐cause mortality · adults with chronic kidney disease
HMG CoA reductase inhibitors (statins) for kidney transplant recipients (2014) · Cochrane
RR 1.08 [0.63, 1.83]6 studies · 2760 participantsLow
Intervention NR
Cardiovascular mortality · adults with chronic kidney disease
HMG CoA reductase inhibitors (statins) for kidney transplant recipients (2014) · Cochrane
RR 0.68 [0.45, 1.01]4 studies · 2322 participantsLow
Intervention NR
All‐cause mortality (8 months) · adults with CKD
Calcimimetics for secondary hyperparathyroidism in chronic kidney disease patients (2014) · Cochrane
RR 0.97 [0.89, 95]14 studies · 6893 participantsHigh
Intervention NR
Parathyroidectomy (9 months) · adults with CKD
Calcimimetics for secondary hyperparathyroidism in chronic kidney disease patients (2014) · Cochrane
RR 0.49 [0.4, 0.59]5 studies · 4893 participantsHigh
Intervention NR
Hypocalcaemia (7 months) · adults with CKD
Calcimimetics for secondary hyperparathyroidism in chronic kidney disease patients (2014) · Cochrane
RR 6.98 [5.1, 9.53]12 studies · 6415 participantsHigh
Intervention NR
Nausea (7 months) · adults with CKD
Calcimimetics for secondary hyperparathyroidism in chronic kidney disease patients (2014) · Cochrane
RR 2.02 [1.45, 2.81]12 studies · 6450 participantsModerate
Intervention NR
GFR category G3a‐G4 · adults with CKD
Calcimimetics for secondary hyperparathyroidism in chronic kidney disease patients (2014) · Cochrane
no estimate extracted3 participantsUngraded
Intervention NR
Haematocrit (%) · adults with the anaemia of chronic kidney disease
Androgens for the anaemia of chronic kidney disease in adults (2014) · Cochrane
no estimate extracted3 studies · 73 participantsLow
Intervention NR
Haemoglobin (g/dL) · adults with the anaemia of chronic kidney disease
Androgens for the anaemia of chronic kidney disease in adults (2014) · Cochrane
no estimate extracted1 study · 32 participantsLow
Intervention NR
Serum albumin (g/L) · adults with the anaemia of chronic kidney disease
Androgens for the anaemia of chronic kidney disease in adults (2014) · Cochrane
no estimate extracted2 studies · 51 participantsVery low
Intervention NR
Adverse events · adults with the anaemia of chronic kidney disease
Androgens for the anaemia of chronic kidney disease in adults (2014) · Cochrane
RR 7.72 [1.45, 41.12]2 studies · 83 participantsVery low
Astragalus and co‐interventions vs same co‐interventions alone
Time to requirement for RRT/initiation of dialysis · patients with CKD
Astragalus (a traditional Chinese medicine) for treating chronic kidney disease (2014) · Cochrane
no estimate extracted0 studies · 0 participantsUngraded
Astragalus and co‐interventions vs same co‐interventions alone
All‐cause mortality · patients with CKD
Astragalus (a traditional Chinese medicine) for treating chronic kidney disease (2014) · Cochrane
no estimate extracted0 studies · 0 participantsUngraded
Astragalus and co‐interventions vs same co‐interventions alone
Creatinine clearance (after treatment) · patients with CKD
Astragalus (a traditional Chinese medicine) for treating chronic kidney disease (2014) · Cochrane
no estimate extracted4 studies · 306 participantsLow
Astragalus and co‐interventions vs same co‐interventions alone
Serum creatinine (after treatment) · patients with CKD
Astragalus (a traditional Chinese medicine) for treating chronic kidney disease (2014) · Cochrane
no estimate extracted14 studies · 841 participantsLow
Astragalus and co‐interventions vs same co‐interventions alone
h proteinuria (after treatment) · patients with CKD
Astragalus (a traditional Chinese medicine) for treating chronic kidney disease (2014) · Cochrane
no estimate extracted11 studies · 706 participantsLow
Astragalus and co‐interventions vs same co‐interventions alone
Albumin · patients with CKD
Astragalus (a traditional Chinese medicine) for treating chronic kidney disease (2014) · Cochrane
no estimate extracted10 studies · 588 participantsLow
Astragalus and co‐interventions vs same co‐interventions alone
Haemoglobin · patients with CKD
Astragalus (a traditional Chinese medicine) for treating chronic kidney disease (2014) · Cochrane
no estimate extracted4 studies · 222 participantsModerate
Intervention NR
All‐cause mortality · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
RR 0.17 [0.02, 1.37]1 study · 43 participantsLow
Intervention NR
Length of hospital stay · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
no estimate extracted1 study · 43 participantsLow
Intervention NR
Serum myoglobin: day 4 · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
no estimate extracted1 study · 36 participantsLow
Intervention NR
Serum myoglobin: day 8 · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
no estimate extracted1 study · 36 participantsLow
Intervention NR
Serum myoglobin: day 10 · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
no estimate extracted1 study · 22 participantsLow
Intervention NR
Serum creatinine: day 4 · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
no estimate extracted1 study · 36 participantsLow
Intervention NR
Serum creatinine: day 8 · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
no estimate extracted1 study · 36 participantsLow
Intervention NR
Serum creatinine: day 10 · patients with rhabdomyolysis
Continuous renal replacement therapy (CRRT) for rhabdomyolysis (2014) · Cochrane
no estimate extracted1 study · 22 participantsLow
Isoniazid vs no treatment
Tuberculosis · kidney transplant recipients
Antibiotic prophylaxis for preventing post solid organ transplant tuberculosis (2014) · Cochrane
RR 0.35 [0.14, 0.89]3 studies · 558 participantsModerate
Isoniazid vs no treatment
INH hepatotoxicity Jaundice, elevated bilirubin, elevated liver enzymes · kidney transplant recipients
Antibiotic prophylaxis for preventing post solid organ transplant tuberculosis (2014) · Cochrane
RR 1.59 [1.06, 2.4]3 studies · 558 participantsModerate
Isoniazid vs no treatment
All‐cause mortality · kidney transplant recipients
Antibiotic prophylaxis for preventing post solid organ transplant tuberculosis (2014) · Cochrane
RR 1.39 [0.7, 2.78]3 studies · 558 participantsLow
Angiotensin receptor blockers (ARBs) vs conventional therapy
Residual kidney function (3 months) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
no estimate extracted1 study · 44 participantsModerate
Angiotensin receptor blockers (ARBs) vs conventional therapy
Diastolic BP · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
no estimate extracted3 studies · 110 participantsModerate
Angiotensin receptor blockers (ARBs) vs conventional therapy
Serum potassium · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
no estimate extracted1 study · 44 participantsLow
Angiotensin receptor blockers (ARBs) vs conventional therapy
Adverse events (episodes of peritonitis) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 0.67 [0.18, 2.54]1 study · 34 participantsLow
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Decline in residual kidney function (12 months) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
no estimate extracted1 study · 60 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Anuria · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 0.32 [0.11, 0.94]1 study · 60 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Mortality · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 1.5 [0.27, 8.34]1 study · 60 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Cardiac events · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 1 [0.37, 3.21]1 study · 60 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Cardiac events (fatal) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 1 [0.15, 6.64]1 study · 60 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Cardiac events (non fatal) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 1 [0.31, 3.27]1 study · 60 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Adverse events (episodes of peritonitis) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 1.13 [0.47, 2.71]1 study · 60 participantsModerate
Angiotensin receptor blockers (ARBs) vs conventional therapy
Residual kidney function (6 months) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
no estimate extracted1 study · 44 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Adverse events (episodes of peritonitis) ‐ treated with an aminoglycoside · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 1.2 [0.41, 3.51]1 study · 60 participantsModerate
Angiotensin‐converting enzyme inhibitors (ACEi) vs conventional therapy
Adverse events (episodes of peritonitis) ‐ not treated with an aminoglycoside · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
RR 1 [0.22, 4.56]1 study · 60 participantsModerate
Angiotensin receptor blockers (ARBs) vs angiotensin‐converting enzyme inhibitors (ACEis)
Residual kidney function (4 weeks) · patients receiving PD
Angiotensin‐converting enzyme inhibitors and angiotensin receptor blockers for preserving residual kidney… (2014) · Cochrane
no estimate extracted1 study · 20 participantsLow