Gap finder
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.
1,886 questions in 74 reviews · Skin
current versionsNo studies 542 · 28.7%Ungraded 130 · 6.9%Very low 326 · 17.3%Low 434 · 23%Moderate 348 · 18.5%High 106 · 5.6%
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.
| Question | Effect | Evidence | Status / GRADE |
|---|---|---|---|
Tacrolimus 0.03% vs pimecrolimus 1% Physician's assessment of global response of improvement · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 1.42 [1.02, 1.98] | 1 study · 139 participants | Low |
Tacrolimus 0.03% vs pimecrolimus 1% Adverse effects ‐ application site reaction · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 1.07 [0.6, 1.91] | 1 study · 141 participants | Low |
Tacrolimus 0.1% vs corticosteroids Physician's assessment of global response of improvement, clear or excellent ‐ tacrolimus 0.1% versus hydrocortisone butyrate: 3 weeks · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 0.95 [0.78, 1.16] | 1 study · 377 participants | Low |
Tacrolimus 0.03% vs pimecrolimus 1% Adverse effects ‐ burning · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 0.87 [0.43, 1.75] | 1 study · 141 participants | Low |
Tacrolimus 0.03% vs pimecrolimus 1% Adverse effects ‐ itching · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 2.37 [0.96, 5.81] | 1 study · 141 participants | Low |
Tacrolimus 0.03% vs pimecrolimus 1% Adverse effects ‐ erythema · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 2.2 [0.89, 5.46] | 1 study · 141 participants | Low |
Tacrolimus 0.1% vs ciclosporin Adverse effects · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 1 [0.31, 3.28] | 1 study · 30 participants | Very low |
Tacrolimus 0.1% vs corticosteroids Physician's assessment of global response of improvement, clear or excellent ‐ tacrolimus 0.1% versus hydrocortisone acetate and butyrate 0.1%: short term (6 months) · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 1.32 [1.17, 1.49] | 1 study · 972 participants | Moderate |
Tacrolimus 0.1% vs corticosteroids Adverse effects: burning ‐ tacrolimus 0.1% versus hydrocortisone acetate 0.1%: 3 weeks · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 2.91 [1.6, 5.28] | 1 study · 371 participants | Moderate |
Tacrolimus 0.1% vs corticosteroids Adverse effects: burning ‐ tacrolimus 0.1% versus hydrocortisone butyrate: 3 weeks · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 4.59 [3.1, 6.78] | 1 study · 377 participants | Moderate |
Tacrolimus 0.1% vs corticosteroids Adverse effects: burning ‐ tacrolimus 0.1% versus hydrocortisone acetate and butyrate 0.1%: 6 months · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 3.79 [2.99, 4.81] | 1 study · 972 participants | Moderate |
Tacrolimus 0.1% vs corticosteroids Participant's self‐assessment of global response of improvement · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 1.21 [1.13, 1.29] | 1 study · 974 participants | Low |
Tacrolimus 0.1% vs pimecrolimus 1% Physician's assessment of global response of improvement, clear or excellent ‐ 6 weeks · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 1.8 [1.34, 2.42] | 2 studies · 506 participants | Moderate |
Tacrolimus 0.1% vs pimecrolimus 1% Adverse effects ‐ 6 weeks · people with atopic dermatitis Topical tacrolimus for atopic dermatitis (2015) · Cochrane | RR 0.89 [0.47, 1.71] | 2 studies · 506 participants | Very low |
Etanercept vs placebo PASI 75 Participants achieving a 75% improvement in the Psoriasis Area and Severity Index · people with paediatric psoriasis Anti‐TNF agents for paediatric psoriasis (2015) · Cochrane | RR 4.95 [2.83, 8.65] | 1 study · 211 participants | High |
Etanercept vs placebo PASI 50 Participants achieving a 50% improvement in the Psoriasis Area and Severity Index · people with paediatric psoriasis Anti‐TNF agents for paediatric psoriasis (2015) · Cochrane | RR 3.26 [2.26, 4.71] | 1 study · 211 participants | High |
Etanercept vs placebo PASI 90 Participants achieving a 90% improvement in the Psoriasis Area and Severity Index · people with paediatric psoriasis Anti‐TNF agents for paediatric psoriasis (2015) · Cochrane | RR 4.1 [1.88, 8.95] | 1 study · 211 participants | High |
Etanercept vs placebo PGA Participants achieving a PGA of 'clear' or 'almost clear' · people with paediatric psoriasis Anti‐TNF agents for paediatric psoriasis (2015) · Cochrane | RR 3.96 [2.36, 6.66] | 1 study · 211 participants | High |
Etanercept vs placebo CDLQI Scores range from 0 to 30. Lower scores indicate better health‐related quality of life. Calculations are based on the change from baseline to week 12 in both groups · people with paediatric psoriasis Anti‐TNF agents for paediatric psoriasis (2015) · Cochrane | no estimate extracted | 1 study · 211 participants | Moderate |
Adalimumab weekly vs placebo Change in DLQI score (imputation) · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 102 participants | Moderate |
Adalimumab every other week vs placebo Frequency of treatment discontinuation · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 4.91 [0.24, 99.74] | 2 studies · 124 participants | High |
Adalimumab every other week vs placebo Proportion of participants with infectious adverse effects · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 1.6 [0.57, 4.53] | 2 studies · 124 participants | High |
Adalimumab every other week vs placebo Change in Pain VAS · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 21 participants | Low |
Adalimumab every other week vs placebo Proportion with improvement in pain · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 1.34 [0.73, 2.43] | 1 study · 95 participants | Moderate |
Adalimumab every other week vs placebo Change in Sartorius scale score (LOCF) · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 2 studies · 124 participants | Moderate |
Infliximab vs placebo At least 50% decrease in HS Severity Index · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 4.8 [0.6, 38.48] | 1 study · 33 participants | Moderate |
Infliximab vs placebo Physician global assessment · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 4.8 [1.66, 13.9] | 1 study · 33 participants | Moderate |
Etanercept vs placebo Dermatology Life Quality Index · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 17 participants | Moderate |
Topical clindamycin vs placebo Adverse effects (non‐serious) · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 0.72 [0.14, 3.64] | 1 study · 27 participants | Moderate |
Oral tetracycline vs topical clindamycin Participant global assessment VAS Visual analogue scale (VAS) (0 to 100 mm) · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 34 participants | Low |
Adalimumab weekly vs placebo Change in DLQI score (LOCF) · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 102 participants | Moderate |
Oral tetracycline vs topical clindamycin Pain VAS VAS (0 to 100 mm) · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 34 participants | Low |
Oral tetracycline vs topical clindamycin Nodules score Nodule count · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 34 participants | Low |
Oral tetracycline vs topical clindamycin Abscesses score Abscess count · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 34 participants | Low |
Oral tetracycline vs topical clindamycin Physician global assessment VAS VAS (0 to 100 mm) · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 34 participants | Low |
Ethinyloestradiol and cyproterone acetate vs ethinyloestradiol and norgestrel Number of participants reporting non‐serious adverse effects · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 0.53 [0.29, 0.98] | 1 study · 18 participants | Moderate |
Ethinyloestradiol and cyproterone acetate vs ethinyloestradiol and norgestrel Participant global assessment VAS Scale from: 0 to 100 · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 17 participants | Moderate |
Gentamicin sponge vs primary closure alone Adverse effects ‐ complication rate at 1 week after surgery · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 0.78 [0.58, 1.05] | 1 study · 200 participants | Moderate |
Gentamicin sponge vs primary closure alone Adverse effects ‐ complication rate at 3 months after surgery · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 0.9 [0.5, 1.62] | 1 study · 200 participants | Moderate |
Gentamicin sponge vs primary closure alone Recurrence rate at 3 months after surgery · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 0.96 [0.68, 1.34] | 1 study · 200 participants | Moderate |
Intense pulsed light vs no treatment Participant global assessment: satisfaction with treatment Questionnaire · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 9.67 [2.01, 46.43] | 1 study · 34 participants | Low |
Adalimumab weekly vs placebo Frequency of serious adverse effects · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 2 [0.38, 10.44] | 1 study · 102 participants | Moderate |
Intense pulsed light vs no treatment Participant global assessment: satisfaction with treatment ‐ axilla Questionnaire · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 21 [1.37, 322.28] | 1 study · 24 participants | Low |
Intense pulsed light vs no treatment Participant global assessment: satisfaction with treatment ‐ groin Questionnaire · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 5 [0.31, 79.94] | 1 study · 8 participants | Low |
Intense pulsed light vs no treatment Participant global assessment: satisfaction with treatment ‐ inframammary Questionnaire · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | RR 3 [0.24, 37.67] | 1 study · 2 participants | Low |
Nd:YAG laser vs topical control Modified HS‐LASI score after 3 months · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 50 participants | Very low |
Nd:YAG laser vs topical control Modified HS‐LASI score after 3 months ‐ axilla · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 20 participants | Very low |
Nd:YAG laser vs topical control Modified HS‐LASI score after 3 months ‐ groin · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 22 participants | Very low |
Nd:YAG laser vs topical control Modified HS‐LASI score after 3 months ‐ inframammary · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 8 participants | Very low |
Nd:YAG laser vs topical control Percentage change in modified HS‐LASI score after 5 months compared with baseline · participants with hidradenitis suppurativa Interventions for hidradenitis suppurativa (2015) · Cochrane | no estimate extracted | 1 study · 50 participants | Very low |