Table D-3. Quality and applicability for KQ 3 studies
Study / Intervention/Comparator / Quality / Limitations to ApplicabilityBadesch, 2000163 /
- Epoprostenol ≤2 ng/kg, then adjusted
- Conventional therapy only
- None
Barst, 199665
Primary Pulmonary Hypertension Study /
- Epoprostenol ≤4 ng/kg, then adjusted
- Conventional therapy only
- None
Barst, 2010164
ASSET-1 /
- Bosentan 62.5 mg BID, then 125 mg BID
- Placebo
- None
Barst, 2010164
ASSET-2 /
- Bosentan 62.5 mg BID, then 125 mg BID
- Placebo
- None
Barst, 2011165
STARTS-1 /
- Low dose sildenafil
- Medium dose sildenafil
- High dose sildenafil
- Placebo
- None
Bharani, 200769 /
- Tadalafil 20 mg daily
- Placebo 20 mg daily
- Intervention (active arm) was not similar to that used in routine clinical practice
Channick, 200175
Badesch, 200276 /
- Bosentan 62.5 mg BID, then 125 mg BID
- Placebo
- Potential adverse events associated with testing or treatment were not measured or reported
Fix, 2007166 /
- Epoprostenol 1 ng/kg/min, then titrated to mean dose of 29 ng/kg/min
- Non-epoprostenol group
- None
Galie, 2005167
Badesch, 2007168
Rubin, 2011169
SUPER /
- Sildenafil 20 mg TID
- Sildenafil 40 mg TID
- Sildenafil 80 mg TID
- Placebo
- None
Galie, 2006170
BREATHE-5 /
- Bosentan 62.5 mg BID, then 125 mg BID
- Placebo
- None
Galie, 2008171
EARLY /
- Bosentan 62.5 mg BID, then 125 mg BID
- Placebo
- None
Galie, 200888
Shapiro, 201290
ARIES-1 /
- Ambrisentan 5 mg daily
- Ambrisentan 10 mg daily
- Placebo
- None
Galie, 200888
Shapiro, 201290
ARIES-2 /
- Ambrisentan 2.5 mg daily
- Ambrisentan 5 mg daily
- Placebo
- None
Galie, 2009172
Barst, 2011173
Oudiz, 2012174
PHIRST /
- Tadalafil 2.5 mg daily
- Tadalafil 10 mg daily
- Tadalafil 20 mg daily
- Tadalafil 40 mg daily
- Placebo
- None
Higenbottam, 1993175 /
- Epoprostenol, initial mean dose 5.2 (0.5) ng/kg/min then titrated up to mean 18.7 (4.5) ng/kg/min
- No epoprostenol
- Study population was inadequately described to assess the applicability of this study
- Study selectively recruited participants who demonstrated a history of favorable or unfavorable response to the drug/intervention of interest
- Included patients did not match the review question
- Potential adverse events associated with testing or treatment were not measured or reported
Hiremath, 2010176
TRUST /
- Treprostinil 4 ng/kg/min, then adjusted
- Placebo
- Study population was inadequately described to assess the applicability of this study
- Cointerventions/treatments did not adequately reflect routine clinical practice
- Care delivery setting was widely divergent from the current typical US setting
Hoeper, 2006177
COMBI /
- Bosentan 125 mg BID + iloprost (aerosolized)
- Bosentan 125 mg
- None
Hoeper, 2007178 /
- Bosentan 62.5 mg BID x 4 weeks, then 125 mg thereafter
- Iloprost (aerosolized) 5 mcg 6x daily
- None
Humbert, 2004179
BREATHE-2 /
- Epoprostenol + bosentan 62.5 mg BID, then 125 mg BID
- Epoprostenol + placebo
- None
Jacobs, 2009106 /
- Epoprostenol titrated to 6-8 ng/kg/min after 1 week (N=6)
- Treprostinil gradually increased to 10 ng/kg/min after 1 week, then 20 ng/kg/min after 6 weeks (N=10)
- None
Jing, 2011180
EVALUATION /
- Vardenafil 5 mg qD, then 5 mg BID
- Placebo
- None
Kemp, 2012181 /
- Epoprostenol/bosentan combined
- Epoprostenol monotherapy
- None
McLaughlin, 2003182 /
- Treprostinil 2.5-5.0 ng/kg/min, then adjusted
- Placebo
- None
McLaughlin, 2006183 /
- Bosentan + iloprost (aerosolized)
- Bosentan + placebo
- None
McLaughlin, 2010119
Frantz, 2012120
TRIUMPH 1 /
- Treprostinil (aerosolized)
- Placebo
- None
Mukhopadhyay, 2011184 /
- Tadalafil 40 mg daily
- Placebo
- Care delivery setting was widely divergent from the current typical US setting
Olschewski, 2002185 /
- Iloprost (aerosolized)
- Placebo
- None
Olschewski, 2010186
AIR /
- Iloprost (aerosolized)
- Standard therapy only
- None
Reichenberger, 2011187 /
- Epoprostenol
- Iloprost up to 20 mcg per breath, max 120 mcg total daily dose
- None
Rich, 2012188 /
- IV treprostinil in epoprostenol diluent
- IV epoprostenol in epoprostenol diluent
- IV treprostinil in native diluent
- Participants had widely differing degrees of disease severity
- Study selectively recruited participants who demonstrated a history of favorable or unfavorable response to the drug/intervention of interest
Rubin, 2002189
Galie, 2003190
Denton, 2006191
BREATHE /
- Bosentan 62.5 mg BID, then 125 mg BID
- Bosentan 62.5 mg BID, then 250 mg BID
- Placebo
- None
Rubin, 1990192
Barst, 1994193 /
- Intravenous epoprostenol 1–2 ng/kg per minute initially, then increased as tolerated
- Conventional therapy
- Study selectively recruited participants who demonstrated a history of favorable or unfavorable response to the drug/intervention of interest
- Current methods for treatment of the disease have changed since the study took place
Sastry, 2007194 /
- Sildenafil 25-50 mg TID
- Conventional therapy
- None
Simonneau, 2002195
Treprostinil Study /
- Treprostinil 1.25 ng/kg/min, then adjusted
- Placebo
- None
Simonneau, 2008196
PACES /
- Sildenafil 20 mg TID, then up to 80 mg TID
- Placebo
- None
Wilkins, 2005155
SERAPH /
- Bosentan 62.5 mg BID, then 125 mg BID
- Sildenafil 50 mg BID, then 50 mg TID
- None
Zeng, 2011197 /
- Sildenafil
- Conventional therapy
- None
Abbreviations: BID=twice daily; kg=kilogram; mcg=microgram; mg=milligram; ng=nanogram; TID=three times daily
D-1