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. 2022 Aug;37(8):1101–1111. doi: 10.1177/08850666221086521

Table 4.

Response to IPVD Therapy in Survivors Versus non-Survivors.

Survivors (n = 33) Non-survivors (n = 26) p-value
Days from admission to IPVD 6 (2-9) 6 (3-9) 0.742
PF ratio at commencing therapy (kPa) 11.39 (9.90-12.92) 11.28 (9.74-12.71) 1.000
Therapy received (n (%))
Iloprost 8 (24.2%) 3 (11.5%) 0.405
NO 4 (12.1%) 5 (19.2%)
NO and Iloprost 21 (63.6%) 18 (69.2%)
NIV or MV at initiation of IPVD (n (%))
NIV 5 (15.2%) 3 (11.5%) 1.000
MV 28 (84.8%) 23 (88.5%)
Percentage change PaO2/FiO2 (%)
+2 hours 14.2 (-5.4-40.6) -2.3 (-17.3-20.5) 0.022*
+6 hours 20.0 (3.0-54.4) 9.6 (-2.9-25.2) 0.106
+12 hours 31.6 (-0.4-80.4) 18.1 (-7.2-46.7) 0.174
+24 hours 34.0 (3.3-60.4) 17.6 (-7.1-44.7) 0.045*
+48 hours 59.5 (9.7-108.1) 6.5 (12.4-27.4) <0.001*
+72 hours 70.8 (35.2-95.5) -4.1 (-19.9-21.3) <0.001*
A-a gradient at commencing therapy (kPa) 54.3 (48.6-67.0) 58.9 (50.0-70.3) 0.376
Percentage reduction A-a gradient (kPa) (%)
 + 2 hours 4.9 (-7.8-15.5) 1.8 (-7.8-7.0) 0.418
 + 6 hours 19.7 (1.8-35.2) 7.3 (-2.9-23.6) 0.109
 + 12 hours 26.4 (3.3-40.9) 21.1 (2.4-32.7) 0.246
 + 24 hours 23.8 (2.5-48.7) 21.3 (4.4-29.3) 0.200
 + 48 hours 38.4 (16.1-62.6) 11.7 (-5.3-25.8) <0.001*
 + 72 hours 44.7 (28.4-58.0) 14.8 (-7.6-31.1) <0.001*