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Table 2 Demographic and clinical characteristics of patients in the follow-up and external validation sets

From: Prediction and prognosis of adverse maternal and foetal/neonatal outcomes in pulmonary hypertension: an observational study and nomogram construction

Variable

Follow-up set (n = 355)

External validation set (n = 221)

Age, median (IQR), year

28.0 (25.0–32.0)

30.0 (27.5–34.0)

follow-up duration, median (IQR), month

64.0 (42.0–83.0)

22.0 (14.5–27.0)

Death or heart failure, No. (%)

 No

266 (74.9)

183 (82.8)

 Yes

89 (25.1)

38 (17.2)

Death, No. (%)

 No

343 (96.6)

217 (98.2)

 Yes

12 (3.4)

4 (1.8)

Heart failure, No. (%)

 No

278 (78.3)

187 (84.6)

 Yes

77 (21.7)

34 (15.4)

Mild preeclampsia, No. (%)

 No

348 (98.0)

210 (95.0)

 Yes

7 (2.0)

11 (5.0)

Severe preeclampsia, No. (%)

 No

308 (86.8)

176 (79.6)

 Yes

47 (13.2)

45 (20.4)

Eclampsia with pregnancy/delivery, No. (%)

 No

318 (89.6)

194 (87.8)

 Yes

37 (10.4)

27 (12.2)

Eclampsia with pre-existing HTN, No. (%)

 No

344 (96.9)

212 (95.9)

 Yes

11 (3.1)

9 (4.1)

Postpartum haemorrhage, No. (%)

 No

341 (96.1)

201 (91.0)

 Yes

14 (3.9)

20 (9.0)

Multiple pregnancies, No. (%)

 No

339 (95.5)

192 (86.9)

 Yes

16 (4.5)

29 (13.1)

Premature rupture of membranes, No. (%)

 No

336 (95.5)

205 (92.8)

 Yes

16 (4.5)

16 (7.2)

Type I respiratory failure, No. (%)

 No

331 (93.2)

207 (93.7)

 Yes

24 (6.8)

14 (6.3)

Type II respiratory failure, No. (%)

 No

353 (99.4)

219 (99.1)

 Yes

2 (0.6)

2 (0.9)

Arrhythmia, No. (%)

 No

220 (62.0)

139 (62.9)

 Yes

135 (38.0)

82 (37.1)

Patent ductus arteriosus, No. (%)

 No

343 (96.6)

209 (94.6)

 Yes

12 (3.4)

12 (5.4)

Ventricular septal defect, No. (%)

 No

285 (80.3)

198 (89.6)

 Yes

70 (19.7)

23 (10.4)

Atrial septal defect, No. (%)

 No

257 (72.4)

182 (82.4)

 Yes

98 (27.6)

39 (17.6)

Pulmonary embolism, No. (%)

 No

347 (97.7)

220 (99.5)

 Yes

8 (2.3)

1 (0.5)

Endocarditis, No. (%)

 No

354 (99.7)

220 (99.5)

 Yes

1 (0.3)

1 (0.5)

Myocardiopathy, No. (%)

 No

340 (95.8)

219 (99.1)

 Yes

15 (4.2)

2 (0.9)

Rheumatic heart disease, No. (%)

 No

326 (91.8)

212 (95.9)

 Yes

29 (8.2)

9 (4.1)

Congenital heart disease, No. (%)

 No

150 (42.3)

134 (60.6)

 Yes

205 (57.7)

87 (39.4)

Eisenmenger syndrome, No. (%)

 No

321 (90.4)

210 (95.0)

 Yes

34 (9.6)

11 (5.0)

Gestational diabetes mellitus, No. (%)

 No

318 (89.6)

194 (87.8)

 Yes

37 (10.4)

27 (12.2)

Infection, No. (%)

 No

313 (88.2)

170 (87.8)

 Yes

42 (11.8)

51 (12.2)

Systemic lupus erythematosus, No. (%)

 No

343 (96.6)

211 (95.5)

 Yes

12 (3.4)

10 (4.5)

Liver insufficiency, No. (%)

 No

349 (98.3)

209 (94.6)

 Yes

6 (1.7)

12 (5.4)

Left to right shunt, No. (%)

 No

344 (96.9)

209 (94.6)

 Yes

11 (3.1)

12 (5.4)

Right-to-left shunt, No. (%)

 No

351 (98.9)

217 (98.2)

 Yes

4 (1.1)

4 (1.8)

Premature delivery, No. (%)

 No

152 (42.8)

87 (39.4)

 Yes

152 (42.8)

107 (48.4)

PH classification, No. (%)

 Group 1

294 (82.8)

191 (86.4)

 Group 2

50 (14.1)

18 (8.1)

 Group 3

2 (0.6)

2 (0.9)

 Group 4

2 (0.6)

0 (0.0)

 Group 5

7 (2.0)

10 (4.5)

Pregnancy outcome, No. (%)

 Termination of pregnancy

51 (14.4)

26 (11.8)

 Vaginal delivery

26 (7.3)

20 (9.0)

 Spinal and/or epidural for C-section

240 (67.6)

164 (74.2)

 General anaesthesia for C-section

38 (10.7)

11 (5.0)

Cardiac surgery, No. (%)

 No

339 (95.5)

204 (92.3)

 Repair of heart defect

16 (4.5)

17 (7.7)

NYHA functional class, No. (%)

 I/II

203 (57.2)

155 (70.1)

 III

91 (25.6)

39 (17.6)

 IV

61 (17.2)

27 (12.2)

NT-proBNP, No. (%), ng/L

 < 1400

268 (75.5)

177 (80.1)

 ≥ 1400

87 (24.5)

44 (19.9)

Gestation times, median (IQR), times

2.0 (1.0–3.0)

2.0 (1.0–3.0)

Parity, median (IQR), times

1.0 (1.0–2.0)

1.0 (1.0–2.0)

Troponin, median (IQR), ng/mL

0.01 (0.00–0.03)

0.01 (0.00–0.15)

Prothrombin time, median (IQR), s

10.1 (9.5–10.8)

10.4 (9.7–11.2)

APTT, median (IQR), s

29.2 (26.8–32.4)

27.9 (26.1–30.7)

Thrombin time, median (IQR), s

13.8 (12.7–15.9)

14.3 (13.1–15.6)

Fibrinogen, median (IQR), g/L

3.7 (3.1–4.3)

3.8 (3.2–4.3)

RBC, median (IQR), × 1012/L

3.9 (3.5–4.3)

3.8 (3.4–4.2)

Haemoglobin, median (IQR), g/L

112.0 (101.0–124.0)

111.5 (100.0–123.0)

Platelet, median (IQR), × 109/L

190.0 (129.8–237.0)

179.0 (137.0–228.0)

D-Dimer, median (IQR), mg/L

0.7 (0.4–1.3)

0.6 (0.3–1.6)

RVD, median (IQR), mm

22.0 (18.0–29.0)

20.0 (18.0–24.0)

LVDs, median (IQR), mm

38.0 (30.0–46.0)

40.0 (33.0–46.0)

mPAD, median (IQR), mm

23.0 (21.0–27.0)

23.0 (21.0–26.0)

AOD, median (IQR), mm

22.0 (20.0–26.0)

25.0 (20.0–25.0)

EF, median (IQR), %

63.0 (60.0–65.0)

63.0 (60.0–66.0)

PASP, median (IQR), mm Hg

53.0 (43.0–79.0)

44.0 (37.0–65.0)

  1. Two-tailed P values < 0.05 were considered statistically significant
  2. APTT activated partial thromboplastin time, AOD aortic diameter, C-section Caesarean section, EF ejection fractions, HR hazard ratio, HTN hypertension, IQR interquartile ratio, LVDs left ventricular systolic diameter, mPAD mean pulmonary artery diameter, NYHA New York Heart Association, NT-proBNP N-terminal pro-brain natriuretic peptide, PASP pulmonary artery systolic pressure, PH pulmonary hypertension, RBC red blood cells, RVD right ventricular diameter