| Literature DB >> 35903438 |
Xuehong Chen1, Xiaoxiao Qiu2, Yaojuan Jin1.
Abstract
Objective: To explore the effect of dydrogesterone tablets combined with Zishen Yutai pills on threatened abortion in early pregnancy and pregnancy outcomes.Entities:
Mesh:
Substances:
Year: 2022 PMID: 35903438 PMCID: PMC9325344 DOI: 10.1155/2022/4593637
Source DB: PubMed Journal: Comput Math Methods Med ISSN: 1748-670X Impact factor: 2.809
Comparison of general data.
| Factors | Observation group | Control group |
|
|
|---|---|---|---|---|
| Age (years) | 27.19 ± 2.16 | 27.23 ± 2.59 | 0.078 | 0.938 |
| BMI (kg/m2) | 0.004 | 0.948 | ||
| ≤23 | 30 (57.69) | 28 (58.33) | ||
| >23 | 22 (42.31) | 20 (41.67) | ||
| Gestation (days) | 6.99 ± 0.47 | 7.1 ± 0.45 | 1.193 | 0.236 |
| Gravida | 0.051 | 0.822 | ||
| ≤1 | 40 (76.92) | 36 (75.00) | ||
| >2 | 12 (23.08) | 12 (25.00) | ||
| Vaginal bleeding time (d) | 0.043 | 0.835 | ||
| ≤3 | 26 (50.00) | 25 (52.08) | ||
| >3 | 26 (50.00) | 23 (47.92) | ||
| Times of abortion | 0.004 | 0.951 | ||
| ≤1 | 42 (80.77) | 39 (81.25) | ||
| >2 | 10 (19.23) | 9 (18.75) |
Comparison of therapeutic effect between two groups of patients.
| Therapeutic effect | Observation group | Control group |
|
|
|---|---|---|---|---|
| Cured | 35 (67.31) | 21 (43.75) | — | — |
| Markedly effective | 10 (19.23) | 12 (25.00) | — | — |
| Effective | 5 (9.62) | 10 (20.83) | — | — |
| Ineffective | 2 (3.85) | 5 (10.42) | — | — |
| Treatment effective rate | 45 (86.54) | 33 (68.75) | 4.603 | 0.032 |
Figure 1Comparison of changes of whole blood high shear viscosity, HCT, and FIB levels before and after treatment between two groups. (a) Comparison of whole blood high shear viscosity of two groups. (b) Comparison of HCT of two groups. (c) Comparison of FIB in two groups. ∗ indicates P < 0.05.
Figure 2Comparison of RI and PI before and after treatment between two groups. (a) RI comparison of two groups. (b) PI comparison of two groups. ∗ means P < 0.05 when the two groups are compared.
Comparison of pain relief time and hemostasis time between two groups of patients.
| Items | Observation group | Control group |
|
|
|---|---|---|---|---|
| Abdominal pain relief time (d) | 4.11 ± 0.26 | 6.56 ± 0.45 | 33.65 | <0.001 |
| Hemostasis time (d) | 4.22 ± 0.22 | 5.4 ± 0.33 | 21.19 | <0.001 |
Figure 3Comparison of progesterone levels between two groups before and after treatment. (a) P comparison in two groups. (b) E2 comparison in two groups. (c) hCG comparison of two groups of patients. ∗ indicates P < 0.05.
Comparison of pregnancy outcomes between two groups.
| Items | Observation group | Control group |
|
|
|---|---|---|---|---|
| Preterm birth rate | 5 (9.62) | 12 (25.00) | 4.187 | 0.041 |
| Miscarriage rate | 2 (3.85) | 8 (16.67) | 4.558 | 0.033 |
| Full-term pregnancy rate | 45 (86.54) | 28 (58.33) | 10.07 | 0.002 |
Comparison of neonatal outcomes between two groups of patients (n (%)).
| Adverse reactions | Observation group | Control group |
|
|
|---|---|---|---|---|
| Fetal macrosomia | 2 (3.85) | 3 (6.25) | — | — |
| Deformity | 1 (1.92) | 4 (8.33) | — | — |
| Respiratory distress | 0 | 4 (8.33) | — | — |
| Term infants with low birth weight | 1 (1.92) | 4 (8.33) | — | — |
| Incidence of adverse outcomes | 4 (7.69) | 15 (31.25) | 9.001 | <0.001 |
Comparison of adverse reaction rates between two groups (n (%)).
| Adverse reactions | Observation group | Control group |
|
|
|---|---|---|---|---|
| Itching | 1 (1.92) | 2 (4.17) | — | — |
| Erythema | 1 (1.92) | 3 (6.25) | — | — |
| Temporary vaginal bleeding | 0 | 3 (6.25) | — | — |
| Incidence of adverse reactions | 2 (3.85) | 8 (16.67) | 4.558 | 0.033 |