| Literature DB >> 32290818 |
Alireza Bagherzadeh Karimi1, Asghar Elmi2, Mojgan Mirghafourvand1,3, Roghaiyeh Baghervand Navid1.
Abstract
BACKGROUND: The rate of cesarean section is increasing in all over the world with different drafts in various countries. This growth increases unpleasant outcomes of delivery. Recent studies explained the benefits of date palm fruit on labor process improvement. Date fruit can be considered as a factor for increasing vaginal delivery and also reducing the frequency of caesarean section in order to prevent its great complications. This systematic review has been designed to review clinical studies that investigate the effects of date palm fruit on labor outcomes (duration of labor stages, bishop score, and frequency of cesarean section) compared with routine cares.Entities:
Keywords: Date fruit; Date palm; Delivery; Labor; Meta-analysis; Phoenix dactiylifera; Systematic review
Mesh:
Year: 2020 PMID: 32290818 PMCID: PMC7157989 DOI: 10.1186/s12884-020-02915-x
Source DB: PubMed Journal: BMC Pregnancy Childbirth ISSN: 1471-2393 Impact factor: 3.007
Fig. 1Flowchart of selection strategy and method (PRISMA statement)
Characteristics of included studies (PICOS)
| Number | Author/ | Study design | Participants and | Intervention | Control | Duration of intervention | Outcomes | Results |
|---|---|---|---|---|---|---|---|---|
| 1 | Ahmed et al., 2018 [ | Randomized, controlled, clinical trial | 57 pregnant women 26 intervention group 31 control group | 7 date’s fruits on the permission | Routine cares | Once | (1–3) Duration of first, second and third stage of labor | 1. ↓ Duration of the first and the third stage of labor in intervention groups significantly compared with control group 2. ↑ Duration of the second stage of labor in intervention groups but not significantly compare with control group |
| 2 | Razali et al.,2017 [ | Randomized controlled clinical trial | 154 nulliparous singleton pregnant women 77 intervention group 77 control group | 7 date’s fruits (approximately 80 g) | Routine cares | 1–4 weeks | (1–3) Duration of first, second and third stage of labor (4) Frequency of caesarian section | 1. ↓ Duration of the first and the third stage of labor in intervention groups but not significantly compare with control group 2. ↑ Duration of the second stage of labor in intervention groups but not significantly compare with control group 3. No significant difference between two groups in mode of delivery |
| 3 | Kariman and Jadidi et al., 2015 [ | Randomized, controlled, clinical trial | 110 nuliparous pregnant women 55 intervention group 55 control group | 7 date’s fruit per day | Routine cares | From week 38 of pregnancy to onset of delivery signs | (1) Duration of active phase of labor (2) Bishop score (3) Frequency of caesarian section | 1. Significant ↓ of active phase of labor in intervention group compared with control group 2. Significant ↓in bishop score after intervention compared with control group 3. No significant differences in mode of delivery between two group 4. ↑ Bishop score significantly after intervention compared with control group 5. ↑ Cervical dilatation significantly after intervention compared with control group 6. ↑ Cervical effacement significantly after intervention compared with control group 7. ↑ Spontaneous labor significantly after intervention compared with control group |
| 4 | Kordi et al.,2013,2014, 2017 [ | Quasi-randomized, controlled, clinical trial | 210 pregnant women with gestational age of 37–38 weeks 105 intervention group 105 control group | 70–75 g date’s fruit per day | Routine cares | 1–3 weeks | (1) Bishop score (2) Frequency of caesarian section (3–5) Duration of first, second and third stage of labor | 1. Significant ↑ of the mean Bishop Score in intervention group compared with control group 2. No significant difference between two groups in mode of delivery (↓ frequency of cesarean section in intervention group) 1. The average length of the second phase and the third phase in the intervention group was significantly lower than the control group 2. Spontaneous start of labor in the intervention group was significantly more than the control group 3. No significant difference between average length of active phase of labor in the two 4. ↑Cervical dilatation in intervention group compared with control group (significant) 5. ↓Length of pregnancy in intervention group compared with control group (significant) |
| 5 | Kordi et al.,2010 [ | Randomized double blinded controlled clinical trial | 60 nuliparous pregnant women with gestational age of 37–42 weeks 30 intervention group 30 control group | 132 g date’s honey syrup from 4 cm cervix dilatation to labor | Routine cares | Maximum 1 day | (1) Duration of active phase of labor (2) Duration of second stage of labor | Significant ↓in duration of active and second phases of labor |
Risk of bias within studies
| Bias | Authors judgment | Support for judgment |
|---|---|---|
| Random sequence generation | Low risk | Simple random sampling has been used |
| Allocation concealment | Unclear risk | No specific information |
| Blinding of participants and personnel | High risk | Open label manner |
| Blinding of outcome assessors | High risk | Open label manner |
| Incomplete outcome data | High risk | Intention to treat analysis has not conducted. |
| Selective reporting | Low risk | Protocol is unavailable but the authors have reported their expected mentioned outcomes |
| Other | High risk | No registered protocol, sample size calculating method is not specified |
| Random sequence generation | Low risk | Sealed envelope numbers has been used |
| Allocation concealment | Low risk | It was done using “sealed envelope” manner |
| Blinding of participants and personnel | High risk | Open label manner |
| Blinding of outcome assessors | High risk | Open label manner |
| Incomplete outcome data | Low risk | The dropped out has been mentioned and intention to treat has been analyzed |
| Selective reporting | Low risk | Protocol is unavailable but the both primary and secondary outcomes have been reported |
| Other | Low risk | Registered protocol exist, sample size calculating method is specified, Ethical approval exist, Specified inclusion and exclusion criteria, specified funding source, no conflict of interest |
| Random sequence generation | Low risk | Random number generator has been used |
| Allocation concealment | Unclear risk | No specific information |
| Blinding of participants and personnel | High risk | Open label manner |
| Blinding of outcome assessors | High risk | Open label manner |
| Incomplete outcome data | Low risk | The dropped out has been mentioned and intention to treat has been analyzed |
| Selective reporting | High risk | Protocol is available but secondary outcomes have not been reported |
| Other | Low risk | Registered protocol exist, sample size calculating method is specified, Ethical approval exist, Specified inclusion and exclusion criteria, specified funding source, no conflict of interest |
| Random sequence generation | High risk | The days of the Week have been used for randomization |
| Allocation concealment | Unclear risk | No specific information |
| Blinding of participants and personnel | High risk | Open label manner |
| Blinding of outcome assessors | High risk | Open label manner |
| Incomplete outcome data | Low risk | The dropped out has been mentioned and intention to treat has been analyzed |
| Selective reporting | Low risk | Protocol is available and both primary and secondary outcomes have been reported |
| Other | Low risk | Registered protocol exist, sample size calculating method is specified, Ethical approval exist, Specified inclusion and exclusion criteria, specified funding source, no conflict of interest |
| Random sequence generation | Low risk | Simple random sampling has been used |
| Allocation concealment | High risk | There was no evidence for allocation concealment |
| Blinding of participants and personnel | High risk | Open label manner |
| Blinding of outcome assessors | High risk | Open label manner |
| Incomplete outcome data | Low risk | There was no lost to follow up |
| Selective reporting | Low risk | Protocol is unavailable but both primary and secondary outcomes have been reported |
| Other | High risk | Conflict of interest didn’t declared, no specified inclusion and exclusion criteria |
The summary of sensitivity analyses
| Number | Measured outcome | Meta-analyses of all studies | Sensitivity Analysesa |
|---|---|---|---|
| 1 | Second stage of labor | P = 0.44 | P = 0.64 |
| 2 | Third stage of labor | P = 0.82 | P = 0.39 |
| 3 | Active phase of labor | ||
| 4 | Bishop score | ||
| 5 | Frequency of cesarean section | P = 0.23 | P = 0.59 |
aquasi-randomized study (Kordi 2013, 2014, 2017) [33–35] removed from meta-analysis
bthe significant values are shown with bold font
Fig. 4Forest plot of the duration of active phase of labor
Fig. 5Forest plot of the duration of first stage of labor
Fig. 6Forest plot of the duration of second stage of labor
Fig. 7Forest plot of the duration of third stage of labor
Fig. 8Forest plot of the bishop score
Fig. 9Forest plot of the caesarian section frequency