| Literature DB >> 35076954 |
Aisling Donnelly1, Federico Foschi1,2,3, Paul McCabe4, Henry F Duncan5.
Abstract
BACKGROUND: Consensus on the treatment of choice for complicated crown fractures of teeth is limited. Recent guidance recommends vital-pulp-therapy; however, the preferred type is not specified. Higher success rates for pulpotomy compared to pulp-capping have been documented, which suggests pulpotomy may be a preferable option for complicated crown-fractures.Entities:
Keywords: complicated crown fractures; dental trauma; follow-up; pulp exposure; pulpotomy; vital pulp therapy
Mesh:
Year: 2022 PMID: 35076954 PMCID: PMC9304243 DOI: 10.1111/iej.13690
Source DB: PubMed Journal: Int Endod J ISSN: 0143-2885 Impact factor: 5.165
FIGURE 1The PRISMA flow diagram details the search and selection process applied during our systematic literature search
Reasons for exclusion
| Reason for exclusion | Number of articles | Author(s), year |
|---|---|---|
| Not available in English | 9 | Ortiz |
| Review article | 5 | Gutmann & Heaton |
| Pulp examined histologically only after pulpotomy | 1 | Cvek & Lundberg |
| Single case description | 1 | Patterson |
| Animal study | 1 | Chiang et al., |
| Did not specify if exposure due to caries or trauma | 2 | Ehrmann |
| Did not provide overall clinical and radiographic success | 1 | Abuelniel et al., |
| Not all teeth included in results were examined clinically and radiographically | 1 | de Blanco |
| Results of pulp capping and pulpotomy not separate | 1 | Robertson et al., |
| Specific number of successful cases not given | 1 | Blanco & Cohen |
| Did not satisfy inclusion criteria for clinical success | 5 | Magnusson et al., |
| Did not specify which teeth were included | 1 | Kunert et al., |
| Study did not include clinical follow‐up | 3 | Winter |
| Insufficient cases of traumatized teeth (per inclusion criteria) | 4 | El‐Meligy & Avery |
| Inadequate follow up time of less than 12 months | 3 | Oulis & Berdouses |
| Subsequent follow‐up study with longer follow up time available | 2 | Cvek |
Included study characteristics
| Author | Study design | Location | Follow up | Intervention | Comparator | Outcome | Funding | Level of evidence |
|---|---|---|---|---|---|---|---|---|
| Caprioglio et al., | Retrospective single arm clinical trial | Italy | 3–42 months | Partial pulpotomy | NA | Clinical and radiographic | NA | 2b |
| Cvek | Retrospective single arm clinical trial | Sweden | 3–15 years | Partial pulpotomy | NA | Clinical and radiographic | NA | 2b |
| Fuks et al., | Retrospective double arm clinical trial | Israel | 3–36 months | Complete pulpotomy | Direct pulp cap | Clinical and radiographic | NA | 2b |
| Klein et al., | Retrospective single arm clinical trial | Israel | 3–36 months | Partial pulpotomy | NA | Clinical and radiographic | NA | 2b |
| Fuks et al., | Retrospective single arm clinical trial | Israel | 7.5–11 years | Partial pulpotomy | NA | Clinical and radiographic | NA | 2b |
| Xu | Retrospective single arm clinical trial | USA | 1 year | Partial pulpotomy | NA | Clinical and radiographic | NA | 2b |
| Rao et al., | Retrospective double arm clinical trial | China | 1–5years | Partial pulpotomy with iRroot BP Plus | Pulpotomy with CH | Clinical and radiographic | Supported by grants from the Natural Science Foundation of China | 2b |
Population characteristics
| Author | No. of patients receiving treatment | No. of teeth treated | Gender M:F | Age (years) | Tooth maturity | Pulpotomy material | Restoration | Follow up (months) | Lost to follow up |
|---|---|---|---|---|---|---|---|---|---|
| Caprioglio et al., | 26 | 27 | Unknown | 8.3 | All immature | MTA | Temporary cement (unspecified) and a composite restoration | 35.1 | 0 at 24 months |
| Cvek | 162 | 209 | Unknown | 6–17 | 90 immature 88 mature | CH | ZOE cement and composite later | 36–180 | 31 at 3 years |
| Fuks et al., | 72 | 76 | Unknown | 7–14 | 38 immature 38 mature | CH | ZOE and unspecified restoration usually amalgam | 6–36 | 22 |
| Klein et al., | 33 | 34 | 21:12 | 7–22 | Unknown distribution | CH | Composite or stainless steel basket crowns | 3–36 | 20 at 13 months |
| Xu | 70 | 70 | Unknown | Unknown | Unknown | CH | Unknown | 12 months | 58 |
| Fuks et al., | 62 | 63 | 35:27 | 7–22 | Unknown distribution | CH | ZOE and composite or stainless‐steel metal basket crown | 6–132 | 19 at 7.5 years |
| Rao et al., | 168 | 205 | Group 1 59:18 | Group 1 9 ± 1.1 | Group 1 62 immature & 43 mature | Group 1root BP, Group 2 | Ketac cement and composite or fragment reattachment | 17.5 ± 4.4 | 50 at 1 year |
| Group 2 65:26 | Group 2 9.1 ± 1.3 | Group 2 66 immature & 34 mature | CH |
Age range as mean age not provided.
Total 76 teeth, 38 immature teeth received pulpotomy and 38 mature teeth received direct pulp cap.
17 in mature group pulp capping group and five in immature group pulpotomy group.
Number of cases treated under 12 h as those over 12 h had unspecified time to treatment so were excluded from the results for this review.
Number of cases treated under 12 h that were lost to follow up.
Figures taken from cross reference to earlier study by Fuks et al. (1987).
Total 205 cases split into two groups after 55 excluded due to failure to attend 12‐month review: group 1 pulpotomy completed with Iroot BP Plus and group 2 pulpotomy completed with CH.
Risk of bias assessment using the Newcastle‐Ottawa Scale for Cohort study
| Study | Selection cohort representative (1 | Selection of non‐exposed cohort (1 | Selection exposure ascertained (1 | Selection outcome of interest not present at start (1 | Comparability (2 | Outcome independent (1 | Outcome follow up (1 | Outcome subjects (1 | Stars (out of 9) | Risk of bias |
|---|---|---|---|---|---|---|---|---|---|---|
| `Caprioglio et al., |
| Not described | Surgical records |
| No controls | Not blinded |
| Complete follow up | 5 | Moderate |
| Cvek |
| Not described | Surgical records |
| No controls | Not blinded |
|
| 4 | Moderate |
| Klein et al., |
| Not described | Surgical records |
| No controls | Not blinded |
| Subjects lost no description | 4 | Moderate |
| Fuks et al., |
| Not described | Surgical records |
| No controls | Not blinded |
| Subjects lost no description | 4 | Moderate |
| Xu |
| Not described | Surgical records |
| No controls | Not blinded |
| Subjects lost no description | 4 | Moderate |
| Rao et al., |
| Not described | Surgical records |
| Some controlled factors |
|
| Complete follow up | 7 | Low |
Newcastle‐Ottawa Scale contains 8 items within 3 domains and the total maximum score is 9. A study with score from 7 to 9, has high quality, 4 to 6, high risk, and 0 to 3 very high risk of bias.
The appraisal was based on the 1 or 2 stars assessed within the selection domain, and 2 stars in comparability and outcome domain.
Quality assessment of the non randomized studies according to Robins‐I tool
| Study | Baseline confounding | Selection of participants | Classification of intervention | Deviation from intended intervention | Missing data | Measurement of outcomes | Selection of reported results | Overall risk of bias |
|---|---|---|---|---|---|---|---|---|
| Fuks et al., | High | Moderate | Low | Low | Moderate | High | Low | Moderate |
Oxford centre for evidence‐based medicine‐levels of evidence employed in this study
| Level | Therapy/Prevention, Aetiology/Harm |
|---|---|
| 1a | SR (with homogeneity) of RCTs |
| 1b | Individual RCT (with narrow Confidence Interval) |
| 1c | All or none |
| 2a | SR (with homogeneity) of cohort studies |
| 2b | Individual cohort study (including low quality RCT; e.g. <80% follow‐up) |
| 2c | ‘Outcomes’ Research; Ecological studies |
| 3a | SR (with homogeneity) of case‐control studies |
| 3b | Individual Case‐Control Study |
| 4 | Case‐series (and poor‐quality cohort and case‐control studies) |
| 5 | Expert opinion without explicit critical appraisal, or based on physiology, bench research or ‘first principles’ |
Pulpotomy success rates ≥12 months
| Author | Number receiving intervention | Observation period (months) | Number available at follow‐up | Failures % ( | Calculated % success ( | Mature success % ( | Immature success % ( |
|---|---|---|---|---|---|---|---|
| Caprioglio et al. ( | 27 | 24–42 | 27 | 0 | 85.1 (23) | 0 (0) | 85.1 (23) |
| Cvek ( | 209 | 36 | 178 | 5 (9) | 95 (169) | 93.75 (90) | 96.70 (88) |
| Fuks et al. ( | 38 | 12–36 | 33 | 7.9 (3) | 90.9 (30) | 0 (0) | 90.9 (30) |
| Klein et al. ( | 34 | 13–36 | 14 | 14.29% (2) | 85.7% | Unknown | Unknown |
| Xu ( | 70 | 12 | 12 | 25% (3) | 75% (9) | Unknown | Unknown |
| Fuks et al. (1993) | 63 | 13–50 | 39 | 10.25 (4) | 89.74 (35) | NA | NA |
| Rao et al. ( | 255 | 12–24 | 205 | 4 (8) | 96 (197) | 97.4 (75) | 95.3 (122) |
Combined healed and healing results as criteria for healing falls under successful criteria for this systematic review.
Only cases which were included in specified time to treat time period of <12 h were included.
Data taken from earlier study in series Fuks et al. (1987).
Success rates in studies with further recorded observation periods
| Author | Number receiving intervention | Observation period (months) | Number available at follow up | Failures % ( | Calculated % success ( | Mature success % ( | Immature success % ( |
|---|---|---|---|---|---|---|---|
| Fuks et al. ( | 38 | ≥36 | 15 | 6.6 (1) | 93.3 (14) | 0 (0) | 93.3 (14) |
| Fuks et al. ( | 63 | 90–132 | 40 | 12.5 (5) | 87.5 (35) | NA | NA |
| Cvek ( | 178 | 37–72 | 162 | 0 | 100 (162) | 100 (84) | 100 (78) |
| Cvek ( | 178 | 73–108 | 85 | 0 | 100 (85) | 100 (43) | 100 (42) |
| Cvek ( | 178 | 109–114 | 52 | 0 | 100 (52) | 100 (27) | 100 (25) |
| Cvek ( | 178 | 145–180 | 29 | 0 | 100 (29) | 100 (12) | 100 (17) |
2 patients diagnosed as failure in first 6 months not included.
4 further patients were diagnosed with pulpal necrosis within 6 months of treatment and were not recalled so are not included in data for this study.
6 patients diagnosed as failure in first 36 months not included in data for this study.
Time interval to treatment
| Study | Observation period (months) | Number available at follow up period | Medicament | Success rate: time interval to treatment <24 h % ( | Success rate: time interval to treatment 25–72 h % ( | Success rate: time interval to treatment >72 h % ( | Overall success rate % ( |
|---|---|---|---|---|---|---|---|
| Cvek ( | 36 | 178 | CH | 95.65 (132) | 95.83 (23) | 87.5 (14) | 95 (169) |
| Fuks et al. ( | 12–36 months | 33 | CH | 100 (21) | 50 (3) | 100 (8) | 90.9 (30) |
| Klein et al. ( | 12–36 months | 14 | CH | 77.7 (7) | 100 (5) | ||
| Fuks et al. ( | 90–132 | 40 | CH | 90.9 (30) | 66.6 (4) | 100 (1) | 87.5 (35) |
Time interval 2–6 days.
Time interval >6 days.
Time interval to treatment 25–96 h.
4 patients who had pulp necrosis within 6 months of treatment were not recalled for this recall and of these four patients 2 were treated within 24 h, one was treated between 1 and 4 days and one was treated after 4 days.
Time interval greater than 96 h.