| Literature DB >> 35419233 |
Mohammad Karam1,2, Ahmad Abul2, Abdulwahab Althuwaini2, Abdulredha Almuhanna2, Talal Alenezi2, Ali Aljadi2, Abdulrahman Al-Naseem3, Abdulmalik Alsaif4,2, Athari Alwael5.
Abstract
This study aimed to compare the outcomes of coblation versus bipolar diathermy in pediatric patients undergoing tonsillectomy. A systematic review and meta-analysis were performed per the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) Guidelines. An electronic search of information was conducted to identify all Randomized Controlled Trials (RCTs) comparing the outcomes of coblation versus bipolar in pediatric patients undergoing tonsillectomy. Primary outcome measures were intraoperative bleeding, reactionary hemorrhage, delayed hemorrhage, and post-operative pain. Secondary outcome measures included a return to a normal diet, effects on the tonsillar bed, operation time, and administration of analgesia. Fixed and random-effects models were used for the analysis. Seven studies enrolling 1328 patients were identified. There was a significant difference between coblation and bipolar groups in terms of delayed hemorrhage (Odds Ratio [OR] = 0.27, P = 0.005) and post-operative pain (standardized mean difference [MD] = -2.13, P = 0.0007). Intraoperative bleeding (MD = -43.26, P = 0.11) and reactionary hemorrhage did not show any significant difference. The coblation group improved analgesia administration, diet and tonsillar tissue recovery, and thermal damage for secondary outcomes. No significant difference was reported in terms of operation time. In conclusion, coblation is comparable to a bipolar technique for pediatric patients undergoing tonsillectomy. It improves postoperative pain and delayed hemorrhage and does not worsen intraoperative bleeding and reactionary hemorrhage.Entities:
Keywords: bipolar diathermy; coblation; hemorrhage; post-operative pain; tonsillectomy
Year: 2022 PMID: 35419233 PMCID: PMC8995054 DOI: 10.7759/cureus.23066
Source DB: PubMed Journal: Cureus ISSN: 2168-8184
Figure 1Prisma Flow Diagram. The PRISMA diagram details the search and selection processes applied during the overview.
PRISMA: Preferred Reporting Items for Systematic Reviews and Meta-Analyses
Baseline Characteristics of the Included Studies.
NR: not reported. † NR: Not Reported ‡ RCT: Randomized Control Trial
| Study (Year) | Country, Journal | Study Design | Sex (Male:Female) | Mean Age ± SD (Range) | Total Study Sample (Control:Intervention) | Interventions Compared |
| Temple et al. (2001) [ | International Journal of Paediatric otorhinolaryngology, UK | RCT‡ | 19:19 | 5.6 years | 38 (18:20) | Standard bipolar versus coblation tonsillectomy |
| Mitic et al. (2007) [ | Clinical Otolaryngology, Norway | RCT | NR† | NR (4-12 years) | 40 (20:20) | Coblator or steel dissecting instruments versus bipolar diathermy |
| Parker et al. (2009) [ | Clinical Otolaryngology, UK | RCT | 35:44 | 8.2 years (4-15 years) | 70 (35:35) | Cold steel dissection with bipolar hemeostasis versus coblator dissection |
| Roje et al. (2009) [ | Collegium antropologicum, Croatia | RCT | 41:31 | 6 years (3-16 years) | 72 (36:36) | Conventional cold steel tonsillectomy with bipolar diathermy coagulation versus coblator |
| Konsulov et al. (2017) [ | International Journal of Otorhinolaryngology, Bulgaria | Prospective Comparative Study | NR | NR (3-18 years) Coblation: 8.16 ± 4.74 Bipolar: 6.87 ± 3.01 | 60 (30:30) | Coblator II system ArthroCare (Smith and Nephew) Evac 70 wand for extracapsular dissection vs. extracapsular blunt dissection with bipolar diathermy |
| Belloso et al. (2010) [ | The Laryngoscope, UK | Cohort | NR | Coblation: 7.76 ± 3.56 years Bipolar: 7.60 ± 3.44 years | 1008 (526:482) | Coblation or blunt dissection versus bipolar diathermy hemostasis |
| Bhardwaj et al. (2018) [ | Indian Journal of Otolaryngology and Head & Neck Surgery, India | RCT | NR | NR (4-14 years) | 100 (50:50) | Coblation Assissted verus Bipolar Diathermy |
Figure 2Forest Plot of Coblation versus Bipolar Tonsillectomy – Intraoperative Bleeding.
Quantitative analysis showing the mean difference in the intraoperative bleeding reported as median by Roje et al. (2009) [16] and Konsulov et al. (2017) [18].
Figure 3Forest Plot of Coblation versus Bipolar – Delayed Haemorrhage.
Quantitative analysis showing the odds ratio in delayed haemorrhage reported by Parker et al. (2009) [15], Roje et al. (2009) [16], Belloso et al. (2010) [17] and Konsulov et al. (2017) [18].
Figure 4Forest Plot of Coblation versus Bipolar – Post-operative Pain by Day 7.
Quantitative analysis showing the odd ratio in delayed haemorrhage reported by Mitic et al. (2007) [14], Konsulov et al. (2017) [18], and Bhardwaj et al. (2019) [19].
Bias analysis of the Randomized Trials using the Cochrane Collaboration’s Tool
| First Author | Bias | Authors’ Judgement | Support for Judgement |
| Temple et al. (2001) [ | Random sequence generation (selection bias) | Unclear Risk | No information given |
| Allocation concealment (selection bias) | Low Risk | Closed opaque envelope technique | |
| Blinding of participants and personnel (performance bias) | High Risk | Single surgeon – not blinded. | |
| Blinding of outcome assessment (detection bias) | Low Risk | Outcome measurement is not likely to be influenced by lack of blinding | |
| Incomplete outcome data (attrition bias) | High Risk | Standard deviation for pain is not reported | |
| Selective reporting (reporting bias) | Unclear Risk | No information given | |
| Other bias | Low Risk | Similar baseline characteristics in both groups. | |
| Mitic et al. (2007) [ | Random sequence generation (selection bias) | Low Risk | A randomised sequence was generated by a statistician of the two interventions. |
| Allocation concealment (selection bias) | Low Risk | Allocation of treatment was envelope sealed by a statistician and was then opened in the surgery room in sequential order by a nurse. | |
| Blinding of participants and personnel (performance bias) | High Risk | Surgeons were not blinded | |
| Blinding of outcome assessment (detection bias) | Low Risk | Outcome assessment was done by parents and nurses whom all were blinded for the operation method. The data from parents and nurses were compared and no difference was identified. | |
| Incomplete outcome data (attrition bias) | Low Risk | All questionnaires were complete. | |
| Selective reporting (reporting bias) | High Risk | Return to normal diet mentioned in abstract was not reported. | |
| Other bias | Low Risk | Similar baseline characteristics in both groups. | |
| Parker et al. (2009) [ | Random sequence generation (selection bias) | Low Risk | Random sequence generated by envelope |
| Allocation concealment (selection bias) | Low Risk | Sealed opaque envelope technique | |
| Blinding of participants and personnel (performance bias) | High risk | Single surgeon. | |
| Blinding of outcome assessment (detection bias) | Low Risk | Double blinded study. The children, the parents and the nursing staff doing the pain assessments and prescribing the analgesia were not informed which technique had been used. The surgeon took no part in the pain assessments. | |
| Incomplete outcome data (attrition bias) | Low Risk | Missing outcome data balanced in numbers across intervention groups, with similar reasons for missing data across groups | |
| Selective reporting (reporting bias) | Low Risk | All outcome data reported | |
| Other bias | Low Risk | Similar baseline characteristics in both groups. | |
| Roje et al. (2009) [ | Random sequence generation (selection bias) | Low Risk | Computer-generated randomisation was used for selection of children and separating them into groups from a large ENT database. |
| Allocation concealment (selection bias) | Unclear Risk | No information given | |
| Blinding of participants and personnel (performance bias) | High Risk | Single blinded (parents). Single surgeon not blinded | |
| Blinding of outcome assessment (detection bias) | Unclear Risk | Parents assessing secondary outcomes did not know which procedure was used. | |
| Incomplete outcome data (attrition bias) | High Risk | Participants lost to follow up (15 total- 7 coblation and 8 bipolar group) | |
| Selective reporting (reporting bias) | Unclear Risk | Insufficient information. | |
| Other bias | Low Risk | Similar baseline characteristics in both groups. | |
| Bhardwaj et al. (2018) [ | Random sequence generation (selection bias) | Unclear Risk | Did not explain the method of obtaining the random numbers |
| Allocation concealment (selection bias) | Unclear Risk | Random numbers but not explicitly concealed | |
| Blinding of participants and personnel (performance bias) | Unclear Risk | Insufficient information | |
| Blinding of outcome assessment (detection bias) | Unclear Risk | Insufficient information | |
| Incomplete outcome data (attrition bias) | Low Risk | No missing information | |
| Selective reporting (reporting bias) | Low Risk | No published protocol but all the expected and pre-specified outcomes are reported | |
| Other bias | Low Risk | No significant demographic difference between the 2 groups. |
Newcastle-Ottawa Scale to Assess the Quality of Non-randomised Studies.
*: stars to indicate points scored
| Study | Selection | Comparability | Exposure |
| Belloso et al. (2010) [ | **** | * | *** |
| Konsulov et al. (2017) [ | **** | * | ** |