| Literature DB >> 36147052 |
Lamiae Hallab1, Asma Azzouzi1, Bassima Chami1.
Abstract
Objective: The objective of this systematic review was to evaluate the impact of mandibular wisdom tooth extraction on a patient's quality of life "QoL".Entities:
Keywords: Extraction; Mandibular wisdom tooth; Quality of life; Systematic review
Year: 2022 PMID: 36147052 PMCID: PMC9486647 DOI: 10.1016/j.amsu.2022.104387
Source DB: PubMed Journal: Ann Med Surg (Lond) ISSN: 2049-0801
Revised Cochrane risk-of-bias tool for randomized trials (RoB 2) [51].
| Study | Risk of Bias Domains | |||||
|---|---|---|---|---|---|---|
| D1 | D2 | D3 | D4 | D5 | Overall | |
Risk of bias for included studies: NIH Quality Assessment Tool for Observational Cohort studies [52].
| NIH Quality Assessment Tool | References of the articles | |||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2 | 3 | 4 | 6 | 7 | 17 | 21 | 23 | 24 | 25 | 26 | 28 | 29 | 30 | 31 | 34 | 35 | 36 | 37 | 39 | 40 | 41 | 42 | 43 | 44 | 45 | 46 | 47 | 48 | 49 | |
| 1 Was the research question or objective in this paper clearly stated? | ||||||||||||||||||||||||||||||
| 2 Was the study population clearly specified and defined? | ||||||||||||||||||||||||||||||
| 3 Was the participation rate of eligible persons at least 50%? | ||||||||||||||||||||||||||||||
| 4 Were all the subjects selected or recruited from the same or similar populations (including the same time period)? Were inclusion and exclusion criteria for being in the study prespecified and applied uniformly to all participants? | ||||||||||||||||||||||||||||||
| 5 Was a sample size justification, power description, or variance and effect estimates Provided? | ||||||||||||||||||||||||||||||
| 6 For the analyses in this paper, were the exposure(s) of interest measured prior to the outcome(s) being measured? | ||||||||||||||||||||||||||||||
| 7 Was the timeframe sufficient so that one could reasonably expect to see an association between exposure and outcome if it existed? | ||||||||||||||||||||||||||||||
| 8 For exposures that can vary in amount or level, did the study examine different levels of the exposure as related to the outcome (e.g., categories of exposure, or exposure measured as continuous variable)? | ||||||||||||||||||||||||||||||
| 9 Were the exposure measures (independent variables) clearly defined, valid, reliable, and implemented consistently across all study participants? | ||||||||||||||||||||||||||||||
| 10 Was the exposure(s) assessed more than once over time? | ||||||||||||||||||||||||||||||
| 11 Were the outcome measures (dependent variables) clearly defined, valid, reliable, and implemented consistently across all study participants? | ||||||||||||||||||||||||||||||
| 12 Were the outcome assessors blinded to the exposure status of participants? | ||||||||||||||||||||||||||||||
| 13 Was loss to follow-up after baseline 20% or less? | ||||||||||||||||||||||||||||||
| 14 Were key potential confounding variables measured and adjusted statistically for their impact on the relationship between exposure(s) and outcome(s)? | ||||||||||||||||||||||||||||||
Systematic search strategy for study selection.
| What is the effect of surgical removal of mandibular third molar on quality on life in the postoperative days | |
| Population | Patients who underwent surgical extraction of mandibular wisdom teeth |
| Intervention | #1 (Third mandibular molar extraction) OR (Third mandibular molar removal) OR (Wisdom Tooth removal) OR (Wisdom Tooth extraction) |
| Comparison | #2 Assessment Quality Of Life |
| Outcome | Surgical removal of wisdom teeth has a negative impact on the physical, psychological and social well-being of the patients which is evaluated by a questionnaire |
| (#1 AND #2) | |
| MEDLINE and ScienceDirect, Cochrane, Ebsco, Scopus and Google Scholar | |
Flow diagram showing the process of inclusion of the studies.
Characteristics of the included studies.
| Authors | Years | Types of studies | Evaluation criteria | The population | Duration of the observation | Questionnaires | The results |
|---|---|---|---|---|---|---|---|
| 2021 | Prospective randomized study | Clinics | 50 patients | 1, 3, and 7 days | OHQoL-UK | Postoperative application of PRF “platelet-rich fibrin” at the extraction site of the impacted lower wisdom tooth has a positive impact on oral health related quality of life. In relation to the effect of PRP « platelet-rich plasma” according to this study there was no significant difference with PRF. | |
| aged between 18 and 55 years | |||||||
| 2021 | Randomized, Double-Blind, Placebo-Controlled Clinical Trial | Clinics | 60 patients | 1–7 days | UK-OHRQoL | Preemptive oral etoricoxib | |
| aged between 18 and 48 years | (60 mg 30 min before intervention) represent an effective therapeutic approach to improving quality of life following surgical extraction of a lower third molar. | ||||||
| 2021 | Prospective study | Clinics | 78 patients | 1, 3, 5, 7 and 14 days | UK-OHRQoL | Quality of life was better in the group of patients who received IM co-administration of 8 mg Dexamethasone and 75 mg Diclofenac.Compared to those who just put ice packs extra-orally | |
| aged between 20 and 49 years | |||||||
| 2021 | Prospective study | Clinics | 100 patients | 1–7 days | UW-QoL v4 | Kinesio Taping has a considerable impact on the quality of life after the extraction of an impacted third molar. | |
| aged between 18 and 59 years | |||||||
| 2021 | Double-blind, split-mouth, randomised controlled trial | Clinics | 52 patients | 1, 3, 7 days and 1 months | OHIP-14 | No significant difference of methylprednisolone or placebo in postoperative sequelae and quality of life after third molar mandibular removal | |
| aged between 18 and 39 years | |||||||
| 2021 | Prospective randomized controlled trial | Clinics | 87 patients | 1–7 days | OHIP-14 | The insertion of an iodine pad into the postoperative socket decreased pain and impact on oral health-related quality of life in the first postoperative week. | |
| Average age 26.47 years | |||||||
| 2021 | Descriptive cross-sectional study | Clinics | 246 patients | 3 months | OHIP-14 | Quality of life after removal of mandibular third molar in asymptomatic patient was better compared to those who were symptomatic. | |
| Aged between 15 and 58 years | |||||||
| 2020 | Randomized, controlled clinical trial | Clinics | 82 patients | 2, 7 days | OHIP-14 | The combination of Kinesio taping with injection of corticosteroides in preoperatively or prescription of anti-inflammatory in postoperative provide results in terms of trismus, | |
| Aged between 18 and 65 years | edema, and QoL after third molar extraction. | ||||||
| 2020 | Randomized, controlled, double-blinded trial | Clinics | 130 patients | 2, 7 days | OHIP-14 | Submucosal administration of dexamethasone has a positive impact on oral health related quality of life and postoperative swelling, pain and trismus after third | |
| Aged between 16 and 40 years | OHRQoL | molar surgery. | |||||
| 2019 | Prospective, crossover, randomized controlled study | Clinics | 54 patients | 1–7 days | OHRQoL | The administration of an iodine-containing tampon in the socket after the extraction of impacted mandibular third molars has a positive impact on the oral health related quality of life. | |
| Average age 25.1 years | |||||||
| 2018 | Observational study | Clinics | 30 patients | 1–7 days | EQ-5D-3L QOL | The use of a home facial cooling system “The Hilotherm” provides an improvement in the quality of life after extraction of the impacted mandibular wisdom tooth. | |
| Aged between 18 and 25 years | |||||||
| 2017 | Observational study | Clinics | 124 patients aged between 18 and 51 years | 1–7 days | OHIP-14 | The patients' quality of life was impaired on days 1 and 3 after extraction of the impacted mandibular wisdom tooth, but was significantly improved on day 7 postoperatively. | |
| 2017 | Retrospective study based on a graph | Clinics | 62 patients aged between 18 and 40 years | 1–5 days | OHIP-14 | The preoperative prescription of the antibiotic combination Amoxicillin/Clavulanic acid would have the same effect on the quality of life when using amoxicillin alone. | |
| 2017 | Randomized controlled trial | Clinics | 280 patients | 1–7 days | OHIP-14 | Irrigation of the surgical site with tap water using a curved syringe after extraction of the impacted mandibular wisdom tooth is effective in reducing the risk of inflammatory complications. | |
| aged under than 26 years old | |||||||
| 2017 | Observational study | Clinics | 135 patients | 1–7 days | UK-OHRQoL | A pre- and postoperative prescription of amoxicillin 875 mg combined with clavulanic acid 625 mg provides an improvement in quality of life after extraction of the impacted mandibular wisdom tooth. This is in contrast to antibiotic prophylaxis with amoxicillin 875 mg and clavulanic acid 125 mg. | |
| aged between 18 et 35 years | |||||||
| 2017 | Observational study | Clinics | 40 patients | 1–7 days | EQ5D3L | The generic EQ3D3L instrument appears to be less used because it does not include the objective measures of pain and swelling contrary to OHIP-14. | |
| aged between 18 and 61 years | OHIP-14 | ||||||
| 2016 | Prospective study | Clinics | 168 patients | 1–7 days | OHIP-14 | Intravenous injection of Prednisolone preoperatively improves quality of life after extraction of the impacted mandibular wisdom tooth compared to oral taken of the same drug. | |
| aged between 21 and 31ans | |||||||
| 2016 | Prospective study | Clinics | 135 patients aged between 18 and 25ans | 1–7 days | UK-OHRQoL | There is a deterioration of the quality of life especially during the first postoperative days. | |
| 2016 | Prospective randomized clinical trial | Clinics | 139 patients | 1–7 days | OHIP-14 | Patients who used the Ice Pack at the operative site expressed a better quality of life after extraction of the impacted mandibular wisdom tooth than those who did not. | |
| Aged between 18 and 49ans | |||||||
| 2016 | Prospective randomized controlled trial | Clinics | 30 patients aged between 17 and 30ans | 1–7 days | OHIP-14 | The quality of life after removal of the suture from the surgical site after the 3rd or 7th postoperative day was the same, under the condition of avoiding any risk of contamination by unsatisfactory oral hygiene. | |
| 2016 | Prospective study | Clinics | 106 patients Older than 15 years | 1–7 days | HRQOL-sp | The quality of life after extraction of the impacted mandibular wisdom tooth was interfered especially in the first days after the operation. But several factors contributed to a good improvement: | |
| Postoperative prescriptions, rest, etc. | |||||||
| 2015 | Prospective study | Clinics | 10 patients | 1–14 days | HRQOL | The technique (Neuronal feedback(NF)) allows to minimize the injury of the inferior alveolar nerve in case of contact of the impacted lower wisdom tooth. It has also been shown that a long time of surgery leads to postoperative complications and an altered quality of life. | |
| 2014 | Observational study | Clinics | 108 patients | 1–30 days | OHIP-14 | Postoperative oral instructions can significantly improve the quality of life after extraction of the impacted mandibular wisdom tooth. | |
| average age of 32 years | |||||||
| 2014 | Prospective study | Clinics | 40 patients | 1–7 days | OHIP-14-CRO | Laser (antimicrobial photodynamic treatment “aPDT”) allows better healing of the operative wound, a diminution of pain, swelling, and temperature especially in the 5th day after the extraction of the impacted mandibular wisdom tooth. | |
| Aged between 19 and 32ans | |||||||
| 2014 | Prospective study | Clinics | 45 patients | 1–7 days | OHIP-14 | Bromelain 250 mg taken pre and postoperatively for 4 days showed a significant improvement in quality of life compared to diclofenac sodium. | |
| Aged between 18 and 35ans | |||||||
| 2013 | Prospective study | Clinics | 60 patients | 1–7 days | OHIP-14 | Ozone therapy showed a significant improvement in quality of life and a reduction in pain after extraction of the impacted mandibular wisdom tooth. Moreover, this treatment had no effect on postoperative swelling and trismus. | |
| Aged between 18 and 25ans | |||||||
| 2013 | Randomized clinical trial | Clinics | 60 patients | 1–7 days | OHIP-14 | Intra- and extra-oral low power laser (LLLT) allows good healing, a significant reduction of pain, trismus, and swelling and improved quality of life on days 2 and 7 after extraction of the impacted mandibular wisdom tooth. | |
| Aged between 18 and 30ans | |||||||
| 2012 | Prospective study | Clinics | 50 patients | 1–7 days | HRQOL-sp | The extraction of the impacted mandibular wisdom tooth affects the quality of life especially in the first 5 days. Intraoperative conscious sedation with Midazolam provides comfort for the patient but has no effect in the postoperative period. | |
| Aged between 18 and 25ans | |||||||
| 2012 | Prospective study | Clinics | 86 patients | 1–7 days | OHIP-14 | A compromised position of the impacted mandibular wisdom tooth (e.g. disto-angular) involves a complex technique for this extraction, which results in a negative alteration of the postoperative quality of life. | |
| aged between 18 and 25 years | |||||||
| 2012 | Prospective study | Clinics | 60 patients | 3 months | OHIP-14 | Quality of life is negatively affected in patients with minor pericoronitis symptomatology after extraction of impacted mandibular wisdom teeth. | |
| aged between 18 and 35 years | |||||||
| 2010 | Prospective study | Clinics | 958 patients aged between 14 and 40 years | 1–14 days | HRQOL | Patients younger than 21 years of age recover more quickly and therefore have a better quality of life compared to those who are older. | |
| 2010 | Prospective study | Clinics | 50 patients | 1–7 days | OHIP-14 | Patients who did not brush their teeth and who smoked cigarettes pre- and postoperatively had intolerable pain in the first 24 h after extraction of the impacted mandibular wisdom tooth. | |
| Aged between 18 and 39 years | |||||||
| 2009 | Prospective study | Clinics | 128 patients | 1–7 days | HRQOL | The quality of life of patients after extraction of impacted mandibular wisdom teeth was deficient in the first 3 days postoperatively and which tended to improve with time. | |
| Aged between 16 and 40 years | |||||||
| 2009 | Randomized controlled trial | Clinics | 72 patients aged between 18 and 45 years | 1–7 days | OHIP-14 | There was a significant deterioration in quality of life during the first 5 days after extraction of the impacted mandibular wisdom tooth, which improved after the 6th day. The use of these two questionnaires in this study identified that there is no difference between them. | |
| OHQoLUK-16 | |||||||
| 2007 | Prospective cohort study | Clinics | 4004 patients | 1–7 days | OHIP-14 | There is an increased risk of complications and deterioration of quality of life in patients over 25 years of age compared to those who were younger. | |
| aged between 13 et 89 ans | |||||||
| 2006 | Prospective observational study | Clinics | 63 patients | 1–7 days | OHIP-14 | The use of these two instruments showed significant results in determining quality of life after extraction of the impacted mandibular wisdom tooth. | |
| under than 25 years old | OHQoL-UK | ||||||
| 2006 | Objective observational study | Clinics | 105 patients average age 25.1 ans | 1–7 days | HRQOL-sp | Women experienced more pain than men, especially in the first 3 days after extraction of the impacted mandibular wisdom tooth. In addition, patients who were followed by telephone and were able to follow the instructions had an improvement in their quality of life postoperatively. | |
| 2006 | Prospective study | Clinics | 63 patients | 1–14 days | HRQOL | Topical application of Minocycline or Ampicillin improves the quality of life after extraction of the impacted mandibular wisdom tooth. | |
| Aged between 18 and 25 years | |||||||
| 2003 | Observational study | Clinics | 740 patients | 1–14 days | HRQOL | After extraction of the impacted mandibular wisdom tooth, most patients reported pain, swelling and deterioration of their quality of life. But this tended to decrease until it disappeared over time. | |
| Aged between 14 and 40 years | |||||||
| 2003 | Prospective observational study | Clinics | 100 patients | 1–7 days | OHIP-14 | The OHIP-14 instrument was more reliable and significant in measuring quality of life after extraction of the impacted mandibular wisdom tooth. This was explained by the significant difference in scores and much more severe changes in the level of perception. | |
| under than 26 years old | OHQOL-UK |
Appraisal tool for Cross-Sectional Studies (AXIS) [50].
| Doni B R et al. [ | |||
|---|---|---|---|
| YES | NOT | Do not know/comment | |
| Introduction | |||
| 1 Were the aims/objectives of the study clear? | + | ||
| Methods | |||
| 2 Was the study design appropriate for the stated aim(s)? | + | ||
| 3 Was the sample size justified? | + | ||
| 4 Was the target/reference population clearly defined? (Is it clear who the research was about?) | + | ||
| 5 Was the sample frame taken from an appropriate population base so that it closely represented the target/reference population under investigation? | + | ||
| 6 Was the selection process likely to select subjects/participants that were representative of the target/reference population under investigation? | + | ||
| 7 Were measures undertaken to address and categorise non-responders? | + | + | |
| 8 Were the risk factor and outcome variables measured appropriate to the aims of the study? | + | ||
| 9 Were the risk factor and outcome variables measured correctly using instruments/measurements that had been trialled, piloted or published previously? | + | + | |
| 10 Is it clear what was used to determined statistical significance and/or precision estimates? (eg, p values, CIs) | |||
| 11 Were the methods (including statistical methods) sufficiently described to enable them to be repeated? | |||
| Results | |||
| 12 Were the basic data adequately described? | + | ||
| 13 Does the response rate raise concerns about non-response bias? | + | ||
| 14 If appropriate, was information about non-responders described? | + | ||
| 15 Were the results internally consistent? | + | ||
| 16 Were the results for the analyses described in the methods, presented? | + | ||
| Discussion | |||
| 17 Were the authors' discussions and conclusions justified by the results? | + | ||
| 18 Were the limitations of the study discussed? | + | ||
| Other | |||
| 19 Were there any funding sources or conflicts of interest that may affect the authors' interpretation of the results? | + | ||
| 20 Was ethical approval or consent of participants attained? | + | ||