| Literature DB >> 31316563 |
Rodrigo Zamboni1, Flávio Renato Reis de Moura2, Myrian Camara Brew3, Elken Gomes Rivaldo2, Marcylene Arruda Braz1, Eduardo Grossmann4, Caren Serra Bavaresco2.
Abstract
Several treatments have been suggested to correct dentofacial abnormalities, including orthognathic surgery. The aim of the present systematic review was to assess the impact of orthognathic surgery on patient satisfaction, overall quality of life, quality of life related to oral health-and to orthognathic surgery in particular-among adult patients. Two investigators independently reviewed the available literature in the databases PubMed/MEDLINE, LILACS, SciELO, EMBASE, Trip, and Google Scholar (gray literature) based on the keywords "orthognathic surgery" and "quality of life." An analysis of bias was performed based on the MINORS (methodological index for nonrandomized studies). A total of 245 relevant studies were retrieved from the databases, and 6 additional studies were located after a manual search of the references. Following selection based on titles, abstracts, and full-text analysis, 30 studies were included in the present systematic review. To evaluate quality of life before and after orthognathic surgery, 12 studies applied the surgery-related Orthognathic Quality of Life Questionnaire (OQLQ), 12 used the Oral Health Impact Profile (OHIP-14), and 4 used the Short Form Health Survey (SF-36). Orthognathic surgery results in improvements in quality of life both physically and psychosocially after surgery and is associated with high rates of patient satisfaction.Entities:
Year: 2019 PMID: 31316563 PMCID: PMC6604419 DOI: 10.1155/2019/2864216
Source DB: PubMed Journal: Int J Dent ISSN: 1687-8728
Figure 1Flow chart for article selection.
Qualitative descriptions of the included studies (n=30).
| Authors/year | Study design | Country | Sample size | Type of orthognathic surgery | Methods for collection of data regarding the outcomes satisfaction and quality of life |
|---|---|---|---|---|---|
| (1) Cunningham et al. [ | Retrospective (postoperative analysis) | United Kingdom | 100 patients (postoperative analysis) | Not reported | (1) Satisfaction: structured questionnaire developed by the authors with ranked responses (very satisfied, moderately satisfied, dissatisfied, very dissatisfied) |
| (2) Forssell et al. [ | Prospective | Finland | Initial sample: 104 patients | Mandibular sagittal split osteotomy (80 patients); Le Fort I maxillary osteotomy (6 patients); bimaxillary osteotomy (14 patients) | (1) Visual analogue scale (VAS): satisfaction with the results |
| (3) Bertolini et al. [ | Prospective | Italy | 20 patients | Not reported | (1) Satisfaction: structured questionnaire developed by the authors with ranked responses (very satisfied, moderately satisfied, dissatisfied, and very dissatisfied) after surgery |
| (4) Busby et al. [ | Retrospective | USA | 79 patients | Mandibular ramus osteotomy; maxillary advancement; combination of both procedures | (1) Satisfaction: 25-item questionnaire to assess satisfaction with postoperative changes, preoperative perception and overall satisfaction with the surgery |
| (5) Lee et al. [ | Prospective | Japan | 36 patients | Bimaxillary osteotomy | (1) SF-36 |
| (6) Al-Ahmad et al. [ | Retrospective | Jordan | 136 patients (35 patients in the postsurgery group) | Not reported | (1) OQLQ |
| (7) Choi et al. [ | Prospective | Japan | 60 patients | Bimaxillary osteotomy | (1) SF-36 |
| (8) Silva et al. [ | Prospective | Brazil | 15 patients | Bimaxillary osteotomy; mandibular setback and maxillary advancement | (1) WHOQOL-Bref |
| (9) Rustemeyer et al. [ | Prospective | Germany | 50 patients | Bimaxillary osteotomy | (1) OHIP-14 |
| (10) Khadka et al. [ | Prospective | China | Total: 158 patients | Group A: sagittal osteotomy; intraoral vertical ramus osteotomy; Le fort I osteotomy; mandibular anterior segmental osteotomy | (1) SF–36 |
| (11) Murphy et al. [ | Prospective | Ireland | Initial sample: 62 patients | Bimaxillary osteotomy, mandibular setback | (1) OQLQ |
| (12) Khattak et al. [ | Retrospective | United Kingdom | 135 patients | Maxillary advancement and mandibular setback; bimaxillary advancement; condylectomy; maxillary posterior impaction; maxillary distraction osteogenesis; mandibular anterior segmental osteotomy | (1) PSQ |
| (13) Rustemeyer and Gregersen [ | Prospective | Germany | 30 patients | Bilateral sagittal split osteotomy of the mandibular ramus | (1) OHIP-14 |
| (14) Trovik et al. [ | Retrospective | Norway | Initial sample: 78 patients | Bilateral sagittal split osteotomy for mandibular advancement | (1) VAS |
| (15) Rustemeyer and Lehmann [ | Retrospective | Germany | Sample total: 60 patients | Bimaxillary osteotomy with or without genioplasty | (1) OHIP-14 |
| (16) Wee and Poon [ | Retrospective | Singapore | Initial sample: 114 patients | Le fort I osteotomy and/or mandibular bilateral sagittal split osteotomy | (1) OQLQ |
| (17) Goelzer et al. [ | Prospective | Brazil | 74 patients | Not reported | (1) OHIP-14 |
| (18) Schwitzer et al. [ | Prospective | USA | Total sample: 49 patients | Le fort I osteotomy and/or mandibular bilateral sagittal split osteotomy | (1) FACE-Q |
| (19) Corso et al. [ | Prospective | Brazil | Control group: 60 patients | Not reported | (1) OHIP-14 |
| (20) Abdullah [ | Retrospective | Saudi Arabia | 17 patients | Mandibular, maxillary or bimaxillary osteotomy | (1) OQLQ |
| (21) Park et al. [ | Prospective | South Korea | Initial sample: 44 patients | Bilateral sagittal split osteotomy of the mandibular ramus; Le fort I osteotomy | (1) OQLQ |
| (22) Baherimoghaddam et al. [ | Prospective | Iran | Initial sample: 75 patients | Le fort I osteotomy; bilateral sagittal split osteotomy of the mandibular ramus | (1) OHIP-14 |
| (23) Kilinc and Ertas [ | Retrospective | Turkey | Total sample: 60 patients | Maxillary advancement, mandibular setback or both procedures and genioplasty | (1) OQLQ |
| (24) Silva et al. [ | Prospective | Sweden | Initial sample: 55 patients | Le fort I osteotomy; bilateral sagittal split osteotomy of the mandibular ramus | (1) OHIP-14 |
| (25) Kurabe et al. [ | Retrospective | Japan | Surgery group: 65 patients | Le fort I osteotomy; bilateral sagittal split osteotomy of the mandibular ramus | (1) OHIPJ-54 |
| (26) Bogusiak et al. [ | Retrospective | Poland | Total sample: 90 patients | Bilateral vertical ramus osteotomy by the external approach; extraoral vertical ramus osteotomy (EVRO); bilateral sagittal split osteotomy of the mandibular ramus by the internal approach; bimaxillary osteotomy | (1) Satisfaction with life scale: SAT |
| (27) Huang et al. [ | Prospective | China | Total sample: 50 patients | Bilateral sagittal split mandibular ramus osteotomy | (1) Dental impact on daily living: DIDL |
| (28) Alanko et al. [ | Prospective | Finland | Initial sample: 60 patients | Bilateral sagittal osteotomy, bimaxillary osteotomy, maxillary osteotomy | (1) OQLQ |
| (29) Pelo et al. [ | Prospective | Italy | Total sample: 30 patients | Le fort I osteotomy, mandibular bilateral sagittal split osteotomy | (1) OQLQ |
| (30) Zingler et al. [ | Prospective | Germany | 9 patients | Maxillary osteotomy, mandibular osteotomy, bimaxillary osteotomy | (1) OQLQ |
Results on patient satisfaction after surgery (n=10).
| Study design | Follow-up duration | Main results | References |
|---|---|---|---|
| (1) Retrospective (postoperative analysis) | At least 9 months after surgery | Of the participants, 95% were satisfied with the results of treatment (very satisfied: 66.7%; moderately satisfied: 28.4%); 7.5% were dissatisfied with the results; and 76.5% stated that they would undergo the surgery again. | Cunningham et al. [ |
| (2) Prospective | T0: 1 month before surgery | The mean VAS score for patient satisfaction was 8.8 (88%); 86% of participants would undergo surgery again. All investigated life aspects improved after surgery: work, livelihood, interpersonal relationships, leisure, mental health, health and perspective on life. | Forssell et al. [ |
| (3) Prospective | T0: 1 week before surgery | 69.2% of participants were satisfied with surgery, and 23.1% were very satisfied; none of the participants reported dissatisfaction. | Bertolini et al. [ |
| (4) Retrospective | Evaluation at 1, 2 and more than 2 years | Of the patients, 92% were satisfied, and 89% were aware of what to expect after discharge. Negative surgery-related outcomes tended to decrease along the follow-up. | Busby et al. [ |
| (5) Prospective | Before surgery | Significant difference in satisfaction before (79.22 ± 18.42) and after (87.56 ± 15.50) ( | Murphy et al. [ |
| (6) Retrospective | 2.54 years after surgery | Participants reported satisfaction with the appearance of their face after treatment; smile, self-confidence (85.3%), social life (46%), eating (60.6%), and speech (39.3%). | Khattak et al. [ |
| (7) Retrospective | T0: baseline | Of the participants, 36% reported that they were very satisfied, 53% were moderately satisfied, and 8% were dissatisfied. | Trovik et al. [ |
| (8) Prospective | T0: before surgery | The scores on the FACE-Q used to assess satisfaction showed a significant increase of patient satisfaction after orthognathic surgery for the domains facial appearance overall (T0: 48.2 ± 3.2; T1: 72.9 ± 3.3), lower face and jawline (T0: 42.6 ± 6.3; T1: 83.3 ± 5.9) and all four chin items ( | Schwitzer et al. [ |
| (9) Retrospective | At least 6 months after surgery | The mean SAT score was 23.9 ± 3.83; 95% of participants would undergo surgery again. The mean SAT score was higher for the participants subjected to sagittal osteotomy compared to that for the patients undergoing bimaxillary osteotomy ( | Bogusiak et al. [ |
| (10) Prospective | T1: before treatment | Satisfaction was substantially lower for the group subjected to the surgery-first approach, but the difference was statistically nonsignificant compared to that of the conventional treatment group. | Huang et al. [ |
Results for the OQLQ global and domain scores (n=12).
| Study design | Follow-up duration | Main results | References |
|---|---|---|---|
| (1) Prospective | T0: baseline | T0-T1: no significant difference in the global score; decrease in the score for the domain facial esthetics. | Lee et al. [ |
| (2) Retrospective | 21 months after surgery | Significant differences in the global score and all 4 domain scores between the pre- and postsurgery groups. However, no difference in the scores was found among the controls, postsurgery group, and patients who declined surgery. | Al-Ahmad et al. [ |
| (3) Prospective | T0: baseline | T0-T1: significant reduction in the global score and scores for the domains social aspects and facial esthetics. | Choi et al. [ |
| (4) Prospective | T0: before surgery | Significant reduction in OQLQ scores after surgery in both groups. | Khadka et al. [ |
| (5) Prospective | T0: during orthodontic treatment | Significant differences in all OQLQ domains before and after surgery. | Murphy et al. [ |
| (6) Retrospective | T0: before surgery | Significant reductions in the global score (T0: 28/T1: 13.51) and all 4 domain scores ( | Wee and Poon [ |
| (7) Retrospective | T0: before surgery | Reduction in the OQLQ global score after surgery. | Abdullah [ |
| (8) Prospective | T0: first visit | Conventional surgery group: significantly higher scores before surgery (T0: 53.87 ± 17.81; T1: 58.07 ± 18.18; | Park et al. [ |
| (9) Prospective | T0: before surgery | Significant reduction in the OQLQ score at T1 (30.5 ± 19.5) and T2 (26.1.±19.3) compared to that of the controls. | Silva et al. [ |
| (10) Prospective | Orthognathic surgery group: T0: before treatment; T1: after orthodontic assessment; T2–T4: during orthodontic treatment; T5: 1 year after surgery | The global score and the score for the domain oral function increased at T2 (35.89 ± 23.39) compared to those at T0 (31.38 ± 20.71) ( | Alanko et al. [ |
| (11) Prospective | T0: before bracket placement | No significant difference between groups at T0 (surgery-first: 57 ± 10/conventional: 52 ± 10) or T2 (surgery-first: 22 ± 3/conventional: 29 ± 9). | Pelo et al. [ |
| (12) Prospective | T0: before surgery | Significant reduction in the score at T1 (18 ± 12.69) compared to that at T0 (36 ± 17.24) ( | Zingler et al. [ |
Results for the global and domain scores on the OHIP-14 (n=12).
| Study design | Follow-up duration | Main results | References |
|---|---|---|---|
| (1) Prospective | T0: baseline | T0-T1: no significant difference in the global score 6 weeks after orthognathic surgery. However, a significant increase was observed for the score on the domain functional limitation and significant decreases were observed for the scores on the domains psychological discomfort and psychological disability. | Lee et al. [ |
| (2) Prospective | T0: baseline | T0-T1: no significant changes in the global score. Significant reductions in the scores on the domains functional limitation and psychological discomfort 6 weeks after surgery. | Choi et al. [ |
| (3) Prospective | 12 months after surgery | Significant reductions in scores on the domains psychological discomfort, dissatisfaction with esthetics and social disability. | Rustemeyer et al. [ |
| (4) Prospective | 8.3 months after surgery | Significant reductions in scores on the domains psychological discomfort and social disability after surgery. | Rustemeyer and Gregersen [ |
| (5) Prospective | T0: 1 week before surgery | Significant differences in all scores (global and domains) at all postsurgery time points; the scores increased 1 month after surgery and substantially decreased 3 months after surgery. | Corso et al. [ |
| (6) Prospective | T0: before treatment | Domain functional limitation: | Baherimoghaddam et al. [ |
| (7) Prospective | T0: before surgery | Significant reductions in OHIP-14 scores at T1 and T2 compared to those of the controls. | Silva et al. [ |
| (8) Retrospective | T0: 1 month before surgery | The scores for social disability, physical pain, psychological discomfort and dissatisfaction with esthetics significantly decreased after surgery in both groups. | Rustemeyer and Lehmann [ |
| (9) Prospective | T0: before surgery | Significant reduction in the global score from T0 (13.23 ± 6.45) to T1 (3.26 ± 4.19) ( | Göelzer et al. [ |
| (10) Retrospective | T0: before surgery | Significant reductions in the global score (T0: 14/T1: 4.68) and all domain scores ( | Wee and Poon [ |
| (11) Prospective | T1: before surgery | The quality of life of the surgery-first group significantly increased at T2 compared to that at T1, but no difference was found from T4 to T6. | Huang et al. [ |
| (12) Prospective | T0: before bracket placement | No significant difference was found between groups at T0 (surgery-first: 16 ± 6/conventional: 13 ± 5) or T2 (surgery-first: 2 ± 1/conventional: 3 ± 1). Significant differences were found in each group among T0, T1 and T2 ( | Pelo et al. [ |
Results for the global and domain scores on the SF-36 (n=4).
| Study design | Follow-up duration | Main results | References |
|---|---|---|---|
| (1) Prospective | T0: baseline | T0-T1: significant reductions in scores for the physical health, mental health, and social domains. | Lee et al. [ |
| (2) Retrospective | 21 months after surgery | Significant differences in the components general health, vitality and mental health between the pre- and postsurgery groups favoring the group of patients who underwent surgery. | Al-Ahmad et al. [ |
| (3) Prospective | T0: baseline | T0-T1: significant reduction in the score for the domain physical health. | Choi et al. [ |
| (4) Prospective | T0: before surgery | Significant differences in the physical and bodily pain components ( | Khadka et al. [ |
Methodological evaluation of the selected studies according to the Methodological Index for Non-Randomized Studies (MINORS). Scores were assigned as follows: 0 (not reported); 1 (reported but inadequate); and 2 (reported and adequate). The ideal global score is 16 for noncomparative studies and 24 for comparative studies [11].
| Criteria | Cunningham et al. [ | Forssell et al. [ | Bertolini et al. [ | Busby et al. [ | Lee et al. [ | Al-Ahmad et al. [ | Choi et al. [ | Silva et al. [ | Rustemeyer et al. [ | Khadka et al. [ | Murphy et al. [ | Khattak et al. [ | Rustemeyer and Gregersen [ | Trovik et al. [ | Rustemeyer and Lehmann, [ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A clearly stated aim | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 |
| Inclusion of consecutive patients | 1 | 2 | 2 | 2 | 2 | 1 | 2 | 1 | 1 | 2 | 2 | 1 | 2 | 1 | 0 |
| Prospective collection of data | 0 | 2 | 2 | 0 | 2 | 0 | 2 | 2 | 2 | 2 | 2 | 0 | 2 | 0 | 0 |
| Endpoints appropriate for the study aim | 1 | 1 | 1 | 1 | 2 | 2 | 2 | 1 | 2 | 2 | 2 | 2 | 2 | 2 | 2 |
| Unbiased evaluation of endpoints | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 |
| Appropriate follow-up | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 2 | 1 | 1 | 2 | 2 | 2 |
| Loss to follow-up of less than 5% | 0 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Prospective sample size calculation | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Adequate control group | NA | NA | NA | NA | NA | 2 | NA | NA | NA | 1 | NA | NA | NA | NA | 2 |
| Contemporary groups | NA | NA | NA | NA | NA | 0 | NA | NA | NA | 2 | NA | NA | NA | NA | 2 |
| Baseline equivalence of groups | NA | NA | NA | NA | NA | 2 | NA | NA | NA | 2 | NA | NA | NA | NA | 2 |
| Adequate statistical analyses | NA | NA | NA | NA | NA | 2 | NA | NA | NA | 2 | NA | NA | NA | NA | 2 |
| Total score | 6 | 11 | 9 | 7 | 12 | 13 | 10 | 7 | 9 | 17 | 10 | 6 | 10 | 7 | 14 |
|
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| Criteria | Wee and Pon [ | Göelzer et al. [ | Schwitzer et al. [ | Abdullah [ | Corso et al. [ | Park et al. [ | Baherimoghaddam et al. [ | Kilinc and Ertas [ | Kurabe et al. [ | Silva et al. [ | Bogusiak et al. [ | Huang et al. [ | Alanko et al. [ | Pelo et al. [ | Zingler et al. [ |
|
| |||||||||||||||
| A clearly stated aim | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 |
| Inclusion of consecutive patients | 1 | 2 | 1 | 1 | 1 | 1 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 1 | 2 |
| Prospective collection of data | 0 | 2 | 2 | 0 | 2 | 2 | 2 | 2 | 2 | 2 | 0 | 2 | 2 | 2 | 2 |
| Endpoints appropriate for the study aim | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 1 | 2 | 2 | 2 | |
| Unbiased evaluation of endpoints | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Appropriate follow-up | 2 | 2 | 1 | 2 | 1 | 2 | 2 | 2 | 2 | 2 | 1 | 2 | 1 | 2 | 2 |
| Loss to follow-up of less than 5% | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 0 | 0 | 0 | 0 | 0 |
| Prospective sample size calculation | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
| Adequate control group | NA | NA | NA | NA | 0 | 2 | 2 | 2 | NA | NA | NA | 0 | 0 | 2 | NA |
| Contemporary groups | NA | NA | NA | NA | 1 | 2 | 2 | 2 | NA | NA | NA | 2 | 1 | 2 | NA |
| Baseline equivalence of groups | NA | NA | NA | NA | 2 | 2 | 2 | 2 | NA | NA | NA | 2 | 2 | 2 | NA |
| Adequate statistical analyses | NA | NA | NA | NA | 2 | 2 | 2 | 2 | NA | NA | NA | 2 | 2 | 2 | NA |
| Total score | 7 | 10 | 6 | 7 | 13 | 18 | 18 | 18 | 10 | 12 | 6 | 15 | 13 | 18 | 10 |