Chirurgische behandeling van obesitas

Initiatief: Cluster Obesitas Aantal modules: 25

Postoperatief leefstijltraject rondom metabole chirurgie

Publicatiedatum: 18-08-2026
Beoordeeld op geldigheid: 18-08-2026

Uitgangsvraag

Wat is de rol van een postoperatieve leefstijlinterventie bij metabole chirurgie?

Aanbeveling

Bied laagdrempelig een postoperatieve leefstijlinterventie (met minimaal een dieet- en beweegcomponent) aan voor duurzame gezondheidswinst bij:

  • Moeite om een gezonde leefstijl te bereiken of vast te houden, gesignaleerd door de arts of ervaren door de patiënt.
  • Suboptimaal gewichtsverlies of gezondheidswinst.
  • Aanwezigheid van eetbuien

Overwegingen

Balans tussen gewenste en ongewenste effecten

Voor de module is de literatuur doorzocht op de effectiviteit van een (gestructureerd) postoperatief leefstijltraject met minimaal een voedings- en beweegcomponent en een vorm van coaching bij patiënten die metabole chirurgie hebben ondergaan.

Een leefstijlinterventie is professionele coaching - niet alleen advies - om een gezondere leefstijl (minimaal voeding en beweging) te bereiken en duurzaam vol te kunnen houden. De precieze invulling van leefstijlinterventies varieert tussen aanbieders.

Daarnaast is het belangrijk te noemen dat de huidige trajecten (standaardzorg) rondom metabole chirurgie ook sterk verschillen tussen centra onderling; er is hiervoor geen afgebakende definitie. Hierdoor is de vergelijking met de standaardzorg in de geïncludeerde studies in de beschreven literatuur (die soms niet te achterhalen was) niet goed te maken.

 

Een systematische review die dezelfde PICO omvatte is gebruikt als uitgangspunt, hoewel hierin geen geschikte studies zijn gevonden (Marshall, 2020). Aanvullend zijn vijf losse trials geïncludeerd (Jassil, 2023; Hanvold, 2019; Lent, 2019; Grilo, 2022; Sockalingham, 2023).

 

Uit de literatuursamenvatting zijn resultaten met lage bewijskracht gevonden voor het ontbreken van een (klinisch relevant) verschil in gewichtsverlies bij het al dan niet inzetten van een (gestructureerd) postoperatieve leefstijlinterventie met minimaal een voedings- en beweegcomponent en een vorm van coaching. Voor de uitkomstmaten obesitas-gerelateerde complicaties, kwaliteit van leven (inclusief eetstoornissen), psychopathologie en emotioneel eetgedrag zijn resultaten met een zeer lage bewijskracht gevonden. Voor de specifiek eetstoornissen dient benoemd te worden dat de interventies hier niet op gericht waren; patiënten met eetstoornissen worden doorgaans uitgesloten voor bariatrie. Vanuit de geïncludeerde studie van Sockalingham (2023) werd voor specifiek de Binge Eating Scale (BES) een klinisch relevant verschil gevonden in voordeel van de leefstijlinterventie. Hoewel dit bewijs beperkt is (en niet separaat beoordeeld middels de GRADE-methodiek) geven deze resultaten de suggestie om een postoperatieve leefstijlinterventie bij aanwezigheid van eetbuien te overwegen in te zetten.

 

Kwaliteit van bewijs

De overall kwaliteit van bewijs is laag. Dit betekent dat we onzeker zijn over het gevonden geschatte effect van de cruciale uitkomstmaten.

 

Er is afgewaardeerd vanwege ernstige of zeer ernstige:

  • Risk of Bias: methodologische beperkingen o.a. vanwege het ontbreken van informatie over blindering bij studiepersoneel en grote verschillen in uitval tussen studiegroepen.
  • Imprecisie: onnauwkeurigheid, omdat het betrouwbaarheidsinterval een of beide grenzen van klinische relevantie overschrijdt, waardoor de effectschatter de mogelijkheid bevat voor een klinisch relevant verschil (in zowel het voordeel van de interventie als de controle).

 

Waarden en voorkeuren van patiënten (en eventueel hun naasten/verzorgers)

De gedachte achter leefstijl interventies na metabole chirurgie is het optimaliseren van de resultaten met name op de langere termijn door compliance aan dieet- en beweegadviezen te vergroten. Het is bekend dat een grote groep patiënten er niet in slaagt om zich aan gezonde dieet- (verminderen van gebruik van ongezonde en calorierijke maaltijden) en beweegadviezen te houden (Aarts, 2015; De Jong, 2017).

 

Hoewel het bij een deel van de patiënten niet noodzakelijk is om leefstijlinterventies aan te bieden in aanvulling op metabole chirurgie zal een subgroep wel degelijk gebaat zijn bij extra zorg om de noodzakelijke gedragsverandering door te voeren en vol te houden. Er treedt gemiddeld op de lange termijn relapse op na bariatrie, hoewel gemiddeld gezien de resultaten nog goed zijn. Er is daarmee op de (zeer) lange termijn een subgroep die veel in gewicht toeneemt, waardoor een aanvullende leefstijlinterventie van meerwaarde kan zijn. Deze termijn is in de geïncludeerde studies niet onderzocht. 

 

Voor een one-size-fits-all benadering lijkt geen steun te bestaan bij patiënten (vanuit klinische praktijkervaring) noch in de wetenschappelijke literatuur.

 

Kostenaspecten

Hoewel metabolische en bariatrische chirurgie (MBS) gemiddeld meer dan 25% totaal gewichtsverlies (TWL) behaald op lange termijn, profiteert niet iedereen. Voor zo’n 1 op de 5 patiënten is op lange termijn sprake van suboptimaal resultaat wat betreft gewicht en daarmee gerelateerde gezondheidsproblemen (zie Obesitas – DATO). Dit gaat gepaard met kosten.

 

In Nederland wordt MBS alleen aangeboden in combinatie met een begeleidingstraject. Dit traject bestaat voornamelijk uit leefstijladviezen. Hoewel een deel van de patiënten daar voldoende aan heeft, kan een aantal patiënten baat hebben bij aanvullende leefstijl interventies om zich aan te passen aan het veranderd eet- en beweegpatroon. Dergelijke leefstijlinterventies overstijgen de gebruikelijke begeleiding en omvatten ook vaker cognitieve gedragstherapie (CBT). Het is aannemelijk dat de kosten van de leefstijlinterventies aan deze groep patiënten aanzienlijk minder zijn dan de kosten en het verlies in kwaliteit van leven wanneer patiënten opnieuw chirurgisch ingrijpen nodig hebben en/of ernstig overgewicht houden. Dit gaat bovendien vaak gepaard gaat met diverse obesitas-gerelateerde complicaties en andere zorgvragen. Een studie van Hecker (2022) van de Universiteit Maastricht laat zien dat ernstig overgewicht jaarlijks gemiddeld 11.500 euro per persoon kost, wat de kosten van een gecombineerde leefstijlinterventie overstijgt.

 

Gelijkheid ((health) equity/equitable)

De interventie leidt niet tot een specifieke verandering van gezondheidsgelijkheid.

 

Aanvaardbaarheid

Ethische aanvaardbaarheid

Er zijn geen ethische bezwaren voor het al dan niet inzetten van een postoperatieve leefstijlinterventie.

 

Duurzaamheid

Bij de interventie spelen de duurzaamheidsaspecten geen belangrijke rol.

 

Haalbaarheid

Voor het tijdig kunnen aanbieden van postoperatieve leefstijlinterventies aan patiënten die daar daadwerkelijk baat bij kunnen hebben omdat zij (dreigen) niet optimaal (te) profiteren van metabole chirurgie is het nodig om gewicht, eet- en beweeggedrag en compliance aan dieet- en beweegadviezen routinematig te monitoren in de tweede lijn. De werkgroep voorziet geen bezwaar van overige relevante stakeholders voor het aanbieden van postoperatieve leefstijlinterventies.

 

Rationale van de aanbeveling: weging van argumenten voor en tegen een leefstijlinterventie na bariatrie.

Er zijn geen duidelijke argumenten voor het aanbieden van een leefstijlinterventie na een metabole chirurgie gevonden in de literatuur. Daarmee is geen aanbeveling te doen om dergelijke interventies standaard aan te bieden in aanvulling op een regulier begeleidingstraject. Op basis van expertise en gegeven dat ongeveer 1 op de 5 patiënten suboptimaal resultaat ervaart op lange termijn (>10 jaar) en het gegeven dat op de nog langere termijn terugval in gewicht en een ongezond leefstijlpatroon gezien wordt (wat in de geïncludeerde studies niet is onderzocht), kan wel zorg op maat zinvol zijn.

 

Eindoordeel:

Conditionele aanbeveling voor

Onderbouwing

Lifestyle advice is important in any obesity treatment modality, but a lifestyle intervention is more than just advice and can be a modality on its own. The value of a lifestyle intervention as a neo-adjuvant treatment in metabolic surgery trajectory has been suggested as an option in a previous guideline.. However, it remained unclear if and when it should be added to the already existing program, typically consisting mainly of lifestyle advice.  New literature on the effectiveness of lifestyle programs surrounding metabolic surgery has emerged, potentially providing more definitive recommendations.

Outcome

Timeframe

Study results and measurements

Absolute effect estimates

Certainty of the evidence

(Quality of evidence)

Summary

Lifestyle intervention

Standard care

Weight loss (%)

Measured as percentage weight loss

Scale: 0 - 100 High better

Based on data from 760 participants in 5 studies

 

 

 

See results under the outcome Weight loss

Low GRADE1

A structured lifestyle intervention with a dietary and exercise component might result in little to no difference on weight loss, compared to standard care.

Obesity-related complications

Measured by: Systolic blood pressure

Low better

Based on data from 165 participants in 1 study

127 (6)

126 (6)

Very Low GRADE2

The evidence is uncertain regarding the effect of a structured lifestyle intervention with a dietary and exercise component on obesity-related complications, compared to standard care.

Difference: MD 1.0 higher

(CI 95% 3.1 lower – 5.1 higher)

Measured by: Diastolic blood pressure

Low better

Based on data from 165 participants in 1 study

80 (11)

79 (11)

Difference: MD 1.0 higher

(CI 95% 2.6 lower – 4.6 higher)

Measured by: Total cholesterol

Low better

Based on data from 165 participants in 1 study

4.8 (0.8)

4.6 (1.0)

Difference: MD 0.2 higher

(CI 95% 0.1 lower – 0.5 higher)

Measured by: Hba1c

Low better

Based on data from 165 participants in 1 study

5.5 (0.8)

5.4 (0.8)

Difference: MD 0.1 higher

(CI 95% 0.2 lower – 0.5 higher)

Quality of life

 

Measured by: EQ-5D (VAS)

Scale: 0 - 100 High better

Based on data from 153 participants in 1 study

 

 

86.0 (12.8)

 

83.5 (13.6)

Very Low GRADE2

 

The evidence is uncertain regarding the effect of a structured lifestyle intervention with a dietary and exercise component on quality of life, compared to standard care.

Difference: MD 2.5 lower

(CI 95% 6.68 lower - 1.68 higher)

Measured by: IWQOL-Lite

Scale: 0 - 100 High better

Based on data from 153 participants in 1 study

88.2 (15.6)

88.1 (15.6)

Difference: MD 0.10 higher

(CI 95% 5.05 lower – 4.85 higher)

 

Measured by: SF36

Scale: 0 - 100 High better

Based on data from 41 participants in 1 study

78.1 (16.3)

66.9 (21.9)

 

Difference: MD 11.2 higher

(CI 95% 0.5 lower – 22.9 higher)

Psychopathology (including eating disorder)

Measured by: BDI-II

Scale: 0 - 63 Low better

Based on data from 237 participants in 2 studies

 

Jassil (2023) reported a difference of -0.80 (-3.7 to 2.1) after 1 year, in favor of the intervention. Grilo (2022) reported a difference of 0.50 (-5.93 to 6.93) after 1 year, in favor of the control group

Very Low GRADE2

The evidence is uncertain regarding the effect of a structured lifestyle intervention with a dietary and exercise component on psychopathology, compared to standard care.

Measured by: PHQ-9

Scale: 0 – 27 Low better

Based on data from 347 participants in 2 studies

 

Lent (2019) reported a difference of -1.9 (-4.8 to 1.0) after 16 months, in favor of the intervention. Sockalingham (2022) reported a difference of -2.0 (-2.1 to -1.9) after 18 months, in favor of the intervention group.

Measured by: GAD-7

Scale: 0 – 27 Low better

Based on data from 306 participants in 1 study

2.0 (0.2)

3.5 (0.4)

Difference: MD 1.5 lower

(CI 95% 1.6 lower – 1.4 lower)

Measured by: LOCES

Scale: 5 - 35 Low better

Based on data from 41 participants in 1 study

11.1 (3.9)

12.4 (4.9)

Difference: MD 1.3 lower

(CI 95% 4.0 lower – 1.4 higher)

Measured by: EES-depression

Scale: 0 - 36 Low better

Based on data from 41 participants in 1 study

7.1 (4.6)

6.1 (3.9)

Difference: MD 1.0 higher

(CI 95% 1.69 lower – 3.69 higher)

Emotional eating

 

Measured by: BES

Scale: 0 - 46 Low better

Based on data from 306 participants in 1 study

6.5 (0.6)

     9.1 (0.8)

Very Low GRADE2

The evidence is uncertain regarding the effect of a structured lifestyle intervention with a dietary and exercise component on emotional eating, compared to standard care.

 

Difference: MD 2.6 lower

(CI 95% 2.8 lower – 2.5 lower)

 

Measured by: EES global score

Low better

Based on data from 306 participants in 1 study

39.7 (1.7)

45.3 (1.8)

 

Difference: MD 5.6 lower

(CI 95% 6.0 lower – 5.2 lower)

 

1. Risk of Bias: serious. Lack of details on possible blinding of outcome assessors and allocation concealment and incorrect blinding of patients in several studies. Frequent of large difference between study groups in loss to follow-up. Imprecision: Serious. Overlap of the 95% CI with the minimal clinically important difference in one of the studies, i.e. boundary of CI includes possibility of benefit or harm and no effect.

2. Imprecision: Extremely serious. Overlap of the 95% CI with the minimal clinically important difference for several outcomes, i.e. boundary of CI includes possibility of benefit or harm and no effect. Only data from one study per (sub) outcome.

Description of studies

Jassil (2023) performed an RCT in the United Kingdom to investigate the impact of a 12-month adjunctive lifestyle intervention (BARI-LIFESTYLE program) on weight loss and health outcomes after bariatric surgery. Patients were selected from an observational cohort from three National Health Service (NHS) bariatric centers. Patients were included if they were aged 18 to 65 years and planning to undergo either primary gastric bypass or sleeve gastrectomy (SG) surgery (study was initiated before surgery), were medically safe to participate in an exercise program, were able to attend a supervised tailored exercise session weekly for 12 weeks, and were willing to wear a Fitbit and ActiGraph. Patients were excluded from participation if they had a body weight ≥200 kg, were non-ambulatory, had a functional limitation or if they had a medical contraindication for exercise. A total of 143 patients were randomized into a lifestyle intervention group (intervention after surgery) or a standard care group (see Table 2).

 

Hanvold (2019) performed an RCT in Norway to evaluate the efficacy of a 2-year group-based lifestyle intervention after bariatric surgery (specifically RYGB) compared with usual care on recurrent weight gain and related metabolic risk factors. Patients were included if they underwent RYGB and attended an information meeting on the study. Patients who participated in other studies were excluded. No further inclusion criteria were described. A total of 165 patients were randomized into a lifestyle intervention group or a usual care group (see Table 2).

 

Lent (2019) performed an RCT in the United States to evaluate the feasibility of a four-month postoperative behavioral intervention program, with a focus on psychosocial outcomes. Patients were included if they were a minimum of 18 years old and completed primary weight-loss surgery within the past 18 months. Patients who underwent surgery revisions, were pregnant or cognitively unable to provide informed consent were excluded. A total of 50 patients were randomized into the intervention group (CBT based) or control group who received usual care (see Table 2). Usual care was not further defined in the study article.

 

Grilo (2022) performed an RCT in the United States to evaluate the effectiveness of two guided-self-help treatments (CBT-based and based on a lifestyle (LEARN) program) for improving loss of control eating (LOC) after bariatric surgery. Adult patients (aged 18-65 years) with regular LOC-eating (≥once weekly) during the past 28 days were included. Exclusion criteria included use of medication known to effectively influence eating/weight, substance dependence, or severe psychiatric illness requiring acute care. A total of 140 patients were randomized into a CBT intervention group (which did not incorporate physical activity, not further considered for the current analysis), a behavioral weight loss intervention group or a usual care group (see Table 2).

 

Sockalingham (2023) performed an RCT in Canada to investigate the efficacy of a telephone-based CBT intervention among patients who underwent bariatric surgery. Adult patients (aged 18 years) with a preoperative BMI of ≥40 or a BMI of ≥35 with at least 1 obesity-related comorbidity were included. Exclusion criteria included severe psychiatric illness (psychosis, suicidality). A total of 306 patients were randomized into a tele-CBT intervention group or a usual care group (see Table 2).

 

Details of the included studies, including details on the intervention and control group, are described in Table 2.

 

Table 2. Characteristics of included studies

Study

Participants

Comparison

Follow-up

Outcome measures

Comments

Risk of bias (per outcome measure)*

Jassil, 2023

N at baseline

Intervention: 79

Control: 74

 

Age (mean, SD)

Intervention: 44.8 (10.8)

Control: 43.6 (10.5)

 

Sex (% male)

Intervention: 61%

Control: 40%

 

Intervention: Lifestyle program combining 17 behavioral (focus on diet and physical activity) tele-counseling sessions of 1 hour with real-time feedback + once-weekly supervised exercise for 12 weeks (started after 3 months). Participants were advised to achieve and maintain ≥150 minutes

of moderate-to-vigorous physical activity per week. Intervention started directly after surgery.

 

Control: Standard post-operative bariatric care according to NICE guidelines, including advice and monitoring on nutrition and physical activity.

12 months

Weight loss, quality of life, psychopathology

Non-commercial funding; several received fees/support from commercial organizations not related to the study.

Low (all outcomes)

Hanvold, 2019

N at baseline

Intervention: 85

Control: 80

 

Age (mean, SD)

Intervention: 45.3 (8.8)

Control: 46.1 (8.5)

 

Sex (% male)

Intervention: 27%

Control: 24%

Intervention: Group meetings (n = 16) of 2 hours, each with guidance of clinical dietitians/students in clinical nutrition, with measurements on body weight, lectures, group assignments and 30 min supervised physical activity (aerobic and resistant exercise).

Starting 14-31 months after surgery, in addition to standard care (see below)

 

Control: Standard care; three follow-up consultations with a clinical dietitian or a doctor on the first year followed by annual consultations on the following years.

24 months

Weight loss, obesity-related complications

Non-commercial funding and potential conflicts of interest

Some concerns (weight loss)

 

 

High (obesity-related complications)

Lent, 2019

N at baseline

Intervention: 24

Control: 26

 

Age (mean, SD)

Intervention: 47.6 (9.1)

Control: 46.2 (12.0)

 

Sex (% male)

Intervention: 17%

Control: 19%

Intervention: Behavioral intervention (CBT based) program with psychologist in group sessions (n = 8) of 1 hour, twice monthly. Focus on coping with potential psychosocial changes after surgery and developing skills for postoperative diet/adherence. Goal setting for diet, physical activity, adherence. 

 

Control: Usual care (not specified)

16 weeks

Weight loss, quality of life, psychopathology

Non-commercial funding. Potential conflicts of interest not reported

High (all outcomes)

Grilo, 2022

N at baseline

Intervention: 60

Control: 26

 

Age (mean, SD)

Intervention: 47.6 (9.1)

Control: 46.2 (12.0)

 

Sex (% male)

Intervention: 17%

Control: 19%

Intervention: Self-care program including lifestyle, exercise, attitudes, relationships, and nutrition delivered via six individual sessions (25–30 minutes) over 12 weeks along with standard bariatric nutrition education provided to participants. Sessions included clinicians’s guidance. Intervention started directly after surgery.

 

Control: Standard care, with 3 monthly assessment sessions of support groups and nutrition education.

24 months

Weight loss, psychopathology

Non-commercial funding and potential conflicts of interest

Some concerns (all outcomes)

Sockalingham, 2023

N at baseline

Intervention: 152

Control: 154

 

Age (mean, SD)

Intervention: 46.9 (10.3)

Control: 48.2 (9.6)

 

Sex (% male)

Intervention: 17%

Control: 16%

Intervention: CBT consisting of 6 weekly 1-hour sessions and a seventh 1-hour booster session delivered 1 month later. Sessions conducted by clinical psychology doctoral students with experience in the assessment and treatment of patients who underwent bariatric surgery. Intervention includes setting goals, identifying and planning for difficult eating scenarios, strategies on planning pleasurable activities and coping with negative thoughts. Participants completed worksheets between sessions and implemented skills taught during sessions. Intervention delivered 1 year after surgery.

 

Control: Standard bariatric care, which included monitoring by a multidisciplinary bariatric surgery team.

18 months

Weight loss, psychopathology

No information on funding or potential conflicts of interest.

 

Focus on dietary behavior.

High (all outcomes)

*For further details, see risk of bias table in the appendix

 

Results

Weight loss

Jassil (2023) reported on weight loss as percentage weight loss at 6-month and 12-month follow-up (post-surgery). Results of 3-month follow-up are also reported but note that the supervised exercise of the intervention was started at three months. At 3 months, only tele-counseling sessions were started in the intervention group. See Table 3 for the results. None of the reported differences between conditions were clinically relevant.

 

Table 3. Mean weight loss (%) and differences at follow-up between study groups (Jassil, 2023)

Outcome

Follow-up

Intervention

Control

Difference (95%CI)

Percentage weight loss (SD)

3 months

14.4 (3.6)

14.3 (3.9)

0.10 (-1.16 to 1.36)

6 months

20.0 (6.1)

21.2 (5.8)

-1.20 (-3.49 to 1.09)

12 months

 

24.9 (9.2)

 

25 (8.8)

 

-0.10 (-3.57 to 3.37)

 

 

Hanvold (2019) reported on weight loss as total weight loss in percentage after two years. The weight loss (SD) in the intervention group was 26.6% (9.8), compared to 27.0% (9.8) in the control group. The corresponding difference is -0.40% (-3.64 to 2.84), which is not clinically relevant. The study did not report results for weight loss after surgery but before the lifestyle intervention.

 

Hanvold reported also on the difference in total weight loss in both groups between start of the study (after surgery) and at the end of the study (24 months). The difference in weight loss (%) in the intervention group was -3.3% (95%CI: -6.2 to -0.4), compared to -3.1% (95%CI: -5.8 to -0.4) in the control group. These numbers indicate relapse (weight regain); the difference between the two groups is not clinically relevant.

 

Lent (2019) reported total weight loss in percentage after follow-up (16 months). The weight loss (SD) in the intervention group was 27.2% (7.6), compared to 30.5% (8.1) in the control group. The corresponding difference is 3.30 (95%CI: -1.61 to 8.21), which is not clinically relevant. The study did not report results for weight loss after surgery but before the lifestyle intervention.

 

Grilo (2022) reported on weight loss as percentage weight loss directly after the intervention, 6-month, 12-month and 24-month follow-up. These results were compared to the total weight at baseline after surgery. See Table 4 for the results. None of the reported differences were clinically relevant .

 

Table 4. Mean weight loss (%) and differences at follow-up between study groups (Grilo, 2023)

Outcome

Follow-up

Intervention

Control

Difference (95%CI)

Percentage weight loss (SD)

Post-intervention

2.1 (3.8)

1.6 (4.2)

 

0.50 (-1.38 to 2.38)

6 months

-0.4 (4.8) 1

-1.4 (4.4)1

 

1.00 (-1.08 to 3.08)

12 months

-2.1 (7.5)1

-3.9 (6.9)1

1.80 (-1.46, 5.06)

24 months

-7.0 (10.5)1

-8.2 (9.3)1

1.20 (-3.25 to 5.65)

1Indicating relapse (weight regain)

 

Sockalingham (2023) reported on total weight loss in percentage after follow-up compared to the total weight at baseline after surgery. The total weight loss in the intervention group was 1.08% (0.44), compared to 0.86 (0.42) in the control group. The corresponding difference is 0.22% (CI 95%: 0.12 to 0.32), which is not clinically relevant. The study did not report results for weight loss after surgery but before the lifestyle intervention.

 

Obesity-related complications

Jassil (2023) reported on obesity-related complications only in term of gastrointestinal adverse events. A total of 7 gastrointestinal events occurred in the intervention group, compared to 2 events in the control group. The number of patients in which these events occurred was not reported. Therefore, these results are not further considered.

 

• Systolic blood pressure (SBP, mmHg)

Hanvold (2019) reported a SBP (SD) of 127 (6) in the intervention group, compared to 126 (16) in the control group. The corresponding difference is 1.0 (-3.1 to 5.1), which is not clinically relevant.

• Diastolic blood pressure (DBP, mmHg)

Hanvold (2019) reported a DBP (SD) of 80 (11) in the intervention group, compared to 79 (11) in the control group. The corresponding difference is 1.0 (-2.6 to 4.6), which is not clinically relevant.

•Total cholesterol (mmol/L)

Hanvold (2019) reported a total cholesterol (SD) of 4.8 (0.8) in the intervention group, compared to 4.6 (1.0) in the control group. The corresponding difference is 0.2 (-0.1 to 0.5), which is not clinically relevant.

• HbA1c (%) (mmol/L)

Hanvold (2019) reported a HbA1c level (SD) of 5.5 (0.8) in the intervention group, compared to 5.4 (0.8) in the control group. The corresponding difference is 0.10 (-0.2 to 0.4), which is not clinically relevant.

 

Quality of life

Jassil (2023) reported on quality of life by the EuroQol-5D (EQ-5D) and the Impact of Weight on Quality of Life-Lite (IWQOL-Lite) questionnaires. For the EQ-5D, the index score ranges from -0.448 (worst) to 1.0). For the EQ-5D VAS and the IWQOL-Lite, these scores are o (worst) to 100 (best). Results for questionnaires were reported at 6-month and 12-month follow-up. See Table 4 for the results. None of the reported differences were clinically relevant, except for the results of the EQ-5D index at 6-month follow-up (scores in favor of the control group).

Note: At baseline, the scores differed substantially between the two groups (e.g. EQ-5D: 0.73 and 0.68 for resp. the intervention and control group), resulting in bias.

 

Table 4. Mean scores and differences between study groups in quality of life, measured by EQ-5D and IWQOL-Lite (Jassil, 2023)

Outcome

Follow-up

Intervention

Control

Mean difference (95%CI)

EQ-5D index (SD)

6 months

0.83 (0.23)

0.88 (0.18)

-0.05 (-0.12 to 0.02)

12 months

0.83 (0.18)

0.85 (0.23)

-0.02 (-0.09 to 0.05)

EQ-VAS (SD)

6 months

79.0 (15.2)

80.8 (13.6)

-1.80 (-6.36 to 2.76)

12 months

83.5 (13.6)

86.0 (12.8)

-2.50 (-6.68 to 1.68)

IWQOL-Lite (SD)

6 months

83.5 (17.6)

86.1 (15.4)

-2.60 (-7.83 to 2.63)

12 months

88.1 (15.6)

88.2 (15.6)

-0.10 (-5.05 to 4.85)

 

Lent (2019) reported on quality of life by the SF36 after follow-up (16 months). The score ranges from 0 (worst) to 100 (best). For the PHQ-9, the score ranges from 0 (best) to 27 (worst).

The SF36 score in the intervention group was 78.1 (16.3), compared to 66.9 (21.9) in the control group. The corresponding difference is 11.2 (CI 95%: -0.5 to 22.9), which is not clinically relevant.

 

Psychopathology

Jassil (2023) reported on psychopathology by the Beck Depression Inventory-II (BDI-II). The score ranges from 0 (best) to 63 (worst). Results are also reported in Table 5. None of the reported differences were clinically relevant.

 

Table 5. Mean scores and differences between study groups in psychopathology, measured by BDI-II (Jassil, 2023)

Outcome

Follow-up

Intervention

Control

Mean difference (95%CI)

BDI-II

6 months

8.0 (9.9)

6.0 (8.1)

2.00 (-0.86 to 4.86)

12 months

7.2 (7.5)

7.3 (10.6)

-0.80 (-3.73 to 2.13)

 

Lent (2019) reported on psychopathology by the PHQ-9 after follow-up (16 months). The score ranges from 0 (best) to 27 (worst). The PHQ-9 score in the intervention group was 4.9 (4.5), compared to 6.8 (4.9) in the control group. The corresponding difference is -1.9 (CI 95%: -4.80 to 1.0), which is not clinically relevant.

 

Grilo (2022) reported on the BDI-II. Results are also reported in Table 6. None of the reported differences were clinically relevant.

 

Table 6. Mean scores and differences between study groups in quality of life, measured by BDI-II (Grilo, 2022)

Outcome

Follow-up

Intervention

Control

Mean difference (95%CI)

BDI-II

Post-intervention

7.6 (8.6)

7.4 (8.2)

0.20 (-3.74 to 4.14)

6 months

8.1 (8.1)

7.3 (8.8)

0.80 (-3.27 to 4.87)

12 months

8.5 (8.7)

8.9 (10.7)

-0.40 (-5.21 to 4.41)

24 months

11.1 (10.6)

10.6 (14.6)

0.50 (-5.93 to 6.93)

 

Sockalingham (2023) reported on psychopathology by PHQ-9 and Generalized Anxiety Disorder 7-item scale (GAD-7). For the GAD-7, the score ranges from 0 (best) to 21 (worst).

 

The PHQ-9 score in the intervention group was 2.7 (0.3), compared to 4.7 (0.4) in the control group. The corresponding difference is -2.0 (CI 95%: -2.1 to 1.9), which is not clinically relevant.

 

The GAD-7 score in the intervention group was 2.0 (0.2), compared to 3.5 (0.4) in the control group. The corresponding difference is -1.5 (CI 95%: -1.6 to -1.4), which is not clinically relevant.

 

• Eating disorder

Grilo (2021/2022) reported on the eating-disorder examination (EDE, global score), which is an interview examination. Results are also reported in Table 7. None of the reported differences were clinically relevant.

 

Table 7. Mean scores and differences between study groups in eating disorder, measured by EDE global score (Grilo, 2022)

Outcome

Follow-up

Intervention

Control

Mean difference (95%CI)

EDE

Post-intervention

1.6 (1.0)

1.7 (1.0)

-0.10 (-0.57 to 0.37)

12 months

1.6 (0.9)

1.3 (1.0)

0.30 (-0.16 to 0.76)

24 months

1.6 (1.0)

1.1 (1.1)

0.50 (-0.01 to 1.01)

 

Sockalingham (2023) reported on the Binge Eating Scale (BES). The score ranges from 0 (best) to 46 (worst). The BES score in the intervention group was 6.5 (0.56), compared to 9.1 (0.8) in the control group. The corresponding difference is -2.6 (CI 95%: -2.8 to -2.5), which is considered clinically relevant.

 

Emotional eating

Lent (2019) reported outcomes of the Loss of control over eating scale-brief (LOCES) and Emotional eating scale (EES, of which the subscale depression is reported here). For the LOCES, the score ranges from 5 (best) to 35 (worst). For the EES-depression, the score ranges from 0 (best) to 36 (worst).

 

The LOCES score in the intervention group was 11.1 (3.9), compared to 12.4 (4.9) in the control group. The corresponding difference is -1.3 (CI 95%: -4.0 to 1.4), in favor of the intervention group, which is not clinically relevant.

 

The EES-depression score in the intervention group was 7.1 (4.6), compared to 6.1 (3.9) in the control group. The corresponding difference is 1.0 (CI 95%: -1.69 to 3.69 higher), in favor of the control group, which is not clinically relevant.

A systematic review of the literature was performed to answer the following question:

What is the effectivity of structured lifestyle intervention program (including coaching, with at least a dietary and exercise component) in adult patients with (morbid) obesity who underwent metabolic surgery?

 

Table 1. PICO

Patients

Adult patients with (morbid) obesity who underwent metabolic surgery

Intervention

Structured lifestyle intervention program with at least a dietary and exercise component1

Control

Standard/usual care (only lifestyle advice)

Outcomes

Weight loss, expressed as % Total or Excess Body Weight Loss

Obesity-related complications

Quality of life, psychopathology, emotional eating

Other selection criteria

Study design: systematic reviews and randomized controlled trials

Intervention duration minimally 10 weeks

1Including motivational interviewing, self-monitoring, learning coping strategies, CBT components, stimulus control, behavioral contracts, reward systems, goal-setting techniques, supermarket visits, cooking classes, food diary discussions, strength training, stress management training, mindfulness-based intervention, sleep interventions, emotional eating interventions

 

Relevant outcome measures

The guideline panel considered weight loss as a critical outcome measure for decision making; and obesity-related complications, quality of life, psychopathology and emotional eating as important outcome measures for decision making.

 

A priori, the guideline panel did not define the outcome measures listed above but used the definitions used in the studies.

 

The guideline panel defined the following thresholds as a minimal clinically (patient) important difference: 

  • Weight loss: Absolute difference of 5%.
  • Obesity-related complications:
    • Systolic blood pressure (SBP): 3 mmHg.
    • Diastolic blood pressure (DBP): 2 mmHg.
    • LDL: 5 mg/dL.
    • HDL: 2 mg/dL.
    • HbA1c: 0.5%.
    • Other complications (inc. triglycerides, total cholesterol): 25% difference (RR <0,75 of >1,25).
  • Quality of life (Warkentin, 2014):
    • EuroQoL-5D (EQ-5D) Index: (MCID = 0.03) and EQ-5D Visual Analog Scale (EQ-5D VAS; MCID = 10) (Warkentin, 2014).
    • Impact of Weight on Quality of Life (IWQOL)-Lite total score (MCID = 12)  (Warkentin, 2014).
    • Short Form (SF)-36): Difference of 11.3 point on total score (Longo, 2025).

Psychopathology

    • Beck Depression Inventory (BDI)-II: Difference of 3 points (based on NICE Clinical guideline on Depression, 2004).
    • Patient Health Questionnaire PHQ)-9, with focus on depression: Difference of 3 points (Lynch, 2021).
    • General Anxiety Disorder (GAD)-7: Difference of 4 points (Toussaint, 2020).
    • Eating disorders: 25% difference (RR <0,75 of >1,25) (standard boundaries).
  • Emotional eating: 25% difference (RR <0,75 of >1,25) (standard boundaries).

Search and select (Methods)

A systematic literature search was performed by a medical information specialist using the following bibliographic databases: Embase.com and Ovid/Medline. Both databases were searched from 2005 to the 2nd of December 2025 for systematic reviews and RCTs. Systematic searches were completed using a combination of controlled vocabulary/subject headings (e.g., Emtree-terms, MeSH) wherever they were available and natural language keywords. The overall search strategy was derived from the following primary search concepts: (1) metabolic surgery; (2) combined lifestyle intervention. Duplicates were removed using EndNote software. After deduplication and removing of retracted articles a total of 3216 records were imported for title/abstract screening. Titles and abstracts were screened using the ASReview software. The settings ELAS u4 (TF-IDF and SVM) were used. The articles were subsequently screened by the guideline methodologist, using the following stopping rule: stop after 10% of the total set subsequent exclusions (indicating all relevant articles have been screened). Initially, only systematic reviews until 2020 were selected. A total of 39 studies were selected based on title and abstract screening. After reading the full text, 38 studies were excluded (see the exclusion table under the tab ‘Evidence tabellen’).

Note: The search was performed for both preoperative and postoperative lifestyle intervention around metabolic surgery. The results of preoperative lifestyle interventions are described in another chapter.

 

For the current module on postoperative lifestyle intervention, one systematic review was selected as starting point (Marshall, 2022). This review focused on both preoperative and postoperative intervention. However, none of the included studies could be included in the current literature analysis on postoperative interventions because of the absence of either a dietary or exercise component, a too short intervention period (less than 10 weeks) or a non-randomized design. The literature search for this review (Marshall, 2022) was performed until July 2018.

 

Additionally, selection was performed for RCT’s published in July 2018 or after (n = 952). This selection was also performed with the ASReview software as described above. Initially, 22 studies were selected based on title and abstract screening. After reading the full text, 17 studies were excluded (see the exclusion table under the tab ‘Evidence Tables) and 5 studies were included. Important study characteristics and results are summarized in Table 2. The assessment of the risk of bias is summarized in the risk of bias tables (under the tab ‘Evidence Tables).

  1. Grilo CM, Ivezaj V, Duffy AJ, Gueorguieva R. 24-Month follow-up of randomized controlled trial of guided-self-help for loss-of-control eating after bariatric surgery. Int J Eat Disord. 2022 Nov;55(11):1521-1531. doi: 10.1002/eat.23804. Epub 2022 Aug 24. PMID: 36054766; PMCID: PMC12498257.
  2. Hanvold SE, Vinknes KJ, Løken EB, Hjartåker A, Klungsøyr O, Birkeland E, Risstad H, Gulseth HL, Refsum H, Aas AM. Does Lifestyle Intervention After Gastric Bypass Surgery Prevent Weight Regain? A Randomized Clinical Trial. Obes Surg. 2019 Nov;29(11):3419-3431. doi: 10.1007/s11695-019-04109-7. PMID: 31363961.
  3. Jassil FC, Carnemolla A, Kingett H, Doyle J, Kirk A, Lewis N, Montagut G, Marvasti P, Boniface D, Brown A, Chaiyasoot K, Zakeri R, Mok J, Devalia K, Parmar C, Batterham RL. Impact of nutritional-behavioral and supervised exercise intervention following bariatric surgery: The BARI-LIFESTYLE randomized controlled trial. Obesity (Silver Spring). 2023 Aug;31(8):2031-2042. doi: 10.1002/oby.23814. Epub 2023 Jul 6. PMID: 37415246.
  4. Hecker J, Freijer K, Hiligsmann M, Evers SMAA. Burden of disease study of overweight and obesity; the societal impact in terms of cost-of-illness and health-related quality of life. BMC Public Health. 2022 Jan 7;22(1):46. doi: 10.1186/s12889-021-12449-2. PMID: 34996413; PMCID: PMC8740868.
  5. Lent MR, Campbell LK, Kelly MC, Lawson JL, Murakami JM, Gorrell S, Wood GC, Yohn MM, Ranck S, Petrick AT, Cunningham K, LaMotte ME, Still CD. The feasibility of a behavioral group intervention after weight-loss surgery: A randomized pilot trial. PLoS One. 2019 Oct 21;14(10):e0223885. doi: 10.1371/journal.pone.0223885. PMID: 31634365; PMCID: PMC6802820.
  6. Longo UG, Campi S, De Salvatore S, Piergentili I, Bandini B, Lalli A, Ammendolia V, de Sire A, Papalia R. Minimum clinically important difference of 36-item short form health survey (SF-36) to assess post-surgery quality of life in knee osteoarthritis. J Back Musculoskelet Rehabil. 2025 Jan;38(1):158-164. doi: 10.1177/10538127241296344. Epub 2025 Jan 9. PMID: 39970460.
  7. Lynch CP, Cha EDK, Jenkins NW, Parrish JM, Mohan S, Jadczak CN, Geoghegan CE, Singh K. The Minimum Clinically Important Difference for Patient Health Questionnaire-9 in Minimally Invasive Transforaminal Interbody Fusion. Spine (Phila Pa 1976). 2021 May 1;46(9):603-609. doi: 10.1097/BRS.0000000000003853. PMID: 33290370.
  8. Marshall S, Mackay H, Matthews C, Maimone IR, Isenring E. Does intensive multidisciplinary intervention for adults who elect bariatric surgery improve post-operative weight loss, co-morbidities, and quality of life? A systematic review and meta-analysis. Obes Rev. 2020 Jul;21(7):e13012. doi: 10.1111/obr.13012. Epub 2020 Mar 20. PMID: 32196906.
  9. NCCMH (2004). Depression: Management of Depression in Primary and Secondary Care. British Psychological Society and Royal College of Psychiatrists: Leicester and London
  10. Sockalingam S, Leung SE, Ma C, Tomlinson G, Hawa R, Wnuk S, Jackson T, Urbach D, Okrainec A, Brown J, Sandre D, Cassin SE. Efficacy of Telephone-Based Cognitive Behavioral Therapy for Weight Loss, Disordered Eating, and Psychological Distress After Bariatric Surgery: A Randomized Clinical Trial. JAMA Netw Open. 2023 Aug 1;6(8):e2327099. doi: 10.1001/jamanetworkopen.2023.27099. PMID: 37535357; PMCID: PMC10401302.
  11. Toussaint A, Hüsing P, Gumz A, Wingenfeld K, Härter M, Schramm E, Löwe B. Sensitivity to change and minimal clinically important difference of the 7-item Generalized Anxiety Disorder Questionnaire (GAD-7). J Affect Disord. 2020 Mar 15;265:395-401. doi: 10.1016/j.jad.2020.01.032. Epub 2020 Jan 15. PMID: 32090765.
  12. Warkentin LM, Majumdar SR, Johnson JA, Agborsangaya CB, Rueda-Clausen CF, Sharma AM, Klarenbach SW, Karmali S, Birch DW, Padwal RS. Weight loss required by the severely obese to achieve clinically important differences in health-related quality of life: two-year prospective cohort study. BMC Med. 2014 Oct 15;12:175. doi: 10.1186/s12916-014-0175-5. PMID: 25315502; PMCID: PMC4212133.

Beoordelingsdatum en geldigheid

Publicatiedatum  : 18-08-2026

Beoordeeld op geldigheid  : 18-08-2026

Initiatief en autorisatie

Initiatief:
  • Cluster Obesitas
Geautoriseerd door:
  • Beroepsvereniging Leefstijl Coaches Nederland
  • Nederlandse Vereniging van Diëtisten
  • Nederlandse Vereniging voor Heelkunde
  • Patiëntenfederatie Nederland
  • Vereniging voor Gedragstherapie en Cognitieve Therapie

Samenstelling werkgroep

Voor het ontwikkelen van de richtlijnmodule is in 2023 een multidisciplinair cluster ingesteld. Het cluster Obesitas bestaat uit meerdere richtlijnen (zie hier de actuele clusterindeling). De stuurgroep bewaakt het proces van modulair onderhoud binnen het cluster. De expertisegroepsleden brengen hun expertise in, indien nodig. De volgende personen uit het cluster zijn betrokken geweest bij de herziening van deze module:

 

Clusterstuurgroepleden

  • Prof. dr. E.L.T. (Erica) van den Akker, kinderarts, Erasmus MC Sophia Kinderziekenhuis, NVK (voorzitter)
  • Dr. I.F. (Ian) Faneyte, chirurg, Ziekenhuisgroep Twente, NVvH
  • Dr. S.W. (Simon) Nienhuijs, chirurg, Catharina Ziekenhuis, NVvH
  • E.C. (Esen) Cingir-Doganer, patiëntvertegenwoordiger, Stichting Kind en Ziekenhuis

Betrokken clusterexpertisegroepleden

  • Prof. dr. A. (Anne) Roefs, Hoogleraar psychologie en neurowetenschappen van abnormaal eetgedrag, Universiteit Maastricht, VGCt
  • Drs. I.J. (Inge) Out-Hoiting, leefstijlcoach, BLCN
  • T. (Talitha) Meine Jansen, diëtist, NVD

Met ondersteuning van

  • Dr. A.N. (Anh Nhi) Nguyen, adviseur, Kennisinstituut van Federatie Medisch Specialisten
  • Drs. J.M.H. (Harm-Jan) van der Hart, adviseur, Kennisinstituut van Federatie Medisch Specialisten
  • Drs. F.A. (Fieke) Pepping, junior adviseur, Kennisinstituut van Federatie Medisch Specialisten
  • Drs. E. (Esther) van der Bijl, medisch informatiespecialist, Kennisinstituut van Federatie Medisch Specialisten

Belangenverklaringen

Een overzicht van de belangen van de clusterleden en het oordeel over het omgaan met eventuele belangen vindt u in onderstaande tabel. De ondertekende belangenverklaringen zijn op te vragen bij het secretariaat van het Kennisinstituut van de Federatie Medisch Specialisten via secretariaat@kennisinstituut.nl.

 

Clusterstuurgroepleden

Tabel Gemelde (neven)functies en belangen stuurgroep

Naam

Hoofdfunctie

Nevenwerkzaamheden

Persoonlijke financiële belangen

Extern gefinancierd onderzoek

Intellectuele belangen en reputatie, overige belangen

Restrictie

Prof. dr. E.L.T. (Erica) van den Akker

Kinderarts endocrinoloog Sophia Kinderziekenhuis

NVK vertegenwoordiger in PON (partnerschap overgewicht NL)-onbetaald

Voorzitter projectgroep internationale richtlijn "endocrine aspects of diagnostics and treatment in children and adolescents with obesity"- onbetaald

Coördinator ESPE (european society of pediatric endocrinology) working group on obesity - onbetaald

Coördinator Erasmus MC EASO-COM (European association for studies on obesity- center of management)-onbetaald

Penvoerder NFU accredited Erasmus MC center of expertise for genetic obesity- onbetaald

Coördinator NVK netwerk farmacotherapie expertisegroep obesitas- onbetaald

Lid EndoERN EuRRECa study group on rare obesities-onbetaald

Geen

Klinische trials met setmelanotide voor indicatie genetische obesitas

Rhythm pharmaceuticals; klinische trial met medicament setmelanotide voor indicatie genetische obesitas, projectleider

 

Europese unie Horizon;

OBCT project sity: Biological, socioCultural, and environmental risk TrajectoriesObesity; projectleider

Geen

Restricties t.a.v. besluitvorming over medicamenteuze behandeling van genetische obesitas; vice-voorzitter bij bespreking van onderwerp van voorgenoemde restrictie

Dr. I.F. (Ian) Faneyte

Chirurg in Ziekenhuisgroep Twente (ZGT) en Saxenburgh Medisch Centrum Hardenberg (SMC), aangesloten bij Chirurgencooperatie Oost-Nederland (ChirCON)

Geen

Geen

Geen

Geen

Geen

Dr. S.W. (Simon) Nienhuijs

Chirurg, Catharina Ziekenhuis Eindhoven

Voorzitter DATO (vacatiegelden); bestuurslid DSMBS (onbetaald); commissie HIPEC register (onbetaald)

Geen

PEACH / SWITCH / educational grant Medtronic aan obesitascentrum / REQUEST studie

Geen

Restrictie t.a.v. besluitvorming over plaatsbepaling remote monitoring devices

E.C. (Esen) Cingir-Doganer

Project-/beleidsmedewerker

Stichting Kind en Ziekenhuis

Geen

Geen

Geen

Geen

Geen

 

Betrokken clusterexpertisegroepleden

Tabel Gemelde (neven)functies en belangen expertisegroep

Naam

Hoofdfunctie

Nevenwerkzaamheden

Persoonlijke financiële belangen

Extern gefinancierd onderzoek

Intellectuele belangen en reputatie, overige belangen

Restrictie

Prof. dr. A. (Anne) Roefs

Professor of Psychology & Neuroscience of Abnormal Eating

Maastricht University

Commissiewerk voor NWO

Geen

NWO VICI, NWO Zwaartekrachtproject en ClickNL project

Geen

Geen

Drs. I.J. (Inge) Out-Hoiting

BLCN

vice voorzitter (deels vrijwillig, deels betaald); beleidsadviseur zorg.

ZZP eigenaar Mijn Leefstijl op recept

Eigenaar Mijn Leefstijl op Recept/ Mijn Leefstijl Academie

online leeromgeving voor GLI deelnemers en coaches

Geen

Geen

Geen

Geen

T. (Talitha) Meine Jansen

Dietist

Bestuurslid Netwerk Kinderdietisten, kennisnetwerk van de Nederlandse Verenging van Dietisten

gastdocent bij Hogeschool Arnhem en Nijmegen, op aanvraag als onderdeel binnen post-HBO onderwijs

Geen

Geen

Geen

Geen

 

Betrokken clusterexpertisegroepleden

Tabel Gemelde (neven)functies en belangen expertisegroep

Naam

Hoofdfunctie

Nevenwerkzaamheden

Persoonlijke financiële belangen

Extern gefinancierd onderzoek

Intellectuele belangen en reputatie, overige belangen

Restrictie

Prof. dr. A. (Anne) Roefs

Professor of Psychology & Neuroscience of Abnormal Eating

Maastricht University

Commissiewerk voor NWO

Geen

NWO VICI, NWO Zwaartekrachtproject en ClickNL project

Geen

Geen

Drs. I.J. (Inge) Out-Hoiting

BLCN

vice voorzitter (deels vrijwillig, deels betaald); beleidsadviseur zorg.

ZZP eigenaar Mijn Leefstijl op recept

/ Mijn Leefstijl Academie

online leeromgeving voor GLI deelnemers en coaches

Geen

Geen

Geen

Geen

T. (Talitha) Meine Jansen

Dietist

Bestuurslid Netwerk Kinderdietisten, kennisnetwerk van de Nederlandse Verenging van Dietisten

gastdocent bij Hogeschool Arnhem en Nijmegen, op aanvraag als onderdeel binnen post-HBO onderwijs

Geen

Geen

Geen

Geen

Inbreng patiëntenperspectief

Er werd aandacht besteed aan het patiëntenperspectief door een afgevaardigde van Stichting Kind en Ziekenhuis in de stuurgroep van het cluster. Daarnaast is de module ter commentaar voorgelegd aan de Nederlandse Vereniging voor Overgewicht en Obesitas en de Patiëntenfederatie.

 

Kwalitatieve raming van mogelijke financiële gevolgen in het kader van de Wkkgz

Bij de richtlijnmodule voerden de clusterleden conform de Wet kwaliteit, klachten en geschillen zorg (Wkkgz) een kwalitatieve raming uit om te beoordelen of de aanbevelingen mogelijk leiden tot substantiële financiële gevolgen. Bij het uitvoeren van deze beoordeling is de richtlijnmodule op verschillende domeinen getoetst (zie het stroomschema bij Werkwijze).

 

Module

Uitkomst raming

Toelichting

Postoperatief leefstijltraject

Geen financiële gevolgen

Uit de toetsing volgt dat de aanbevelingen niet breed toepasbaar zijn (<5.000 patiënten) en daarom naar verwachting geen substantiële financiële gevolgen zullen hebben voor de collectieve uitgaven.

Werkwijze

Voor meer details over de gebruikte richtlijnmethodologie verwijzen wij u naar de Werkwijze. Relevante informatie voor de ontwikkeling/herziening van deze richtlijnmodule is hieronder weergegeven.

Volgende:
Psychologie rondom metabole chirurgie