Abstract
Introduction
Constipation and bloating are common bothersome gastrointestinal (GI) symptoms that frequently occur concurrently. It is important to recognize the underlying condition(s) and tailor therapeutic interventions appropriately. This review discusses the evaluation and management of patients with constipation who also have bloating as a predominant symptom.
Discussion
Key areas reviewed are potential etiologies for constipation with bloating and clinical evaluation, including differentiation between common underlying causes such as chronic idiopathic constipation (CIC) and irritable bowel syndrome with constipation (IBS-C). Management approaches discussed include dietary modification, biofeedback, and pharmacologic therapy, including over-the-counter treatments, plecanatide, linaclotide, lubiprostone, tenapanor, neuromodulators, and antibiotics.
Conclusions
Constipation and bloating are common GI symptoms; however, bloating is a relatively nonspecific symptom with a complex pathophysiology. While specifically treating constipation may also improve bloating, this strategy does not improve bloating in all patients. There is a need for additional research to further understand the physiology of bloating. In an era when personalized medicine is becoming increasingly emphasized, understanding the pathophysiology of bloating for an individual patient, be it alongside constipation or other GI and non-GI symptoms, will be paramount to improve treatment outcomes.
Keywords: Bloating, chronic idiopathic constipation, IBS-C, intestinal methanogen overgrowth, irritable bowel syndrome, pelvic floor dysfunction
Key Messages
Patients presenting with constipation, with bloating as a predominant symptom, should be evaluated for underlying conditions, including irritable bowel syndrome with constipation (IBS-C), chronic idiopathic constipation (CIC), pelvic floor dysfunction, and microbial overgrowth (e.g. intestinal methanogen overgrowth), among other causes
If food intolerances are suspected, a trial of dietary restriction, such as a low-fermentable oligosaccharides, disaccharides, monosaccharides, and polyols diet, can be suggested
Improvement in bloating has been demonstrated in large, randomized trials of several gastrointestinal-targeted pharmacologic therapies (e.g. secretagogues) in patients with IBS-C or CIC
Pelvic floor physical therapy with biofeedback should be considered for patients with dyssynergic defecation
Introduction
Constipation and bloating are common bothersome gastrointestinal (GI) symptoms [1,2]. The estimated prevalence of constipation has ranged from 6% to 9% in Asian countries to 15% to 17% in Europe and North America [3]. The estimated prevalence of bloating has ranged from approximately 11% in East Asian countries to approximately 20% in European, Latin American, Middle Eastern, and North American countries [4]. Sociocultural factors likely contribute to differences in patient perception of symptoms and reported prevalence rates [3,5].
Constipation and bloating frequently present concurrently [6,7]. In a global survey of 51,425 people with nonorganic causes of GI symptoms, approximately one-third of individuals reporting constipation with ≥30% of their bowel movements also reported bloating at least once per week [4]. Rates of bloating were higher among individuals with irritable bowel syndrome with constipation (IBS-C) or chronic idiopathic constipation (CIC), with 71% and 36% of these populations, respectively, reporting bloating at least once weekly [4]. In another global survey (N = 20,099), among 10,425 (51.9%) individuals who reported having constipation in the previous 6 months, 65% reported also having bloating/distention [7]. Of note, a study in Italy of patients with IBS-C (n = 369) or CIC (n = 1834) identified substantially higher bloating prevalence rates of 96% and 91%, respectively, based on a 2-week recall period [1]. Although patients may often experience bloating and abdominal distention concurrently, these are distinct phenomena. Distension refers to an objective measurable increase in abdominal girth, whereas bloating refers to a subjective sensation of gassiness or fullness/pressure within the abdomen and does not include visible distension [2]. The underlying pathophysiology of bloating is complex and diverse, as will be discussed latter in the manuscript, whereas abdominal distension may result from an increased volume of gas or stool within the intestines. Abdominophrenic dyssynergia, in which the diaphragm inappropriately contracts and the anterior wall muscles inappropriately relax in response to intestinal gas load, leading to distension, remains an underrecognized cause of abdominal distension, particularly in disorders of gut-brain interaction [8]. Data have shown that both constipation and bloating impair patient health-related quality of life (QoL) [1,9]. Constipation is associated with pronounced detriments to general health, social functioning, and mental health, leading to impairments in health-related QoL that are comparable to those associated with chronic diseases, such as diabetes and osteoarthritis [10]. Chronic constipation has been associated with poor QoL and impaired general well-being [11–13], with a strong negative correlation between symptom severity and QoL [12]. Individuals with CIC experience markedly impaired QoL compared with individuals without constipation [10,14]; likewise, individuals with IBS-C report greater impairments in health-related QoL, work productivity, and activity compared with those without IBS-C [15]. Notably, patients with bloating have impaired QoL, independent of CIC or IBS-C [1]. In a US survey of patients with IBS-C (n = 328) or CIC (n = 552), bloating was reported as a ‘very/extremely bothersome’ symptom in 56% of patients with IBS-C and 46% of patients with CIC (p < 0.03 between the 2 groups) [16]. Additionally, the frequency of bloating was higher in patients with IBS-C vs CIC (2.8 vs 1.4 mean days/week, p < 0.0001). A systematic literature review of studies of CIC that used validated or disease-specific QoL measures, including the Patient Assessment of Constipation Quality of Life questionnaire, concluded that increased intensity of symptoms of constipation, including bloating, correlated with impaired QoL [17].
Given that constipation and bloating are common symptoms that can occur with a range of medical conditions, it is crucial to recognize the underlying condition(s) and tailor therapeutic interventions appropriately. The objective of this narrative review is to highlight key considerations in the evaluation and management of adults with constipation who also have the subjective sensation of bloating as a clinically predominant (i.e. bothersome) symptom.
Methods
PubMed was searched for English-language publications on constipation with bloating during a 10-year period (January 2015 through August 2025). The search string applied was ‘constipation’ AND ‘bloating’ AND (‘irritable bowel syndrome’ OR ‘chronic idiopathic constipation’ OR ‘functional constipation’). For pharmacologic treatments indicated for IBS-C or CIC, evidence was prioritized from randomized controlled trials (RCTs), pooled analyses of RCTs, and meta-analyses. When RCT data were not consistently available (e.g. nonpharmacologic therapies), other clinical trials and meta-analyses were also reviewed. Study appraisal prioritized publications on relevant therapies that reported both constipation and bloating as individual outcomes. Reference lists of all included articles were manually screened to identify additional relevant publications not captured in the primary search. Given the narrative design, a formal risk-of-bias assessment was not performed.
Etiology of constipation with bloating symptoms
Several GI disorders should be considered in an adult experiencing constipation with bloating, including CIC, IBS (predominant constipation [IBS-C] or mixed type [IBS-M]), pelvic floor dysfunction (PFD; e.g. dyssynergic defecation and structural pelvic floor abnormalities), and intestinal microbial overgrowth, specifically intestinal methanogen overgrowth (IMO). Additionally, though bloating can occur in the setting of impaired GI motility, motility disorders, such as gastroparesis and chronic intestinal pseudo-obstruction, are relatively uncommon (Figure 1) [6,18–30]. Non-GI, secondary causes of constipation should also be considered [20]. Constipation may be secondary to or exacerbated by metabolic disorders (e.g. diabetic neuropathy and hypothyroidism), electrolyte imbalances/abnormalities (e.g. hypercalcemia, hypokalemia, and hypomagnesemia), endometriosis, and neurologic disorders (e.g. Parkinson’s disease and small fiber neuropathy), among other causes [20,26–29,31]. Inquiry about prescription and over-the-counter (OTC) product use is important because many commonly administered medications, such as anticholinergics, calcium-containing antacids, opioid analgesics, and dietary supplements (e.g. iron, calcium) may cause constipation [20]. This article focuses on potential GI-related causes; readers seeking additional information on secondary etiologies should consider reviewing these cited references [32–34]. Celiac disease (i.e. autoimmunity characterized by abnormal reaction to gluten in genetically susceptible individuals), nonceliac gluten sensitivity (i.e. reaction to gluten that is not mediated by allergy or autoimmunity), and food intolerance are potential underlying contributors to bloating; however, these conditions more commonly present with diarrhea than constipation [19,35].
Figure 1.
Etiology of constipation with bloating [6,18–29]. CIC: chronic idiopathic constipation; CIPO: chronic intestinal pseudo-obstruction; GI: gastrointestinal; GLP-1: glucagon-like peptide-1; IBS-C: irritable bowel syndrome with constipation; IBS-M: irritable bowel syndrome mixed type; IMO: intestinal methanogen overgrowth; PFD: pelvic floor dysfunction.
Approach to evaluation and management of constipation with bloating
An approach to evaluating and managing a patient presenting with constipation with bloating, including medical history, basic laboratory testing, physical examination, and primary diagnostic considerations, is outlined in Figure 2 [2,19,20,36–39].
Figure 2.
Clinical approach to constipation with bloating [2,19,20,36–39].
aTime frame for criteria is within the previous 3 months, with onset ≥6 months before diagnosis.
bBristol Stool Form Scale Types 1 or 2 [37].
cBristol Stool Form Scale Types 6 or 7 [37].
CBC: complete blood count; CIC: chronic idiopathic constipation; CRC: colorectal cancer; IBS-C: irritable bowel syndrome with constipation; IBS-M: irritable bowel syndrome mixed type; IMO: intestinal methanogen overgrowth; PFD: pelvic floor dysfunction; SIBO: small intestinal bacterial overgrowth.
Evaluation
History and physical
In a patient presenting with constipation and bloating, an initial evaluation should include identification of alarm symptoms (e.g. iron-deficiency anemia of unknown etiology, GI bleeding, vomiting, unintentional loss of >10% of body weight, and a family history of GI cancer or inflammatory bowel disease), as the aforementioned factors should influence testing [2,19]. Diagnostic workup should begin with a detailed history. In women, obstetric history is crucial, given that more than half of women may have PFD within the decade following childbirth [40]. Vaginal delivery, in particular, is associated with an increased risk of PFD [41], potentially due to pudendal nerve damage and persistent functional impairment in the pelvic floor sphincter musculature [42].
A physical, including a digital rectal examination (DRE) is essential, and a comprehensive 10-step approach to a DRE in GI practice has been described previously [43]. A DRE may reveal stricture, spasm, tenderness, mass, blood, and/or presence of stool [21] and can also help identify pertinent structural factors (e.g. rectocele in the anterior wall) [44]. During the DRE, for GI-related assessment, the patient should lie on their left side [43], and they should push and bear down as though having a bowel movement, so the examiner can assess for appropriate anal sphincter and puborectalis muscle relaxation and perineal descent, as well as any obvious extrinsic compression. Simultaneously, the examiner should place their hand on the patient’s abdomen to assess for a strong abdominal push effort. If the examiner does not detect appropriate relaxation of the anal sphincter muscles with the bear-down maneuver, an evacuation disorder should be suspected. To further assess for PFD, the provider may consider testing with high-resolution anorectal manometry (ARM), ideally with balloon expulsion testing. Notably, ARM testing is not widely available, but it is commonly offered at referral practices and academic institutions. If ARM testing is not available, a careful DRE should be performed, as described above, to assess for PFD.
Data suggest that ARM detects the health status (i.e. presence/absence of dyssynergic defection) in only approximately 60% of patients [45,46]. When resources are available, defecography can be considered a first-line diagnostic test to determine whether structural abnormalities contribute to chronic constipation [45]. Additional diagnostic modalities that may be useful in evaluating patients with constipation and bloating include wireless motility capsules (e.g. ingestible gas-sensing capsule) and radionucleotide scintigraphy, which assesses GI transit and motility [47–49].
Constipation and bloating are both characteristic bowel symptoms of PFD [50]. Structural pelvic floor abnormalities (e.g. rectocele, enterocele, and cystocele) can cause obstructed defecation [51–53], which, in turn, may contribute to bloating. Clinically relevant rectoceles (>2 cm) are common in women with constipation and can impair rectal emptying, particularly when large in size [30]. Even in patients with constipation who do not exhibit overt outlet obstruction, it is important to consider dyssynergic defecation when bloating is a predominant symptom. Dyssynergic defecation is a type of PFD characterized by impaired coordination between the pelvic floor muscles, anal sphincter, and abdominal wall during attempted defecation [20]. Symptoms most predictive of dyssynergic defecation include a sense of incomplete evacuation or blockage, excessive straining, and the use of digital maneuvers [54]. Abdominal bloating is also common in this population and is reported as occurring ‘often’ to ‘always’ by almost three-fourths of patients [55]. Additionally, patients may have urinary or sexual symptoms (i.e. dyspareunia) that are associated with other conditions under the umbrella term of PFD [21].
Of interest, a 2024 study in patients with chronic constipation identified a minimally invasive and reliable approach for determining which individuals may benefit from early referral to biofeedback. Two findings were strongly associated with dyssynergic defection: (1) failed anal relaxation during simulated defection on DRE, particularly when abdominal palpation is added during straining, and (2) response of ‘anal muscles’ when asked, ‘What muscles do you mainly use when you push to defecate?’ [56].
After obtaining a detailed medical history and conducting a comprehensive physical exam, a basic laboratory workup could be considered, especially in patients who have not had recent testing. This may include a complete blood count, a comprehensive metabolic panel, thyroid function tests (i.e. thyroid-stimulating hormone and free thyroxine levels), and celiac screening [57] (i.e. tissue transglutaminase immunoglobulin A and total serum immunoglobulin A levels). These evaluations may be performed in a primary care or specialty setting as part of the initial diagnostic assessment. It is important, however, to tailor laboratory testing to the individual, as not all patients require the same level of investigation.
IBS and CIC
Differentiation among IBS-C, IBS-M, and CIC as potential underlying causes of constipation with bloating is important (see Figure 2 for diagnostic criteria). IBS-C and CIC have multiple overlapping symptoms; however, a key point of distinction is that patients with IBS, by definition, have recurrent abdominal pain, whereas pain is not fundamental to the diagnosis of CIC [36]. When pain is present in CIC, it is relatively less frequent and less intense. Patients with IBS-C also report a higher frequency and intensity of bloating compared with individuals with CIC [58].
Other considerations
Colonoscopy may be advised for patients who are not current with age-appropriate screening for colorectal cancer, but it would not be recommended for evaluation of bloating and constipation symptoms, particularly without alarm features, in a young, otherwise healthy individual. In patients in whom dyssynergic defecation is ruled out, a colonic transit study (e.g. Sitz marker test) may be considered, if available, to assess for slow-transit constipation or colonic inertia; however, this is a relatively uncommon condition [20,24]. In patients with clear risk factors for intestinal microbial overgrowth (e.g. conditions associated with abnormal small intestinal motility or anatomic abnormalities such as small bowel diverticula or procedures including surgeries of the ileocecal valve and Roux-en-Y gastric bypass) [59] or severe symptoms, breath testing (utilizing glucose or lactulose as substrate) may be warranted [19,59]. While both IMO and small intestinal bacterial overgrowth (SIBO) are associated with bloating, IMO has a much stronger association with constipation than SIBO [18,59–61]. Methanobrevibacter smithii is the predominant methanogen in the human GI tract, and in patients with IMO, M. smithii produces excess methane, which causes bloating, distention, and worsening constipation [18,60,62–64].
Breath testing is a noninvasive diagnostic tool that may be considered in select patients with supportive clinical features and a high symptom burden, although its use is supported by limited evidence. Because there is a lack of consensus on optimal cutoff times, diagnostic thresholds, and substrate dosing, routine breath testing may not be warranted for the evaluation of bloating/distention, unless a patient has clear risk factors or severe symptoms [2,19]. Glucose and lactulose are the primary substrates used for breath testing; glucose, due to its rapid absorption, is associated with fewer false-positive results, although false positives can still occur [65–67]. Exhaled breath hydrogen and methane serve as biomarkers of metabolically active gut microbes – a hydrogen-predominant result suggests SIBO and a methane-predominant result indicates IMO [65,66]. In patients with IBS-C, bloating may be caused by IMO, and the North American consensus document recommends a diagnostic methane threshold of ≥10 parts per million at any time point during testing [61]. A 2022 study showed high sensitivity and specificity for diagnosing IMO using a methane threshold of ≥10 parts per million [68]. However, the optimal criterion for defining excessive methane production is still being debated, and further validation studies are warranted [61].
Key limitations of breath testing include its indirect measurement of microbial overgrowth, reliance on patient adherence to pretesting preparation protocols (e.g. avoidance of fermentable foods for 24 h and avoidance of exercise and smoking on test day), and impaired substrate transit in those with comorbid conditions, such as gastroparesis [66]. For SIBO, variable orocecal transit time can further confound interpretation [65]. Clinically, IMO can only be diagnosed with breath testing, whereas SIBO may also be diagnosed by small bowel aspirate. However, aspirate culture, often described as the gold standard, is rarely performed due to its invasiveness, susceptibility to contamination from oropharyngeal or gastric flora [66,69], and the fact that >60% to 70% of gut microbes cannot be identified or cultured using conventional techniques [69,70]. The lack of a validated gold standard test for diagnosing SIBO has been identified as a key challenge in breath testing [61]. Notably, diagnostic criteria for methane breath tests have never been validated [71]. Several recent publications further delve into the role of breath testing, including controversies [66,67,71].
For patients with a high pretest probability of celiac disease (e.g. first-degree relative with the condition, presence of associated autoimmune disorders), serologic testing using tissue transglutaminase and immunoglobulin A is warranted [2,72]. Although celiac disease is typically associated with diarrhea rather than constipation, health care providers should consider serologic testing for celiac disease if a patient with constipation continues to have persistent bloating after initiation of treatment (see the Management section below) [2,36].
Management
Several treatment options are available to manage symptoms in patients with constipation and bloating. Interventions include dietary modification, pharmacologic treatments, and psychotherapeutic approaches (e.g. cognitive-behavioral therapy [CBT] or gut-directed hypnotherapy for IBS; biofeedback for dyssynergic defecation) [2,39,73–75]. It has been suggested that certain OTC products for constipation, including psyllium fiber and the laxative polyethylene glycol, may worsen bloating [76,77]; however, a minimal or neutral impact on bloating has also been described [78–80]. That said, soluble fiber and polyethylene glycol have favorable safety profiles and may be considered reasonable first-line treatments for patients with constipation and bloating.
Dietary modification
If food intolerance is suspected, a brief (e.g. 2-week) trial of dietary restriction can be employed to assess for resolution of symptoms [19]. However, dietary restriction should generally be avoided in individuals with a history of an eating disorder (e.g. avoidant restrictive food intake disorder) and approached with caution in those at increased risk for disordered eating [81]. The low-fermentable oligosaccharides, disaccharides, monosaccharides, and polyols (FODMAP) diet has been shown to improve bloating and distention in patients with IBS as well as non-IBS etiologies [2,82–84]. If symptom resolution does not occur during the trial, the diet should be discontinued and other treatment options considered [81]. If symptoms improve, the global restriction of FODMAP intake should be continued for a total of 4 to 8 weeks before transitioning to the gradual reintroduction phase. During reintroduction, previously eliminated foods are methodically added back while monitoring for recurrence of symptoms, with the goal of avoiding nutritional deficiencies [85].
Practical challenges of the low-FODMAP diet include patients finding it too complicated to follow, as well as it being expensive and unpalatable [86]. In a study of individuals with IBS (n = 131) or inflammatory bowel disease (n = 49), approximately one-quarter (26%) of the participants with IBS discontinued the diet before completing the initial dietary period, and fewer than half (47%) remained on it at follow-up (median, 15 months) [86]. Long-term maintenance is particularly difficult, given the extent of food exclusions and the protracted nature of the weekly food reintroduction process [87]. An umbrella review of 16 low-FODMAP diet meta-analyses of approximately 10,000 adults with IBS reported reduced overall symptom severity and improved QoL [88]. However, no statistically significant effect was demonstrated on key symptoms, including bloating and bowel movement frequency, and the majority of data were from short-term trials with variable adherence reporting.
Because reducing consumption of high FODMAP fruits and vegetables can decrease fiber intake, some patients may be at risk of constipation unless the restricted items are replaced with lightly fermentable, high-fiber alternatives (e.g. oat or rice bran) [85]. Notably, the 2021 guideline from the American College of Gastroenterology recommends that soluble, but not insoluble, fiber be used to treat global IBS symptoms [89]. This recommendation may be particularly helpful for patients with IBS-C, as fiber may improve stool frequency and viscosity. However, the data supporting this rationale in IBS-C is considered weak [89].
Collaboration with a skilled, qualified dietician is essential to guide patients through the restriction and reintroduction phases of the low FODMAP diet, ensure adequate nutrition, and support long-term diet personalization. While the role of gluten in bloating is less established than that of FODMAPs [2], a gluten-free diet should be instituted, under the guidance of a dietician, in patients with confirmed celiac disease. In cases in which nonceliac gluten sensitivity is suspected, a gluten-free diet can be implemented for at least 2 weeks to assess symptom improvement, followed by a gluten challenge for diagnostic confirmation [19,35].
In 2025, the British Dietetic Association published the first evidence-based guidelines on the dietary management of chronic constipation in adults [78]. Among the dietary options recommended as effective for constipation, psyllium supplements, select probiotic strains, and kiwifruit did not demonstrate an effect on bloating, whereas administration of magnesium oxide supplements was associated with reduced bloating severity in patients with constipation [78,90]. The guidelines did not recommend whole diet approaches, such as a high-fiber diet, because of insufficient evidence supporting their efficacy [78].
Pharmacologic treatments indicated for the management of IBS-C and CIC
Several medications indicated for the treatment of IBS-C and/or CIC have had findings reported for the treatment of bloating, independent of constipation symptom management (Table 1) [74,91–102]. Of note, a meta-analysis (n = 13 trials; 10,091 patients) affirmed the effectiveness of prosecretory agents as an overall class for the treatment of bloating in patients with IBS-C [73]. The secretagogue plecanatide, a guanylate cyclase-C agonist indicated for the treatment of IBS-C and CIC in adults, was evaluated in two identically designed, phase 3, randomized, double-blind, placebo-controlled trials in patients with IBS-C [74]. In a pooled analysis, plecanatide 3 mg once daily for 12 weeks significantly improved bloating from baseline compared with placebo as early as Week 1, with sustained significant improvement across the 12-week treatment period (p < 0.001) [74]. Plecanatide was also evaluated in two identically designed, phase 3, randomized, double-blind, placebo-controlled trials in patients with CIC [95,96]. In both trials, plecanatide 3 mg once daily for 12 weeks significantly improved bloating versus placebo (p < 0.01) [95,96]. A set of subgroup analyses from these trials, of individuals meeting criteria for severe constipation, reported significant reductions in bloating with plecanatide 3 mg versus placebo in both IBS-C (p = 0.001) and CIC (p < 0.001) [100].
Table 1.
Impact on bloating: pharmacologic agents indicated for IBS-C and/or CIC.
| Pharmacologic agent | Mechanism | Population(s) | Impact on bloatinga |
|---|---|---|---|
| Plecanatide [74,95,96,100] | Guanylate cyclase-C agonist | IBS-C; CIC |
|
| Linaclotide [91,92,97,98] | Guanylate cyclase-C agonist | IBS-C; CIC |
|
| Lubiprostone [93,99] | Chloride channel activator | IBS-C; CIC |
|
| Tenapanor [94,102] | Sodium/hydrogen exchanger isoform 3 inhibitor | IBS-C |
|
| Prucalopride [101] | Prokinetic selective serotonin-4 receptor agonist | CICb |
|
a”Significant” refers to comparisons of active treatment with placebo with p values < 0.05 in clinical trials or pooled analyses.bIndividuals with moderate to very severe bloating. CIC: chronic idiopathic constipation; IBS-C: irritable bowel syndrome with constipation.
Another guanylate cyclase-C agonist, linaclotide, which is indicated for the treatment of IBS-C and CIC in adults and functional constipation in patients aged 6–17 years, was evaluated in two phase 3, double-blind, placebo-controlled IBS-C trials – a 12-week study and a 26-week study [91,92]. Both studies reported significant improvement from baseline in bloating with linaclotide 290 µg once daily compared with placebo (p < 0.0001) [91,92]. Additionally, two randomized, double-blind, placebo-controlled CIC trials reported that linaclotide 145 µg significantly improved bloating versus placebo (p < 0.01) [97]. In a randomized, double-blind, 12-week, placebo-controlled CIC trial in individuals with moderate to severe bloating, a significantly greater improvement from baseline in bloating was observed for linaclotide 145 µg versus placebo (p < 0.001) [98].
The chloride channel activator lubiprostone, indicated for the treatment of women with IBS-C, adults with CIC, and adults with opioid-induced constipation and chronic noncancer pain, was evaluated in two phase 3, randomized, double-blind, placebo-controlled IBS-C trials [93]. Significant improvement from baseline in bloating was noted with lubiprostone 8 µg twice daily for 12 weeks compared with placebo at Month 2 (p = 0.04) but not at Months 1 or 3 (pooled analysis). A meta-analysis (n = 9 trials) of 2309 patients with IBS-C or CIC treated with lubiprostone (dose range, 24–72 µg daily) reported that improvement in bloating was significantly greater with lubiprostone versus placebo (both conditions pooled; p < 0.001) [99]. However, when analyzed by condition, improvement in bloating with lubiprostone versus placebo was significant in patients with CIC (n = 900; p = 0.004) but not in those with IBS-C (n = 1409; p = 0.05) [99].
Tenapanor, the sodium/hydrogen exchanger isoform 3 inhibitor, is indicated for the treatment of IBS-C in adults and was evaluated in phase 3, double-blind, placebo-controlled trials lasting 12 and 26 weeks [94,102]. The 12-week study (n = 629) examined the impact of tenapanor 50 mg twice daily on bloating and identified that the bloating responder rate (≥30% improvement from baseline in average weekly score for ≥6 of 12 weeks) was significantly higher for tenapanor compared with placebo (p = 0.014), whereas the 26-week study did not evaluate tenapanor on the individual symptoms of bloating.
The prokinetic selective serotonin-4 receptor agonist prucalopride is indicated for the treatment of CIC in adults and was evaluated in a post hoc analysis of randomized, double-blind, placebo-controlled CIC trials (five phase 3 trials; one phase 4 trial) in 1931 patients with moderate to very severe bloating at baseline [101]. An approximately 20% greater improvement from baseline in bloating scores was observed with prucalopride 2 mg once daily compared with placebo during Weeks 2 through 12 (p values were not provided) [101].
Neuromodulators
Neuromodulators (e.g. antidepressants) have been shown to improve bloating in patients with IBS (including IBS-C and IBS-M), but data have generally been limited to small trials (<50 patients) [103,104]. In an RCT of patients with IBS-C (n = 44), the selective serotonin reuptake inhibitor fluoxetine 20 mg daily for 12 weeks significantly improved both constipation and bloating compared with placebo (p < 0.05) [103]. The largest RCT of tricyclic antidepressants (TCAs) in the management of IBS (ATLANTIS; Amitriptyline at Low-Dose and Titrated for Irritable Bowel Syndrome as Second-Line Treatment) included 463 patients with IBS (17% IBS-C, 41% IBS-M, 39% IBS-D, 3% unsubtyped) treated with amitriptyline (10–30 mg/day) or placebo for 6 months [105]. A significant decrease was observed for amitriptyline versus placebo in the IBS severity scoring system score and adequate relief of IBS symptoms (both p = 0.008). However, effects on abdominal distension were not statistically significant, and outcomes specific to bloating were not reported. Because the anticholinergic properties of tertiary amine TCAs such as amitriptyline and imipramine may worsen constipation, it has been proposed that neuromodulators with a lower potential to reduce intestinal motility, such as secondary amine TCAs (e.g. desipramine, nortriptyline) or serotonin-norepinephrine reuptake inhibitors (e.g. duloxetine, venlafaxine) may be more appropriate for patients with IBS-C, although supporting data remain limited [106,107].
Nonpharmacologic mechanical stimulation and neural modulation
Data are limited on the efficacy of mechanical and neuronal stimulation modalities for treating constipation with bloating. Direct mechanical stimulation of the colon using a vibrating capsule, indicated for the treatment of CIC in adults, did not improve mean bloating scores from baseline at Week 8 versus a placebo capsule (−0.3 vs −0.2; p = 0.55) in a phase 3 randomized trial of 312 adults with CIC (1 capsule/day, 5 days/week, for 8 weeks) [108]. Investigational therapies, including transabdominal electrical stimulation (randomized, double-blind, sham-controlled phase 3 trial) and sacral neuromodulation (randomized, open-label trial versus conservative treatment) have been evaluated in patients with chronic constipation, but changes in the symptom of bloating were not reported [109,110]. A preliminary nonrandomized trial of 55 women with chronic constipation refractory to biofeedback reported that sacral nerve stimulation improved both constipation and abdominal bloating [111]; however, a meta-analysis of RCTs demonstrated only marginal relief of constipation [112].
Antibiotic treatment for IMO
For patients diagnosed with IMO, combination antibiotic regimens can be considered, although the evidence base is limited [19] and practices vary. In one small (n = 32) randomized, double-blind, placebo-controlled trial of patients with IBS-C who had a methane-positive breath test result (i.e. indicative of IMO), treatment with the nonsystemic antibiotic rifaximin 1650 mg plus neomycin 1000 mg for 2 weeks significantly improved the severity of constipation (p < 0.001) and bloating (p = 0.02) from baseline compared with treatment with neomycin (plus placebo) over the course of the 4-week study [63]. Of interest, 10 of 15 patients treated with rifaximin plus neomycin had methane levels ≤3 ppm posttreatment and significantly lower constipation severity compared with those who had methane levels >3 ppm at the last visit (p = 0.02).
Use of antibiotics may be limited by concerns regarding the risk of Clostridioides difficile colitis and antimicrobial resistance, although the risk may be reduced with targeted, short-term treatment regimens. Because neomycin has the potential to cause ototoxicity and nephrotoxicity, even with short-term oral dosing, patients should be monitored for proteinuria, elevations in serum creatinine levels, and decreases in auditory acuity, with immediate discontinuation of therapy if toxicity is suspected. For patients who are not candidates for antibiotic therapy, it has been suggested that a 2-week course of an elemental diet (typically consisting of free amino acids, medium-chain triglycerides, monosaccharides or easily digestible saccharide polymers, and required vitamins/minerals) may provide some symptom benefit [113,114].
Psychotherapeutics
Several psychotherapeutics have been investigated for the management of IBS, including CBT (e.g. in-person, teleconference, self-administered/minimal contact, and group CBT), contingency management, dynamic psychotherapy, gut-directed hypnotherapy, stress management, and face-to-face multicomponent psychological therapy [39]. A meta-analysis of psychological therapies for IBS (n = 41 randomized clinical trials; 4072 participants) concluded that while several therapies showed efficacy, CBT and gut-directed hypnotherapy had a greater evidence base and long-term improvement in IBS symptoms [39]. Individual symptom (e.g. bloating) data are limited [115,116] because studies of psychological therapies in IBS typically have focused on global, rather than distinct, symptom outcome measures [117–122]. Of interest, a 2025 pilot trial that assessed a 12-week, self-guided hypnotherapy program in 25 patients with nonorganic GI disorders (e.g. functional bloating/distention, IBS, or functional dyspepsia) with predominant chronic bloating reported that bloating scores were significantly reduced from baseline to end of treatment (p = 0.003) and that 69.6% of patients had a treatment response (≥30% reduction from baseline) for bloating [123]. Although the effects of hypnotherapy on bloating were promising, the findings were limited by the small sample size and lack of a control group [123]. Questions have been raised regarding the lack of oversight governing hypnotherapy practice and insufficient training of some practitioners delivering gut-directed hypnotherapy [124].
Biofeedback may be considered for treatment of constipation in patients with dyssynergic defecation; however, long-term data are limited [125,126]. In patients with PFD and constipation, biofeedback to teach relaxation of the pelvic floor and anal sphincter muscles increased bowel movement frequency and reduced straining and bloating frequency [75]. After five weekly sessions, patients with constipation due to PFD/dyssynergia (n = 34) had significantly greater improvements from baseline in stool frequency (p < 0.001) and bloating frequency (p < 0.01) per week at 1-, 6-, and 12-month follow-up compared with patients with constipation due to slow transit in the absence of dyssynergia (n = 12) [75]. Another study of 50 patients with constipation due to PFD (n = 36), slow transit (n = 8), or mixed etiology (n = 6) reported that biofeedback (electromyography- or manometry-based) 2 times weekly (total, five sessions) significantly reduced the percentage of patients with ‘difficult evacuation’ (i.e. constipation), from all patients at baseline to fewer than 35% at both 10 days and 1 year after completion of biofeedback sessions (p < 0.01 for both timepoints) [127]. Similarly, the percentage of patients with symptoms of ‘distension or bloating’ was significantly reduced, from 84% of patients at baseline to ≤30% after biofeedback (p < 0.05 for both timepoints). Furthermore, in a trial of 156 patients with a disorder of gut-brain interaction and severe bloating as a primary complaint, 105 (67.3%) patients did not respond to dietary advice, and 104 underwent a standardized balloon expulsion test [128]. Of the 67 (64.4%) who failed the balloon expulsion test, 65 underwent pelvic floor biofeedback therapy. After therapy, 53.8% of the 65 patients experienced fair improvement or major improvement/cure (i.e. responded [score, 3 or 4 on a 0- to 4-point scale]), and all responders had at least a 50% reduction in bloating intensity. Collectively, these findings support the potential utility of pelvic floor biofeedback in individuals with PFD experiencing constipation and/or bloating. However, the evidence is limited by relatively small sample sizes, lack of a control group, and short duration of follow-up. Outcomes may be further impacted by therapist skill and experience, as well as variability in the specific training techniques implemented [75]. For patients with PFD who do not respond to or are not candidates for biofeedback, sacral neuromodulation, discussed previously, has been suggested as a safe alternative [129,130].
Discussion
Although constipation and bloating are both common GI symptoms that present together, bloating is a relatively nonspecific symptom with a complex pathophysiology. For example, while bloating in the presence of constipation can occur as the result of luminal distension of the intestines by excess stool and gas, there can be other factors, such as visceral hypersensitivity and alterations in the gut microbiome, as well as dietary and psychological influences, which can affect symptom presentation in the individual patient. Thus, while simply treating constipation via the use of medications (such as a secretagogue, chloride channel activator, or sodium/hydrogen exchanger isoform 3 inhibitor) or pelvic floor physical therapy (with biofeedback therapy in the setting of PFD) can improve bloating, unfortunately, effective treatment of constipation does not resolve bloating for all patients. In these cases, there is likely another underlying factor(s) contributing to the manifestation of bloating symptoms. Therefore, there is a need for additional research aimed at understanding the physiology of bloating to improve treatment options for patients with and without constipation.
Because bloating is common in patients with disorders of gut-brain interaction, such as IBS and functional dyspepsia, it is reasonable to hypothesize that interventions focused on modulating the brain-gut axis, such as neuromodulators and psychological therapies (e.g. CBT and hypnotherapy), as well as other novel techniques (e.g. virtual reality) are treatment strategies ripe for further exploration with regard to the treatment of bloating. Additionally, the identification of other pathophysiological causes of bloating, such as altered intestinal barrier function and colonic dysbiosis, may help to identify new treatment targets for bloating. Furthermore, while SIBO and increasingly IMO are being considered in the diagnostic strategy for patients with bloating, the true prevalence among patients with bloating as a predominant symptom is unknown. Substantial debate surrounds the ideal testing parameters (i.e. breath testing) for accurate diagnosis of SIBO and IMO. Additional research is needed to better understand the true prevalence of SIBO and IMO in patients with bloating as a primary symptom, as well as to clarify ideal testing strategies to allow for more educated and judicious use of antibiotic treatment in clinical practice. Finally, while patients often attribute symptoms of bloating to diet, many fail to achieve adequate symptom relief with various diet elimination trials. A low FODMAP diet currently has the best evidence for use as a diet strategy to manage symptoms of IBS, including bloating, but it does not work for all patients. For example, data are lacking regarding the utility of the low FODMAP diet to manage specific symptoms of IBS-C. Based on available evidence, no diet can be universally recommended for the treatment of bloating as a primary symptom. Further research assessing diet to treat bloating, particularly in the setting of constipation, is needed. In an era when personalized medicine is more commonly emphasized, understanding how and why bloating presents in an individual patient (whether with constipation or other concomitant GI and non-GI symptoms) will be paramount to improve treatment outcomes for this common, frequently vexing symptom.
Conclusions
Constipation and bloating are common GI symptoms that frequently occur together. While the etiology for constipation and bloating is diverse, specific GI causes that should be considered in the evaluation of bloating and constipation include CIC, IBS-C, IBS-M, PFD, and IMO. In cases for which food intolerance is suspected, a 2-week trial of dietary restriction to assess response (e.g. low FODMAP diet) can be considered, ideally with the assistance of a qualified dietician. Furthermore, soluble fiber and polyethylene glycol are safe and reasonable first-line treatment considerations. Among pharmacologic options, secretagogues indicated for the treatment of IBS-C and CIC have demonstrated significant improvements in constipation and bloating symptoms in robust RCTs. Other treatments that may have a role for patients with constipation and bloating include antibiotics (bacterial overgrowth), psychotherapeutic approaches (IBS-C), and pelvic floor physical therapy with biofeedback (PFD); however, data are relatively limited, and more well-designed RCTs are needed. An individualized approach, based on available evidence, is advised to best address the common and frequently bothersome symptoms of constipation and bloating.
Looking ahead, additional research is needed to better understand the prevalence of SIBO and IMO in patients with bloating, as these remain popular and oft-debated topics in the field of gastroenterology and the true prevalence of these conditions remains unclear. Further studies are needed to establish the most effective treatment strategies for microbial overgrowth conditions, such as SIBO and IMO. In addition, clinical trials evaluating new therapeutic approaches for bloating – particularly dietary interventions, neuromodulators, and psychologically based therapies – would be valuable, as these modalities are likely to play an increasingly prominent role in managing bloating and constipation in the future.
Acknowledgments
Editorial assistance and medical writing assistance were provided, under the direction of the authors, by Katie Singh, PharmD, and Mary Beth Moncrief, PhD, Synchrony Medical Communications, LLC, West Chester, PA, with funding from Salix Pharmaceuticals, Bridgewater, NJ. Support for development of this manuscript was provided by Salix Pharmaceuticals in the form of editorial assistance and medical writing assistance supplied by Synchrony Medical Communications, LLC, and payment of relevant publication charges. AP Laitman and O Faiman received salaries as employees of Salix Pharmaceuticals. Other than these authors, Salix Pharmaceuticals did not actively contribute to content or have a role in the decision to submit, but reviewed for medical accuracy. The authors did not receive any financial compensation for manuscript development, and there was no additional funding related to this work.
Funding Statement
No funding was received for this work.
Disclosure statement
DJ Cangemi reports having no competing interests to declare.
AP Laitman and O Faiman are employees of Salix Pharmaceuticals.
BW Chang reports having no competing interests to declare.
Data availability statement
Data sharing is not applicable to this article, as no data were created or analyzed in this research.
References
- 1.Neri L, Iovino P, Laxative Inadequate Relief Survey (LIRS) Group . Bloating is associated with worse quality of life, treatment satisfaction, and treatment responsiveness among patients with constipation-predominant irritable bowel syndrome and functional constipation. Neurogastroenterol Motil. 2016;28(4):581–591. doi: 10.1111/nmo.12758. [DOI] [PubMed] [Google Scholar]
- 2.Lacy BE, Cangemi D, Vazquez-Roque M.. Management of chronic abdominal distension and bloating. Clin Gastroenterol Hepatol. 2021;19(2):219–231.e1. doi: 10.1016/j.cgh.2020.03.056. [DOI] [PubMed] [Google Scholar]
- 3.Chuah KH, Mahadeva S.. Cultural factors influencing functional gastrointestinal disorders in the East. J Neurogastroenterol Motil. 2018;24(4):536–543. doi: 10.5056/jnm18064. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Ballou S, Singh P, Nee J, et al. Prevalence and associated factors of bloating: results from the Rome Foundation Global Epidemiology Study. Gastroenterology. 2023;165(3):647–655.e4. doi: 10.1053/j.gastro.2023.05.049. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Gwee KA, Gonlachanvit S, Ghoshal UC, et al. Second Asian consensus on irritable bowel syndrome. J Neurogastroenterol Motil. 2019;25(3):343–362. doi: 10.5056/jnm19041. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Said H, Nee J, Iturrino J, et al. Clinical characteristics of patients presenting with bloating as a predominant symptom. J Clin Gastroenterol. 2023;57(8):830–834. doi: 10.1097/MCG.0000000000001767. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Lacy BE, Delfini R, Fladung B, et al. Prevalence and patterns of laxative use in subjects with self-reported constipation: results from a multinational digestive health survey. Ther Adv Gastroenterol. 2024;17:17562848241232605. doi: 10.1177/17562848241232605. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Damianos JA, Tomar SK, Azpiroz F, et al. Abdominophrenic dyssynergia: a narrative review. Am J Gastroenterol. 2023;118(1):41–45. doi: 10.14309/ajg.0000000000002044. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Pinto Sanchez MI, Bercik P.. Epidemiology and burden of chronic constipation. Can J Gastroenterol. 2011;25 Suppl B(Suppl B):11B–15B. doi: 10.1155/2011/974573. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Belsey J, Greenfield S, Candy D, et al. Systematic review: impact of constipation on quality of life in adults and children. Aliment Pharmacol Ther. 2010;31(9):938–949. doi: 10.1111/j.1365-2036.2010.04273.x. [DOI] [PubMed] [Google Scholar]
- 11.Sun SX, Dibonaventura M, Purayidathil FW, et al. Impact of chronic constipation on health-related quality of life, work productivity, and healthcare resource use: an analysis of the National Health and Wellness Survey. Dig Dis Sci. 2011;56(9):2688–2695. doi: 10.1007/s10620-011-1639-5. [DOI] [PubMed] [Google Scholar]
- 12.Glia A, Lindberg G.. Quality of life in patients with different types of functional constipation. Scand J Gastroenterol. 1997;32(11):1083–1089. doi: 10.3109/00365529709002985. [DOI] [PubMed] [Google Scholar]
- 13.O’Keefe EA, Talley NJ, Zinsmeister AR, et al. Bowel disorders impair functional status and quality of life in the elderly: a population-based study. J Gerontol A Biol Sci Med Sci. 1995;50(4):M184–M189. doi: 10.1093/gerona/50a.4.m184. [DOI] [PubMed] [Google Scholar]
- 14.Wald A, Sigurdsson L.. Quality of life in children and adults with constipation. Best Pract Res Clin Gastroenterol. 2011;25(1):19–27. doi: 10.1016/j.bpg.2010.12.004. [DOI] [PubMed] [Google Scholar]
- 15.DiBonaventura M, Sun SX, Bolge SC, et al. Health-related quality of life, work productivity and health care resource use associated with constipation predominant irritable bowel syndrome. Curr Med Res Opin. 2011;27(11):2213–2222. doi: 10.1185/03007995.2011.623157. [DOI] [PubMed] [Google Scholar]
- 16.Heidelbaugh JJ, Stelwagon M, Miller SA, et al. The spectrum of constipation-predominant irritable bowel syndrome and chronic idiopathic constipation: US survey assessing symptoms, care seeking, and disease burden. Am J Gastroenterol. 2015;110(4):580–587. doi: 10.1038/ajg.2015.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Nag A, Martin SA, Mladsi D, et al. The humanistic and economic burden of chronic idiopathic constipation in the USA: a systematic literature review. Clin Exp Gastroenterol. 2020;13:255–265. doi: 10.2147/CEG.S239205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Mehravar S, Takakura W, Wang J, et al. Symptom profile of patients with intestinal methanogen overgrowth: a systematic review and meta-analysis. Clin Gastroenterol Hepatol. 2025;23(7):1111–1122.e9. doi: 10.1016/j.cgh.2024.07.020. [DOI] [PubMed] [Google Scholar]
- 19.Moshiree B, Drossman D, Shaukat A.. AGA Clinical Practice Update on evaluation and management of belching, abdominal bloating, and distention: expert review. Gastroenterology. 2023;165(3):791–800.e3. doi: 10.1053/j.gastro.2023.04.039. [DOI] [PubMed] [Google Scholar]
- 20.Wilkinson JM, Cozine EW, Loftus CG.. Gas, bloating, and belching: approach to evaluation and management. Am Fam Physician. 2019;99(5):301–309. [PubMed] [Google Scholar]
- 21.Rao SSC, Patcharatrakul T.. Diagnosis and treatment of dyssynergic defecation. J Neurogastroenterol Motil. 2016;22(3):423–435. doi: 10.5056/jnm16060. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Jiang X, Locke GR, III, Choung RS, et al. Prevalence and risk factors for abdominal bloating and visible distention: a population-based study. Gut. 2008;57(6):756–763. doi: 10.1136/gut.2007.142810. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Parkman HP, Sharkey E, McCallum RW, et al. Constipation in patients with symptoms of gastroparesis: analysis of symptoms and gastrointestinal transit. Clin Gastroenterol Hepatol. 2022;20(3):546–558.e5. doi: 10.1016/j.cgh.2020.10.045. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Frattini JC, Nogueras JJ.. Slow transit constipation: a review of a colonic functional disorder. Clin Colon Rectal Surg. 2008;21(2):146–152. doi: 10.1055/s-2008-1075864. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Gabbard SL, Lacy BE.. Chronic intestinal pseudo-obstruction. Nutr Clin Pract. 2013;28(3):307–316. doi: 10.1177/0884533613485904. [DOI] [PubMed] [Google Scholar]
- 26.Ek M, Roth B, Ekström P, et al. Gastrointestinal symptoms among endometriosis patients – a case-cohort study. BMC Womens Health. 2015;15:59. doi: 10.1186/s12905-015-0213-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Chan ACY, Siah KTH.. Can small fiber neuropathy explain the overlap gastrointestinal and non-gastrointestinal symptoms in some irritable bowel syndrome patients? J Neurogastroenterol Motil. 2024;30(1):116–118. doi: 10.5056/jnm23039. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Safarpour D, Sharzehi K, Pfeiffer RF.. Gastrointestinal dysfunction in Parkinson’s disease. Drugs. 2022;82(2):169–197. doi: 10.1007/s40265-021-01664-1. [DOI] [PubMed] [Google Scholar]
- 29.Fasano A, Visanji NP, Liu LWC, et al. Gastrointestinal dysfunction in Parkinson’s disease. Lancet Neurol. 2015;14(6):625–639. doi: 10.1016/S1474-4422(15)00007-1. [DOI] [PubMed] [Google Scholar]
- 30.Karlbom U, Påhlman L, Nilsson S, et al. Relationships between defecographic findings, rectal emptying, and colonic transit time in constipated patients. Gut. 1995;36(6):907–912. doi: 10.1136/gut.36.6.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Yu QJ, Yu SY, Zuo LJ, et al. Parkinson disease with constipation: clinical features and relevant factors. Sci Rep. 2018;8(1):567. doi: 10.1038/s41598-017-16790-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Bharucha AE, Lacy BE.. Mechanisms, evaluation, and management of chronic constipation. Gastroenterology. 2020;158(5):1232–1249.e3. doi: 10.1053/j.gastro.2019.12.034. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Nelson AD, Camilleri M.. Chronic opioid induced constipation in patients with nonmalignant pain: challenges and opportunities. Ther Adv Gastroenterol. 2015;8(4):206–220. doi: 10.1177/1756283X15578608. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Andrews CN, Storr M.. The pathophysiology of chronic constipation. Can J Gastroenterol. 2011;25 Suppl B(Suppl B):16B–21B. doi: 10.1155/2011/169319. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Serena G, D’Avino P, Fasano A.. Celiac disease and non-celiac wheat sensitivity: state of art of non-dietary therapies. Front Nutr. 2020;7:152. doi: 10.3389/fnut.2020.00152. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Lacy BE, Mearin F, Chang L, et al. Bowel disorders. Gastroenterology. 2016;150(6):1393–1407.e5. doi: 10.1053/j.gastro.2016.02.031. [DOI] [PubMed] [Google Scholar]
- 37.Lewis SJ, Heaton KW.. Stool form scale as a useful guide to intestinal transit time. Scand J Gastroenterol. 1997;32(9):920–924. doi: 10.3109/00365529709011203. [DOI] [PubMed] [Google Scholar]
- 38.Cotter TG, Gurney M, Loftus CG.. Gas and bloating-controlling emissions: a case-based review for the primary care provider. Mayo Clin Proc. 2016;91(8):1105–1113. doi: 10.1016/j.mayocp.2016.04.017. [DOI] [PubMed] [Google Scholar]
- 39.Black CJ, Thakur ER, Houghton LA, et al. Efficacy of psychological therapies for irritable bowel syndrome: systematic review and network meta-analysis. Gut. 2020;69(8):1441–1451. doi: 10.1136/gutjnl-2020-321191. [DOI] [PubMed] [Google Scholar]
- 40.González-Timoneda A, Valles-Murcia N, Muñoz Esteban P, et al. Prevalence and impact of pelvic floor dysfunctions on quality of life in women 5–10 years after their first vaginal or caesarian delivery. Heliyon. 2025;11(3):e42018. doi: 10.1016/j.heliyon.2025.e42018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Handa VL, Blomquist JL, Knoepp LR, et al. Pelvic floor disorders 5–10 years after vaginal or cesarean childbirth. Obstet Gynecol. 2011;118(4):777–784. doi: 10.1097/AOG.0b013e3182267f2f. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Lee SJ, Park JW.. Follow-up evaluation of the effect of vaginal delivery on the pelvic floor. Dis Colon Rectum. 2000;43(11):1550–1555. doi: 10.1007/bf02236737. [DOI] [PubMed] [Google Scholar]
- 43.Talley NJ. How to do and interpret a rectal examination in gastroenterology. Am J Gastroenterol. 2008;103(4):820–822. doi: 10.1111/j.1572-0241.2008.01832.x. [DOI] [PubMed] [Google Scholar]
- 44.Forootan M, Bagheri N, Darvishi M.. Chronic constipation: a review of literature. Medicine (Baltimore). 2018;97(20):e10631. doi: 10.1097/MD.0000000000010631. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Grossi U, Di Tanna GL, Heinrich H, et al. Systematic review with meta-analysis: defecography should be a first-line diagnostic modality in patients with refractory constipation. Aliment Pharmacol Ther. 2018;48(11-12):1186–1201. doi: 10.1111/apt.15039. [DOI] [PubMed] [Google Scholar]
- 46.Staller K, Neshatian L, Lembo A, et al. AGA Clinical Practice Update on evaluation and management of refractory constipation: expert review. Clin Gastroenterol Hepatol. 2026;24(2):296–305. doi: 10.1016/j.cgh.2025.09.031. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Zhou J, Thwaites PA, Gibson PR, et al. Comparison of gas-sensing capsule with wireless motility capsule in motility disorder patients. J Neurogastroenterol Motil. 2024;30(3):303–312. doi: 10.5056/jnm23157. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Kuo B, Lee AA, Abell T, et al. The assessment of gastrointestinal transit by the Atmo Capsule: a comparison with the SmartPill capsule. Clin Gastroenterol Hepatol. 2025;23(9):1633–1641.e8. doi: 10.1016/j.cgh.2024.12.013. [DOI] [PubMed] [Google Scholar]
- 49.Alame AM, Bahna H.. Evaluation of constipation. Clin Colon Rectal Surg. 2012;25(1):5–11. doi: 10.1055/s-0032-1301753. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Faubion SS, Shuster LT, Bharucha AE.. Recognition and management of nonrelaxing pelvic floor dysfunction. Mayo Clin Proc. 2012;87(2):187–193. doi: 10.1016/j.mayocp.2011.09.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Tan C, Geng J, Tang J, et al. The relationship between obstructed defecation and true rectocele in patients with pelvic organ prolapse. Sci Rep. 2020;10(1):5599. doi: 10.1038/s41598-020-62376-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Baessler K, Schuessler B.. Obstructed defecation caused by a cystourethrocele and mobile posterior vaginal wall: a case report. Int Urogynecol J Pelvic Floor Dysfunct. 2001;12(5):349–351. doi: 10.1007/pl00004042. [DOI] [PubMed] [Google Scholar]
- 53.Tsunoda A, Takahashi T, Kusanagi H.. Reappraising the role of enterocele in the obstructed defecation syndrome: is radiological impaired rectal emptying significant in enterocele? J Anus Rectum Colon. 2022;6(2):113–120. doi: 10.23922/jarc.2021-064. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Jain M, Agrawal V.. A simple four symptom-based BEDS score to predict dyssynergic defecation in patients with chronic constipation. Indian J Gastroenterol. 2025;44(3):330–335. doi: 10.1007/s12664-024-01697-w. [DOI] [PubMed] [Google Scholar]
- 55.Rao SSC, Tuteja AK, Vellema T, et al. Dyssynergic defecation: demographics, symptoms, stool patterns, and quality of life. J Clin Gastroenterol. 2004;38(8):680–685. doi: 10.1097/01.mcg.0000135929.78074.8c. [DOI] [PubMed] [Google Scholar]
- 56.Chiarioni G, Lambiase C, Whitehead WE, et al. Difficult defecation in constipated patients: diagnosis by minimally invasive diagnostic tests. Dig Liver Dis. 2024;56(3):429–435. doi: 10.1016/j.dld.2023.06.004. [DOI] [PubMed] [Google Scholar]
- 57.Rubio-Tapia A, Hill ID, Semrad C, et al. American College of Gastroenterology Guidelines update: diagnosis and management of celiac disease. Am J Gastroenterol. 2023;118(1):59–76. doi: 10.14309/ajg.0000000000002075. [DOI] [PubMed] [Google Scholar]
- 58.Shah ED, Almario CV, Spiegel BMR, et al. Lower and upper gastrointestinal symptoms differ between individuals with irritable bowel syndrome with constipation or chronic idiopathic constipation. J Neurogastroenterol Motil. 2018;24(2):299–306. doi: 10.5056/jnm17112. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Quigley EMM, Murray JA, Pimentel M.. AGA Clinical Practice Update on small intestinal bacterial overgrowth: expert review. Gastroenterology. 2020;159(4):1526–1532. doi: 10.1053/j.gastro.2020.06.090. [DOI] [PubMed] [Google Scholar]
- 60.Banaszak M, Górna I, Woźniak D, et al. Association between gut dysbiosis and the occurrence of SIBO, LIBO, SIFO and IMO. Microorganisms. 2023;11(3):573. doi: 10.3390/microorganisms11030573. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Rezaie A, Buresi M, Lembo A, et al. Hydrogen and methane-based breath testing in gastrointestinal disorders: the North American Consensus. Am J Gastroenterol. 2017;112(5):775–784. doi: 10.1038/ajg.2017.46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Ghoshal U, Shukla R, Srivastava D, et al. Irritable bowel syndrome, particularly the constipation-predominant form, involves an increase in Methanobrevibacter smithii, which is associated with higher methane production. Gut Liver. 2016;10(6):932–938. doi: 10.5009/gnl15588. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Pimentel M, Chang C, Chua KS, et al. Antibiotic treatment of constipation-predominant irritable bowel syndrome. Dig Dis Sci. 2014;59(6):1278–1285. doi: 10.1007/s10620-014-3157-8. [DOI] [PubMed] [Google Scholar]
- 64.Chatterjee S, Park S, Low K, et al. The degree of breath methane production in IBS correlates with the severity of constipation. Am J Gastroenterol. 2007;102(4):837–841. doi: 10.1111/j.1572-0241.2007.01072.x. [DOI] [PubMed] [Google Scholar]
- 65.Hammer HF, Fox MR, Keller J, et al. European guideline on indications, performance, and clinical impact of hydrogen and methane breath tests in adult and pediatric patients: European Association for Gastroenterology, Endoscopy and Nutrition, European Society of Neurogastroenterology and Motility, and European Society for Paediatric Gastroenterology Hepatology and Nutrition consensus. Unit Eur Gastroenterol J. 2022;10(1):15–40. doi: 10.1002/ueg2.12133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Lim J, Rezaie A.. Pros and cons of breath testing for small intestinal bacterial overgrowth and intestinal methanogen overgrowth. Gastroenterol Hepatol (NY). 2023;19(3):140–146. [PMC free article] [PubMed] [Google Scholar]
- 67.Kholwadwala AS, Quigley EMM.. Small intestinal bacterial overgrowth and intestinal methanogen overgrowth: are they overdiagnosed? Acta Gastroenterol Latinoam. 2025;55(4):276–291. doi: 10.52787/agl.v55i4.570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Takakura W, Pimentel M, Rao S, et al. A single fasting exhaled methane level correlates with fecal methanogen load, clinical symptoms and accurately detects intestinal methanogen overgrowth. Am J Gastroenterol. 2022;117(3):470–477. doi: 10.14309/ajg.0000000000001607. [DOI] [PubMed] [Google Scholar]
- 69.Silva BCD, Ramos GP, Barros LL, et al. Diagnosis and treatment of small intestinal bacterial overgrowth: an official position paper from the Brazilian Federation of Gastroenterology. Arq Gastroenterol. 2025;62:e24107. doi: 10.1590/S0004-2803.24612024-107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Ghoshal UC, Sachdeva S, Ghoshal U, et al. Asian-Pacific consensus on small intestinal bacterial overgrowth in gastrointestinal disorders: an initiative of the Indian Neurogastroenterology and Motility Association. Indian J Gastroenterol. 2022;41(5):483–507. doi: 10.1007/s12664-022-01292-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Kashyap P, Moayyedi P, Quigley EMM, et al. Critical appraisal of the SIBO hypothesis and breath testing: a clinical practice update endorsed by the European Society of Neurogastroenterology and Motility (ESNM) and the American Neurogastroenterology and Motility Society (ANMS). Neurogastroenterol Motil. 2024;36(6):e14817. doi: 10.1111/nmo.14817. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 72.Husby S, Murray JA, Katzka DA.. AGA Clinical Practice Update on diagnosis and monitoring of celiac disease-changing utility of serology and histologic measures: expert review. Gastroenterology. 2019;156(4):885–889. doi: 10.1053/j.gastro.2018.12.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73.Nelson AD, Black CJ, Houghton LA, et al. Systematic review and network meta-analysis: efficacy of licensed drugs for abdominal bloating in irritable bowel syndrome with constipation. Aliment Pharmacol Ther. 2021;54(2):98–108. doi: 10.1111/apt.16437. [DOI] [PubMed] [Google Scholar]
- 74.Brenner DM, Fogel R, Dorn SD, et al. Efficacy, safety, and tolerability of plecanatide in patients with irritable bowel syndrome with constipation: results of two phase 3 randomized clinical trials. Am J Gastroenterol. 2018;113(5):735–745. doi: 10.1038/s41395-018-0026-7. [DOI] [PubMed] [Google Scholar]
- 75.Chiarioni G, Salandini L, Whitehead WE.. Biofeedback benefits only patients with outlet dysfunction, not patients with isolated slow transit constipation. Gastroenterology. 2005;129(1):86–97. doi: 10.1053/j.gastro.2005.05.015. [DOI] [PubMed] [Google Scholar]
- 76.Cash BD. Understanding and managing IBS and CIC in the primary care setting. Gastroenterol Hepatol (NY). 2018;14(5 suppl 3):3–15. [PMC free article] [PubMed] [Google Scholar]
- 77.Quigley EMM, Neshatian L.. Advancing treatment options for chronic idiopathic constipation. Expert Opin Pharmacother. 2016;17(4):501–511. doi: 10.1517/14656566.2016.1127356. [DOI] [PubMed] [Google Scholar]
- 78.Dimidi E, van der Schoot A, Barrett K, et al. British Dietetic Association guidelines for the dietary management of chronic constipation in adults. J Hum Nutr Diet. 2025;38(5):e70133. doi: 10.1111/jhn.70133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 79.Seinelä L, Sairanen U, Laine T, et al. Comparison of polyethylene glycol with and without electrolytes in the treatment of constipation in elderly institutionalized patients: a randomized, double-blind, parallel-group study. Drugs Aging. 2009;26(8):703–713. doi: 10.2165/11316470-000000000-00000. [DOI] [PubMed] [Google Scholar]
- 80.Rao SSC, Brenner DM.. Efficacy and safety of over-the-counter therapies for chronic constipation: an updated systematic review. Am J Gastroenterol. 2021;116(6):1156–1181. doi: 10.14309/ajg.0000000000001222. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Chey WD, Hashash JG, Manning L, et al. AGA Clinical Practice Update on the role of diet in irritable bowel syndrome: expert review. Gastroenterology. 2022;162(6):1737–1745.e5. doi: 10.1053/j.gastro.2021.12.248. [DOI] [PubMed] [Google Scholar]
- 82.Halmos EP, Power VA, Shepherd SJ, et al. A diet low in FODMAPs reduces symptoms of irritable bowel syndrome. Gastroenterology. 2014;146(1):67–75.e5. doi: 10.1053/j.gastro.2013.09.046. [DOI] [PubMed] [Google Scholar]
- 83.Staudacher HM, Whelan K, Irving PM, et al. Comparison of symptom response following advice for a diet low in fermentable carbohydrates (FODMAPs) versus standard dietary advice in patients with irritable bowel syndrome. J Hum Nutr Diet. 2011;24(5):487–495. doi: 10.1111/j.1365-277X.2011.01162.x. [DOI] [PubMed] [Google Scholar]
- 84.Biesiekierski JR, Tuck CJ.. Low FODMAP diet beyond IBS: evidence for use in other conditions. Curr Opin Pharmacol. 2022;64:102208. doi: 10.1016/j.coph.2022.102208. [DOI] [PubMed] [Google Scholar]
- 85.Bellini M, Tonarelli S, Nagy AG, et al. Low FODMAP diet: evidence, doubts, and hopes. Nutrients. 2020;12(1):148. doi: 10.3390/nu12010148. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 86.Maagaard L, Ankersen DV, Végh Z, et al. Follow-up of patients with functional bowel symptoms treated with a low FODMAP diet. World J Gastroenterol. 2016;22(15):4009–4019. doi: 10.3748/wjg.v22.i15.4009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 87.Catassi G, Lionetti E, Gatti S, et al. The low FODMAP diet: many question marks for a catchy acronym. Nutrients. 2017;9(3):292. doi: 10.3390/nu9030292. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88.Bogdanowska-Charkiewicz D, Malinowska U, Daniluk J.. An umbrella review of meta-analyses on the low-FODMAP diet in IBS. Front Nutr. 2026;12:1714281. doi: 10.3389/fnut.2025.1714281. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Lacy BE, Pimentel M, Brenner DM, et al. ACG Clinical Guideline: management of irritable bowel syndrome. Am J Gastroenterol. 2021;116(1):17–44. doi: 10.14309/ajg.0000000000001036. [DOI] [PubMed] [Google Scholar]
- 90.van der Schoot A, Creedon A, Whelan K, et al. The effect of food, vitamin, or mineral supplements on chronic constipation in adults: a systematic review and meta-analysis of randomized controlled trials. Neurogastroenterol Motil. 2023;35(11):e14613. doi: 10.1111/nmo.14613. [DOI] [PubMed] [Google Scholar]
- 91.Rao S, Lembo AJ, Shiff SJ, et al. A 12-week, randomized, controlled trial with a 4-week randomized withdrawal period to evaluate the efficacy and safety of linaclotide in irritable bowel syndrome with constipation. Am J Gastroenterol. 2012;107(11):1714–1724; quiz p.1725. doi: 10.1038/ajg.2012.255. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92.Chey WD, Lembo AJ, Lavins BJ, et al. Linaclotide for irritable bowel syndrome with constipation: a 26-week, randomized, double-blind, placebo-controlled trial to evaluate efficacy and safety. Am J Gastroenterol. 2012;107(11):1702–1712. doi: 10.1038/ajg.2012.254. [DOI] [PubMed] [Google Scholar]
- 93.Drossman DA, Chey WD, Johanson JF, et al. Clinical trial: lubiprostone in patients with constipation-associated irritable bowel syndrome—results of two randomized, placebo-controlled studies. Aliment Pharmacol Ther. 2009;29(3):329–341. doi: 10.1111/j.1365-2036.2008.03881.x. [DOI] [PubMed] [Google Scholar]
- 94.Chey WD, Lembo AJ, Rosenbaum DP.. Efficacy of tenapanor in treating patients with irritable bowel syndrome with constipation: a 12-week, placebo-controlled phase 3 trial (T3MPO-1). Am J Gastroenterol. 2020;115(2):281–293. doi: 10.14309/ajg.0000000000000516. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Miner PB, Jr., Koltun WD, Wiener GJ, et al. A randomized phase III clinical trial of plecanatide, a uroguanylin analog, in patients with chronic idiopathic constipation. Am J Gastroenterol. 2017;112(4):613–621. doi: 10.1038/ajg.2016.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 96.DeMicco M, Barrow L, Hickey B, et al. Randomized clinical trial: efficacy and safety of plecanatide in the treatment of chronic idiopathic constipation. Ther Adv Gastroenterol. 2017;10(11):837–851. doi: 10.1177/1756283X17734697. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 97.Lembo AJ, Schneier HA, Shiff SJ, et al. Two randomized trials of linaclotide for chronic constipation. N Engl J Med. 2011;365(6):527–536. doi: 10.1056/NEJMoa1010863. [DOI] [PubMed] [Google Scholar]
- 98.Lacy BE, Schey R, Shiff SJ, et al. Linaclotide in chronic idiopathic constipation patients with moderate to severe abdominal bloating: a randomized, controlled trial. PLoS One. 2015;10(7):e0134349. doi: 10.1371/journal.pone.0134349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 99.Li F, Fu T, Tong WD, et al. Lubiprostone is effective in the treatment of chronic idiopathic constipation and irritable bowel syndrome: a systematic review and meta-analysis of randomized controlled trials. Mayo Clin Proc. 2016;91(4):456–468. doi: 10.1016/j.mayocp.2016.01.015. [DOI] [PubMed] [Google Scholar]
- 100.Cash BD, Sharma A, Walker A, et al. Plecanatide for the treatment of chronic idiopathic constipation and irritable bowel syndrome with constipation: post hoc analyses of placebo-controlled trials in adults with severe constipation. Neurogastroenterol Motil. 2023;35(9):e14632. doi: 10.1111/nmo.14632. [DOI] [PubMed] [Google Scholar]
- 101.Staller K, Hinson J, Kerstens R, et al. Efficacy of prucalopride for chronic idiopathic constipation: an analysis of participants with moderate to very severe abdominal bloating. Am J Gastroenterol. 2022;117(1):184–188. doi: 10.14309/ajg.0000000000001521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 102.Chey WD, Lembo AJ, Yang Y, et al. Efficacy of tenapanor in treating patients with irritable bowel syndrome with constipation: a 26-week, placebo-controlled phase 3 trial (T3MPO-2). Am J Gastroenterol. 2021;116(6):1294–1303. doi: 10.14309/ajg.0000000000001056. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 103.Vahedi H, Merat S, Rashidioon A, et al. The effect of fluoxetine in patients with pain and constipation-predominant irritable bowel syndrome: a double-blind randomized-controlled study. Aliment Pharmacol Ther. 2005;22(5):381–385. doi: 10.1111/j.1365-2036.2005.02566.x. [DOI] [PubMed] [Google Scholar]
- 104.Tack J, Broekaert D, Fischler B, et al. A controlled crossover study of the selective serotonin reuptake inhibitor citalopram in irritable bowel syndrome. Gut. 2006;55(8):1095–1103. doi: 10.1136/gut.2005.077503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 105.Ford AC, Wright-Hughes A, Alderson SL, et al. Amitriptyline at Low-Dose and Titrated for Irritable Bowel Syndrome as Second-Line Treatment in Primary Care (ATLANTIS): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2023;402(10414):1773–1785. doi: 10.1016/S0140-6736(23)01523-4. [DOI] [PubMed] [Google Scholar]
- 106.Hanna-Jairala I, Drossman DA.. Central neuromodulators in irritable bowel syndrome: why, how, and when. Am J Gastroenterol. 2024;119(7):1272–1284. doi: 10.14309/ajg.0000000000002800. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 107.Drossman DA, Tack J, Ford AC, et al. Neuromodulators for functional gastrointestinal disorders (disorders of gut-brain interaction): a Rome Foundation Working Team report. Gastroenterology. 2018;154(4):1140–1171.e1. doi: 10.1053/j.gastro.2017.11.279. [DOI] [PubMed] [Google Scholar]
- 108.Rao SSC, Quigley EMM, Chey WD, et al. Randomized placebo-controlled phase 3 trial of vibrating capsule for chronic constipation. Gastroenterology. 2023;164(7):1202–1210.e6. doi: 10.1053/j.gastro.2023.02.013. [DOI] [PubMed] [Google Scholar]
- 109.Vitton V, Mion F, Leroi AM, et al. Interferential therapy for chronic constipation in adults: the CON-COUR randomized controlled trial. United European Gastroenterol J. 2023;11(4):337–349. doi: 10.1002/ueg2.12373. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110.Heemskerk SCM, Dirksen CD, van Kuijk SMJ, et al. Sacral neuromodulation versus conservative treatment for refractory idiopathic slow-transit constipation: the randomized clinical no.2-trial. Ann Surg. 2024;279(5):746–754. doi: 10.1097/SLA.0000000000006158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 111.Kamm MA, Dudding TC, Melenhorst J, et al. Sacral nerve stimulation for intractable constipation. Gut. 2010;59(3):333–340. doi: 10.1136/gut.2009.187989. [DOI] [PubMed] [Google Scholar]
- 112.Emile SH, Dourado J, Wignakumar A, et al. Meta-analysis of randomized controlled trials on the efficacy of sacral neuromodulation in chronic constipation. Neuromodulation. 2025;28(5):737–745. doi: 10.1016/j.neurom.2025.03.001. [DOI] [PubMed] [Google Scholar]
- 113.Nasser J, Mehravar S, Pimentel M, et al. Elemental diet as a therapeutic modality: a comprehensive review. Dig Dis Sci. 2024;69(9):3344–3360. doi: 10.1007/s10620-024-08543-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 114.Pimentel M, Constantino T, Kong Y, et al. A 14-day elemental diet is highly effective in normalizing the lactulose breath test. Dig Dis Sci. 2004;49(1):73–77. doi: 10.1023/b:ddas.0000011605.43979.e1. [DOI] [PubMed] [Google Scholar]
- 115.Blanchard EB, Lackner JM, Sanders K, et al. A controlled evaluation of group cognitive therapy in the treatment of irritable bowel syndrome. Behav Res Ther. 2007;45(4):633–648. doi: 10.1016/j.brat.2006.07.003. [DOI] [PubMed] [Google Scholar]
- 116.Peters SL, Yao CK, Philpott H, et al. Randomised clinical trial: the efficacy of gut-directed hypnotherapy is similar to that of the low FODMAP diet for the treatment of irritable bowel syndrome. Aliment Pharmacol Ther. 2016;44(5):447–459. doi: 10.1111/apt.13706. [DOI] [PubMed] [Google Scholar]
- 117.Everitt HA, Landau S, O’Reilly G, et al. Cognitive behavioural therapy for irritable bowel syndrome: 24-month follow-up of participants in the ACTIB randomised trial. Lancet Gastroenterol Hepatol. 2019;4(11):863–872. doi: 10.1016/S2468-1253(19)30243-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 118.Lee HH, Choi YY, Choi MG.. The efficacy of hypnotherapy in the treatment of irritable bowel syndrome: a systematic review and meta-analysis. J Neurogastroenterol Motil. 2014;20(2):152–162. doi: 10.5056/jnm.2014.20.2.152. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 119.Flik CE, Laan W, Zuithoff NPA, et al. Efficacy of individual and group hypnotherapy in irritable bowel syndrome (IMAGINE): a multicentre randomised controlled trial. Lancet Gastroenterol Hepatol. 2019;4(1):20–31. doi: 10.1016/S2468-1253(18)30310-8. [DOI] [PubMed] [Google Scholar]
- 120.Ford AC, Lacy BE, Harris LA, et al. Effect of antidepressants and psychological therapies in irritable bowel syndrome: an updated systematic review and meta-analysis. Am J Gastroenterol. 2019;114(1):21–39. doi: 10.1038/s41395-018-0222-5. [DOI] [PubMed] [Google Scholar]
- 121.Lackner JM, Jaccard J, Radziwon CD, et al. Durability and decay of treatment benefit of cognitive behavioral therapy for irritable bowel syndrome: 12-month follow-up. Am J Gastroenterol. 2019;114(2):330–338. doi: 10.1038/s41395-018-0396-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 122.Lackner JM, Jaccard J, Keefer L, et al. Improvement in gastrointestinal symptoms after cognitive behavior therapy for refractory irritable bowel syndrome. Gastroenterology. 2018;155(1):47–57. doi: 10.1053/j.gastro.2018.03.063. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 123.Wang XJ, Philpot L, Ebbert J, et al. Digital therapeutic combining hypnosis and diaphragmatic breathing intervention for functional abdominal bloating: a feasibility study. Clin Transl Gastroenterol. 2025;16(4):e00811. doi: 10.14309/ctg.0000000000000811. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 124.Pemberton L, Kita L, Andrews K.. Practitioners’ experiences of using gut directed hypnosis for irritable bowel syndrome: perceived impact upon client wellbeing: a qualitative study. Complement Ther Med. 2020;55:102605. doi: 10.1016/j.ctim.2020.102605. [DOI] [PubMed] [Google Scholar]
- 125.Woodward S, Norton C, Chiarelli P.. Biofeedback for treatment of chronic idiopathic constipation in adults. Cochrane Database Syst Rev. 2014;2014(3):CD008486. doi: 10.1002/14651858.CD008486.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 126.Rao SS, Valestin J, Brown CK, et al. Long-term efficacy of biofeedback therapy for dyssynergic defecation: randomized controlled trial. Am J Gastroenterol. 2010;105(4):890–896. doi: 10.1038/ajg.2010.53. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 127.Wang J, Luo M, Qi Q, et al. Prospective study of biofeedback retraining in patients with chronic idiopathic functional constipation. World J Gastroenterol. 2003;9(9):2109–2113. doi: 10.3748/wjg.v9.i9.2109. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 128.Iovino P, Neri MC, D’Alba L, et al. Pelvic floor biofeedback is an effective treatment for severe bloating in disorders of gut-brain interaction with outlet dysfunction. Neurogastroenterol Motil. 2022;34(5):e14264. doi: 10.1111/nmo.14264. [DOI] [PubMed] [Google Scholar]
- 129.Al-Sannan B, Banakhar M, Hassouna MM.. The role of sacral nerve stimulation in female pelvic floor disorders. Curr Obstet Gynecol Rep. 2013;2(3):159–168. doi: 10.1007/s13669-013-0052-9. [DOI] [Google Scholar]
- 130.Serra J, Pohl D, Azpiroz F, et al. European Society of Neurogastroenterology and Motility guidelines on functional constipation in adults. Neurogastroenterol Motil. 2020;32(2):e13762. doi: 10.1111/nmo.13762. [DOI] [PubMed] [Google Scholar]
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