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Contamination of single fluid-filled intragastric balloons with orogastric fluid is not associated with hyperinflation: an ex-vivo study and systematic review of literature

BMC Gastroenterology volume 21, Article number: 286 (2021) Cite this article

Abstract

Background

Spontaneous hyperinflation is reported to the Food and Drug Administration as a complication of intragastric balloons. It is postulated that orogastric contamination of the intragastric balloon may cause this phenomenon. We sought to investigate the effects of intentional balloon contamination with gastric contents on intragastric balloon perimeter and contents, whether methylene blue plays a role in preventing spontaneous hyperinflation, and review the available literature on spontaneous hyperinflation.

Methods

Four pairs of balloons with different combinations of sterile saline, orogastric contaminants, and methylene blue were incubated in a 37 °C water bath for six months to simulate physiological conditions with serial measurements of balloon perimeter. Our findings were compared against a systematic review across multiple databases to summarize the available literature.

Results

Balloon mean perimeter decreased from 33.5 cm ± 0.53 cm to 28.5 cm ± 0.46 cm (p < 0.0001). No significant differences were seen with the methylene blue group. Only 11 cases were found reported in the literature.

Conclusions

Despite contaminating intragastric balloons with gastric aspirates, hyperinflation did not occur, and other factors may be in play to account for this phenomenon, when observed. Rates of hyperinflation remain under-reported in the literature. Further controlled experiments are needed.

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Background

Obesity is the second leading cause of preventable death in the United States, behind tobacco use [1]. Traditional obesity management techniques, such as lifestyle interventions (e.g., diet and physical activity), which remain the foundation of any weight loss program, are often ineffective in inducing clinically significant weight loss alone [2]. On the other hand, bariatric surgery is considered most effective but is reserved for severe obesity classes (class II and III obesity), with low penetration [3].

In this context, endoscopic bariatric therapies (EBTs) emerged as an effective and less-invasive alternative to surgery [4]. This field has the potential to bridge the gap in patients who fail lifestyle interventions or who are intolerant to weight loss pharmacotherapy and are not surgical candidates. Furthermore, in addition to being less-invasive, endoscopic therapies for weight loss are potentially reversible, repeatable, and of lower cost than other medical and surgical alternatives [5].

Among EBTs, the intragastric balloon (IGB) is a minimally invasive, temporary weight loss method that has become one of the most common procedures performed for the less severe cases of obesity (class I and class II obesity with body mass index (BMI) of 30–40 kg/m2) [6]. Its efficacy and safety have been demonstrated in the literature for inducing weight loss and reducing obesity-related comorbidities in the adult population [7,8,9,10]. Single fluid-filled IGBs were shown to be the most effective type of space-occupying devices in promoting weight loss [11]. The most commonly reported adverse events (AEs) associated with this device are mild accommodative gastrointestinal symptoms, while serious AEs occur in < 1% of cases (e.g., perforation, prosthesis migration) [11,12,13].

In February 2017, the Food and Drug Administration (FDA) issued an update regarding potential risks with fluid-filled IGBs [14]. It advised close patient monitoring for acute onset of nausea, vomiting, and abdominal pain that could be a sign of spontaneous hyperinflation of the IGB. The FDA defined hyperinflation as the spontaneous filling of IGBs with additional air or liquid while inside a patient’s stomach, typically resulting in the need for early device removal. The onset of symptoms can be as early as seven days and up to 23 weeks after balloon placement. The mechanism behind this AE remains unclear, with reports postulating that orogastric (OG) contamination with microorganisms during IGB insertion is the likely culprit [15, 16]. In this ex-vivo study, we investigate the effects of intentional contamination of the single fluid-filled IGBs with OG contents on balloon perimeter and contents and whether methylene blue (MB) plays a role in preventing spontaneous hyperinflation. A systematic review across multiple databases was also performed to summarize the available literature.

Methods

An ex-vivo study using eight single fluid-filled IGBs (Orbera, Apollo Endosurgery, Austin, TX, USA) was designed to simulate physiological conditions during device placement for a total of six months. IGBs were filled with a combination of sterile saline, OG contaminants, and MB.

The eight IGBs were divided into four pairs (A1, A2, B1, B2, C1, C2, D1, D2). The first pair (A1, A2) was filled with 650 ml sterile saline; the second pair (B1, B2) was filled with 650 ml sterile saline and inoculated with 3 ml of OG contaminants; the third (C1, C2) and fourth pairs (D1, D2) were filled with 650 ml sterile saline, 3 ml of OG contaminants in addition to 0.5 ml and 2 ml of MB, respectively (Table 1).

Table 1 Intragastric balloons pairs with respective contents
Full size table

The IGBs were filled using standard equipment delivered with the Orbera balloon system. Each IGB was filled independently without re-use of equipment to avoid cross-contamination. The OG contaminants were obtained during a routine upper endoscopy procedure using standard aspirate techniques. After filling with the respective contents, the IGBs were placed in a water bath incubated in a 37 °C rotating incubator to mimic physiological conditions for the study's planned duration (6 months). Serial balloon perimeter measurements in two dimensions and changes in visual appearance were taken every 7 to 14 days to monitor hyperinflation signs (Fig. 1). The measurements were taken twice by one individual (EJV) using a flexible tape measure.

Fig. 1
figure 1

Intragastric balloons. Panel (A): Four pairs of intragastric balloons (A1/A2, B1/B2, C1/C2, D1/D2). Panel (B): Intragastric balloons within the heated water bath with the formation of an initial air bubble

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At the conclusion of the study, the final IGBs mean perimeter was compared to their baseline perimeter using the non-parametric version of the paired t-test. In addition, the mean perimeter difference between IGBs with or without MB, and those with and without sterile saline alone were compared. P < 0.05 was considered statistically significant.

In order to identify published case reports/series of spontaneous IGB hyperinflation, a medical reference librarian conducted an extensive search of multiple databases without any restriction of language from the inception of the database to February 10, 2021. The data sources and search terms are provided in Additionl file 1. A manual review of the reference lists of relevant publications was done for additional publications. One reviewer (FH) selected the case studies reporting spontaneous IGB hyperinflation and extracted the relevant data onto a standardized form. Data included the year of publication, patient age, sex, and initial BMI, type of IGB used, IGB filling volume, use of MB, hyperinflation symtoms, timing of hyperinflation symptoms post-IGB placement, management approach, management outcome, and IGB fluid culture results.

The quality of the included cases was determined using the methodological quality and synthesis of case series and case reports tool, since all included studies were non-comparative single case reports [17]. According to this instrument, each study is evaluated based on four domains: selection of study groups, ascertainment, causality, and reporting (Additional file 1: Table S1). This resulted in a five-item tool to assess whether the methodological quality of the included studies is good, unclear, or low based on three possible answers for each item (yes, cannot tell, no). This tool has been previously applied with consistency among reviewers [18,19,20,21,22].

Results

Results of the ex-vivo study

Eight (four pairs) IGBs were used in the ex-vivo study, and serial measurements of the perimeter of the balloon were documented over 165 days. Each pair was filled with its unique contents with the formation of an initial “air bubble” that subsequently disappeared two weeks into the incubation period (Fig. 2).

Fig. 2
figure 2

Disappearance of the “air bubble” within 2 weeks into the experiment

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All balloons were maintained inside the heated water bath during the study. At two months (56 days), the balloons began to deflate and develop an air-fluid level (Fig. 3).

Fig. 3
figure 3

Balloon deflation and development of air-fluid levels at 2 months

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Thereafter, balloons continued to decrease in perimeter over the study period (Fig. 4).

Fig. 4
figure 4

Intragastric balloons perimeter (centimeters) trends over time (days)

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At 165 days, the deflation precluded further consistent measurements. Mean perimeter of the balloons dropped from 33.5 cm ± 0.53 cm to 28.5 cm ± 0.46 cm (p < 0.0001). The MB groups final mean perimeter was similar to other balloons [28.9 cm ± 0.25 cm vs 28.3 cm ± 0.5 cm (p = 0.19)]. The sterile saline group (A1, A2) trended to display a higher final mean perimeter when compared to the other groups with OG contaminants [29.3 cm ± 0.4 cm versus 28.3 cm + 1.3 cm (p = 0.07)]. No spontaneous balloon ruptures occurred during the study period.

Results of the systematic review

Figure 5 shows the flow diagram of the systematic review.

Fig. 5
figure 5

Flow diagram showing the different phases of the systematic review

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A total of 10 publications (11 cases) [15, 23,24,25,26,27,28,29,30,31] describing spontaneous IGB hyperinflation were identified in the literature despite a reported rate of approximately 2% in post-marketing studies [13]. All identified cases shared a common definition of spontaneous IGB hyperinflation which is consistent with the FDA’s statement [14]. Patient baseline characteristics, type of IGB, clinical presentation and subsequent management are detailed in Table 2.

Table 2 Case reports with spontaneous intragastric balloon hyperinflation
Full size table

The assessment of the case reports’ methodological quality is shown in Additional file 1: Table S2, and the overall evaluation of the methodological quality is shown in Additional file 1: Figure S1. For the selection domain, none of the authors mentioned whether the reported case(s) represented the entire experience of their center. Overall, none of the case reports had a good methodological quality in all domains, with the majority having low or unclear methodological quality.

Discussion

Intragastric balloon therapy has become one of the most commonly used bariatric endoscopic techniques since its approval by the FDA in 2015, with fluid-filled IGBs being the most effective thus far [6, 11]. IGBs are placed endoscopically for 6 months to promote weight loss, not only by inducing early satiation but also by delaying gastric emptying and restoring satiety between meals [32]. Indeed randomized controlled trials and meta-evidence have demonstrated their higher efficacy in weight loss when combined with dietary interventions and physical activity, compared to the latter alone [11, 33]. The safety of IGBs has also been evaluated in the literature; Genco et al. [34] reported an overall AEs rate of 2.8% in 2515 patients who underwent balloon placement with esophagitis as the most common AE. Furthermore, the American Society for Gastrointestinal Endoscopy bariatric endoscopy task force pooled the rate of AEs after implantation of the Orbera IGB from 68 studies (~ 8500 patients) and found that pain and nausea were the most frequent side effects, occurring in 33.7% of subjects with an early removal rate approximating 7% [7]. This was followed by the Brazilian IGB consensus statement of over 40,000 cases, which reported an AE rate of 2.5%, with the most common being spontaneous hyperinflation of the IGB, with an early removal rate due to intolerance of 2.2% [13].

Worldwide, over 200 AE reports of IGB hyperinflation were received by the FDA with few published reports in the literature [15, 23,24,25,26,27,28,29,30,31, 35]. Accordingly, the FDA issued an updated letter to providers regarding the potential risk of spontaneous hyperinflation based on the post-approval study of the Orbera IGB [35, 36]. The study found that 6 out of 258 patients (2.3%) experienced balloon hyperinflation; however, the precise mechanism behind this phenomenon remains unknown.

De Souza et al. [16] relayed iatrogenic causes as a possible explanation, which can occur at the time of placement if the prosthesis is filled beyond the recommended amount of saline (> 700 ml). Other investigators have conjectured that it may be due to the permeability of the IGB, which results in the entry of fluids and gases by osmosis as the balloon is filled with saline solution [24]. A defective balloon valve allowing air entry or a manufacturing defect of the filling fluid has also been proposed [30, 37]. However, the most widely accepted hypothesis is fungal and/or bacterial contamination of the balloon, a process that can potentially produce gas secondary to fermentation and thus resulting in hyperinflation of the IGB [16].

In our ex-vivo experiment, we aimed to evaluate the effects of purposely inoculating OG contaminants into single fluid-filled IGBs with or without the use of MB, an agent postulated to have antimicrobial effects [38]. The IGBs were placed in a heated water bath to 37 °C to simulate physiological conditions during device placement, and change in the balloons’ perimeter was followed over 165 days (until balloon deflation prevented further measurements). After the study, we noticed that the balloons did not hyperinflate over time but rather decreased in mean perimeter from a mean of 33.5 cm ± 0.53 cm to 28.5 cm ± 0.46 cm (p < 0.0001), with the formation of air-fluid levels. Furthermore, the addition of MB did not appear to affect the final IGB mean perimeter (28.9 cm ± 0.25 cm versus 28.3 cm ± 0.5 cm, p = 0.19). Similarly, filling the balloon purely with sterile saline only did not result in a different final IGB mean perimeter, compared to the other groups [29.3 cm ± 0.4 cm versus 28.3 cm ± 1.3 cm (p = 0.07)].

Intragastric balloons are liable to fungal and bacterial contamination during the passage of the device through the oral cavity secondary to the direct exposure to oral microbiota [39]. Furthermore, the IGB is made of a silicone elastomer, susceptible to colonization by anaerobic bacteria and Candida species. Such colonization results in biofilm formation and subsequent invasion into the balloon contents [40,41,42]. Saray et al. [43] experimented to compare fungal translocation across silicone tissue expanders with intact injection ports to those with multi-punctured ports. The experiment showed that an intact silicone membrane is impermeable to fungi, while a multi-punctured injection port allows the entry of fungi into the implant. Nonetheless, our systematic review of literature identified multiple case studies reporting asymptomatic microbial colonization of the IGB without balloon hyperinflation [41, 44, 45]. In contrast, others described bacterial or fungal colonization with associated symptomatic spontaneous balloon hyperinflation [25, 27,28,29, 31]. In combination with the results of our experiment, these observations suggest that IGB contamination and ensuing microbial fermentation may not be the sole cause of hyperinflation, and the presence of additional factors is likely involved.

Silicone is considered a permeable elastomer to gas, water, and protein molecules [42, 46]. In our experiment, we noticed balloon deflation with the simultaneous formation of air-fluid levels. This could be attributed to intra-luminal fluid extrusion or evaporation occurring concurrently with slow air entry into the balloon; hence, it resulted in balloon shrinkage. Alternatively, the relatively higher final mean perimeter of the balloons containing sterile saline only, may suggest a degradative effect of OG contaminants on the balloon structure.

Based on our experiment results, we cannot conclude whether a gas-forming process (fermentation) secondary to OG contamination contributed to the development of the air-fluid levels or not, even though it occurred in all balloons. This observation, and others, point out certain limitations of our study. First, spontaneous hyperinflation is a relatively rare complication of IGB placement. Therefore, using only four pairs of IGBs given the experimental nature of the study may not be adequate to fully investigate the causative factors for spontaneous hyperinflation. Second, the OG contaminants were obtained from random patients without a history of spontaneous IGB hyperinflation. However, the experimentation, being agnostic to the patient from whom the aspirates were collected, simulates the real-life scenario and ignorance of the patient’s fate in term of IGB hyperinflation. Third, the OG contaminants were not cultured prior to inoculating the IGBs or after the conclusion of the study. Furthermore, these contaminants do not fully resemble the gastric contents of patients with IGB placement, largely due to the use proton pump inhibitors (PPIs) post-IGB placement which results in less acidic gastric contents as compared to the OG contaminants used in this experiment. Lastly, it should be noted that the water bath is not a perfect surrogate of post-IGB placement intragastric environment which may have affected the results of the experiment.

We hypothesize that spontaneous IGB hyperinflation occurs in the setting of a multifactorial process rather than secondary to a single culprit. First, the stomach can be considered a confined system, given the intrinsic lower esophageal sphincter tone and the pylorus tone. This anatomy generates an intragastric pressure, and hence favors air diffusion into the balloon rather than fluid extrusion; these circumstances were not available in our water bath environment. Second, the suppressed acid production in the stomach secondary to PPI use in addition to the delayed gastric emptying induced by the IGB can provide a nutritive environment to promote rapid colonization of Candida and bacteria [27, 44, 45]. Third, endoscopic placement of IGB may compromise the silicone elastomer and/or balloon valve integrity, thus resulting in higher permeability of the balloon to air and opportunistic microorganisms [37]. Lastly, bile reflux may still occur into an acid-suppressed stomach while the IGB is in place, which may provide protective effects to fungal growth as has been illustrated by Hsieh and Brock [47].

Irrespective of the etiology of spontaneous hyperinflation, early recognition of this phenomenon in patients with IGB and acute abdomen is paramount. This should be followed by prompt removal of the IGB [24]. De Souza et al. [16] and Usuy et al. [31] proposed adding Nystatin or antibacterial agents to the balloon solution as prophylaxis or treatment for fungal and bacterial colonization. This practice, however, was not recommended by the Brazilian consensus due to a lack of proof that fungal colonization is the culprit behind this phenomenon [13]. Unfortunately, the low incidence of this complication will make it difficult to evaluate in a randomized controlled trial.

Conclusions

Spontaenous IGB hyperinflation precise pathophysiology remains unclear. However, in combination with the results of our ex-vivo experiment, the current literature suggests that balloon contamination may not be the sole contributor, and the phenomenon is rather a multifactorial process. Additional risk factors and etiologies need to be considered and investigated. Early recognition of this phenomenon and subsequent removal of the IGB is paramount to avoid sinister outcomes.

Availability of data and materials

The datasets used and analyzed during the current study (ex-vivo study and systematic review) are available from the corresponding author upon request. Systematic review registration: The systematic review was not registered.

Abbreviations

AEs:

Adverse events

BMI:

Body mass index

EBT:

Endoscopic bariatric therapies

FDA:

Food and drug administration

IGB:

Intragastric balloon

MB:

Methylene blue

OG:

Orogastric

PPI:

Proton pump inhibitor

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Acknowledgements

The authors acknowledge Apollo Endosurgery for providing the intragastric balloons for experimental purposes at no cost. The authors thank Ms. Jillah Biza for conducting the librarian systematic review of literature.

Funding

Not applicable. No specific grant was received from any public, commercial, or not-for-profit sectors for this research activity.

Author information

Authors and Affiliations

  1. Department of Internal Medicine, St. Joseph Mercy Ann Arbor Hospital, 5333 McAuley Drive, Suite 3009, Ypsilanti, MI, 48197, USA

    Fadi Hawa

  2. Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA

    Eric J. Vargas, Andres Acosta, Alison McRae & Barham K. Abu Dayyeh

  3. Division of Gastroenterology and Hepatology, St. Cloud Hospital, 1406 6th Ave N, St Cloud, MN, 56303, USA

    Fateh Bazerbachi

Authors
  1. Fadi Hawa
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  2. Eric J. Vargas
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  3. Andres Acosta
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  4. Alison McRae
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  5. Fateh Bazerbachi
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  6. Barham K. Abu Dayyeh
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Contributions

FH analyzed and interpreted the data and was a major contributor in writing the manuscript. EJV collected, analyzed, and interpreted the data, and was a major contributor in writing the methods section of the manuscript. AA analyzed and interpreted the data and critically revised the article. AM helped care for the balloons between measurements and critically revised the article. FB analyzed and interpreted the data, and was a major contributor in revising the discussion section of the article. BKAD conceptualized and designed the study, and critically revised the article. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Barham K. Abu Dayyeh.

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Not applicable.

Competing interests

AA: Founder and stockholder: Gila Therapeutics, Phenomix Sciences. Consultant: Rhythm Pharmaceuticals, and General Mills. BKAD: Consultant: Metamodix, BFKW, DyaMx, Boston Scientific, USGI Medical, Hemostasis. Research support: Apollo Endosurgery, USGI, Spatz Medical, Boston Scientific, GI Dynamics, Cairn Diagnostics, Aspire Bariatrics, Medtronic. Speaker: Johnson and Johnson, Endogastric solutions, Olympus. The remaining authors declare that they have no competing interests.

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Hawa, F., Vargas, E.J., Acosta, A. et al. Contamination of single fluid-filled intragastric balloons with orogastric fluid is not associated with hyperinflation: an ex-vivo study and systematic review of literature. BMC Gastroenterol 21, 286 (2021). https://doi.org/10.1186/s12876-021-01863-w

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  • DOI: https://doi.org/10.1186/s12876-021-01863-w

Keywords

BMC Gastroenterology

ISSN: 1471-230X

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