Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1033_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
31.08.2026
Размер:
24 Мб
Скачать
192
https://t.me/medicina_free
9. Banks M. The modern investigation and management of gastro­oesophageal reux disease (GORD). Clin Med. 2009;9(6):600–4. Epub 2010/01/26.
10. Shaheen NJ, Weinberg DS, Denberg TD, Chou R, Qaseem A, et al.; Clinical guidelines Committee of the American College of Physicians. Upper endoscopy for gastroesophageal reux disease: best practice advice from the clinical guidelines committee of the American College of Physicians. Ann Intern Med. 2012;157:808–16.
11. Martinez SD, Malagon IB, Garewal HS, Cui H, Fass R. Non-erosive reux disease (NERD)--acid reux and symptom patterns. Aliment Pharmacol Ther. 2003;17:537–45.
12. Lundell LR, Dent J, Bennett JR, etal. Endoscopic assessment of oesoph­agitis: clinical and functional correlates and further validation of the Los Angeles Classication. Gut. 1999;45:172–80.
13. Hartono JL, Qua CS, Goh KL. Non-erosive reux disease (NERD), symptomatic and asymptomatic erosive reux disease (ERD): from hypersensitive to hyposensitive esophagus. Dig Dis Sci. 2011;56(1):90–
6. Epub 2010/05/15.
14. Dean BB, Gano AD Jr, Knight K, et al. Effectiveness of proton pump inhibitors in nonerosive reux disease. Clin Gastroenterol Hepatol. 2004;2:656–64.
15. Vaezi MF.Laryngeal manifestations of gastroesophageal reux disease. Curr Gastroenterol Rep. 2008;10(3):271–7. Epub 2008/07/16.
16. Mathus-Vliegen EMH, Smit CF, Devriese PP.Artifacts in 24-h pharyn­geal and oesophageal pH monitoring: is simplication of pH data analy­sis feasible? Scand J Gastroenterol. 2004;39(1):14–9.
17. Adhami T, Goldblum JR, Richter JE, Vaezi MF.The role of gastric and duodenal agents in laryngeal injury: an experimental canine model. Am J Gastroenterol. 2004;99(11):2098–106. Epub 2004/11/24.
18. Ahmed T, Vaezi MF.The role of pH monitoring in extraesophageal gas­troesophageal reux disease. Gastrointest Endosc Clin N Am. 2005;15:319–31.
19. Lim PL, Gibbons MJ, Crawford EJ, Watson RGP, Johnston BT. The effect of lifestyle changes on results of 24-h ambulatory oesophageal pH monitoring. Eur J Gastroenterol Hepatol. 2000;12(6):655–6.
20. Jamieson JR, Stein HJ, DeMeester TR, etal. Ambulatory 24-h esophageal pH monitoring: normal values, optimal thresholds, specicity, sensitivity, and reproducibility. Am J Gastroenterol. 1992;87:1102–11.
21. Schwameis K, Lin B, Roman J, Olengue K, Siegal S, DeMeester SR.Is pH testing necessary before Antireux surgery in patients with endo­scopic erosive esophagitis? J Gastrointest Surg. 2018;22(1):8–12.
22. Hong S-KS, Vaezi MF.Gastroesophageal reux monitoring: pH (catheter and capsule) and impedance. Gastrointest Endosc Clin N Am. 2009;19(1):1–22.
F. Fontan et al.
13 Catheter-Based pH Testing
https://t.me/medicina_free
23. Kavanagh R, Smith J, Bashir U, etal. Optimizing bariatric surgery out­comes: a novel preoperative protocol in a bariatric population with gas­troesophageal reux disease. Surg Endosc. 2020;34:1812–8.
24. Charbel S, Khandwala F, Vaezi MF.The role of esophageal pH monitor­ing in symptomatic patients on PPI therapy. Am J Gastroenterol. 2005;100:283–9.
25. Gyawali CP, Kahrilas PJ, Savarino E, etal. Modern diagnosis of GERD: the Lyon consensus. Gut. 2018;67:1351–62. https://doi.org/10.1136/
gutjnl- 2017- 314722.
26. Wiener GJ, Richter JE, Copper JB, Wu WC, Castell DO.The symptom index: a clinically important parameter of ambulatory 24-hour esopha­geal pH monitoring. Am J Gastroenterol. 1988;83:358–61.
27. Weusten BL, Roelofs JM, Akkermans LM, Van Berge-Henegouwen GP, Smout AJ.The symptom-association probability: an improved method for symptom analysis of 24-hour esophageal pH data. Gastroenterology. 1994;107:1741–5.
28. Richter JE, et al. Normal 24-hr ambulatory esophageal pH values. Inuence of study center, pH electrode, age, and gender. Dig Dis Sci. 1992;37:849–56.
193
Wireless pH Testing
https://t.me/medicina_free
14
JennwoodChen andKyleA.Perry
While gastroesophageal reux disease (GERD) is a common dis­order, making the diagnosis can be challenging because symp­toms are often vague. Symptom presentations can be variable between patients, and manifestations of GERD overlap with other foregut pathologies including functional dyspepsia, esophagitis, and gastroparesis [14]. Consequently, identifying GERD based on symptoms alone leads to the wrong diagnosis in 30–50% of patients [57]. Similarly, esophageal acid exposure alone is insuf­cient to predict the presence of GERD symptoms or their sever­ity; however, it can help predict response to anti-reux surgery [8,
9]. Therefore, it is imperative to document objective pathologic
reux in GERD patients, especially for those being considered for anti-reux surgery (ARS) [6, 10].
J. Chen Division of Gastroesophageal and Bariatric Surgery, University of Utah, Salt Lake City, UT, USA e-mail: Jennwood.Chen@hsc.utah.edu
K. A. Perry (*) Division of General and Gastrointestinal Surgery, Ohio State University, Columbus, OH, USA e-mail: Kyle.Perry@osumc.edu
© Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) 2023 A. D. Patel et al. (eds.), The SAGES Manual of Physiologic Evaluation of Foregut Diseases,
https://doi.org/10.1007/978-3-031-39199-6_14
195
196
https://t.me/medicina_free
In the absence of clear endoscopic evidence, the current gold standard test to diagnose GERD is the 24-h ambulatory esophageal pH metry or alternatively, the wireless esophageal pH monitoring probe (Bravo™, Medtronic, Shoreview, MN) which most con­sider an equivalent option [11]. In fact, the recent GERD consen­sus panel in Lyon recommends that the optimal diagnostic for initial proton pump inhibitor (PPI) non-responders without prior endoscopic demonstration of GERD is pH monitoring done while withholding anti-secretory therapy [12]. In this chapter, we will discuss the evolution, interpretation, and utility of wireless pH monitoring.
J. Chen and K. A. Perry
A Brief History of pH Monitoring
The diagnosis of gastroesophageal reux has been evolving for over a century since 1884, when Reichmann lowered a sponge in the esophagus of patient with heartburn and showed that it con­tained acid [13]. In 1958, using a modied manometry probe, Tuttle and Grossman measured the in situ pH of the esophagus 2cm above the “respiratory inection point” [14]. Based on their work, pH would eventually become the standard metric to quan­tify gastroesophageal reux.
Designed to measure the hydrogen-ion concentration through­out the gastrointestinal tract, the rst wireless pH capsule was cre­ated by Jacobson and Mackay in 1957 [15]. Although not specically geared toward detecting esophageal reux, its cre­ation provided the fundamentals for what would later become the ambulatory wireless pH monitoring device [16]. In 1974, DeMeester and Johnson studied gastroesophageal reux in nor­mal individuals and patients with GERD symptoms. Their land­mark study established the modern parameters of pH monitoring to diagnose GERD. In particular, they established the location at which the pH sensor is to be placed (5cm above the lower esoph­ageal sphincter), dened the threshold pH (4) for acid reux, and created a composite score (Johnson- DeMeester Score) to cat­egorize patients as having pathologic acid reux [1719].
14 Wireless pH Testing
https://t.me/medicina_free
197
Catheter-Based pH Monitoring
Until the early 2000s, the primary options for ambulatory esopha­geal pH monitoring were catheter-based systems. First introduced in the 1970s, these require passage of a nasopharyngeal catheter placed 5cm above the endoscopically or manometrically identi­ed lower esophageal sphincter (LES) [20]. The catheter runs over and behind the ear and is taped securely to the nose. The catheter connects to a portable digital data recorder that the patient wears around the waist or over the shoulder. The patient is instructed to refrain from changing their daily routine, abstain from bathing, and remain upright until bedtime. Using the digital data recorder, a virtual diary of events is kept which includes symptom events (e.g., heartburn, regurgitation, cough, and sore throat), beginning and end of mealtimes, each time the patient lays down and gets up, and duration of events.
Interpreting the output of the digital recorder involves analyzing both graphical and numerical data. The graphical output comprises a pH tracing that shows acid reux episodes (drops in pH to a level below pH of 4) over time. The recording system is calibrated to a sampling rate (usually 4s) at which the pH data are recorded [21]. The numerical data include the percent time of reux over the mon­itoring period, percent time of reux in the upright and supine posi­tions, total number of reux episodes, number of episodes that last longer than 5min, duration of the longest episode, and a composite score [22]. The composite score, commonly referred to as the DeMeester score, is based on the standard deviation of the mean of each of the six components measured in normal subjects [23]. Finally, the data also include three measures of symptom correla­tion: symptom index (SI) dened as the percentage of reux-related symptom episodes, symptom-sensitivity index (SSI), dened as the percentage of symptom-associated reux episodes, and symptom association probability (SAP) which is a measure of correlation between symptoms and reux episodes [21]. Of the three symptom correlation schemes, the SAP and the SI, interpreted in conjunction, are the most statistically valid for symptom-reux association [24].
The normative thresholds for diagnosing pathologic reux, as agreed upon by professional consensus groups, are as follows: (1)
198
https://t.me/medicina_free
24-h total % time pH < 4 greater than 4–5.5% (2) DeMeester score14.7 (3) SAP>95% for primary symptom, SI>50% for primary symptom [25].
The total duration of the catheter-based ambulatory pH study is typically 24h. This allows for measurements to be characterized over a complete circadian cycle and captures the effect of physical activity and body position on esophageal acid exposure [26].
It should be apparent from the above description that the abil­ity of ambulatory pH monitors to accurately detect abnormal reux is largely dependent on patient’s tolerance of the test, adherence to a “normal routine,” and adequate duration of moni­toring. It is these areas which catheter-based systems tend to be most problematic.
Patient discomfort and social embarrassment from the passage and xation of the nasoesophageal pH catheter are ubiquitous [27,
28]. In fact, up to 10% of patients fail to complete the 24-h moni-
toring period due to intolerance [29, 30]. For those that are able to endure the duration of the test, studies have shown that patients do signicantly alter their daily routine [31, 32]. In particular, patients are more sedentary and spend less time eating, drinking, and being physically active [33]. Unfortunately, these compensa­tory behaviors may alter the reliability of the test [27, 32]. Finally, it has been suggested that limiting the test to 24h decreases the diagnostic yield due to the high day-to-day variability in acid exposure and symptom reporting [29, 34, 35]. Studies comparing repeated 24-h monitoring estimated the reproducibility to be 77–83% which may explain why a signicant portion of patients with erosive reux have a normal ambulatory 24-h pH study [28,
36, 37]. Furthermore, studies reporting on the detection perfor-
mance of catheter-based systems vary widely with reported sensi­tivities ranging between 73 and 96% [28, 38, 39].
J. Chen and K. A. Perry
Wireless pH Monitoring
In response to these limitations, the Bravo™ wireless pH moni­toring device was developed in 2001 and approved by the US Food and Drug Administration in 2005 for the evaluation of patients with GERD [40].
14 Wireless pH Testing
https://t.me/medicina_free
199
The Bravo™ wireless pH monitoring system utilizes a radio­telemetry pH sensing capsule that is attached to the mucosa of the distal esophagus. The capsule measures 6mm×5.5mm×25mm and contains an antimony pH electrode, a reference electrode, a battery, and a radio-transmitter [40]. The capsule is mounted onto the end of a delivery catheter for oral or nasal insertion, with the former being the preferred method [41].
Prior to insertion, an upper endoscopy is generally performed and the squamocolumnar junction (SCJ) is identied and mea­sured from the incisors. Ideally, the capsule is deployed 6 cm proximal to the SCJ [42]. This is due to the fact that the SCJ is approximately 1cm distal to the proximal border of the LES [43]. Therefore, endoscopic placement of the Bravo™ capsule 6cm proximal to the SCJ corresponds to manometric placement of the traditional pH catheter 5cm proximal to the LES.Transoral place­ment of the capsule based on manometric landmarks is an alterna­tive option. However, the positioning requires a correction factor to account for the longer pathway of the transnasal manometry catheter [44].
Once the device is activated and calibrated, the delivery catheter is inserted with or without direct endoscopic guidance. With the cathe­ter in its desired location, a vacuum pump is used to apply suction to the wall of the capsule. A pressure between 510 and 700mmHg is applied for approximately 10–30 s, after which time an activation button is pressed to deploy a spring-loaded pin that attaches the Bravo™ capsule to the mucosa [40, 45, 46]. If placed without direct endoscopic guidance, a repeat endoscopy may be performed to con­rm placement. The capsule measures pH and transmits data to a pager-sized receiver that can be worn on the patient’s belt [47]. As long patients stay within signal detection range of the receiver (approximately 1m or 3ft.), patients are encouraged to follow their daily routine, including bathing. Patients keep a virtual diary of their reux-related symptoms and events.
The parameters measured during wireless pH monitoring are similar to catheter-based systems [19, 48]. However, in contrast to the 4s sampling rate of catheter-based systems, the Bravo™ cap­sule samples esophageal pH every 6s [27]. Another important difference is that the duration of wireless pH monitoring can be extended to 96h.
200
https://t.me/medicina_free
J. Chen and K. A. Perry
Wireless Versus Catheter-Based pH Monitoring
The clear advantage of wireless pH monitoring over traditional catheter-based systems is patient comfort and ability to adhere to routine activities. In a randomized cross-over trial, Wenner etal. showed that 87% of patients undergoing esophageal pH monitor­ing preferred the wireless pH capsule over the catheter-based technique, citing less interference with normal activities and social embarrassment [32]. In a study of 133 patients who under­went pH monitoring (78 catheter-based; 55 wireless), Grigolon etal. found that the wireless technique was far better tolerated than the catheter-based, with minor impact on daily activities including food intake [31]. Sweis et al. showed that 96% of patients, who were previously unable to tolerate 24-h catheter­based monitoring, successfully completed 48h of wireless testing and due to less restriction in activities of daily living, nasopharyn­geal discomfort, dysphagia, and chest pain [30]. Finally, in a meta-analysis of randomized control trials that included 167 patients, authors concluded that the Bravo™ wireless pH monitor interfered less with daily activities compared to the catheter­system system [49].
Second, proponents of wireless pH monitoring often discuss the potential increased sensitivity for detecting reux events due to the prolonged monitoring capability. While catheter-based monitoring is carried out over a 24-h cycle, which typically pro­vides 20–22h of interpretable data, the Bravo™ capsule captures pH levels for up to 96h [25]. In a study of 186 patients undergoing wireless pH monitoring, extended monitoring for 48h identied 22% more patients with abnormal esophageal acid exposure [50]. Sweis etal. found that 96-h monitoring using the Bravo™ capsule diagnosed GERD in 76% of patients with typical reux symptoms but with previously negative 24-h catheter-based pH studies [51]. Authors comparing 48 to 96-h wireless pH monitoring reported a
23.5% increase in GERD diagnosis when the test was extended by 2 days [52]. Similarly, in a study of 99 patients undergoing 96-h wireless pH testing, Capovilla etal. found an increase in diagnos­tic yield of 12% when the wireless testing interval was extended
14 Wireless pH Testing
https://t.me/medicina_free
201
to 96 h. However, at long-term follow-up, only 25% of these patients, who would have otherwise had negative tests at 48h, reported good outcomes post-fundoplication. The authors con­cluded that while prolonged testing does increase diagnostic yield, it comes at the expense of potentially recruiting complex patients who may not respond to surgical therapy [53]. Currently, the most widely adopted duration for wireless testing is 48h.
Head-to-head studies comparing performance of wireless ver­sus catheter-based pH monitoring are intriguing. Pandolno etal. subjected 25 asymptomatic patients to simultaneous 24-h catheter­based and 48-h wireless pH monitoring [54]. Digitized uoro­scopic images were employed to ensure proper and equivalent positioning of the pH electrodes. A pH reference was established using swallows of orange juice (pH= 3.88). The result of the study showed that the catheter-based system over-reported the number of acid exposure events by nearly three times (117.0 vs.
41.8). Forty percent of this discrepancy was attributable to awed software calibration while the majority of the remainder were brief events with poor reproducibility between systems. In an almost identical study, Pandolno etal. again noted a signicant discrepancy between the two systems [55]. In terms of percent time, the pH was less than 4; Pandolno found that the catheter­based system reported acid exposure values twice those reported by the Bravo™ capsule. The tendency of catheter-based systems to over-report esophageal acid exposure has been a consistent nding in additional studies [48, 56]. Further examination reveals that the majority of the reux episodes missed by the Bravo™ capsule are short-duration events that are attributable to the longer sampling rate of the wireless system (6 vs. 4s), the signicance of which, is questionable [20]. Moreover, unlike the Bravo™ cap­sule which moves with the esophageal mucosa, catheter-based probes can “dip down” toward the stomach with each swallow [26]. Therefore, what is perceived to be an increase in reux events is simply artifact [57].
Wireless pH monitoring does have limitations. Despite the overall comfort of the Bravo™ capsule, chest pain can be signi­cant and is reported much more often when compared to catheter­based systems [49, 58]. Unintended and early detachment of the
202
https://t.me/medicina_free
J. Chen and K. A. Perry
capsule can be as high as 10% [59]. Furthermore, when positioned endoscopically, misplacement is common. In a retrospective study of 161 patients, investigators reported that nearly 30% of Bravo™ capsules placed were mal-positioned. The majority of which were >3 cm proximal to the ideal location [42]. Interestingly, upon reanalysis, the authors concluded that even misplacement of 5cm did not affect the frequency of positive pH studies. Finally, com­pared to catheter-based systems, the Bravo™ wireless capsule is considerably more expensive [40, 45].
Conclusion
Ambulatory pH monitoring is an invaluable tool in the diagnosis of GERD. The primary end points of pH monitoring are esopha­geal acid exposure time, number of reux events, and, to a lesser extent, the association between symptoms and episodes. Wireless pH monitoring is particularly useful for those patients who are unable to tolerate catheter-based testing. Extending the duration of monitoring time to 48 or 96h may increase diagnostic yield and reproducibility. However, wireless pH monitoring is consid­erably more expensive and thus may be cost-prohibitive in some instances.
References
1. Johnson LF, DeMeester TR.Development of the 24-hour intraesophageal pH monitoring composite scoring system. J Clin Gastroenterol. 1986;8:S52–8.
2. Penagini R, Sweis R, Mauro A, etal. Inconsistency in the diagnosis of functional heartburn: usefulness of prolonged wireless pH monitoring in patients with proton pump inhibitor refractory gastroesophageal reux disease. J Neurogastroenterol Motil. 2015;21:265–72.
3. Clayton S, Emerson JF.Eosinophilic esophagitis: a mimic of gastro­esophageal reux disease. Am Fam Physician. 2018;97:628–9.
4. Savarino E, de Bortoli N, De Cassan C, et al. The natural history of gastro- esophageal reux disease: a comprehensive review. Dis Esophagus. 2016;22:331–9.