What Is Known
- Abdominal pain is a leading complaint in the emergency department, and constipation a frequent etiology.
- Optimal therapy for pediatric fecal disimpaction in the acute setting remains unknown.
- The current literature on soap suds enema is primarily based on small case reports in adults describing adverse events.
What Is New
- The present study is the largest study of soap suds enema use in children in the acute setting.
- Soap suds enema was effective in 82% of children with fecal impaction.
- No serious attributable adverse events occurred.
- Soap suds enemas offer an effective and safe therapy for fecal impaction in the acute setting.
See “Do We Really Need Soap to Clean the Rectum?” by Koppen and Di Lorenzo on page 1.
Abdominal pain is a leading chief complaint for patients seen in the emergency department (ED), and constipation is a frequent etiology (1). Published guidelines, such as those from the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN), on the evaluation and treatment of childhood constipation are primarily focused on the outpatient, non-acute evaluation and management of constipation (2–4). The optimal therapy for pediatric fecal disimpaction in the acute setting remains unknown.
In the ED, there is often a need to rapidly evaluate for potential life-threatening etiologies of abdominal pain, including appendicitis (5–7). This may result in a diagnostic and therapeutic approach toward suspected constipation that varies from algorithms used in the standard outpatient setting. Children undergoing disimpaction in the acute setting are more likely to experience pain relief compared with less aggressive therapies, and thus disimpaction per rectum is often employed (7–12). Published guidelines support oral therapies, such as polyethylene glycol (PEG) 3350, and rectal enemas as equally effective for fecal disimpaction; however, oral therapy may take several days (2,7,12). Children may tolerate rectal therapy enemas well without adverse events, and these may be employed for a more rapid onset of action (11).
Soap suds enema (SSE) is a hypertonic solution that provides a large-volume and detergent-based mucosal irritation to stimulate defecation. SSE has been the standard enema therapy administered in the ED setting of our institution with good anecdotal results. However, information regarding its efficacy is based primarily on small case reports, many of which report adverse events such as discomfort, colitis, and hemorrhage following SSE (13–18). To our knowledge, large studies reporting SSE usage in children are unavailable. We hypothesized that SSE is safe and effective; thus, the objective of the present study was to evaluate the safety and efficacy of SSE for fecal impaction in a large population of children presenting to a pediatric ED.
The present study was conducted on the basis of data from a quaternary children's hospital ED with an average annual volume of approximately 85,000 visits. The present retrospective cross-sectional study was approved by the Baylor College of Medicine institutional review board. All patients receiving SSE in the ED during one calendar year (from June 2011 to June 2012) were included. Patients were identified from electronic medical record orders for SSE within the ED. Included subjects presented with abdominal pain and were clinically suspected of having a fecal impaction by the attending physician. Patient demographics, medical history, disposition, return visits within 72 hours, and stool output were systematically recorded from review of nursing and physician notes. A significant medical history was defined as the presence of a prominent comorbidity including cystic fibrosis, cerebral palsy or muscle disorders, hypothyroidism, spina bifida or other spine anomalies, gastric anomalies, anal atresia or Hirschsprung disease, cardiac anomalies, or previous abdominal surgery. Data abstractors (E.H.B. and K.L.V.) were trained by the principal investigator. To minimize bias associated with data abstraction, we used specific, restrictive key words for subjective data fields. Unavailable data were coded as missing except for medical history and laboratory testing, for which the absence of specific description was interpreted as “not present” or “not done.” When multiple documentation sources were present, that of the most senior physician was used. Historical variables were documented before reviewing the outcome, investigations, adverse events, laboratory results, and disposition status.
SSE was ordered and delivered in the standard manner described below for the treatment of clinically suspected fecal impaction in children with abdominal pain. The decision to use an SSE and the amount given were made by the treating physician and administered by the nursing team. The SSE consisted of an average of 20 mL/kg (maximum: 1 L) tap water and one packet of soap (castile soap, Amsino International, Inc, Pomona, CA) administered by gravity using an enema bucket and a clear catheter tip inserted (up to 10 cm) into the rectum (19). One packet of soap was added regardless of volume administered; thus, detergent concentration varied. The patient was asked to retain the liquid as long as possible until they felt they must evacuate the liquid and stool.
The primary outcome was presence (treatment success) or absence (failure) of stool output following administration of the enema. Any stool output was considered a treatment success. If no stool output was documented, there was assumed to be no stool output, and this was coded as a failure. Secondary outcomes were adverse events, admissions, and return emergency visits. Mild adverse events were defined as nausea, vomiting, abdominal pain, or any untoward effect documented by the physician or the nurse attributed to the SSE following enema administration. Serious adverse events were defined a priori as severe colitis, hypotension, or hemorrhage. All patients with adverse events were reviewed by the first two authors to determine severity.
Comparisons of baseline demographic data, comorbidities, laboratory, treatment effect, and adverse events were evaluated using the χ2 or Fisher exact test comparing those with versus without successful output. Descriptive statistics including mean, median, and proportional frequencies were used to analyze the adverse events as appropriate. Continuous data including age were evaluated using the 2-sided independent Student t test with parametric data and Mann-Whitney U with nonparametric data. A P-value <0.05 was considered statistically significant using SPSS version 21 (SPSS, Inc, Chicago, IL).
Six hundred thirty-three potential patients were reviewed, of which 512 received SSE in the ED (Fig. 1). The median age was 7.8 years (range 8 months–23 years); with a slight female predominance (Table 1). A majority of children had a significant medical history, including 193 (38%) with a history of constipation (Table 1).
Efficacy and Discharges Following SSE Therapy
Productive stool was documented in 419 (82%) following SSE (Fig. 1). Sex, age, and history of constipation were not associated with SSE therapy success or failure (data not shown). A large majority of subjects were discharged from the ED following SSE therapy (Fig. 1). Of the 405 patients initially discharged from the ED following enema administration, 15 (3.7%) returned to the ED within 72 hours. This included 11 patients who had been discharged following stool output from an SSE and 4 discharged without documented output following SSE. Of those returning, 8 (53%) were admitted: 7 for observation with medical management and 1 for appendectomy. Patients with pain improvement were discharged according to provider's clinical impression.
Admissions Following SSE Therapy
Following the enema, 107 patients (21%) were subsequently admitted. Children who failed to have output following SSE were more likely to be admitted (39/93) than those who had a productive stool (68/419; P < 0.001). Of those admitted, 83 (78%) had a significant medical history and 52 (49%) had a history of constipation. The majority of admissions were to the observation unit (N = 63, 59%). In the observation unit, 47 (75%) received a cleanout using PEG solution and were discharged home without event.
Overall in those admitted further constipation therapies (of any type) were used in 75 (70%). Of these, PEG therapy failed for 4 patients, who required a manual disimpaction by the surgical team, and an additional 5 patients went to the operating room for other reasons (supplementary table, https://links.lww.com/MPG/A586). Non-abdominal pain-related admissions occurred in 6 patients (supplementary table, https://links.lww.com/MPG/A586), and the remaining admissions, both observation and inpatient, were related to serial abdominal examinations for abdominal pain with subsequent discharge. Patients were discharged according to provider clinical judgment with improvement in pain.
Adverse events were documented in 37 (7.2%) patients and included nausea, vomiting, and abdominal pain (Table 2). Those may all be attributed to the primary problem of increased stool burden as well. Children with adverse events were more likely to be admitted following SSE than children without an adverse event (28/37 vs 79/475, respectively; P < 0.001). No serious adverse events were noted that were attributed to SSE.
Respiratory complications unrelated to SSE occurred in 2 (0.4%) patients, who were subsequently transferred to the intensive care unit. A 14-year-old girl with nausea and abdominal pain developed hives with respiratory distress, as well as lip and eye swelling 4 hours after enema administration subsequently attributed to ondansetron by the allergy and immunology service. A second patient with a ventriculoperitoneal shunt developed respiratory distress following morphine administration. The respiratory distress was attributed to morphine and improved after naloxone administration. The same patient required an exploratory laparotomy for small bowel obstruction attributed by the attending surgeon to adhesions at the abdominal ventriculoperitoneal shunt site 3 days later. There was a 7-year-old patient who had 4 large bowel movements after SSE, tolerated 26 ounces of Gatorade and reported no abdominal pain on discharge that returned the next day with a perforated appendicitis. The appendicitis was not attributed to the SSE therapy by the attending surgeon.
SSE volume was recorded in 413 of the patients, with the median volume (20 mL/kg) of enema given (range 2–35 mL/kg; 10–20 mL/kg [25%–75%]). In those with a recorded SSE volume, the volume did not differ in those with productive stool versus those without (data not shown). The volume of SSE given did not differ between those with or without adverse events (data not shown).
Identifying rapid, safe, and efficacious modalities for therapy of fecal impaction prompting ED visits for pain in the pediatric setting is important. To our knowledge, our study is the largest of its kind to evaluate SSE as a therapeutic modality in any population. We found that SSE is efficacious in a large majority of children receiving SSE for suspected fecal impaction in the ED setting. This was seen both with our primary outcome of documented stool output and our secondary outcome of initial discharge from the ED. In addition, we found a limited number of adverse events. None were serious in nature, suggesting SSE is safe to use in the ED setting for childhood constipation.
SSE therapy is not included in recent guidelines for functional constipation (3). In addition recent NASPGHAN pediatric gastroenterology guidelines for the treatment of constipation recommend against the use of SSE due to potential toxicity, although did not grade the evidence for the recommendation (1). We suspect that omission of SSE is based on a lack of large studies to date evaluating its efficacy and safety. Rather the literature on SSE is primarily based on case reports, with a few articles identifying severe colitis as an adverse event; often in adult patients with significant underlying medical conditions (13–16). However, caustic colitis from SSE is believed to be rare because the strength of the enema solution is seldom strong enough to cause corrosive effects on the colon (15). Our study, using a readily available SSE solution, supports the rare nature of serious adverse events as we found none in more than 500 SSE administrations. All adverse events attributable to SSE were mild and occurred at a rate comparable to the 10% to 30% reported in other enema types in children in the ED setting (8,11). Given the relatively low number of adverse events related to SSE in our study, we suggest SSE may be as safe as other commonly used disimpaction therapies in the ED setting.
The ED setting differs from a typical outpatient setting in many ways. This may include more frequent vital sign monitoring, nursing assessments, and additional therapies such as intravenous fluids. These and other potential differences may help ensure safety of SSE therapy in the acute care setting. Future studies in other outpatient settings may be needed before SSE therapy is adopted outside the ED.
Recent NASPGHAN guidelines on the treatment of functional constipation state that enema therapy is as effective as PEG-based oral therapies for disimpaction (2,6). Although one productive stool following enema was the measure of success in the present study, a complete rectal disimpaction was unlikely completed in most children. This outcome measure was chosen in the ED setting, as the resulting clinical improvement following a bowel movement may be reassuring to both clinicians and families with respect to the correct diagnosis and therapy needed. Therefore, we felt this outcome best exemplified whether SSE therapy was successful as an end point lending to a safe disposition for the child as others have done when evaluating ED-based therapies (8). The large number of children able to be discharged home with only a few returning to the ED reinforces the efficacy of this therapy in the ED setting. Further oral therapy is required in the majority of discharged children, a finding consistent with previously reported laxatives on discharge (8).
As expected SSE was not completely successful in all patients. We hypothesize that some children were too impacted to respond sufficiently to one SSE enema alone. Other possibilities include an incorrect diagnosis of fecal impaction as a contributing factor for the abdominal pain, insufficient enema volume used, or other technical issues such as lack of retention of the enema following administration. Future studies investigating diagnostic algorithms or higher volumes or concurrent therapies with SSE may be warranted in this population.
There are several strengths to the study. First, this is the largest cohort of patients in which SSE therapy has been reported to date. Second, the data were obtained from the medical record; as such the results are likely to be generalizable and applicable in the clinical setting as the SSE therapy was given as part of routine clinical practice. SSE provides a less expensive and readily available enema alternative. In addition, in our setting, this enema solution does not come from pharmacy and thus is more rapidly administered than other enema types. Finally, outcomes related to short-term efficacy as well as longer-term efficacy with relation to return visits allowed for an increased opportunity to capture a wide evaluation of efficacy and safety of the SSE therapy.
The primary limitation to this retrospective study is the lack of prospective standardization (eg, SSE volume administered, concentration, diagnostic criteria, and discharge criteria.) There may have been bias in how some variables (eg, adverse events, quantification for amount of stool output) were documented, as it is based on provider and nurse determinations. However, we thoroughly reviewed all ED provider and nursing notes as well as hospital notes from admitted patients in an attempt to capture all documented events. In addition, there is the possibility that the discharged patients sought care elsewhere and were not captured on follow-up. Future prospective trials, perhaps comparing SSE to other therapeutic modalities will be needed to capture outcome evaluations more thoroughly.
In conclusion, SSE is an effective and safe means of treating fecal impaction in the pediatric ED setting. The adverse events of SSE are comparable to those seen with other laxative therapies, and no serious attributable adverse events were found in more than 500 SSE administrations. We suggest consideration of SSE as a potential therapy for fecal impaction in the ED setting.
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