Abstract
Purpose
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For many decades, patients recovering from wound closure have been instructed not to bathe. Although studies have shown that earlier postoperative bathing does not increase the risk of wound infection, it remains rare in practice for patients to be allowed earlier postoperative bathing. We performed this meta-analysis to determine how earlier bathing affected rates of wound infection, other complications, and patient satisfaction.
Methods
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This systematic review conforms to PRISMA guidelines. The PubMed, EMBASE, Medline, Web of Science, and the Cochrane Central Register of Controlled Trials were searched from their inception dates to December 31, 2022. We estimated pooled values for the efficacy of trial of earlier bathing versus delayed bathing using the odds ratio and their associated 95% CI, and we used the I 2 statistic to assess heterogeneity between studies contributing to these estimates.
Results
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Of the 1813 articles identified by our search, 11 randomized controlled trials including 2964 patients were eligible for inclusion. The incidence of wound infection did not differ significantly between the earlier bathing and delayed bathing groups, nor did rates of other wound complications such as redness and swelling, or wound dehiscence. However, the incidence of hematoma in the delayed bathing group was higher than in the earlier bathing group. Reported patient satisfaction was significantly higher in the earlier bathing group.
Conclusion
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The medical community, health authorities, and government should create and disseminate clinical practice guidelines to guide patients to evidence-based beneficial treatment.
Introduction
In outpatient or emergency department settings, patients recovering from sutured wound closure often ask whether and when the direct water contact with the skin wound is permitted. If regular bathing and body cleaning are not carried out during long-term treatment, body odor and negative emotions can result, especially in areas with high humidity and high temperature (1). Not bathing for a week or even several months significantly affects a patient’s comfort and reduces their quality of life.
In the 1980s, numerous authoritative studies addressed the question of whether wounds without stitches could be soaked in water and bathed. The traditional practice was to keep the wounds dry until the stitches were removed (2). However, guidance issued by an expert panel at the U.S. National Institutes of Health (NIH) states that it is relatively safe to bathe the epidermis and cover the wound within 48 h of wound closure (3). Furthermore, studies have found that earlier postoperative bathing does not increase the risk of suturing wound infection compared with bandaging without bathing (4, 5, 6).
Therefore, the possibility of earlier postoperative bathing has become the focus of international controversy (7), mainly concerning the potential for infection and its potential effects on healing the injured tissue if the wound surface becomes wet. The risk of infection depends on the type of wound (open wounds are more susceptible to infection than epidermal wounds), medical complications, type and quality of water used, and wound complications. However, because it is clinically difficult to determine the exact probability of infecting a sutured wound, it is difficult to fully determine whether bathing truly increases the probability of wound infection. Although as early as 1976, earlier postoperative bathing was reported not to increase the incidence of postoperative complications (8), over the years, surgeons have been reluctant to let patients bathe.
To further investigate the evidence or lack thereof regarding the timing of postoperative bathing, we conducted a systematic review of the literature to clarify whether and how direct water contact influences the healing of closed wounds, providing a reliable proof for the later formulation of guidelines and the promotion of concepts.
Methods
The study conforms to the principles outlined in the Handbook of the Cochrane Collaboration (9), along with the guidelines established by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement (10). The protocol for this meta-analysis was registered on PROSPERO (Registration No.: CRD 42022303738).
Inclusion criteria
We measured trials to be eligible if they compared earlier exposure to water on the surgical incision site with delayed exposure, and if the patients had clean or clean-contaminated incisions.
Exclusion criteria
We excluded studies if they were letters, case reports, reviews, observational studies, animal trials, or republished studies; if they recruited patients with current infection status, open wounds, or severe immunocompromised status; if the patients were taking immunosuppressive drugs; if the patients underwent a flap or 2-layer procedure, or had contamination incision; and if the articles had missing data.
Outcomes
The primary outcome was the incidence of surgical site infection (SSI). Secondary outcomes included satisfaction and the incidence of other wound complications.
Search strategy
Two of the authors (WJP and HY) performed the search in PubMed, EMBASE, Medline, Web of Science, and the Cochrane Central Register of Controlled Trials from the inception dates to December 31, 2022.
PubMed search strategy
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#1 (Wound or suture* or stitch* or incision* or excision) [All Fields].
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#2 (Wet or water or bath* or shower* or swimming) [All Fields].
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#3 postoperat* [All Fields].
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#4 (randomized controlled trial[pt] OR controlled clinical trial[pt] OR randomized[tiab] OR placebo[tiab] OR randomly[tiab] OR randomised[tiab]).
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#5 (#1 AND #2 AND #3 AND #4).
We also searched the International Clinical Trials Registry Platform (ICTRP) portal maintained by the World Health Organization to identify ongoing or unpublished eligible trials and the reference lists of articles retrieved from the electronic search for related articles. No language restrictions were applied during the search. Reviewers were blind to each other's decisions and assessments to minimize the risk of bias.
Study selection
After the removal of duplicates, two independent researchers (YR and WJP) screened all titles and abstracts, performed the searches, and made decisions regarding inclusion and exclusion criteria. When studies were considered eligible, they obtained full texts and performed further screening. If the two researchers had different opinions about the eligibility of a study for inclusion and a consensus was not reached, the senior researcher (HL) decided after a group discussion.
Data collection process
Two investigators (YR and HL) used a standard data extraction form to independently extract all related data from selected trials. When the randomized controlled trials had more than two groups and permitted multiple comparisons, we pooled only the data and information of interest reported in the original article. Data extracted included the first author’s name, year of publication, country, type of study, sample size, age, surgical site, and the number of infections. Disagreements were resolved by consensus.
Assessment of risk of bias and quality of evidence
Two researchers (LC and HL) independently assessed the quality of all included trials based on Cochrane risk-of-bias criteria (11). Researchers decided whether those assessing the risk of bias would be blinded to the names of the authors, institutions, journals, and results of a study when they assessed its methods. Disagreements were resolved by consensus.
Data synthesis
The meta-analysis was performed using Stata software (version 17; StataCorp, 2021). The heterogeneity was assessed by using the Q test and I 2 value calculation. The random-effects model was used for our analyses. The odds ratio (OR) and their associated 95% CI were used to assess outcomes, and a P value less than 0.05 suggested that the difference was statistically significant.
Subgroup analyses
We performed subgroup analyses for similar subsets of patients across trials.
Sensitivity analyses
We performed a sensitivity analysis by excluding the largest trial; excluding cluster randomized or quasi-randomized trials; excluding trials with a high risk of bias; using random-effect models.
Results
Eligible studies and study characteristics
We initially identified a total of 1801 unique published studies via the search methods detailed above and finally included 11 eligible trials in the meta-analysis, all of which reported surgical site infection (5, 8, 12, 13, 14, 15, 16, 17, 18, 19, 20). The reference flow is shown in Fig. 1. The details of included trials are shown in Table 1. These trials comprised 2964 participants, of whom 122 developed an infection at the surgical site. To ensure reliable study data, we evaluated the risk of bias and quality of evidence for each of the included studies. Figure 2 presents the risk of bias for each study.
Characteristics of included studies. Values are presented as the mean ± s.d., unless otherwise indicated.
Study | Country | Study design | Participants, n | Age, mean ± s.d. | Surgical site | Definition of SSI | Intervention | ||
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Earlier bathing | Delayed bathing | Earlier bathing | Delayed bathing | ||||||
Fraser et al. (8) | England | RCT | 108 | NA | NA | Miscellaneous | Own definition | Bath 48 h PO | Bath-forbidden |
Ghandi et al. (18) | Iran | RCT | 468 | 28 ± 8.1 | 31 ± 6.9 | Dermatological surgeries | Defined by two dermatologists | Wet 24 h PO | Wet 48 h PO |
Gök et al. (19) | Turkey | RCT | 51 | NA | NA | Coronary artery bypass graft | CDC criteria | Bath 48–72 h PO | Bath-forbidden |
Goldberg et al. (5) | USA | RCT | 200 | NA | NA | Clean head and neck lacerations or incisions | Not defined | Bath 8–24 h PO | Bath-forbidden |
Heal et al. (12) | Australia | RCT | 857 | 56.5 ± 16.2 | 55.9 ± 16.6 | Minor skin excision | CDC criteria | Bath 12 h PO | Bath 48 h PO |
Hsieh et al. (13) | Taiwan | RCT | 440 | 55.3 ± 14.2 | 55.6 ± 13.8 | Miscellaneous | CDC definitions | Bath 48 h PO | Bath-forbidden |
Neues & Haas (14) | Germany | RCT | 572 | 39 (22–78)* | 53 (23–81)* | Varicose surgery | Not defined | Bath 48 h PO | Bath-forbidden |
Palese et al. (15) | Italy | RCT | 53 | 51.4 ± 17.6 | 52.5 ± 15.6 | Neurosurgical surgery | CDC criteria | Bath 72 h PO | Bath-forbidden |
Riederer & Inderbitzi (16) | Germany | RCT | 101 | NA | NA | Inguinal hernia | Not defined | Bath 24 h PO | Bath-forbidden |
Voorhees et al. (17) | USA | RCT | 82 | NA | NA | Miscellaneous | Own definition | Bath 48 h PO | Bath-forbidden |
Yu et al. (20) | USA | RCT | 32 | NA | NA | Total knee arthroplasty | Not defined | Bath 48 h PO | Bath-forbidden |
*Median (range).
RCT, randomized controlled trials; CDC, Centers for Disease Control and Prevention; NA, not applicable; PO, post-operation.
Primary outcome: surgical site infection
The pooled infection rate was 3.57% (55/1542) in the earlier postoperative bathing group and 4.71% (67/1422) in the delayed postoperative bathing group. There was no statistically significant difference in the proportion of participants who developed surgical site infection between these two groups (OR: 0.84, 95% CI: 0.58–1.22, P = 0.368, I2 = 0%; Fig. 3) The Harbord test showed no small-study effects (P = 0.117).
Cumulative meta-analysis
Cumulative meta-analyses were performed in order of years of publication. The results showed that the cumulative effect size stabilized, and the 95% CI narrowed gradually. The cumulative effect OR was 0.57, and the 95% CI was 0.27–1.19 (Fig. 4), indicating no difference between groups in the rate of infection.
Other wound complications
Rates of other wound complications were reported in three of the included studies. These mostly included redness and swelling, wound dehiscence, secretion, and hematoma. For the incidence of hematoma, there was a significant difference between the earlier and delayed postoperative bathing groups (OR: 0.25; 95% CI: 0.09–0.73, P = 0.01; Fig. 5); for the other wound complications, no significant difference was found.
Satisfaction
Four of the included studies evaluated patient satisfaction (13, 14, 15, 16). Data from the study by Palate et al. were not pooled because no data were provided (15). In the remaining three studies, the earlier postoperative bathing group showed a significant increase in satisfaction compared with the control group (OR: 101.91, 95% CI: 36.92–281.29, P < 0.0001, I2 = 62.3%; Fig. 6).
Discussion
Earlier bathing improves patient satisfaction, reduces the incidence of respiratory infections and venous thrombosis (7), and does not increase the incidence of wound complications. To provide stronger evidence supporting this opinion, we conducted a meta-analysis to assess the effect of earlier postoperative bathing on wound healing. In this meta-analysis of 11 randomized controlled trials with a total of 2964 participants, all included patients who underwent elective surgery and underwent strict sterilization before surgery. As a result, patients were well prepared for surgery. Except for two articles comparing earlier water exposure (after 12 or 24 h post procedure) and late (after 48 h post procedure) (12, 18), all other comparisons were made between contact post-surgery and no contact with water before suture removal. The pooled results show that earlier bathing is not significantly associated with surgical site infections. Furthermore, the findings suggest that earlier bathing improves patient satisfaction but does not increase the rate of other wound complications such as redness and swelling, wound dehiscence, and secretion. Although a statistically significant increase was found for hematoma, only one study reported this rate, and the sample size was small, with the potential for bias being large, and the evidence level being low. To speculate on potential reasons for the observed lower incidence of hematoma in the early bathing group, we can consider several hypotheses based on existing knowledge and clinical experience such as improved wound healing due to better blood flow and oxygenation, enhanced removal of inflammatory mediators or debris, and reduced bacterial colonization through early cleansing and subsequent wound care. As shown in Fig. 2, the risk of bias assessment revealed a high-risk level. This classification is primarily attributed to performance bias. It is imperative to acknowledge that high risk of bias may have introduced limitations to the reliability of our findings, potentially leading to overestimation or underestimation of results. We have conducted sensitivity analyses to assess the actual impact of high-bias risk on our results. While highlighting this limitation, we also emphasize the need for cautious interpretation. It is essential to consider other aspects such as the number of studies, consistency, and effect size when evaluating the overall evidence. Additionally, we suggest future research directions, including stricter methodology, comprehensive reporting, and enhanced quality control measures, to mitigate the influence of high bias risk in similar studies.
Besides, the included study by Yu et al. provides valuable insights into patient bathing practices specifically related to total knee arthroplasty and its implications for orthopedic practice. The findings from the study by Yu et al. suggest that early showering, starting at 2 days post operation, does not increase the risk of bacterial recolonization at the surgical site in total knee arthroplasty (TKA) patients. There was no significant difference in the rate of colonization or bacterial type between the early showering group and the delayed showering group. This finding supports the consideration of early showering as a safe practice for TKA patients, enhancing their comfort, facilitating early mobilization, and aligning with patient preferences. Early showering can contribute to improved patient satisfaction, psychological well-being, and compliance with infection control measures. These findings, along with the conclusions drawn from other studies in abdominal surgery, neurosurgery, and various surgical subspecialties, suggest that patient bathing practices may not significantly impact surgical site outcomes in terms of bacterial recolonization. However, it is important to acknowledge the heterogeneity in the available literature and the need for further research specifically focused on patient bathing after orthopedic surgical procedures. While the conclusions for orthopedic patients based on the current evidence may be limited, the collective evidence suggests that patient bathing practices can be approached cautiously and individualized based on the specific surgical context and patient preferences.
Studies have shown that bathing earlier postoperatively can effectively remove sweat, dirt, microorganisms, and necrotic tissue, thereby accelerating wound healing and reducing the risk of infection. Not bathing for 2 or 3 days after surgery has a negative impact on patient comfort and can lead to the risk of infection (2). The traditional recommendation is to cover the wound with a dressing for at least 48 h, as this is the period when wound epithelialization occurs (21). Post-bathing, there is no evidence of increased growth of bacteria on the skin around the wound (20). Considering all the above evidence, it seems illogical to prohibit patients from taking an earlier postoperative bath. However, more than half of doctors nonetheless reject the evidence and say they will not apply it to the clinic, especially in cardiovascular surgery, orthopedics, and neurosurgery. In clinics, the wound was either taped over, or the patient was advised to wait until the wound had healed before bathing. In addition, most patients do not realize that the wound can be exposed to water, and even after receiving the doctor’s explanation, they may be nonetheless worried about the occurrence of complications such as wound infection.
There have been relevant meta-analysis studies in the past to explore this scientific problem (7, 22), but each has had their own shortcomings. Copeland-Halperin et al. searched only within PubMed and restricted the publication language to English, thereby increasing the potential bias of the report. Additionally, they included only seven articles (one retrospective study and six randomized clinical trials (RCTs)), concluding that earlier postoperative bathing did not increase the risk of infection (22). In 2018, Yu et al. also conducted a meta-analysis, which included a total of 12 articles (two retrospective and ten RCTs), and came to the same conclusion (7). However, this article included a study on the use of saunas; we investigated whether bathing affects wound infection, mainly because the wound increases the risk of infection when exposed to water. Because sauna use mainly implies contact with sweat, which is relatively sterile, it is not the focus of our discussion, and our study excluded it (23). Unlike previously published studies, our meta-analysis only included RCT studies, did not restrict language, and searched multiple databases. Additionally, as years have passed and published evidence has accumulated, our analysis was able to include more published RCT studies with larger sample sizes are larger and higher evidence levels.
Although we conclude that earlier postoperative exposure to water has no significant effect on wounds, most of these studies were conducted in developed countries. Sanitation conditions vary from place to place, and some developing areas or island communities may still be living with rainwater, well water, and other sources when groundwater is scarce or polluted. Rainwater is the source of drinking water most likely to be contaminated by feces, and during collection, it can be contaminated by roofs and other collection surfaces, and often has no mobility, which can easily lead to bacterial growth when stored (24). In developing countries, tap water may not be disinfected, and the number of bacteria in tap water may greatly exceed the standard. Even if tap water is disinfected, water can become susceptible to infection during storage and pipeline transportation (25). Further, the bacterial requirements for domestic water are developed based on levels of common pathogenic bacteria that are pathogenic to the human digestive system after drinking. For water used to clean wounds, the requirements for bacteria should be higher. It is generally accepted in the medical profession that wounds can become infected when the bacterial colonies per gram of tissue or per milliliter of liquid exceed 105 colony-forming units (CFUs) (26). In summary, if the patient is given permission for earlier postoperative bathing, we recommend the following: First, for these patients, it is best to choose intradermal sutures or use smooth silk threads or leather nails for sutures, because if silk thread is used, the water will be immersed in the deep tissue along the silk thread. Secondly, the bathroom used for bathing should be disinfected. Thirdly, domestic water should be boiled and cooled before use, which further eliminates most of the bacteria. Fourthly, rubbing the wound should be avoided during bathing. Fifthly, it is recommended to carry out local disinfection of the wound after bathing. Sixthly, the patient’s pain should be managed because wound pain will reduce the likelihood of bathing (27). RCTs involving more countries are needed to further support these recommendations.
Based on the available studies, our findings provide a high level of evidence that earlier bathing does not increase the incidence of infection and improves patient comfort. However, a gap between evidence-based knowledge and decision-making exists at all levels of health care. Some patients may still refuse earlier postoperative access to water, mainly because of a lack of awareness, the treating team’s hesitance to allow an earlier bath, and the lack of advocacy from a trusted institution. Therefore, the medical community and government health authorities should develop and disseminate, including via social media, clinical practice guidelines that allow clinicians to agree and adhere to recommendations, and guide patients to make correct, beneficial treatments to promote proper care.
Limitations
While our analysis provides findings with a high level of medical evidence, it does have the following limitations: First, SSI has been defined as an infection related to surgical procedures occurring at or near a surgical incision within 90 days postoperative (28). However, some of the included studies had follow-up periods of less than 90 days (15), which may have resulted in incomplete outcome data and increased bias. Besides, some studies lacked diagnostic specifications for SSI or had differing diagnostic criteria for SSI, resulting in increased heterogeneity and influencing outcome indicators. Secondly, except for one study conducted in Taiwan, most of the other studies were reported in developed countries. The sanitary conditions and the degree of bacterial contamination of water in different regions varied, which may have increased publication bias. Thirdly, due to the scarcity of available literature focusing on patient bathing practices in relation to implantation and infection outcomes, our study lacked the necessary data to draw definitive conclusions regarding the impact of implantation on infection risks. It is important to highlight that the inclusion of a larger number of studies specifically addressing the effect of implantation on infection would be essential to conducting meaningful subgroup analyses. This would provide a more comprehensive understanding of the relationship between implantation and infection risks associated with patient bathing practices. Besides, the importance of longer follow-up periods, ideally spanning 1, 2, or even 3 years, to thoroughly evaluate the occurrence of implant-associated infections. Future studies with extended follow-up durations are warranted to capture these delayed infections and provide a more comprehensive understanding of their association with patient bathing practices. Fourthly, the included studies included very heterogeneous types of surgery from abdominal surgery, dermatological surgeries, coronary artery bypass graft, head and neck lacerations or incisions, varicose surgery, neurosurgical surgery, with only one study by Yu et al. specifically addressing TKA. The limited number of studies conducted in orthopedic patients poses a challenge in drawing definitive conclusions and making robust recommendations for patient bathing in orthopedic practice. Orthopedic surgical procedures, such as joint replacements, may have unique considerations and variations in practice that need to be explored to optimize patient outcomes. To address this gap in knowledge, further research specifically targeting orthopedic surgical patients is necessary. Future studies should aim to investigate the impact of different patient bathing practices on surgical site outcomes, infection rates, patient satisfaction, and other relevant clinical parameters in orthopedics. Besides, the limited availability of studies within each subgroup hindered our initial plan of conducting subgroup analyses based on different surgical populations. This scarcity of data prevented us from performing the pre-planned subgroup analyses. As a result, our ability to draw definitive conclusions specific to these subgroups was restricted. It is important to acknowledge that this limitation might have implications for the generalizability of our findings to distinct surgical cohorts. Fifthly, large-scale randomized controlled trials with rigorous methodology and standardized protocols are needed to provide high-quality evidence and enable more precise recommendations for patient bathing in the orthopedic setting. By emphasizing the need for further research focused on orthopedic surgical patients, we can highlight the importance of bridging the gap in knowledge and addressing the specific requirements of the orthopedic field. This will contribute to the development of more robust guidelines and recommendations tailored to the unique needs of orthopedic surgical patients.
Conclusion
This meta-analysis shows that earlier postoperative bathing does not increase the risk of wound infection and other complications, and can improve patient satisfaction with medical care. Given this medical evidence, the medical community, health authorities, and governments should develop and disseminate clinical practice guidelines that allow clinicians to adhere to recommendations that guide patients to evidence-based and beneficial treatment.
ICMJE Conflict of Interest Statement
The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the study reported.
Funding Statement
This work did not receive any specific grant from any funding agency in the public, commercial, or not-for-profit sector.
Author contribution statement
YR and HL collected data, performed data analysis, interpreted results, and wrote the first draft of the manuscript. WJP and HY reviewed the protocol, screened articles, extracted data, and reviewed the results and manuscript. LC and HL contributed to the systematic review protocol and critically reviewed the results and manuscript. HL contributed to the protocol development and reviewed the manuscript. ZW provided critical advice during the revision process. All authors contributed to the conception and design of the study and reviewed all documents and materials.
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