a School of Medical Sciences and Bosch Institute, University of Sydney, Sydney, New South Wales, Australia.
Find articles by Brian J Morrisb University of Washington School of Medicine and VA Puget Sound Health Care System, Section of Urology, Seattle, WA, USA.
Find articles by John N Kriegerc Department of Epidemiology, Jonathan and Karin Fielding School of Public Health, University of California, Los Angeles, CA, USA.
Find articles by Jeffrey D Klausnera School of Medical Sciences and Bosch Institute, University of Sydney, Sydney, New South Wales, Australia.
b University of Washington School of Medicine and VA Puget Sound Health Care System, Section of Urology, Seattle, WA, USA.
c Department of Epidemiology, Jonathan and Karin Fielding School of Public Health, University of California, Los Angeles, CA, USA.
Correspondence to Brian J Morris (ua.ude.yendys@sirrom.nairb). Received 2016 Dec 2; Accepted 2017 Jan 31. Copyright © Morris et al.This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly cited. To view a copy of the license, visit http://creativecommons.org/licenses/by/3.0/. When linking to this article, please use the following permanent link: https://doi.org/10.9745/GHSP-D-16-00390
Frisch and Earp, opponents of male circumcision, have criticized draft recommendations from the CDC that advocate counseling men and parents of newborn boys in the United States about the benefits and risks of male circumcision. We provide a rebuttal to Frisch and Earp's criticisms and contend that the recommendations are entirely appropriate and merit consideration for policy development.
Frisch and Earp, opponents of male circumcision, have criticized draft recommendations from the CDC that advocate counseling men and parents of newborn boys in the United States about the benefits and risks of male circumcision. We provide a rebuttal to Frisch and Earp's criticisms and contend that the recommendations are entirely appropriate and merit consideration for policy development.
After an extensive evaluation of the scientific evidence, the United States Centers for Disease Control and Prevention (CDC) released draft policy recommendations in December 2014 affirming male circumcision (MC) as an important public health measure. 1 – 3 The CDC's summary 1 (Box 1) was accompanied by a 61-page literature review. 2 The CDC supported the 2012 American Academy of Pediatrics (AAP) infant MC policy 4 , 5 (Box 2) and recommended that providers: (1) give parents of newborn boys comprehensive counseling about the benefits and risks of MC; (2) inform all uncircumcised adolescent and adult males who engage in heterosexual sex about the significant, but partial, efficacy of MC in reducing the risk of acquiring HIV and some sexually transmitted infections (STIs) through heterosexual sex, as well as about the potential harms of MC; and (3) inform men who have sex with men (MSM) that while it is biologically plausible that MC could benefit MSM during insertive sex, MC has not been proven to reduce the risk of acquiring HIV or other STIs during anal sex. 3
These recommendations are intended to assist health care providers in the United States who are counseling men and parents of male infants, children and adolescents in decision-making about male circumcision. Such decision-making is made in the context of not only health considerations, but also other social, cultural, ethical, and religious factors. Although data have been accumulating about infant male circumcision for many years, clinical trials conducted between 2005–2010 have demonstrated safety and significant efficacy of voluntary adult male circumcision performed by clinicians for reducing the risk of acquisition of human immunodeficiency virus (HIV) by a male during penile-vaginal sex (“heterosexual sex”). Three randomized clinical trials showed that adult male circumcision reduced HIV infection risk by 50–60% over time. These trials also found that adult circumcision reduced the risk of men acquiring two common sexually transmitted infections (STIs), herpes simplex virus type-2 (HSV–2) and types of human papilloma virus (HPV) that can cause penile and other anogenital cancers, by 30%. Since the release of these trial data, various organizations have updated their recommendations about adult male and infant male circumcision.
Systematic evaluation of English-language peer-reviewed literature from 1995 through 2010 indicates that preventive health benefits of elective circumcision of male newborns outweigh the risks of the procedure. Benefits include significant reductions in the risk of urinary tract infection in the first year of life and, subsequently, in the risk of heterosexual acquisition of HIV and the transmission of other sexually transmitted infections.
The procedure is well tolerated when performed by trained professionals under sterile conditions with appropriate pain management. Complications are infrequent; most are minor, and severe complications are rare. Male circumcision performed during the newborn period has considerably lower complication rates than when performed later in life.
Although health benefits are not great enough to recommend routine circumcision for all male newborns, the benefits of circumcision are sufficient to justify access to this procedure for families choosing it and to warrant third-party payment for circumcision of male newborns. It is important that clinicians routinely inform parents of the health benefits and risks of male newborn circumcision in an unbiased and accurate manner.
Parents ultimately should decide whether circumcision is in in the best interests of their male child. They will need to weigh medical information in the context of their own religious, ethical, and cultural beliefs and practices. The medical benefits alone may not outweigh these other considerations for individual families.
Findings from the systematic evaluation are available in the accompanying technical report. The American College of Obstetricians and Gynecologists has endorsed this statement.
The CDC has a mandate to use the best available evidence to inform the public on interventions for disease prevention. In the case of early infant MC, there are few public health interventions in which the scientific evidence in favor is now so compelling. Despite this, opponents of MC do not accept the CDC's position. Two prominent opponents, Frisch and Earp, published arguments that led them to conclude that “from a scientific and medical perspective, current evidence suggests that circumcision is not an appropriate public health measure for developed countries such as the United States.” 6
Here, we critically assess the evidence used by Frisch and Earp to support their thesis and respond to their main criticisms (summarized in Box 3).
In a recently published article, Frisch and Earp 6 oppose the 2014 draft MC recommendations from the U.S. Centers for Disease Control and Prevention (CDC), 3 referring to what they believe are “numerous scientific and conceptual shortcomings.” Here, we quote these 7 criticisms by Frisch and Earp and provide our response to each criticism.
Failure to provide a thorough description of the normal anatomy and functions of the penile structure being removed at circumcision (i.e., the foreskin)Response: There seems to be no need for the CDC to provide a thorough description of the anatomy and functions of the foreskin.
Failure to consider the intrinsic value to some men of having an unmodified genital organResponse: While some men may believe there is “an intrinsic value to having an unmodified genital organ,” those men should be made aware of the risks posed by their foreskin.
Undue reliance on findings from sub-Saharan Africa concerning circumcision of adult males (as opposed to infants or children)Response: The evidence shows the CDC is correct in concluding that findings from sub-Saharan Africa concerning circumcision of adult males for protection against heterosexually-acquired HIV and certain other STIs also apply to men in the United States. The findings also apply to boys when they grow up. Moreover, the cumulative lifetime benefit is greatest if circumcision is performed early in infancy since early infant circumcision is simpler, more convenient, and carries lower risk than when performed later, and circumcision confers immediate protection against urinary tract infections, phimosis, balanitis, and, when older, specific STIs and genital cancers. MC also protects the female partners, as confirmed in randomized controlled trials.
Uncritical reliance on a prima facie implausible benefit-risk analysis performed by a self-described circumcision advocateResponse: The benefit-risk analysis used by the CDC is based on the best current evidence relevant to the United States, and the results are plausible.
Reliance on misreported statistics to downplay the problem of pain in the youngest of boysResponse: While procedural pain can occur during circumcision, the evidence cited by the CDC indicates that, with use of local anesthetic, pain is negligible in the first week of a boy's life. Frisch and Earp misconstrue pain statistics to overplay the issue of pain.
Reliance on incomplete register data to assess the frequency of short-term post-operative complications associated with circumcision, leading to a likely underestimation of their true frequencyResponse: By selective citation and misrepresentation of findings, Frisch and Earp overstate the frequency of short-term postoperative complications associated with MC while ignoring data from large high-quality studies such as those published recently by CDC researchers.
Serious underestimation of the late-occurring harms of circumcision presenting months to years after the operation (most notably meatal stenosis).Response: Frisch and Earp selectively cite small, outdated, weak studies, often involving traditional circumcisers, and misrepresent data while ignoring large, high-quality studies. As a result, they overestimate the frequency of meatal stenosis occurring years after the MC procedure.
MC confers immediate and lifelong protection against numerous medical conditions (Box 4). 1 , 2 , 4 , 5 , 7 – 9 For example, MC protects against a number of STIs including HIV, and it partially protects against oncogenic types of human papillomavirus (HPV) 10 – 15 that together with phimosis, balanitis, and smegma are major risk factors for penile cancer, 10 , 16 – 18 as shown in meta-analyses that found 12-, 4-, and 3-fold statistically significant higher risks of penile cancer for phimosis, balanitis, and smegma, respectively. 16 Infancy is the ideal time for MC and there are cogent reasons why it should not be delayed until the boy or man can make up his own mind 19 ( Table ).
Why Infant Male Circumcision Is Preferable to Male Circumcision at a Later Age
Infant Male Circumcision | Male Circumcision of Older Boys and Men |
---|---|
Simple | More complex |
Quick (a few minutes) | Takes half an hour or more |
Low cost | Expensive (often unaffordable) |
Low risk (adverse events 0.4%) 20 | Moderate risk (adverse events 4%–8%) 20 |
Bleeding is minimal | Bleeding more common, requiring cautery or other interventions |
No need for sutures | Sutures or tissue glue needed |
Convenient (baby mostly sleeps) | Inconvenient (time off school or work required) |
Local anesthesia for those | General anesthesia for those >2 months to 9 years of age; local anesthesia for men, although general anesthesia sometimes preferred by surgeon |
Healing is fast (2 weeks) 21 | Healing takes 6 weeks or more |
Cosmetic outcome usually good | Stitch marks may be seen |
No long-term memory of procedure | Fear of undergoing an operation |
Abstinence from sexual intercourse for the 6-week healing period |
Male circumcision confers immediate and lifelong protection against numerous medical conditions.
Sexually transmitted infections including high-risk human papillomavirus (HPV), genital herpes simplex virus (HSV), trichomoniasis, mycoplasma, syphilis, chancroid, and HIV
Physical injuries to the foreskin, including coital injuries Cancers of the penis, prostate, and cervixSources: CDC technical review 2 and draft policy recommendations, 3 AAP review 5 and infant MC policy statement, 4 risk-benefit analyses by Morris et al. 7 – 9
Disputing the value of MC's protection against STIs, Frisch and Earp argue that less invasive STI prevention strategies should instead be promoted, such as encouraging safe sex practices. But we argue that public health messages normally include all effective measures for protection against disease, and in the case of STIs, MC complements current safe sex messages. The effectiveness of each approach should, moreover, be considered in real-world settings.
Frisch and Earp also contend that many STIs can be treated effectively if they do occur. We dispute that logic and instead argue that prevention is preferable to treatment, especially for viruses for which there is no cure (e.g., HIV, herpes simplex virus [HSV], and HPV). And for bacterial STIs and urinary tract infection (UTI), antibiotic-resistant strains mean that infections that were once easily treatable can now be life threatening. 22 – 25
The benefits of medical procedures should always, of course, be weighed with the potential risks. Frisch and Earp question whether the potential benefits of MC are “worth” the risk, pointing to potential risks of surgical accidents and supposed adverse psychological or sexual effects. The risk of major surgical mishaps with MC, however, is extremely low and the benefits gained from MC far exceed risks. 2 , 5 , 8 , 9 Furthermore, there is no long-term adverse effect of infant MC on psychological 26 , 27 or sexual 28 – 33 outcomes. Systematic reviews have found no adverse effect of MC on sexual function, 28 , 29 , 33 sensitivity, or satisfaction. 29 A meta-analysis of all common male sexual dysfunctions found none were related to MC status. 28 Furthermore, the third British National Survey of Sexual Attitudes and Lifestyles (Natsal-3), a large national probability survey, which used a new, comprehensive, validated measure of sexual function, the Natsal-SF, presented findings for 6,293 men and 8,869 women aged 16–74 years, broadly representative of the British population. The survey concluded that MC is not associated with men's overall sexual function. 31 In addition, a recent survey of 1,000 adults by an Internet-based market research firm that is a member of the British Polling Council found 29% of uncircumcised men wished they had been circumcised, compared with only 10% of circumcised men who wished they had not been circumcised (margin of error ±4%). 34 A randomized controlled trial (RCT) of uncircumcised men in Kenya found sexual pleasure increased in most men after MC. 35 It is possible some circumcised men may be unhappy due to exposure to misleading propaganda that dominates the Internet.
The benefits gained from male circumcision far exceed risks.
A risk-benefit analysis 8 cited by the CDC 2 found that benefits of infant MC exceed risks by over 100:1. A letter 36 questioning this risk-benefit analysis that Frisch and Earp cite contained misunderstandings, as pointed out in the response to the letter. 37 A large study by CDC researchers found frequency of adverse events for newborn MC was 0.4%. 20 These data are robust and withstand Frisch and Earp's non-evidence-based speculation to the contrary. Frisch and Earp refer to analysis conducted by the Canadian Paediatric Society (CPS) that tabulated risks and benefits of newborn MC, concluding the risk-benefit ratio was “closely balanced.” 38 But risk figures in the CPS analysis were exaggerated because they were drawn from a global study that included data from traditional (non-medical) MCs 39 and outlier studies while ignoring a more recent study by CDC researchers of 1.4 million (mostly newborn) MCs. 20 In addition, multiple benefits (phimosis, balanitis, balanoposthitis, prostate cancer, some STIs, candidiasis, and lifetime prevalence of urinary tract infections) were omitted, and the actual risk-benefit ratio was not determined. (See critique 40 for further details.)
In addition to potential risks from the surgical procedure, Frisch and Earp point to other potential negative consequences of MC, namely, “the loss of healthy, functional tissue” (i.e., the foreskin). But they fail to acknowledge that the healthy foreskin of an uncircumcised male remains vulnerable to adverse medical conditions, infections, and genital cancers. We draw attention to a Danish study by Sneppen and Thorup that found “significant morbidity related to foreskin problems in a predominantly uncircumcised population.” 41 It pointed out that the reason most Danish boys might go through infancy, childhood, and adolescence without being circumcised reflects “the strict foreskin-preserving culture of Denmark.” 41 “More than 5% … were admitted to the pediatric surgical department with foreskin-related problems [mainly phimosis] and at least 1.66% of the boys needed surgical procedures in [sic] general anesthesia.” 41 Of these, 24% initially received a circumcision and another 5% received circumcision after alternative treatment failed. Moreover, foreskin-preserving preputioplasty had to be repeated in 5.5% of cases (repeat surgery for MC was lower, at 2%), further exposing the boy to surgical risks.
The uncircumcised foreskin remains vulnerable to adverse medical conditions, infections, and genital cancers.
Foreskin problems continue into adulthood, as does MC for medical and cosmetic reasons. Since some men might not seek medical attention, especially for sexual or genital conditions, foreskin problems will always be more common than evident in case studies such as the one by Sneppen and Thorup. Infant MC would prevent later foreskin problems and obviate the need for later MC which is more costly and risky. 19 Risk-benefit analyses calculated that half of uncircumcised males will, over their lifetimes, suffer from an adverse medical condition attributable to their foreskin. 8 , 42 One such condition among uncircumcised men is lichen sclerosus (a condition that creates patchy, white skin that is thinner than normal, most often affecting the genital area). 43 This had a prevalence of 0.37% in the Danish study. 41 Lichen sclerosus is difficult to treat, and treatment has a low success rate. 43 Frisch and Earp go into a lengthy argument that another condition, meatal stenosis (a subcategory of urethral stricture disease), is one of the most common complications after MC, citing numerous studies. But most of the studies they cite to support their claim are small, quite old, comprised of MC performed by non-medical personnel, lack a control group of uncircumcised males, and either include no statistical analyses or include P values that were not statistically significant. Furthermore, meatal stenosis is seen in uncircumcised males as well. In the Danish study, risk of developing meatal stenosis in uncircumcised boys before 18 years of age was 0.17%. 41 Prevalence was 0.01% in a large U.S. 20 study of infants and a U.K. 44 study of boys aged 0–15 years, although follow-up in each study was only 6 months. Among the lichen sclerosus patients in the Danish study, 37.5% developed meatal stenosis. 40
Finally, Frisch and Simonsen reported that circumcised boys may be at increased risk for autism spectrum disorder (ASD) due to MC-related pain. 45 Their conclusion was based on their finding of ASD prevalence of 6.3% in circumcised and 1.5% in uncircumcised Danish boys. That report has been criticized. 41 , 46 , 47 Sneppen and Thorup, in particular, found ASD prevalence was 7.2% in uncircumcised Danish boys and suggested Frisch's study suffered from confounding. 41
Frisch and Earp criticize (without scientific evidence) the CDC's draft recommendations for not discussing the “protective and sexual functions” of the foreskin. A study by Frisch claiming sexual dysfunctions in circumcised men 48 was one-sided and suffered from confounding and statistical flaws. 29 , 49 In this Danish study, MC of the mostly (89%) Lutheran or non-religious Danish men surveyed was likely for medical conditions that often affect sexual function, either directly or from a preexisting psychological aversion that develops because the condition causes difficulties with intercourse. 29 , 49 , 50 Participation bias, small sample sizes for cases among the 5% who were circumcised, and failure to correct for multiple testing were also noted. 29 , 49 Confounding and statistical flaws were also noted for a study of penile sensitivity by Sorrells et al. 51 That study was severely criticized for a multitude of reasons, including failure to correct for multiple testing that, if performed, would have rendered the age-adjusted P value of .014 non-significant; mode of recruitment; large discrepancies in subject numbers between the methods and results sections; and failure to compare comparable sites on the penis of circumcised and uncircumcised men (which when performed by the critics were shown to be not statistically significant). 29 , 52 A recent Canadian study concluded that “if sexual function is related to circumcision status, this relationship is not likely the result of decreased penile sensitivity stemming from neonatal circumcision.” 32 It has also been found that sensory nerve endings (Meissner's corpuscles) in the foreskin are lower in density and smaller in size than those in other glabrous (hairless) epithelia of the body. 53
Sensitivity to vibration (not tested by either Bossio et al. 32 or Sorrells et al. 51 ) correlates with sexual response and is similar in uncircumcised and circumcised men. 30 Studies of histological correlates of sexual sensation concluded that the glans, not the foreskin, is involved in sexual sensation. 30 , 54 C-fibers (activated by thermal stimuli and punctate pain) may be involved in erotic sensation and sexual arousal. 55 Similar unmyelinated free nerve endings predominate in the glans, not the foreskin. 30
Thus, speculation and outdated opinion pieces claiming special properties of the foreskin, such as in penile function and masturbation, should be viewed with skepticism. Perhaps sensitivity of the foreskin to fine touch (which activates Aβ, large diameter, myelinated nerve fibers) might have served as an “early warning system” in our naked upright forebears from the intrusion of biting insects and parasites while protecting the glans. 56
The area of the outer and inner foreskin combined spans a wide range: 7–100 cm 2 (n=965) 57 and 18–68 cm 2 (n=8), 58 respectively. In discussing vestigial structures, Charles Darwin stated, “An organ, when rendered useless, may well be variable, for its variations cannot be checked by natural selection.” 59 The variability in foreskin size is consistent with the foreskin being a vestigial structure. Larger foreskins place uncircumcised men at increased risk for HIV infection. 56
Arguments by MC opponents disputing the validity of the large African RCTs showing that MC provides substantial protection against heterosexually-acquired HIV infection have been exposed as fallacious. 60 – 72 Frisch and Earp instead question the CDC for applying the African trial findings to the United States. Although the proportion of HIV infections acquired heterosexually in the United States is far less than in sub-Saharan Africa, in some U.S. localities heterosexually-acquired HIV incidence is high. Furthermore, 2014 CDC figures show 24% of new HIV infections in the United States involved heterosexual contact. 73 It was estimated that if all boys in the 2011 annual U.S. male birth cohort were circumcised, 5,530 HIV infections would be prevented over their lifetime. 74 Lifetime risk of HIV diagnosis in heterosexual males in the United States is currently 1 in 524. 75 The increase in HIV infections in African-Americans, in particular, has been faster than in all other groups. 76 Modeling by the CDC found MC could reduce heterosexual HIV risk by approximately 21% in African-Americans and by approximately 12% in Hispanics, and costs would be saved in each group. 77 Actual MC-related risk reduction in heterosexual African-American men with known HIV exposure was 51%. 78
Male circumcision could reduce heterosexual HIV risk by about 21% in African-Americans and 12% in Hispanics.
Comparison of HIV and MC prevalence in high-income countries also suggest MC has a protective effect, providing further support to the applicability of the African MC trials to the United States and other high-income countries. For example, HIV prevalence in the mostly uncircumcised populations of France and the Netherlands was much higher than in Israel where almost all men are circumcised, despite all other risk factors being comparable. 79 In Australia, where MC is less common than in the United States and Israel, the number of HIV infections related to heterosexual contact has increased by 28% over the past decade, representing 25% of new diagnoses in 2013, 29% being in Australian-born patients. 80 In Canada, where infant MC prevalence has, like in Australia, declined in recent decades, 9.5% of new HIV infections involve men infected heterosexually. 81
As well as substantial protection against HIV, data from the African RCTs reinforced the ability of MC to protect against several other STIs in heterosexual males, 10 , 11 , 13 , 16 , 71 , 82 – 90 as well as their female sex partners 10 , 91 – 95 and among MSM who are insertive-only. 96 – 100 With regard to MSM in particular, a Cochrane analysis of MC and HIV prevalence among MSM found results were statistically significant among 3,465 men in 7 studies reporting an insertive role (odds ratio, 0.27; 95% confidence interval, 0.17 to 0.44; I 2 =0%), but were not significant among 1,792 men in 3 studies reporting a receptive role (odds ratio, 1.20; 95% confidence interval, 0.63 to 2.29; I 2 = 0%).” 1 , 80 MC also reduces the risk of potentially fatal penile, prostate, and cervical cancer. 10 , 16 – 18 , 101 – 104 Partial protection against prostate cancer incidence was seen in U.S. 101 and Canadian 103 studies and in a meta-analysis of all studies, 104 the protective effect being strongest (36% 101 and 60% 103 ) in North American men of African heritage.
It is misleading to compare HIV prevalence in the United States, where MC is common, with a similar or slightly lower prevalence in Europe, where MC is uncommon, and conclude that MC does not make a difference, as Frish and Earp do. Unlike Africa, most HIV infections in the United States and Europe occur in MSM. HIV subtype B arrived in Haiti from Africa between 1961 and 1970, reaching the United States in the mid-1970s after Haiti became a popular destination for sex tourism. 105 The United States thus had a “head-start” on Europe and the rest of the developed world.
Because Frisch and Earp dispute the low prevalence of adverse events with MC, they disagree with the conclusions from a cost-benefit study by authors from the Johns Hopkins University. 74 This study found that if infant MC prevalence in the United States decreased from the current 80% prevalence 106 to the levels of 10% typical in Europe, the additional direct medical costs in infancy and later for treatment of UTIs and STIs would exceed US$4.4 billion over 10 annual birth cohorts, after accounting for the cost of the MC procedure and treatment of MC complications. 74 If early infant MC rates decreased to 10%, lifetime prevalence of infant UTIs would increase by 211.8%, high- and low-risk human HPV by 29.1%, HSV-2 by 19.8%, and HIV by 12.2%. 74 Among females, lifetime prevalence of bacterial vaginosis would increase by 51.2%, trichomoniasis by 51.2%, high-risk HPV by 18.3%, and low-risk HPV by 12.9%. 74
Frisch and Earp also take issue with the CDC's modeling findings 77 that MC in the United States was cost-saving for HIV prevention among black and Hispanic males but not necessarily among, what Frisch and Earp refer to as, “the majority population of white males.” The CDC found that “for all males, circumcision resulted in undiscounted lifetime HIV-related health care savings of $2,070 per male and discounted lifetime HIV-related health care savings of $427.” 77 As pointed out in the CDC study, the lack of cost-effectiveness for white males may be because white males in the United States already have a high prevalence of MC, a low lifetime risk of HIV, and a low risk of acquiring HIV through heterosexual sex compared with black and Hispanic males. We also contend that if other factors were considered in the model, including medical conditions associated with lack of MC, infections and genital cancers in both sexes, and indirect costs, MC would likely be cost-saving among U.S. whites as well. For example, in the absence of MC in the United States, there would be 24%–40% more prostate cancer cases and US$0.8–1.1 billion extra in costs for treatment and terminal care per year. 107 Annual cost-savings for genital cancer prevention by a shift from the current rate of 10%–20% for infant MC in Australia to 80% was calculated as $1–2 million for direct medical costs, unadjusted for inflation. 108
The U.S. state of Florida provides an illustrative case study of the cost-savings benefits of MC. In 2003, the state withdrew Medicaid health insurance coverage for infant MC. That resulted in a 6-fold increase in medical costs for publicly funded MCs for medical indications, because later MCs are substantially more expensive than early infant MCs. 109 In response, Florida restored Medicaid coverage in 2014.
Thus, in contrast to the assertions by Frisch and Earp, the cost-savings estimated by the CDC 77 and Johns Hopkins researchers 74 appear conservative. Moreover, cost-savings from infant MC apply to whites, blacks, and Hispanics.
Claims of long-term psychological, emotional, and sexual impediments from infant MC “pain” are anecdotal. 110 , 111 In contrast, in a longitudinal study of New Zealand boys circumcised in 1977, MC had no adverse effect on breastfeeding outcomes or cognitive ability later in childhood. 26 In another follow-up study, of Swedish boys after MC, the boys showed no adverse psychological effect of MC. 112
There are many painful experiences encountered by the child before, during, and after birth. 113 MC, if performed without anesthetic, is one of these. Cortisol levels, heart rate, and respiration have registered an increase during and shortly after infant MC. 114 , 115 Adequate anesthesia is essential for pain management during MC at any age. Most MC procedures can be performed under local anesthesia. General anesthesia involves risks, is usually unnecessary, and is falling out of favor. The AAP 5 and CDC 2 recommend local anesthesia for infant MC.
Frisch and Earp take issue with a study the CDC cited related to the issue of pain associated with the MC procedure, arguing that the figures cited from the study were inaccurate. The study objectively scored pain experienced by newborns when undergoing MC and concluded that “painless circumcision [by Gomco clamp] is possible in almost all newborns if it is performed during the first week of life.” 116 It is regrettable that there were indeed some errors in the figures reported in the study—in the abstract of the article, 6.5% of infants 1 week old or younger were reported to have pain scores of 2 or greater, whereas the source table in the main body of the article reports the figure of 6.7% and the raw data indicate the figure should actually be 7.1%. However, the error is trivial, resulting in a minor difference of up to 0.6 percentage points and thus does not negate the study's overall conclusion.
In addition, Frisch and Earp highlight that infants may also experience pain from administration of the anesthesia itself before the MC. Pain does occur during injection of local anesthetics, but it can be reduced by prior application of readily available topical anesthetic creams containing lidocaine and prilocaine (EMLA, or the more potent LMX4). In a clinical trial, application of EMLA cream 2 hours prior to Plastibell MC resulted in near absence of evidence of pain during and for 4 hours after infant MC, by which time nerves at the ablation site would have died, meaning a pain-free MC. 117 Furthermore, we contend that any pain associated with injection of local anesthetic is no greater than pain incurred with injection of a vaccine.
While infants may experience pain from administration of a local anesthetic before circumcision, the pain can be reduced by prior application of topical anesthetic creams.
A small telephone survey, misconstrued by Frisch and Earp, actually found parents' (subjective) perception of level of discomfort among infants circumcised at 4–167 days of age (mean, 41.7 days) was mild in 84% of cases, moderate in 11%, and severe in only 5%. 118 The average discomfort score for MC was less than for other simple ambulatory pediatric procedures evaluated in the study. Similarly, Frisch and Earp summarize results of another telephone survey 119 by stating that “71% of parents reported varying degrees of circumcision-related pain in their infants … up to six weeks after surgery.” When analyzing the study's results in detail, however, one finds that only about 2% of parents whose sons were circumcised using a Gomco clamp reported “more than acceptable pain” (1.5%) or “much more pain” (0.9%). In comparison, 29% reported “no pain,” 15% reported “minimal pain,” and 53% reported “acceptable pain.” For Plastibell MC, these figures were 32% (no pain), 11% (minimal pain), 50% (acceptable pain), 3.2% (more than acceptable pain), and 3.8% (much more pain). 119
Men circumcised as adults are well placed to communicate MC-related pain. In the 3 large RCTs of adult MC conducted in sub-Saharan Africa, only 0.8%, 120 0.3%, 121 and 0.2% 122 of men reported severe pain.
In the 3 large RCTs of adult male circumcision conducted in sub-Saharan Africa, less than 1% of men reported severe pain with the procedure.
Frisch and Earp speculate about adverse MC-related events after discharge from hospital and over the long-term. They considered meatal stenosis to be “particularly worrying,” but misconstrue data on its prevalence, which, as noted earlier in this article, we argue will not affect “between 5% and 20% of boys undergoing non-therapeutic circumcision.” A recent study by Frisch and Simonsen found meatal stenosis incidence in Denmark to be very much lower than those figures and higher in uncircumcised than in circumcised elderly men, 123 possibly contributed by lichen sclerosus. A critical evaluation of the literature suggests prevalence is in the order of 0.01%–1%, with a similarly low frequency among both circumcised and uncircumcised boys. 13 , 20 , 44 , 124
Frisch and Earp also point to findings of retrospective case study that 4.7% of cases operated on in the pediatric surgery department of the MassGeneral Hospital for Children between 2003 and 2007 were for late complications related to newborn MC. 125 Since that hospital serves the wider Boston area and receives cases following MC elsewhere, the sample is not representative. Besides vaccination, newborn MC is the most common pediatric procedure among males in the United States. Frisch and Earp concede that the “total number of circumcisions [that these figures relate to are] unknown.” In contrast, a recent study of 95,046 elective MCs from 2004 to 2013 in ambulatory surgery centers of 43 U.S. tertiary care pediatric hospitals found only 0.1% underwent a second ambulatory procedure within the first 7 days, being higher for older boys than for infants. 126
The draft CDC recommendations advocate informing parents of newborn boys and adolescent and adult men about the benefits and risks of MC, 3 and the accompanying technical report 2 refers to an analysis that finds the benefits of MC exceed the risks. 8 The AAP policy also concluded that benefits of MC exceed the risks. Policy statements from Australian, British, and Dutch medical bodies, however, are more conservative or even negative about MC. Frisch and Earp point to these differences as a “lack of international agreement with the U.S. view,” 6 but they fail to mention that none of these other bodies go to the level of claiming that MC detracts from sexual pleasure or function, oppose MC in high-HIV prevalence countries, or recommend that MC should be legislated against in their own countries. One negative policy, by the Royal Australasian College of Physicians, even maintains a relatively balanced view on MC, stating that 127 :
It is reasonable for parents to weigh the benefits and risks of circumcision.To make the decision whether or not to circumcise their sons, the medical attendant is obliged to provide accurate, unbiased, and up-to-date information on the risks and benefits of the procedure.
Parental choice should be respected.The operation should be undertaken in a safe, child-friendly environment by an appropriately trained competent practitioner, capable of dealing with the complications and using appropriate analgesia.
And while the CPS (Canada) newborn MC position statement 38 does not recommend routine MC of every newborn male, it does acknowledge that “there may be a benefit for some boys in high-risk populations and circumstances where the procedure could be considered for disease reduction or treatment.”
The policy statements by the CDC and AAP have raised the bar. Policy statements on MC by medical bodies should follow their lead and rely on a thorough evaluation of the medical evidence to support their conclusions.
Policy statements on male circumcision by medical bodies should rely on medical evidence.
We find major shortcomings in the criticisms by Frisch and Earp of the CDC's draft MC recommendations. In summary, the current scientific evidence shows that MC provides protection against numerous adverse medical conditions and infections, and the benefits of the procedure, including cost-savings over the long-term, greatly exceed risks, with benefits found in both poor and wealthy countries such as the United States. In addition, MC has no adverse effect on sexual function, sensitivity, or pleasure, nor is there reliable evidence for any long-term adverse psychological effect of MC. Furthermore, complication rates following the procedure are low, especially following early infant MC. Finally, pain that may be associated with the procedure during the first week of life can be negligible when local anesthesia is used.
Criticisms of the AAP and CDC policies by MC opponents have been consistently exposed as flawed (AAP policy 42 , 128 – 131 ; CDC policy 132 , 133 ). Convincing arguments have been made that it would be unethical to withhold information about the risks and benefits of MC from parents of boys. 130 – 132 , 134 , 135 as recommended by the AAP and CDC. Curiously, those who condemn parent-approved infant MC are not as quick to condemn procedures that provide no medical benefit to children (e.g., cosmetic orthodontia, correction of harelip, surgery for tongue-tie, treatment of dwarfism by growth hormone injections, and surgery for removal of supernumerary digits). 135 Why then do some regard MC as controversial? 135 Article 24(1) of the United Nations Convention on the Rights of the Child states, “States Parties recognize the right of the child to the enjoyment of the highest attainable standard of health” and “shall strive to ensure that no child is deprived of his or her right of access to health care services.” 136 Therefore, we assert that the CDC's draft MC recommendations do nothing more than advocate appropriately the right of male infants, children, adolescents, and adults to access health care services with medical benefits—that is, MC—and that adoption of the draft CDC recommendations into formal policy should improve public health in the United States.
Convincing arguments have been made that it would be unethical to withhold information about the risks and benefits of male circumcision from parents of boys.
Adoption of the draft CDC recommendations into formal policy should improve public health in the United States.
Peer Reviewed
Competing Interests: Dr. Morris reports that he is a member of the Circumcision Academy of Australia, a government registered incorporated association whose Constitution states that it is “a non-profit organization” whose objectives are to “educate health professionals and the general public about male circumcision, including but not limited to the benefits, the risks and methods of male circumcision” and “to promote ease of access and affordability of male circumcision in Australia.” Dr. Krieger reports that he performs male circumcision in his clinical practice as a urologist, outside the submitted work. In addition, Dr. Krieger has a patent pending for a male circumcision device. Dr. Klausner has nothing to disclose.
Cite this article as: Morris BJ, Krieger JN, Klausner JD. CDC's male circumcision recommendations represent a key public health measure. Glob Health Sci Pract. 2017;5(1):15-27. https://doi.org/10.9745/GHSP-D-16-00390
1. U.S. Centers for Disease Control and Prevention (CDC). Recommendations for providers counseling male patients and parents regarding male circumcision and the prevention of HIV infection, STIs, and other health outcomes. A notice by the Centers for Disease Control and Prevention on 12/02/2014. [Docket No. CDC–2014–0012] . Fed Regist . 2014; 79 ( 231 ):71433 https://www.federalregister.gov/documents/2014/12/02/2014-27814/recommendations-for-providers-counseling-male-patients-and-parents-regarding-male-circumcision-and Accessed September 14, 2016. [Google Scholar]
2. U.S. Centers for Disease Control and Prevention (CDC). Background, methods, and synthesis of scientific information used to inform the "Recommendations for providers counseling male patients and parents regarding male circumcision and the prevention of HIV infection, STIs, and other health outcomes." [Docket No. CDC-2014-0012-0002] . https://www.regulations.gov/document?D=CDC-2014-0012-0002 Accessed September 14, 2016.
3. U.S. Centers for Disease Control and Prevention (CDC). Recommendations for providers counseling male patients and parents regarding male circumcision and the prevention of HIV infection, STIs, and other health outcomes. [Docket No. CDC-2014-0012-0002] . https://www.regulations.gov/document?D=CDC-2014-0012-0003 Accessed September 14, 2016.
4. American Academy of Pediatrics Task Force on Circumcision. Circumcision policy statement . Pediatrics . 2012; 130 ( 3 ):585–586. 10.1542/peds.2012-1989. [PubMed] [CrossRef] [Google Scholar]
5. American Academy of Pediatrics Task Force on Circumcision. Male circumcision . Pediatrics . 2012; 130 ( 3 ):e756–e785. 10.1542/peds.2012-1990. [PubMed] [CrossRef] [Google Scholar]
6. Frisch M, Earp BD. Circumcision of male infants and children as a public health measure in developed countries: a critical assessment of recent evidence . Glob Public Health . 2016:1–16. 10.1080/17441692.2016.1184292. [PubMed] [CrossRef] [Google Scholar]
7. Morris BJ, Wodak AD, Mindel A, et al. Infant male circumcision: an evidence-based policy statement . Open J Prevent Med . 2012; 02 ( 1 ):79–92. 10.4236/ojpm.2012.21012 [CrossRef] [Google Scholar]
8. Morris BJ, Bailis SA, Wiswell TE. Circumcision rates in the United States: rising or falling? What effect might the new affirmative pediatric policy statement have? Mayo Clin Proc . 2014; 89 ( 5 ):677–686. 10.1016/j.mayocp.2014.01.001. [PubMed] [CrossRef] [Google Scholar]
9. Morris BJ, Kennedy SE, Wodak AD, et al. Early infant male circumcision: systematic review, risk-benefit analysis, and progress in policy . World J Clin Pediatr . 2017; 6 ( 1 ):89–102. 10.5409/wjcp.v6.i1.89 [PMC free article] [PubMed] [CrossRef] [Google Scholar]
10. Castellsagué X, Bosch FX, Muñoz N, et al.; International Agency for Research on Cancer Multicenter Cervical Cancer Study Group. Male circumcision, penile human papillomavirus infection, and cervical cancer in female partners . N Engl J Med . 2002; 346 ( 15 ):1105–1112. 10.1056/NEJMoa011688. [PubMed] [CrossRef] [Google Scholar]
11. Backes DM, Bleeker MCG, Meijer CJLM, et al.. Male circumcision is associated with a lower prevalence of human papillomavirus-associated penile lesions among Kenyan men . Int J Cancer . 2012; 130 ( 8 ):1888–1897. 10.1002/ijc.26196. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
12. Tobian AAR, Serwadda D, Quinn TC, et al.. Male circumcision for the prevention of HSV-2 and HPV infections and syphilis . N Engl J Med . 2009; 360 ( 13 ):1298–1309. 10.1056/NEJMoa0802556. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
13. Auvert B, Sobngwi-Tambekou J, Cutler E, et al.. Effect of male circumcision on the prevalence of high-risk human papillomavirus in young men: results of a randomized controlled trial conducted in Orange Farm, South Africa . J Infect Dis . 2009; 199 ( 1 ):14–19. 10.1086/595566 [PMC free article] [PubMed] [CrossRef] [Google Scholar]
14. Gray RH. Infectious disease: male circumcision for preventing HPV infection . Nat Rev Urol . 2009; 6 ( 6 ):298–299. 10.1038/nrurol.2009.96. [PubMed] [CrossRef] [Google Scholar]
15. Gray RH, Wawer MJ, Serwadda D, Kigozi G. The role of male circumcision in the prevention of human papillomavirus and HIV infection . J Infect Dis . 2009; 199 ( 1 ):1–3. 10.1086/595568 [PubMed] [CrossRef] [Google Scholar]
16. Morris BJ, Gray RH, Castellsague X, et al.. The strong protection afforded by circumcision against cancer of the penis . Adv Urol . 2011; 2011 :812368. 10.1155/2011/812368. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
17. Larke NL, Thomas SL, dos Santos Silva I, Weiss HA. Male circumcision and penile cancer: a systematic review and meta-analysis . Cancer Causes Control . 2011; 22 ( 8 ):1097–1110. 10.1007/s10552-011-9785-9. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
18. Schoen EJ, Oehrli M, Colby CJ, Machin G. The highly protective effect of newborn circumcision against invasive penile cancer . Pediatrics . 2000; 105 ( 3 ):e36. [PubMed] [Google Scholar]
19. Morris BJ, Waskett JH, Banerjee J, et al.. A ‘snip' in time: what is the best age to circumcise? BMC Pediatr . 2012; 12 :20. 10.1186/1471-2431-12-20. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
20. El Bcheraoui C, Zhang X, Cooper CS, Rose CE, Kilmarx PH, Chen RT. Rates of adverse events associated with male circumcision in U.S. medical settings, 2001 to 2010 . JAMA Pediatr . 2014; 168 ( 7 ):625–634. 10.1001/jamapediatrics.2013.5414. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
21. World Health Organization (WHO), Jhpiego. Manual for Early Infant Male Circumcision Under Local Anaesthesia . Geneva: WHO; 2010. http://apps.who.int/iris/bitstream/10665/44478/1/9789241500753_eng.pdf Accessed February 10, 2017. [Google Scholar]
22. Pallett A, Hand K. Complicated urinary tract infections: practical solutions for the treatment of multiresistant Gram-negative bacteria . J Antimicrob Chemother . 2010; 65 ( suppl 3 ):iii25–iii33. 10.1093/jac/dkq298. [PubMed] [CrossRef] [Google Scholar]
23. Fasugba O, Gardner A, Mitchell BG, et al. Ciprofloxacin resistance in community- Fasugba O, Gardner A, Mitchell BG, Mnatzaganian G. Ciprofloxacin resistance in community- and hospital-acquired Escherichia coli urinary tract infections: a systematic review and meta-analysis of observational studies . BMC Infect Dis . 2015; 15 ( 1 ):545. 10.1186/s12879-015-1282-4 [PMC free article] [PubMed] [CrossRef] [Google Scholar]
24. Bryce A, Hay AD, Lane IF, Thornton HV, Wootton M, Costelloe C. Global prevalence of antibiotic resistance in paediatric urinary tract infections caused by Escherichia coli and association with routine use of antibiotics in primary care: systematic review and meta-analysis . BMJ . 2016; 352 :i939. 10.1136/bmj.i939. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
25. Looke DFM, Gottlieb T, Jones CA, Paterson DL. Gram-negative resistance: can we combat the coming of a new Red Plague? Med J Aust . 2013; 198 ( 5 ):243–244. 10.5694/mja13.10190. [PubMed] [CrossRef] [Google Scholar]
26. Fergusson DM, Boden JM, Horwood LJ. Neonatal circumcision: effects on breastfeeding and outcomes associated with breastfeeding . J Paediatr Child Health . 2008; 44 ( 1–2 ):44–49. 10.1111/j.1440-1754.2007.01202.x. [PubMed] [CrossRef] [Google Scholar]
27. Stenram A, Malmfors G, Okmian L: Circumcision for phimosis: a follow-up study . Scand J Urol Nephrol . 1986; 20 ( 2 ):89–92. [PubMed] [Google Scholar]
28. Tian Y, Liu W, Wang JZ, Wazir R, Yue X, Wang KJ. Effects of circumcision on male sexual functions: a systematic review and meta-analysis . Asian J Androl . 2013; 15 ( 5 ):662–666. 10.1038/aja.2013.47. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
29. Morris BJ, Krieger JN. Does male circumcision affect sexual function, sensitivity, or satisfaction? A systematic review . J Sex Med . 2013; 10 ( 11 ):2644–2657. 10.1111/jsm.12293. [PubMed] [CrossRef] [Google Scholar]
30. Cox G, Krieger JN, Morris BJ. Histological correlates of penile sexual sensation: does circumcision make a difference? Sex Med . 2015; 3 ( 2 ):76–85. 10.1002/sm2.67. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
31. Homfray V, Tanton C, Mitchell KR, et al.. Examining the association between male circumcision and sexual function: evidence from a British probability survey . AIDS . 2015; 29 ( 11 ):1411–1416. 10.1097/QAD.0000000000000745. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
32. Bossio JA, Pukall CF, Steele SS. Examining penile sensitivity in neonatally circumcised and intact men using quantitative sensory testing . J Urol . 2016; 195 ( 6 ):1848–1853. 10.1016/j.juro.2015.12.080. [PubMed] [CrossRef] [Google Scholar]
33. Shabanzadeh DM, Düring S, Frimodt-Møller C. Male circumcision does not result in inferior perceived male sexual function – a systematic review . Dan Med J . 2016; 63 ( 7 ):A5245. [PubMed] [Google Scholar]
35. Krieger JN, Mehta SD, Bailey RC, et al.. Adult male circumcision: effects on sexual function and sexual satisfaction in Kisumu, Kenya . J Sex Med . 2008; 5 ( 11 ):2610–2622. 10.1111/j.1743-6109.2008.00979.x. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
36. Jenkins I. Bias and male circumcision . Mayo Clin Proc . 2014; 89 ( 11 ):1588. 10.1016/j.mayocp.2014.09.001. [PubMed] [CrossRef] [Google Scholar]
37. Morris BJ, Bailis SA, Wiswell TE. In reply–Bias and male circumcision . Mayo Clin Proc . 2014; 89 ( 11 ):1588–1589. 10.1016/j.mayocp.2014.09.002. [PubMed] [CrossRef] [Google Scholar]
38. Sorokan ST, Finlay JC, Jeffries AL; Canadian Paediatric Society. Newborn male circumcision. Position statement . Paediatr Child Health . 2015; 20 ( 6 ):311–315. http://www.cps.ca/documents/position/circumcision Accessed February 15, 2017. [PMC free article] [PubMed] [Google Scholar]
39. Weiss HA, Larke N, Halperin D, Schenker I. Complications of circumcision in male neonates, infants and children: a systematic review . BMC Urol . 2010; 10 :2. 10.1186/1471-2490-10-2. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
40. Morris BJ, Klausner JD, Krieger JN, Willcox BJ, Crouse PD, Pollock N. Canadian Pediatrics Society position statement on newborn circumcision: a risk-benefit analysis revisited . Can J Urol . 2016; 23 ( 5 ):8495–8502. [PubMed] [Google Scholar]
41. Sneppen I, Thorup J. Foreskin morbidity in uncircumcised males. Pediatrics . 2016; 137 ( 5 ):e20154340. 10.1542/peds.2015-4340. [PubMed] [CrossRef] [Google Scholar]
42. Morris BJ, Krieger JN, Klausner JD. Critical evaluation of unscientific arguments disparaging affirmative infant male circumcision policy . World J Clin Pediatr . 2016; 5 ( 3 ):251–261. 10.5409/wjcp.v5.i3.251. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
43. Morris BJ, Krieger JN. Penile inflammatory skin disorders and preventive role of circumcision . Int J Prev Med . 2017. In press. [PMC free article] [PubMed] [Google Scholar]
44. Cathcart P, Nuttall M, van der Meulen J, Emberton M, Kenny SE. Trends in paediatric circumcision and its complications in England between 1997 and 2003 . Br J Surg . 2006; 93 ( 7 ):885–890. 10.1002/bjs.5369. [PubMed] [CrossRef] [Google Scholar]
45. Frisch M, Simonsen J. Ritual circumcision and risk of autism spectrum disorder in 0- to 9-year-old boys: national cohort study in Denmark . J R Soc Med . 2015; 108 ( 7 ):266–279. 10.1177/0141076814565942. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
46. Morris BJ, Wiswell TE. 'Circumcision pain' unlikely to cause autism . J R Soc Med . 2015; 108 ( 8 ):297. 10.1177/0141076815590404. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
47. Bauer AZ. PubMed Commons comment on: Ritual circumcision and risk of autism spectrum disorder in 0- to 9-year-old boys: national cohort study in Denmark . J R Soc Med . 2015; 108 ( 7 ):266–79. https://www.ncbi.nlm.nih.gov/pubmed/25573114#comments. Published April 15, 2015 Accessed February 15, 2017. [PMC free article] [PubMed] [Google Scholar]
48. Frisch M, Lindholm M, Gronbaek M. Male circumcision and sexual function in men and women: a survey-based, cross-sectional study in Denmark . Int J Epidemiol . 2011; 40 ( 5 ):1367–1381. 10.1093/ije/dyr104. [PubMed] [CrossRef] [Google Scholar]
49. Morris BJ, Waskett JH, Gray RH. Does sexual function survey in Denmark offer any support for male circumcision having an adverse effect? Int J Epidemiol . 2012; 41 ( 1 ):310–326, author reply 312-314. 10.1093/ije/dyr180. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
50. Mao LM, Templeton DJ, Crawford J, et al.. Does circumcision make a difference to the sexual experience of gay men? Findings from the Health in Men (HIM) Cohort . J Sex Med . 2008; 5 ( 11 ):2557–2561. 10.1111/j.1743-6109.2008.00845.x. [PubMed] [CrossRef] [Google Scholar]
51. Sorrells ML, Snyder JL, Reiss MD, et al.. Fine-touch pressure thresholds in the adult penis . BJU Int . 2007; 99 ( 4 ):864–869. 10.1111/j.1464-410X.2006.06685.x. [PubMed] [CrossRef] [Google Scholar]
52. Waskett JH, Morris BJ. Fine-touch pressure thresholds in the adult penis . BJU Int . 2007; 99 ( 6 ):1551–1552. 10.1111/j.1464-410X.2007.06970_6.x. [PubMed] [CrossRef] [Google Scholar]
53. Bhat GH, Bhat MA, Kour K, Shah BA. Density and structural variations of Meissner's corpuscles at different sites in human glaborous skin . J Anat Soc India . 2008; 57 :30–33. http://medind.nic.in/jae/t08/i1/jaet08i1p30.pdf Accessed February 15, 2017. [Google Scholar]
54. Bleustein CB, Fogarty JD, Eckholdt H, Arezzo JC, Melman A. Effect of neonatal circumcision on penile neurologic sensation . Urology . 2005; 65 ( 4 ):773–777. 10.1016/j.urology.2004.11.007. [PubMed] [CrossRef] [Google Scholar]
55. Jönsson EH, Backlund Wasling H, Wagnbeck V, et al.. Unmyelinated tactile cutaneous nerves signal erotic sensations . J Sex Med . 2015; 12 ( 6 ):1338–1345. 10.1111/jsm.12905. [PubMed] [CrossRef] [Google Scholar]
56. Morris BJ, Krieger JN.. Letter from Morris and Kriger Re: Examining penile sensitivity in neonatally circumcised and intact men using quantitative sensory testing: J.A. Bossio, C.F. Pukall and S.S. Steele J Urol 2016; 195 :1848–1853. J Urol. 2016;196(6):1824–1825. 10.1016/j.juro.2016.05.127. [PubMed] [CrossRef] [Google Scholar]
57. Kigozi G, Wawer M, Ssettuba A, et al.. Foreskin surface area and HIV acquisition in Rakai, Uganda (size matters) . AIDS . 2009; 23 ( 16 ):2209–2213. 10.1097/QAD.0b013e328330eda8. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
58. Werker PMN, Terng ASC, Kon M. The prepuce free flap: dissection feasibility study and clinical application of a super-thin new flap . Plast Reconstr Surg . 1998; 102 ( 4 ):1075–1082. 10.1097/00006534-199809020-00024. [PubMed] [CrossRef] [Google Scholar]
59. Darwin C. The Origin of Species by Means of Natural Selection . London, UK: John Murray; 1859. [Google Scholar]
60. Halperin DT, Wamai RG, Weiss HA, et al. Male circumcision is an efficacious, lasting and cost-effective strategy for combating HIV in high-prevalence AIDS epidemics: time to move beyond debating the science . Future HIV Therapy . 2008; 2 ( 5 ):399–405. 10.2217/17469600.2.5.399 [CrossRef] [Google Scholar]
61. Tobian AAR, Serwadda D, Gray RH. Male circumcision for the prevention of HSV-2 and HPV infections and syphilis. Authors reply . N Engl J Med . 2009; 361 :307–308. 10.1056/NEJMc090844 [CrossRef] [Google Scholar]
62. Banerjee J, Klausner JD, Halperin DT, et al.. Circumcision denialism unfounded and unscientific. [Critique of Green et al., "Male circumcision and HIV prevention: Insufficient evidence and neglected external validity"] . Am J Prev Med . 2011; 40 ( 3 ):e11–e12, author reply e13-e14. 10.1016/j.amepre.2010.12.005. [PubMed] [CrossRef] [Google Scholar]
63. Morris BJ, Waskett JH, Gray RH, et al. Exposé of fallacious claims that male circumcision will increase HIV infections in Africa . J Public Health Africa . 2011; 2 ( 2 ):e28 10.4081/jphia.2011.e28 [PMC free article] [PubMed] [CrossRef] [Google Scholar]
64. Wamai R, Morris BJ. How to contain generalized HIV epidemics article misconstrues the evidence . Int J STD AIDS . 2011; 22 ( 7 ):415–416, author reply 416-417. 10.1258/ijsa.2010.010460. [PubMed] [CrossRef] [Google Scholar]
65. Wamai RG, Morris BJ, Bailis SA, et al.. Male circumcision for HIV prevention: current evidence and implementation in sub-Saharan Africa . J Int AIDS Soc . 2011; 14 :49. [PMC free article] [PubMed] [Google Scholar]
66. Morris BJ. Boyle and Hill's circumcision Phallusies . BJU Int . 2012; 110 ( 3 ):e153–e154. 10.1111/j.1464-410X.2012.10674_2.x. [PubMed] [CrossRef] [Google Scholar]
67. Wamai RG, Morris BJ, Waskett JH, et al.. Criticisms of African trials fail to withstand scrutiny: male circumcision does prevent HIV infection . J Law Med . 2012; 20 ( 1 ):93–123. [PubMed] [Google Scholar]
68. Morris BJ, Hankins CA, Tobian AA, Krieger JN, Klausner JD. Does male circumcision protect against sexually transmitted infections? Arguments and meta-analyses to the contrary fail to withstand scrutiny . ISRN Urol . 2014; 2014 : 684706. 10.1155/2014/684706. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
69. Wamai RG, Morris BJ, Bailey RC, Klausner JD, Boedicker MN. Male circumcision for protection against HIV infection in sub-Saharan Africa: the evidence in favour justifies the implementation now in progress . Glob Public Health . 2015; 10 ( 5-6 ):639–666. 10.1080/17441692.2014.989532. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
70. Wamai RG, Morris BJ, Bailey RC, Klausner JD, Boedicker MN. Debating male circumcision for HIV prevention: a one-sided argument does not represent a legitimate controversy analysis–Reply to de Camargo et al . Glob Public Health . 2015; 10 ( 5-6 ):672–678. 10.1080/17441692.2015.1014827. [PubMed] [CrossRef] [Google Scholar]
71. Morris BJ, Wamai RG, Krieger JN, Banerjee J, Klausner JD. Male circumcision to prevent syphilis in 1855 and HIV in 1986 is supported by the accumulated scientific evidence to 2015: Response to Darby . Glob Public Health . 2015 Nov 13:1–19. Epub ahead of print. 10.1080/17441692.2015.1104371. [PubMed] [CrossRef] [Google Scholar]
72. Morris BJ, Barboza G, Wamai RG, Krieger JN. Circumcision is a primary preventive against HIV infection: critique of a contrary meta-regression analysis by Van Howe . Glob Public Health . 2016:1–11. 10.1080/17441692.2016.1164737. [PubMed] [CrossRef] [Google Scholar]
73. U.S. Centers for Disease Control and Prevention. HIV Surveillance Report: Diagnoses of HIV Infection in the United States and Dependent Areas , 2014. Volume 26 http://www.cdc.gov/hiv/pdf/library/reports/surveillance/cdc-hiv-surveillance-report-us.pdf. Published November 2015 Accessed September 14, 2016. [Google Scholar]
74. Kacker S, Frick KD, Gaydos CA, Tobian AAR. Costs and effectiveness of neonatal male circumcision . Arch Pediatr Adolesc Med . 2012; 166 ( 10 ):910–918. 10.1001/archpediatrics.2012.1440. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
75. Hess KL, Hu X, Lansky A, et al. Lifetime risk of a diagnosis of HIV infection in the United States . Ann Epidemiol . 2017. In press. [PMC free article] [PubMed] [Google Scholar]
76. U.S. Centers for Diseases Control and Prevention. HIV Surveillance Report: Diagnoses of HIV Infection in the United States and Dependent Areas , 2011. Volume 23 http://www.cdc.gov/hiv/pdf/statistics_2011_HIV_Surveillance_Report_vol_23.pdf. Published February 2013 Accessed July 25, 2015. [Google Scholar]
77. Sansom SL, Prabhu VS, Hutchinson AB, et al.. Cost-effectiveness of newborn circumcision in reducing lifetime HIV risk among U.S. males . PLoS One . 2010; 5 ( 1 ):e8723. 10.1371/journal.pone.0008723. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
78. Warner L, Ghanem KG, Newman DR, Macaluso M, Sullivan PS, Erbelding EJ. Male circumcision and risk of HIV infection among heterosexual African American men attending Baltimore sexually transmitted disease clinics . J Infect Dis . 2009; 199 ( 1 ):59–65. 10.1086/595569. [PubMed] [CrossRef] [Google Scholar]
79. Chemtob D, Op de Coul E, Van Sighem A, Mor Z, Cazein F, Semaille C. Impact of male circumcision among heterosexual HIV cases: comparison between three low prevalence countries . Israel J Health Policy Res . 2015; 4 :36. 10.1186/s13584-015-0033-8. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
80. Kirby Institute. HIV in Australia: Australia Annual Surveillance Report 2014 Supplement . Sydney, New South Wales, Australia: Kirby Institute; 2014. http://kirby.unsw.edu.au/sites/default/files/hiv/resources/HIVASRsuppl2014_online.pdf Accessed July 2015. [Google Scholar]
81. Public Health Agency of Canada. Summary: Estimates of HIV Incidence, Prevalence and Proportion Undiagnosed in Canada, 2014 . Ottawa, Ontario, Canada: Public Health Agency of Canada; 2015. http://www.catie.ca/sites/default/files/2014-HIV-Estimates-in-Canada-EN.pdf Accessed September 14, 2016. [Google Scholar]
82. Morris BJ, Castellsague X. The role of circumcision in preventing STIs . In: Gross GE, Tyring SK, eds. Sexually Transmitted Infections and Sexually Transmitted Diseases . Berlin and Heidelberg: Springer-Verlag; 2011:715–739. [Google Scholar]
83. Morris BJ, Wamai RG. Biological basis for the protective effect conferred by male circumcision against HIV infection . Int J STD AIDS . 2012; 23 ( 3 ):153–159. 10.1258/ijsa.2011.011228. [PubMed] [CrossRef] [Google Scholar]
84. Tobian AAR, Quinn TC. Herpes simplex virus type 2 and syphilis infections with HIV: an evolving synergy in transmission and prevention . Curr Opin HIV AIDS . 2009; 4 ( 4 ):294–299. 10.1097/COH.0b013e32832c1881. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
85. Tobian AAR, Gray RH. The medical benefits of male circumcision . JAMA . 2011; 306 ( 13 ):1479–1480. 10.1001/jama.2011.1431. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
86. Mehta SD, Gaydos C, Maclean I, et al.. The effect of medical male circumcision on urogenital Mycoplasma genitalium among men in Kisumu, Kenya . Sex Transm Dis . 2012; 39 ( 4 ):276–280. 10.1097/OLQ.0b013e318240189c. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
87. Bailey RC, Mehta SD. Circumcisions place in the vicious cycle involving herpes simplex virus type 2 and HIV . J Infect Dis . 2009; 199 ( 7 ):923–925. 10.1086/597209. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
88. Bailey RC, Plummer FA, Moses S. Male circumcision and HIV prevention: current knowledge and future research directions . Lancet Infect Dis . 2001; 1 ( 4 ):223–231. 10.1016/S1473-3099(01)00117-7. [PubMed] [CrossRef] [Google Scholar]
89. Homfray V, Tanton C, Miller RF, et al.. Male circumcision and STI acquisition in Britain: evidence from a national probability sample survey . PLoS One . 2015; 10 ( 6 ):e0130396. 10.1371/journal.pone.0130396. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
90. Larke N, Thomas SL, dos Santos Silva I, Weiss HA. Male circumcision and human papillomavirus infection in men: a systematic review and meta-analysis . J Infect Dis . 2011; 204 ( 9 ):1375–1390. 10.1093/infdis/jir523. [PubMed] [CrossRef] [Google Scholar]
91. Hallett TB, Alsallaq RA, Baeten JM, et al.. Will circumcision provide even more protection from HIV to women and men? New estimates of the population impact of circumcision interventions . Sex Transm Infect . 2011; 87 ( 2 ):88–93. 10.1136/sti.2010.043372. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
92. Castellsagué X, Peeling RW, Franceschi S, et al.; IARC Multicenter Cervical Cancer Study Group. Chlamydia trachomatis infection in female partners of circumcised and uncircumcised adult men . Am J Epidemiol . 2005; 162 ( 9 ):907–916. 10.1093/aje/kwi284. [PubMed] [CrossRef] [Google Scholar]
93. Bosch FX, Albero G, Castellsagué X. Male circumcision, human papillomavirus and cervical cancer: from evidence to intervention . J Fam Plann Reprod Health Care . 2009; 35 ( 1 ):5–7. 10.1783/147118909787072270. [PubMed] [CrossRef] [Google Scholar]
94. Cherpes TL, Meyn LA, Krohn MA, Hillier SL. Risk factors for infection with herpes simplex virus type 2: role of smoking, douching, uncircumcised males, and vaginal flora . Sex Transm Dis . 2003; 30 ( 5 ):405–410. 10.1097/00007435-200305000-00006. [PubMed] [CrossRef] [Google Scholar]
95. Cherpes TL, Hillier SL, Meyn LA, Busch JL, Krohn MA. A delicate balance: risk factors for acquisition of bacterial vaginosis include sexual activity, absence of hydrogen peroxide-producing lactobacilli, black race, and positive herpes simplex virus type 2 serology . Sex Transm Dis . 2008; 35 ( 1 ):78–83. 10.1097/OLQ.0b013e318156a5d0. [PubMed] [CrossRef] [Google Scholar]
96. Templeton DJ, Jin F, Prestage GP, et al.. Circumcision and risk of sexually transmissible infections in a community-based cohort of HIV-negative homosexual men in Sydney, Australia . J Infect Dis . 2009; 200 ( 12 ):1813–1819. 10.1086/648376. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
97. Wiysonge CS, Kongnyuy EJ, Shey M, et al.. Male circumcision for prevention of homosexual acquisition of HIV in men . Cochrane Database Syst Rev . 2011;( 6 ):CD007496. 10.1002/14651858.CD007496.pub2. [PubMed] [CrossRef] [Google Scholar]
98. Templeton DJ, Jin F, Mao L, et al.. Circumcision and risk of HIV infection in Australian homosexual men . AIDS . 2009; 23 ( 17 ):2347–2351. 10.1097/QAD.0b013e32833202b8. [PubMed] [CrossRef] [Google Scholar]
99. Templeton DJ, Millett GA, Grulich AE. Male circumcision to reduce the risk of HIV and sexually transmitted infections among men who have sex with men . Curr Opin Infect Dis . 2010; 23 ( 1 ):45–52. 10.1097/QCO.0b013e328334e54d. [PubMed] [CrossRef] [Google Scholar]
100. Poynten IM, Jin F, Templeton DJ, et al.. Prevalence, incidence, and risk factors for human papillomavirus 16 seropositivity in Australian homosexual men . Sex Transm Dis . 2012; 39 ( 9 ):726–732. 10.1097/OLQ.0b013e31825d5cb8. [PubMed] [CrossRef] [Google Scholar]
101. Wright JL, Lin DW, Stanford JL. Circumcision and the risk of prostate cancer . Cancer . 2012; 118 ( 18 ):4437–4443. 10.1002/cncr.26653. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
102. Wachtel M, Yang S, Morris B. Countries with high circumcision prevalence have lower prostate cancer mortality . Asian J Androl . 2016; 18 ( 1 ):39–42. 10.4103/1008-682X.159713. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
103. Spence AR, Rousseau MC, Karakiewicz PI, Parent MÉ. Circumcision and prostate cancer: a population-based case-control study in Montréal, Canada . BJU Int . 2014; 114 ( 6b ):e90–e98. 10.1111/bju.12741. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
104. Pabalan N, Singian E, Jarjanazi H, Paganini-Hill A. Association of male circumcision with risk of prostate cancer: a meta-analysis . Prostate Cancer Prostatic Dis . 2015; 18 ( 4 ):352–357. 10.1038/pcan.2015.34. [PubMed] [CrossRef] [Google Scholar]
105. Gilbert MTP, Rambaut A, Wlasiuk G, Spira TJ, Pitchenik AE, Worobey M. The emergence of HIV/AIDS in the Americas and beyond . Proc Natl Acad Sci USA . 2007; 104 ( 47 ):18566–18570. 10.1073/pnas.0705329104. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
106. Introcaso CE, Xu F, Kilmarx PH, Zaidi A, Markowitz LE. Prevalence of circumcision among men and boys aged 14 to 59 years in the United States, National Health and Nutrition Examination Surveys 2005-2010 . Sex Transm Dis . 2013; 40 ( 7 ):521–525. 10.1097/01.OLQ.0000430797.56499.0d. [PubMed] [CrossRef] [Google Scholar]
107. Morris BJ, Waskett J, Bailis SA. Case number and the financial impact of circumcision in reducing prostate cancer . BJU Int . 2007; 100 ( 1 ):5–6. 10.1111/j.1464-410X.2007.06875.x. [PubMed] [CrossRef] [Google Scholar]
108. Morris BJ, Mindel A, Tobian AAR, et al.. Should male circumcision be advocated for genital cancer prevention? Asian Pac J Cancer Prev . 2012; 13 ( 9 ):4839–4842. 10.7314/APJCP.2012.13.9.4839. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
109. Gutwein LG, Alvarez JF, Gutwein JL, Kays DW, Islam S. Allocation of healthcare dollars: analysis of nonneonatal circumcisions in Florida . Am Surg . 2013; 79 ( 9 ):865–869. [PubMed] [Google Scholar]
110. Williams N, Kapila L. Complications of circumcision . Br J Surg . 1993; 80 ( 10 ):1231–1236. 10.1002/bjs.1800801005. [PubMed] [CrossRef] [Google Scholar]
111. Moses S, Bailey RC, Ronald AR. Male circumcision: assessment of health benefits and risks . Sex Transm Infect . 1998; 74 ( 5 ):368–373. 10.1136/sti.74.5.368. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
112. Stenram A, Malmfors G, Ókmian L. Circumcision for phimosisindications and results . Acta Paediatr . 1986; 75 ( 2 ):321–323. 10.1111/j.1651-2227.1986.tb10207.x. [PubMed] [CrossRef] [Google Scholar]
113. McIntosh N. Pain in the newborn, a possible new starting point . Eur J Pediatr . 1997; 156 ( 3 ):173–177. 10.1007/s004310050576. [PubMed] [CrossRef] [Google Scholar]
114. Taddio A, Katz J, Ilersich AL, Koren G. Effect of neonatal circumcision on pain response during subsequent routine vaccination . Lancet . 1997; 349 ( 9052 ):599–603. 10.1016/S0140-6736(96)10316-0. [PubMed] [CrossRef] [Google Scholar]
115. Taddio A, Stevens B, Craig K, et al.. Efficacy and safety of lidocaine-prilocaine cream for pain during circumcision . N Engl J Med . 1997; 336 ( 17 ):1197–1201. 10.1056/NEJM199704243361701. [PubMed] [CrossRef] [Google Scholar]
116. Banieghbal B. Optimal time for neonatal circumcision: an observation-based study . J Pediatr Urol . 2009; 5 ( 5 ):359–362. 10.1016/j.jpurol.2009.01.002. [PubMed] [CrossRef] [Google Scholar]
117. Russell CT, Chaseling J. Topical anaesthesia in neonatal circumcision: a study of 208 consecutive cases . Aust Fam Physician . 1996; 25 ( suppl 1 ):S30–S34. [PubMed] [Google Scholar]
118. Smith C, Smith DP. Office pediatric urologic procedures from a parental perspective . Urology . 2000; 55 ( 2 ):272–276. 10.1016/S0090-4295(99)00571-3. [PubMed] [CrossRef] [Google Scholar]
119. Freeman JJ, Spencer AU, Drongowski RA, Vandeven CJM, Apgar B, Teitelbaum DH. Newborn circumcision outcomes: are parents satisfied with the results? Pediatr Surg Int . 2014; 30 ( 3 ):333–338. 10.1007/s00383-013-3430-5. [PubMed] [CrossRef] [Google Scholar]
120. Auvert B, Taljaard D, Lagarde E, Sobngwi-Tambekou J, Sitta R, Puren A. Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: the ANRS 1265 Trial . PLoS Med . 2005; 2 ( 11 ):e298. 10.1371/journal.pmed.0020298. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
121. Gray RH, Kigozi G, Serwadda D, et al.. Male circumcision for HIV prevention in men in Rakai, Uganda: a randomised trial . Lancet . 2007; 369 ( 9562 ):657–666. 10.1016/S0140-6736(07)60313-4. [PubMed] [CrossRef] [Google Scholar]
122. Bailey RC, Moses S, Parker CB, et al.. Male circumcision for HIV prevention in young men in Kisumu, Kenya: a randomised controlled trial . Lancet . 2007; 369 ( 9562 ):643–656. 10.1016/S0140-6736(07)60312-2. [PubMed] [CrossRef] [Google Scholar]
123. Frisch M, Simonsen J. Cultural background, non-therapeutic circumcision and the risk of meatal stenosis and other urethral stricture disease: two nationwide register-based cohort studies in Denmark 1977-2013 . Surgeon . 2016; pii :S1479–666X (16)30179-2. 10.1016/j.surge.2016.11.002. [PubMed] [CrossRef] [Google Scholar]
124. Simforoosh N, Tabibi A, Khalili SA, et al.. Neonatal circumcision reduces the incidence of asymptomatic urinary tract infection: a large prospective study with long-term follow up using Plastibell . J Pediatr Urol . 2012; 8 ( 3 ):320–323. 10.1016/j.jpurol.2010.10.008. [PubMed] [CrossRef] [Google Scholar]
125. Pieretti RV, Goldstein AM, Pieretti-Vanmarcke R. Late complications of newborn circumcision: a common and avoidable problem . Pediatr Surg Int . 2010; 26 ( 5 ):515–518. 10.1007/s00383-010-2566-9. [PubMed] [CrossRef] [Google Scholar]
126. Roth JD, Keenan AC, Carroll AE, et al.. Readmission characteristics of elective pediatric circumcisions using large-scale administrative data . J Pediatr Urol . 2016; 12 ( 1 ):27.e1–6. 10.1016/j.jpurol.2015.10.006. [PubMed] [CrossRef] [Google Scholar]
127. Royal Australasian College of Physicians. Circumcision of infant males . Sydney, New South Wales, Australia: Royal Australasian College of Physicians; 2010. https://www.racp.edu.au/docs/default-source/advocacy-library/circumcision-of-infant-males.pdf Accessed May 5, 2015. [Google Scholar]
128. Task Force on Circumcision. Cultural bias and circumcision: the AAP Task Force on Circumcision responds . Pediatrics . 2013; 131 ( 4 ):801–804. 10.1542/peds.2013-0081. . [PubMed] [CrossRef] [Google Scholar]
129. Morris BJ, Tobian AAR, Hankins CA, et al.. Veracity and rhetoric in paediatric medicine: a critique of Svoboda and Van Howes response to the AAP policy on infant male circumcision . J Med Ethics . 2014; 40 ( 7 ):463–470. 10.1136/medethics-2013-101614. [PubMed] [CrossRef] [Google Scholar]
130. Brady MT. Newborn male circumcision with parental consent, as stated in the AAP circumcision policy statement, is both legal and ethical . J Law Med Ethics . 2016; 44 ( 2 ):256–262. . [PubMed] [Google Scholar]
131. Morris BJ, Krieger JN, Klausner JD, Rivin BE. The ethical course is to recommend infant male circumcision–Arguments disparaging American Academy of Pediatrics affirmative policy do not withstand scrutiny . J Law Med Ethics . In press. [Google Scholar]
132. Rivin BE, Diekema DS, Mastroianni AC, Krieger JN, Klausner JD, Morris BJ. Critical evaluation of Adler's challenge to the CDC's male circumcision recommendations . Int J Child Rights . 2016; 24 :265–303. 10.1163/15718182-02402004 [CrossRef] [Google Scholar]
133. Morris BJ. Commentary: do the benefits of male circumcision outweigh the risks? A critique of the proposed CDC guidelines . Front Pediatr . 2015; 3 :88. 10.3389/fped.2015.00088. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
134. Bates MJ, Ziegler JB, Kennedy SE, et al.. Recommendation by a law body to ban infant male circumcision has serious worldwide implications for pediatric practice and human rights . BMC Pediatr . 2013; 13 :136. 10.1186/1471-2431-13-136. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
135. Jacobs AJ. The ethics of circumcision of male infants . Isr Med Assoc J . 2013; 15 ( 1 ):60–65. [PubMed] [Google Scholar]
136. United Nations General Assembly. Convention on the Rights of the Child . A/RES/44/25. November 20, 1989. http://www.un.org/documents/ga/res/44/a44r025.htm Accessed March 2, 2017.
Articles from Global Health: Science and Practice are provided here courtesy of The Johns Hopkins Bloomberg School of Public Health Center for Communication Programs