Case Study - Chlorhexidine for Umbilical Cord Care

Publication date: 2012

  WORKING PAPER March  2012   Prepared  for  the  United  Nations   Commission  on  Life-­‐Saving  Commodities   for  Women  and  Children   This  is  a  working  document.  It  has  been  prepared  to  facilitate  the  exchange  of  knowledge  and  to  stimulate  discussion.     The  findings,  interpretations  and  conclusions  expressed  in  this  paper  are  those  of  the  authors  and  do  not  necessarily  reflect  the   policies  or  views  of  the  United  Nations  Commission  on  Life-­‐Saving  Commodities  for  Women  and  Children,  or  the  United  Nations.       The  text  has  not  been  edited  to  official  publication  standards,  and  the  Commission  accepts  no  responsibility  for  errors.     The  designations  in  this  publication  do  not  imply  an  opinion  on  legal  status  of  any  country  or  territory,  or  of  its  authorities,  or  the   delimitation  of  frontiers.   C A S E   S T U D Y   Newborn  Re su s c i t a t i on  Dev i c e s   2     C A S E S T U D Y Chlorhexidine for Umbilical Cord Care February  2012   Prepared  for  the  United  Nations   Commission  on  Life-­‐Saving   Commodities  for  Women  and   Children   ii   Authors Joel Segrè1, Patricia Coffey2, Mutsumi Metzler2, Shirley Villadiego2, Neal Brandes3, Steve Hodgins4, Luke Mullany5, Saul Morris6. 1Consultant to the Bill & Melinda Gates Foundation; 2PATH; 3United States Agency for International Development; 4Maternal and Child Integrated Program; 5The Johns Hopkins University Bloomberg School of Public Health; 6the Bill & Melinda Gates Foundation. Acknowledgments The authors would like to thank the following individuals for their contributions: Abra Greene, Janet Saulsbury, Jill Sherman-Konkle, and Gretchen Shively. PATH’s contribution to this case study was made possible by the generous support of the American people through the United States Agency for International Development (USAID) under the terms of the HealthTech Cooperative Agreement # AID-OAA-A-11-00051. The contents provided by PATH are the responsibility of PATH and do not necessarily reflect the views of USAID or the US Government. Cover photograph credits Photograph 1: A mother in Nepal lies with her baby. © 2008 Suaahara/JHUCCP; courtesy of Photoshare. Photograph 2: A baby in Djoliba, Mali. © 2000 Hannah Koenker; courtesy of Photoshare. Photograph 3: A newborn child sleeps next to his mother at the Tinh Gia District Health Center in Vietnam. © 2004 Philippe Blanc; courtesy of Photoshare. C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     iii   Acronyms ASHA Accredited social health activist CDK Clean delivery kit CHX Chlorhexidine EMA European Medicines Agency EMLc Pediatric essential medicines list or model list of essential medicines for children FCHV Female Community Health Volunteer HDPE High-density polyethylene ICH International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use RCT Randomized controlled trial RH Relative humidity TBA Traditional birth attendant USFDA United States Food and Drug Administration WHO World Health Organization WTP Willingness to pay C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     iv   Table of Contents Executive Summary . v 1. Efficacy and Effectiveness of Chlorhexidine . 1 1.1. Historical use of the product and safety record. 1 1.2. Completed studies for umbilical cord care . 2 1.3 Additional studies under way on umbilical cord care. 3 2. Global Policy and Regulation . 3 2.1 WHO guidelines for umbilical cord care . 3 2.2. The World Health Organization Model List of Essential Medicines for Children. 4 3. National Regulatory Policy. 5 3.1. South Asian countries: Nepal, India, Bangladesh. 6 3.2. African countries: Zambia, Tanzania, others . 7 4. Financing Chlorhexidine. 7 4.1 Cost and cost-effectiveness data . 7 4.2 Current use in Nepal . 7 4.3 Potential for public procurement. 8 4.4 Potential for private purchase . 8 5. User Centered Product Design: What Women Want. 9 5.1 Formulation considerations. 9 5.2 Packaging considerations. 9 5.3 Bundling with clean delivery kits . 11 6. Manufacturing. 11 6.1 The global chlorhexidine industry . 11 6.2 The finished product manufacturer’s business case. 12 6.3 Local versus centralized manufacturing of finished products . 12 6.4 Formulation details . 13 6.5 Packaging details. 14 7. Supply Chain Management. 14 7.1 Shipping considerations . 14 7.2 Shelf life . 14 8. Cultivating demand from caregivers. 15 9. Cultivating demand from consumers . 16 10. Monitoring and Evaluation . 17 11. Recommendations. 18 C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     v   Executive Summary Globally, neonatal infections are estimated to account for over 1 million newborn deaths annually (over a third of the total burden). In many regions, infection is the leading cause of neonatal mortality, and in high-mortality regions infections are responsible for around half of all newborn deaths. Many of these infections come from contamination of the umbilical cord stump. Chlorhexidine digluconate is a widely used, low-cost antiseptic effective against major agents of neonatal infection. Since its introduction in the 1950s, it has been used regularly as a surgical and detail antiseptic and carefully studied for safety and efficacy. Recent community-level randomized controlled trials in Nepal, Pakistan, and Bangladesh have shown that applying a 4% chlorhexidine product (7.1% chlorhexidine digluconate) to the umbilical cord saves lives (the Pakistan and Bangladesh findings were published in The Lancet on February 8, 2012). Across the three countries, data from over 54,000 newborns showed an aggregate 23% reduction in neonatal mortality (not including deaths in the first few hours of life) and a 68% reduction in severe infections for the chlorhexidine intervention groups. These are some of the largest effect sizes seen in any neonatal intervention. There are literally dozens of manufacturers currently making chlorhexidine-based products around the world, at concentrations from <1% to 20%. Chlorhexidine digluconate—used to make a variety of chlorhexidine finished products—is readily available on every inhabited continent at low cost. The finished product for care of the umbilical cord stump (4% free chlorhexidine, or 7.1% chlorhexidine digluconate) can cost less than US$0.01 in raw materials per baby. It has a long shelf life, requires no cold chain, and is extremely easy to apply with minimal training and no equipment. These factors make it suitable for hospital, health center, and home care alike. Few other interventions have demonstrated such potential for rapidly reducing newborn mortality across so many settings for such a low cost. While there have been efforts to improve umbilical cord hygiene by advocating “dry cord care,” these efforts have not always had the intended effect in all settings. Millions of mothers around the world continue to have a strong desire to apply something to the umbilical cord stump of their newborns. In the absence of a specifically recommended product, they resort to a variety of traditional and non-traditional substances including edible oils, ash, dirt, and feces. Where consumer research has been conducted, mothers have shown a strong latent demand for a purpose-made antiseptic like chlorhexidine and also have demonstrated the ability to use chlorhexidine correctly. Nepal is the first country to have registered a chlorhexidine product specifically for umbilical cord stump care. Additionally, Nepal has included chlorhexidine in their 2011 national list of essential medicines. One of the largest pharmaceutical producers in the country manufactures it for newborn care programs. The government of Nepal has plans to allocate funds in the coming year for procuring the product for broader use. Several actions are required to take advantage of this opportunity, beyond Nepal, and to address one of the leading causes of neonatal mortality: C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     vi   • Add 4% chlorhexidine (7.1% chlorhexidine digluconate) for umbilical cord care to the WHO model list of essential medicines for children. • Correct the common misconception that WHO advocates dry cord care only. The WHO umbilical cord care guidelines recommend that antimicrobials be used “…as a temporary measure, according to a local situation (e.g., in neonatal tetanus-endemic areas or to replace a harmful traditional substance).” These exceptions are rarely cited in discussions of WHO’s dry cord care recommendation but may apply to more than half of all births around the world. • Fast track registration of 4% chlorhexidine (7.1% chlorhexidine digluconate) for umbilical cord care with national regulatory authorities and encourage additional manufacturers to produce the drug with guaranteed minimum volumes. • Train birth attendants to correctly apply chlorhexidine to the umbilical cord, as part of newborn care training programs. • Allocate resources to integrate chlorhexidine for umbilical cord care into essential newborn care programs in order to generate sustainable demand and attractive manufacturing volumes for the product. Through these actions, we are much more likely to see increased use of this overlooked intervention, thereby contributing to hundreds of thousands of newborns lives saved annually. C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     1   1. Efficacy and Effectiveness of Chlorhexidine 1.1. Historical use of the product and safety record Chlorhexidine (digluconate or gluconate)1 is a broad-spectrum antiseptic, effective against major agents of neonatal sepsis. Since its development in 1950, chlorhexidine (CHX) has been widely used in a range of applications including hand washes, preoperative body shower, wound care, cosmetics, oral hygiene, general disinfection, and veterinary care. Common formulations can be water-based, alcohol-based, gels, or powders and are commonly applied to adult, infant, and neonatal skin. Considering the extent of its use as a topical antiseptic on humans, reported side effects are rare, but have included delayed reactions such as contact dermatitis and photosensitivity. Today, topical 4% chlorhexidine solutions are commonly used for wound care and are widely available over the counter in the United States and in other countries under multiple branded and generic labels. In the 1970s CHX became popular for neonatal use in the United States and elsewhere as hexachlorophene was discontinued. Bathing of newborns in CHX-based solutions quickly became routine practice in many clinical settings to reduce the occurrence of staphylococcal outbreaks in nurseries.2,3,4,5 Additionally, the World Health Organization (WHO) has recognized CHX as a suitable antimicrobial for cord care where necessary and especially to displace harmful cord care practices.6 In recent years, tens of thousands of neonates have received a range of CHX-based cleansing interventions, including full-body and umbilical cord cleansing, without reported adverse effects.7 There are no reports of adverse health consequences as a result of absorption of CHX in neonates, and there is no data to suggest that the levels of absorption reported have any clinical importance. Transient contact dermatitis has been reported in preterm very-low-birth-weight infants after long-term (>7 days) placement of chlorhexidine-impregnated dressings for central venous catheters, and thus this type of application in these infants should be monitored carefully. Overall, CHX is very safe.8                                                                                                                                         1NOTE:  It  is  common  practice  to  use  ‘chlorhexidine  gluconate’  and  ‘chlorhexidine  digluconate’  interchangeably  when   referring  to  the  concentrated  chemical  antiseptic.  ‘Chlorhexidine  digluconate’  is  used  throughout  this  document  for   precision  and  consistency.   2  Mullany  LC,  Darmstadt  GL,  Tielsch  JM.  Safety  and  impact  of  chlorhexidine  antisepsis  interventions  for  improving   neonatal  health  in  developing  countries.  Pediatric  Infectious  Disease  Journal.  2006;25:665–675.   3  Maloney  MH.  Chlorhexidine:  a  hexachlorophane  substitute  in  the  nursery.  Nursing  Times.  1975;71(37):21.     4  Rosenberg  A,  Alatary  SD,  Peterson  AF.  Safety  and  efficacy  of  the  antiseptic  chlorhexidine  gluconate.  Surgery,   Gynecology,  &  Obstetrics.  1976;143(5):789–792.     5  Tuke  W.  Hibiscrub  in  the  control  of  staphylococcal  infection  in  neonates.  Nursing  Times.  1975;71(37):20.   6  World  Health  Organization.  Care  of  the  Umbilical  Cord:  A  Review  of  the  Evidence.  Geneva:  WHO/RHT/MSM;  1999.   Available  at:  https://apps.who.int/rht/documents/MSM98-­‐4/MSM-­‐98-­‐4.htm.   7  Mullany  LC,  Khatry  SK,  Sherchand  JB,  et  al.  Bacterial  colonization  of  hospital-­‐born  infants  in  Nepal  and  impact  of   chlorhexidine  skin  cleansing:  a  randomized  controlled  trial.  Pediatric  Infectious  Disease  Journal.  2008;27(6):505–511.   8  Mullany  LC,  Darmstadt  GL,  Tielsch  JM.  Safety  and  impact  of  chlorhexidine  antisepsis  interventions  for  improving   neonatal  health  in  developing  countries.  Pediatric  Infectious  Disease  Journal.  2006;25:665–675.   C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     2   1.2. Completed studies for umbilical cord care In 2004, a Cochrane review concluded that there was insufficient evidence to recommend topical antiseptics for prevention of umbilical cord infection (RR=0.53 [0.25−1.13]).9 Of the 21 studies included in the most recent version of the review, all but one took place in developed countries (one was in a Bangkok tertiary care teaching hospital). In such environments, only seven studies reported cord infection, and the overall rate of infection was low. CHX was only used in one study. No deaths were reported in any of the studies. This combination of factors limits the extent to which that Cochrane review can inform decision-making about optimal cord care practices in the developing world contexts where neonatal infection is highest. In recent years, three large community-based randomized controlled trials (RCT) evaluating the effectiveness of CHX for umbilical cord care as part of a package of newborn interventions have been conducted in Nepal, Pakistan, and Bangladesh. A simplified summary of each study is provided in Table 1 below. Table 1. Clinical trials evaluating the effectiveness of chlorhexidine for umbilical cord care. Study Characteristic Nepal Bangladesh Pakistan Overall NMR* (at time of study) 30/1000 36/1000 30/1000 Percent of Births at Home (at time of study) 92% 88% 80% Total Sample Size 15,123 29,760 9,741 Primary Outcomes Neonatal mortality Omphalitis Neonatal mortality Omphalitis Neonatal mortality Omphalitis Comparison Group Dry cord care Dry cord care Dry cord care Frequency of Multiple Applications (day) 1,2,3,4,6,8,10 1,2,3,4,5,6,7 Daily for 14 days Intervention Provider Project staff Project staff TBA† and caretaker *Neonatal mortality rate. †Traditional birth attendant. The full details of the Nepal study were published in The Lancet in 200610 while results of the other two trials were published online on February 8, 2012.11,12 All three studies showed substantial reductions in neonatal mortality (20% to 38%) and even greater reductions in omphalitis (24% to 75%) in the CHX groups. Several groups have conducted meta-analyses using the data as reported, and the unpublished                                                                                                                                         9  Zupan  J,  Garner  P,  Omari  AA.Topical  umbilical  cord  care  at  birth.  Cochrane  Database  of  Systematic  Reviews.   2004;(3):CD001057.   10  Mullany  LC,  Darmstadt  GL,  Khatry  SK,  et  al.  Topical  applications  of  chlorhexidine  to  the  umbilical  for  prevention  of   omphalitis  and  neonatal  mortality  in  southern  Nepal:  a  community-­‐based,  cluster-­‐randomized  trial.  The  Lancet.   2006;367:910–918.   11  Soofi  S,  Cousens  S,  Imdad  A,  Bhutto  N,  Ali  N,  Bhutta  ZA.  Topical  application  of  chlorhexidine  to  neonatal  umbilical   cords  for  prevention  of  omphalitis  and  neonatal  mortality  in  a  rural  district  of  Pakistan:  a  community-­‐based,  cluster-­‐ randomised  trial.  The  Lancet.  Published  online  February  8,  2012.   12  El  Arifeen  S,  Mullany  LC,  Shah  R,  et  al.  The  effect  of  cord  cleansing  with  chlorhexidine  on  neonatal  mortality  in  rural   Bangladesh:  a  community-­‐based,  cluster-­‐randomised  trial.  The  Lancet.  Published  online  February  8,  2012.   C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     3   analyses suggest reduction in mortality of approximately 20% to 23%. More formal meta-analyses are due for publication in the coming months. Additionally, Hodgins et al. published a trial showing the non-inferiority of 4% CHX gel to 4% CHX liquid. The study, based in Kathmandu, recruited 653 neonates in a hospital setting and showed that 24 hours after application, liquid CHX offered a 64% reduction in the proportion of samples positive for bacteria, whereas gel CHX offered an 86% reduction in the proportion of samples positive for bacteria.13 Overall, there is currently sufficient evidence to recommend a 4% CHX product (7.1% CHX digluconate) for umbilical cord cleansing as a strategy to reduce neonatal mortality in settings with poor hygiene and high neonatal mortality. 1.3 Additional studies under way on umbilical cord care Two additional RCTs are under way to determine the effectiveness of CHX in Africa. Both are expected to report results in 2014. Table 2. Clinical trials currently under way. Pemba (Tanzania) Zambia Institutional Lead The Johns Hopkins University Boston University Trial Type Individually randomized, double-blind, placebo-controlled trial Cluster randomized, unmasked comparison versus “dry” cord care Sample Size 24,000 + additional 4,000 42,570 (90 clusters) Product Type 10-mL dropper bottle of liquid 4% CHX (7.1% CHX digluconate) 10-mL dropper bottle of liquid 4% CHX (7.1% CHX digluconate) Delivery Method Project staff demonstrate for mothers four times, mothers apply in other cases Mothers Intervention Duration 10 days, or three days after the stump separates, whichever is longer Ten days, or three days after the stump separates, whichever is longer Outcomes Primary: mortality. Sub-study will examine impact on omphalitis as well as the etiology, sensitivity, and specificity of diagnosing omphalitis Primary: mortality, Secondary: Incidence of omphalitis through 28 days 2. Global Policy and Regulation 2.1 WHO guidelines for umbilical cord care There is a common misconception that the WHO guidelines advocate for the exclusive use of dry cord care. In fact, in the 1999 WHO document entitled “Care of the Umbilical Cord: A Review of the Evidence” WHO recommends that topical antimicrobials be used on the stump after cutting in home deliveries “…as a temporary measure, according to a local situation (e.g., in neonatal tetanus-endemic                                                                                                                                         13  Hodgins  S,  Thapa  K,  Khanal  L,  et  al.  Chlorhexidine  lotion  vs.  aqueous  for  preventative  use  on  umbilical  stump:  a   randomized  non-­‐inferiority  trial.  Pediatric  Infectious  Disease  Journal.  2010;29(11):999–1003.   C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     4   areas or to replace a harmful traditional substance).”14 Additionally, WHO recommends that in institutional deliveries, antimicrobials may be used “according to local situation” and specifically identifies CHX as one of five recommended antimicrobial agents. 2.2. The World Health Organization Model List of Essential Medicines for Children The 2011 WHO Model List of Essential Medicines for Children (EMLc)15 includes CHX for umbilical cord care under section 15. DISINFECTANTS AND ANTISEPTICS, subsection 15.1 Antiseptics. The listing is as follows: Chlorhexidine Solution: 5% (digluconate); 20% (digluconate) (needs to be diluted prior to use for cord care). The 17th Expert Committee on the Selection and Use of Essential Medicines convened by WHO in 2009 concluded that data from a community-based, cluster-randomized trial in Nepal showed a significant reduction in neonatal mortality after use of a 4% CHX solution (7.1% CHX digluconate) for umbilical cord care. This was sufficient to include such a product and indication for use in the WHO EMLc. Nevertheless, due to the absence of a commercially available 4% CHX product at that time, this recommendation of the expert review committee resulted in listing 20% CHX (digluconate) with an instruction to dilute for umbilical cord care use. At the time of publication of the 2009 WHO model list, PATH and the US Agency for International Development submitted a joint letter to the WHO expert review committee stating that the indication was not clear and suggesting that it should be revised to stipulate use of 4% CHX for umbilical cord care. WHO responded by saying that such an issue would be taken up during the next review of the EMLc in 2010–2011. Clarity on the use of 4% CHX for umbilical cord care is critical because there is a very common confusion around the concentrations of free chlorhexidine versus chlorhexidine digluconate. The conversion between the two is listed in Table 3 below. It is worth noting that the current listing of 5% CHX digluconate would deliver approximately 2.8% free CHX, a level lower than what was used in the RCTs for umbilical cord care. If one is not aware of this difference, one may see 5% CHX on the EMLc and incorrectly think that one does not have to go through any in-country regulatory process because the 5% is higher than the 4% for umbilical cord care.                                                                                                                                         14  World  Health  Organization.  Care  of  the  Umbilical  Cord:  A  Review  of  the  Evidence.  Geneva:  WHO/RHT/MSM;  1999.   Available  at:  https://apps.who.int/rht/documents/MSM98-­‐4/MSM-­‐98-­‐4.htm.  Accessed  February  10,  2012.   15  World  Health  Organization.  Model  List  of  Essential  Medicines  for  Children.  3rd  list.  Geneva:  WHO;  March  2011.   Available  at:  http://whqlibdoc.who.int/hq/2011/a95054_eng.pdf.  Accessed  February  10,  2012.   C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     5   Table 3. Free chlorhexidine versus chlorhexidine digluconate. Chlorhexidine Diluconate Free Chlorhexidine Notes 20% 11.3% Concentration listed on the EMLc 7.1% 4.0% Concentration used in the RCTs in five countries 5% 2.8% Concentration listed on the EMLc To avoid this confusion, the EMLc should state: Chlorhexidine 7.1% chlorhexidine digluconate solution or gel, delivering 4% chlorhexidine for umbilical cord care. In 2010, PATH submitted an amendment with additional data to the WHO expert review committee to support the clarification of the indication for use of CHX for umbilical cord care by stipulating use of 4% CHX in either gel or aqueous solution. The expert committee decided to maintain the previous listing for CHX until a product of the strength and formulation used in the trials is commercially available (i.e., availability of the product on the open market, not just for trial purposes). Specifically, The Unedited Report of 18th Expert Committee on the Selection and Use of Essential Medicines (21 to 25 March, 2011) noted that: “The problem remains that, as in 2009, a commercially available preparation of 7.1% chlorhexidine digluconate solution or gel (delivering 4% chlorhexidine) is not yet available. While the 20% requires dilution and manipulation and is clearly not optimal, until there is a commercially available product of the strength and formulation used in the trials, the current listing cannot be amended. However, the Committee noted that an optimized 4% chlorhexidine is listed as one of the priority products for development by WHO on the Priority Medicines list for maternal and child health and therefore flagged it as a ‘missing’ essential medicine, given the impact on mortality suggested in the trials.” Today, there is one company, Lomus Pharmaceuticals Pvt. Ltd (Kathmandu, Nepal), producing a 4% CHX product commercially. It has been in use in four districts (and a larger procurement is currently underway), but could be made available for sale anywhere in the country and for export. Lomus has registered the product with the Department of Drugs Administration in Nepal. Additionally, 4% CHX (7.1% CHX digluconate) is on Nepal’s national essential medicines list for 2011 as a solution or gel for umbilical cord care. This data may help to add 4% CHX (7.1% CHX digluconate) to the WHO EMLc. 3. National Regulatory Policy CHX is included in some national essential medicines lists, but Nepal is the only country known to have added it to their national essential medicines list at a 4% concentration for umbilical cord care. In other countries it is not at the correct concentration for umbilical cord care. Experience in Bangladesh and Nepal to date demonstrates that CHX for umbilical cord care has been classified by country regulatory agencies as a medicine, and the product is required to be registered in country with the appropriate drug authority. Over-the-counter distribution of the product is independent of the need to register the product as a medicine. C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     6   In 2011, PATH reviewed various global regulatory pathways for CHX for umbilical cord care. Pathways investigated included United States Food and Drug Administration (USFDA), European Medicines Agency (EMA), WHO prequalification of medicines, and a country-by-country approach. The results of this review suggest that the EMA procedure (termed Article 58) might appear to be promising in certain respects. Article 58 was established in 2004 to facilitate developing-country registration of medicines to prevent or treat diseases of major public health interest. Per Article 58 requirements, since the CHX product is a simple formulation, regulatory assessment of the manufacture and control of this drug product would be considered to be standard. Results from clinical trials in South Asia are also available; however, certain factors make this option less than desirable: • Significant resources are required to complete an Article 58 application and maintain the positive scientific opinion resulting from successful submission. It is questionable whether such cost could be justified when using public funds. Also, it might not make sense to make such an investment of several hundreds of thousands of dollars when revenues are expected to be low. • The holder of the positive opinion has substantial responsibilities, including post-opinion submission of results from any ongoing and future clinical trials and provision of additional information on the product’s efficacy and safety. Although a nonprofit organization can be an opinion holder, it is questionable whether a nonprofit organization would be willing to assume those substantial responsibilities on an ongoing basis. • Manufacturers would need to ensure manufacture of the product from certified sources of active ingredients if the manufacturers were to pursue Article 58. This might increase costs and therefore pricing of the product. • Registration of the CHX product on a country-by-country basis would still need to be undertaken. Considering the above, a country-by-country approach would appear to be the better approach to take to secure registration for a CHX product. An expert consultation with WHO should take place after publication of recent RCT results in Bangladesh and Pakistan. Favorable findings from this consultation, along with an updated listing on the EMLc, will likely facilitate regulatory reviews at the country and/or regional level. Obtaining WHO prequalification could be explored concurrently if this approach is determined to be reasonable considering time and resource requirements. 3.1. South Asian countries: Nepal, India, Bangladesh Country-level regulatory processes vary from country to country. A country-level registration process should only be undertaken where the CHX product intervention will be rolled out in the same country. This is the case, for example, in Nepal, where the intervention has been recently approved by the Ministry of Health and Population and the product has obtained registration in country. In Bangladesh, for example, registration would be very straightforward to obtain by Popular Pharmaceutical Ltd, the manufacturer of the product used in the most recent study. However, they would need an incentive to do (i.e., assurance of market demand) that could be demonstrated by an enabling policy environment and firm support for the intervention on the part of the Ministry of Health and other key stakeholders. While India may appear to be a good entry point for product registration in the region, product registration is C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     7   subject to approval by the Drug Controller General of India, and the data requirements for approval are yet to be determined. 3.2. African countries: Zambia, Tanzania, others Given the status of ongoing RCTs in Zambia and Tanzania, national regulatory authorities will likely be most interested in product registration after the RCTs are completed. If RCT results are favorable, and corollary ministry of health policy and stakeholders are supportive of the intervention, it is possible that that the product could be registered relatively easily. Regulatory approval obtained in one country may be applied to other countries thereby facilitating market clearance in the sub-Saharan Africa region. Some countries in the region, however, may prefer to have more localized data about the intervention before giving market clearance for the CHX product. 4. Financing Chlorhexidine 4.1 Cost and cost-effectiveness data Assuming that every baby requires 3 g of a 4% CHX product (as is provided in the Nepal programs), a finished pharmaceutical product costs less than $0.005 in raw materials and an additional $0.09-0.15 in packaging costs. Preliminary estimates of cost effectiveness from a cost effectiveness study in Sylhet, Bangladesh, suggest that when umbilical cord cleansing with a 4% CHX product is added to a platform of community-based maternal and newborn health services, the mean incremental cost per disability- adjusted life year (DALY) averted is less than US$10.00.16,17,18 4.2 Current use in Nepal CHX for umbilical cord care is currently used in four districts of Nepal (Parsa, Banke, Jumla, and Bajhang). To date, the programs have been donor financed, effectively working as “at scale” demonstrations. Given the strong results in these pilots, the Government of Nepal is in the process of creating a budget to procure CHX from a local manufacturer (Lomus Pharmaceuticals) for distribution primarily via Female Community Health Volunteers (FCHV). Donor funding is likely to support continued procurement for the FCHVs until government funding is available (expected in 2013). The Lomus product is listed with a maximum retail price of 18 Nepali Rupees (approximately US$0.22) for a                                                                                                                                         16  NOTE:  Costs  were  derived  incrementally  on  top  of  existing  platforms  of  maternal  and  newborn  health  services,  from  a   program  perspective  and  included  operational  and  support  costs  as  well  as  costs  associated  with  product  delivery   through  village  health  workers  and  supervising  community  health  workers.  Costs  may  be  higher  or  lower  in   non-­‐effectiveness  trial  settings,  and/or  where  an  existing  platform  and  infrastructure  for  community-­‐based  maternal   and  newborn  health  does  not  exist.   17  NOTE:  This  estimate  falls  between  childhood  immunizations  for  TB,  DPT,  polio  and  measles  ($8.00);  and  other   common  programs  like  HIV/AIDS  services  voluntary  testing  and  counseling,  ARVs  to  prevent  vertical  transmission,  etc.   ($68);  surgical  services  and  emergency  care  ($109);  community  case  management  of  childhood  pneumonia  ($146);  and   maternal  and  newborn  care,  inclusive  of  increased  primary  care,  targeted  newborn  care,  and  improved  emergency  and   newborn  care  ($261).   18  Musgrove  P,  Fox-­‐Rushby  J.  Cost-­‐effectiveness  analysis  for  priority  setting.  In:  Jamison  D,  Breman  JG,  Measham  AR,  et   al.,  eds.  Disease  Control  Priorities  in  Developing  Countries  (2nd  edition).  Washington,  DC:  The  World  Bank  and  Oxford   University  Press;  2006.   C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     8   single application, but the actual transfer price between Lomus and the Government of Nepal is not known at this time. Additionally, Lomus hopes to sell the product via its traditional retail channels. 4.3 Potential for public procurement The low cost of CHX—and particularly the low cost per life saved—makes it among the “best buys” in neonatal health and an excellent candidate for public procurement in countries with high mortality due to neonatal infection. 4.4 Potential for private purchase The majority of health care expenditure in much of the developing world is private expenditure, and the countries where neonates die from infections are no exception. Table 4 below shows private expenditure on health as a percentage of total expenditure on health for selected countries. Table 4. Private expenditure on health as a percentage of total expenditure on health. Country Annual Estimated Neonatal Deaths from Infection* % Private Expenditure † India 405,848 68% Nigeria 150,459 63% Pakistan 119,122 68% DR Congo 109,091 46% Ethiopia 66,159 48% Bangladesh 45,722 69% Tanzania 32,037 28% Zambia 14,461 38% Nepal 9,004 62% *Source: Partnership for Maternal, Newborn & Child Health. †Source: WHO; 2008. Private-sector sales are often an important complement to public-sector provision. As a relatively low- cost, easy-to-use product with a long shelf life, CHX may be particularly well suited to private-sector sales. Data on willingness to pay (WTP) specifically for CHX is scarce, but the data in Table 5 provides some indication for South Asia. Table 5. Willingness to pay in South Asia. Country WTP Range in US$ Type Source Year Nepal $0.05–$0.06 TBAs’ stated WTP Tuladhar et al. 2007 Bangladesh $0.42–$0.70 Actual purchases Winch et al. 2009 Bangladesh $0.21–$0.85 Mothers’ stated WTP ICDDR,B 2010 India (urban) $0.50–$0.70 Mothers’ stated WTP Synovate 2011 India (rural) $0.30–$0.40 Mothers’ stated WTP Synovate 2011 C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     9   These WTP figures are 50% to 200% greater than the projected wholesale cost of CHX, leaving potential retail margins for private-sector delivery. 5. User Centered Product Design: What Women Want Umbilical cord care is a culturally mediated practice wherein consumer preferences are a key driver of what products are ultimately adopted and discarded. In many communities, there is a deep desire to dress the cord with something, but practices vary widely. Thoughtful combination of formulation and packaging may increase the product’s adoption in a specific community. 5.1 Formulation considerations Based on the clinical trials conducted in South Asian countries and a subsequent test to establish non- inferiority of the 4% CHX gel, the product can be formulated into either aqueous solution (liquid) or gel. Table 6 illustrates several efforts to assess user preferences in regions of interest. Table 6. Efforts to understand user preferences. Country Preference Notes Bangladesh Gel In 2010, PATH and ICDDR,B assessed the demand for the product among potential users (women who were currently pregnant or had a child over the last six months, and their husbands). The study showed that 63% of the respondents, or 1,109 people, preferred gel formulation over aqueous solution. However, the price they were willing to pay did not differ significantly between the two formulations. Nepal Gel The randomized non-inferiority trial conducted in Nepal in 2009 included questions regarding user preference of dosage forms. Of the 30 subjects originally given gel (excluding those woman reporting a negative experience), 2 preferred aqueous. However, over half of those using aqueous indicated they would have preferred gel (17/30), believing that it would stay in place more easily and be longer lasting. India Gel In 2011, a consumer research group polled mothers, mothers-in-law, and caregivers in Uttar Pradesh for product preferences using an unlabeled tube of Lomus 4% gel and an unlabeled 70-ml bottle of aqueous. The majority of respondents across all participant groups preferred the gel. Tanzania Liquid The Pemba study looked at consumer preferences for aqueous formulations in 10- ml and 100-ml bottles as well as tubes of gel formulations. 44.6% of mothers preferred the 10-ml bottle, 33.9% preferred the tube of gel, and 21.5% preferred the 100-ml bottle. Zambia Liquid The Zambia study looked at 10-ml and 100-ml liquid presentations as well as tubes that would contain a gel formulation. Unfortunately, the tubes did not contain CHX gel (a major limitation of the study) and were therefore not popular among respondents. 5.2 Packaging considerations Primary container for liquid. Both the Nepal and Bangladesh trials used a white Boston round bottle as the primary container (a Boston round bottle can be seen in Figure 1 below) and a cotton ball as the applicator. In the operations research conducted in Bangladesh, a white high-density polyethylene (HDPE) bottle with a nozzle was selected as the material for the primary container for the 4% CHX aqueous solution because: 1) HDPE is the most common plastic material for CHX digluconate-based C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     10   drugs, 2) the color white protects CHX digluconate from sunlight, and 3) the nozzle minimizes occasions in which users directly contact the umbilical cord. The results from the following two studies led to selecting the white HDPE bottle with a nozzle: • PATH conducted a product attribute study in 2008. This study compared these three options: 1) white HDPE bottle with a nozzle, 2) white Boston round bottle, and 3) amber glass bottle. Results indicated that the white HDPE bottle with a nozzle was the option most preferred by users and service providers (141 out of 165 respondents [or 85.5%] chose this option). • The pretesting that the Projahnmo study group conducted with health counselors in 2008 indicated that the 4% CHX aqueous solution was properly applied to the umbilical cord with a nozzle bottle and confirmed their decision to select a nozzle bottle as the primary container. Primary container for gel. In Nepal, a preprinted aluminum tube (a common primary container for semi- solid drug products) was selected for the 4% CHX gel formulation. While other types of primary containers could be applicable for 4% CHX gel including sachets and plastic tubes, consumer research suggested that mothers and caregivers associated this type of packaging with pharmaceutical products and good health. Secondary packaging. The operations research in Bangladesh did not utilize a secondary package. The information required by the drug authority in Bangladesh was printed on a label designed by the manufacturer, which was attached to the primary container. Pictorial instructions for use were developed through collaboration among Projahnmo study group members, PATH, and Popular Pharmaceuticals in order to supplement the instructions-for-use text printed on the label. These supplemental pictorial instructions were then attached to the container with a rubber band. In Nepal, the aluminum tube containing 4% CHX gel was packaged in a small paper box preprinted with labeling information. Please see Figure 1 below for packaging examples and Figure 2 for examples of instructions for use. Figure 1. Liquid primary packaging as produced by a manufacturer in Bangladesh for study purposes only (left); primary and secondary packaging of gel product as produced by Lomus in Nepal (right). C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     11   Figure 2. Pictorial instructions for use used in Nepal (left) and Bangladesh (right). 5.3 Bundling with clean delivery kits Some have advocated the bundling of a CHX product with clean delivery kits (CDK) as a way to increase availability and use of the product. To date, such bundling has not occurred. In Nepal, CHX will not be bundled with the clean delivery kit currently being distributed by Contraceptive Sales Company. In Bangladesh, physically bundling a 4% CHX product with a CDK (putting CHX and CDK into the same package) will likely require additional regulatory approval since CHX is a pharmaceutical product and the other contents of the CDK are not. Instead of bundling the two products, nongovernmental organizations that distribute CDKs may use their own depot holders or community workers to present the CHX and CDK concurrently and explain how using both could be beneficial. 6. Manufacturing 6.1 The global chlorhexidine industry Chlorhexidine digluconate is broadly available around the world both in its bulk drug form of 20% chlorhexidine digluconate and in myriad finished products. In India alone there are over 70 brands of finished CHX products for sale from over 60 different companies. The product has applications as both a preservative and active ingredient across a broad range of veterinary, dental, and other health care applications, as summarized in Table 7. Table 7. Various uses for chlorhexidine. Application Concentration Veterinary 20% Mouthwashes, toothpastes, oral rinses 0.12%–0.2% Skin prep for surgery, procedural hand washing 0.5%–4% Wound treatment 4% The drug monograph of 20% chlorhexidine digluconate is listed in Unites States, Unites Kingdom, European, and Japanese pharmacopeias. There are also more than 50 vendors of bulk 20% chlorhexidine C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     12   digluconate concentrate, several of which have Drug Master Files with USFDA. The bulk product is typically sold in 200 kg drums, and there are sufficient buffer stocks on every inhabited continent. Commodity pricing for this product is often in the range of US$4.50 per kilogram. Assuming that every baby requires 3 g of a 4% CHX product (as is provided in the Nepal programs), the total requirement of 20% CHX digluconate would be just over 1,000 L per million children treated, or just five drums of active pharmaceutical ingredient per million newborns. Global supply of the active pharmaceutical ingredient, therefore, is unlikely to be a concern. 6.2 The finished product manufacturer’s business case CHX for umbilical cord care is a low-volume, low-margin product with few barriers to entry. If the product is used in all births in a given region, annual sales would correlate with crude birth rates of 30–50 births per thousand in high fertility areas. This is a relatively low sales volume when compared with other pharmaceutical manufacturing opportunities for more commonly used over-the-counter products. Margins for CHX are likely to be similarly lackluster for a product which is in the public domain (not patentable) and quite simple to make. The combination of these factors means that large pharmaceutical companies are unlikely to take an interest in independent manufacture and distribution of CHX for umbilical cord care. Institutional buyers and large volume orders are more likely to attract the attention of potential manufacturers, similar to what took place with Lomus Pharmaceuticals in Nepal. 6.3 Local versus centralized manufacturing of finished products There are several reasons to consider local manufacturing of a CHX product for umbilical cord care. Capital costs of manufacturing are relatively low, and standard equipment found in most pharmaceutical companies would be used. The manufacturing process is simple and robust enough to be easily replicated. Bulk chlorhexidine digluconate can be purchased in 200-kg drums or even 20-kg pails. Small amounts of the bulk drug yield a large volume of finished CHX product for umbilical cord care. For example, a 20-kg pail of chlorhexidine digluconate can serve about 20,000 newborns at the dose and duration used in Nepal. Local manufacturing can also simplify local regulation where indigenous pharmaceutical companies may be better equipped than foreign firms to navigate an approval process. Central manufacturing also has some benefits. A single, central manufacturer may be more compelled by the business case of manufacturing a very high-volume, low-cost product. And should there be a pooled procurement, a centralized manufacturer would also simplify logistics and quality control. The shelf life at 40°C with 75% relative humidity (RH) is sufficient to withstand warehousing and shipping in most climates. Ultimately, the choice of local versus central manufacturing should be made for business reasons, depending on what type of manufacturer is able to offer the most competitive price on the shortest timeline. C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     13   6.4 Formulation details CHX for umbilical cord care may be formulated as a topical gel or liquid, which have very similar manufacturing processes, as diagrammed below in Figure 3, with the only difference in the dotted lines where guar gum is added to thicken the product into a gel if desired. Figure 3. Potential manufacturing processes. Some manufacturers have chosen to add small amounts of benzalkonium chloride to CHX products as a preservative, but stability tests conducted by PATH have shown that this may not be a crucial addition. Additionally, some manufacturers have added perfume and coloring as per consumer preferences. Over all, the inputs for CHX manufacturing are inexpensive. One representative formulation for gel is detailed below in Table 8. Table 8. A representative formulation for chlorhexidine gel. Formula Component Formulation Cost in US$ per 3 g Source 20% CHX gluconate, BP* 7.10% $0.004795 Viporchemicals.com 50% benzalkonium chloride (optional) 0.10% $0.000000 Alibaba.com Guar gum, NF† 1% $0.000060 Alibaba.com Sodium hydroxide, NF pH to 6.0 $0.000009 Alibaba.com Purified water, USP‡ Remainder $0.000001 (estimated water tariffs) Total $0.004865 *British Pharmacopoeia. †National formulary. ‡United States Pharmacopeia. C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     14   6.5 Packaging details Packaging is responsible for most of a CHX product’s cost. For liquid formulations, bottles or sachets may be used. Dropper bottles have been used in all of the RCTs to date and typically cost around US$0.15 each including filling. Sachets may pack more tightly and ship more easily and often have packing and filling costs in the range of US$0.01 in India. The only CHX product packaged for retail sales is made by Lomus Pharmaceuticals in Kathmandu. Based on user feedback, their packaging includes a tube for the gel, a full color instructional package insert, and an outer box (please refer to Figures 1 and 2 above), totaling approximately US$0.09 (Table 9). Table 9. Packaging costs example. Packaging Component US$ per Unit Source Preprinted collapsible aluminum tube $0.04 Perfect Tubes Pvt Printed paperboard box $0.04 Lomus Pharmaceuticals Printed color package insert <$0.01 Lomus Pharmaceuticals Total $0.09 7. Supply Chain Management 7.1 Shipping considerations Temperature, pH level, and exposure to sunlight adversely affect the stability of CHX digluconate, the active ingredient of 4% CHX for umbilical cord care. When CHX digluconate is kept under suboptimal conditions, it degrades to p-chloroaniline and its purity is compromised. According to the US Pharmacopeia, a 20% aqueous solution of CHX digluconate should maintain its pH range between 5.5 and 7.0. It also states that 20% CHX digluconate should be preserved in a tight container at room temperature and be protected from light. These requirements should also be maintained for shipping and storing 4% CHX for umbilical cord care. In addition, selecting an appropriate primary container is important in order not only to maintain the quality of the product but to minimize its shipping cost. The quality of the CHX digluconate would be best preserved with neutral glass or polypropylene. Also, transparent primary containers should be avoided in order to protect CHX digluconate from light. A commonly used primary container for commercially available CHX digluconate-based products is HDPE since it is lighter than glass (thus reduces shipping cost) and it maintains product quality. As an example, Medichem S.A. (Barcelona, Spain), one of the 20% CHX digluconate manufacturers listed in the Drug Master File submitted to the USFDA, provides its product in a 200-kg HDPE drum. In any case, manufacturers should perform compatibility tests according to local regulations in order to confirm the appropriateness of the selected primary containers. 7.2 Shelf life A drug product’s shelf life is the length of time during which it is considered suitable for sale, use, or consumption. Shelf life is affected by temperature, humidity, and light. For this reason, according to C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     15   International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), each country is classified into one of four climatic zones with defined storage conditions for drug substances and products (see table below). Based on this classification, in South Asia, Bangladesh and India are both assigned to Zone IV, whereas Nepal is assigned to Zone II. In Africa, Tanzania is assigned to Zone IV whereas Zambia is assigned to Zone II. Table 10. Climatic zones for shelf life. Climatic Zone Definition Storage Condition I Temperate climate 21°C/45% RH II Subtropical and Mediterranean climates 25°C/60% RH III Hot, dry climate 30°C/35% RH IV Hot, humid climate 30°C/70% RH Source: ICH Q1F Guideline, “Stability Data Package for Registration in Climatic Zones III and IV.” Manufacturers of 4% CHX products must perform stability tests using the primary container that they selected for their products in order to establish their product shelf life under the storage conditions assigned to the country in which the products will be distributed and used. Stability tests can be performed using accelerated conditions (e.g., in general, 40°C ± 2°C/75% RH ± 5% RH for 6 months for climatic zones III and IV). In addition to this ICH guideline, manufacturers need to check with their local drug regulatory authority to ascertain whether there are any additional requirements. In 2009, PATH commissioned a contract laboratory in the United States to perform stability tests on the 4% CHX aqueous solution and gel. Testing was conducted under the following protocol: • Primary container: 4-mL HDPE bottle and polypropylene screw closure (materials commonly used for commercial CHX-based products). • Testing conditions: 5oC, 25oC/60% RH and 40oC/75% RH to establish 24-month stability. • Tested at: 0, 1, 3, and 6 months. • Tested for: appearance, pH, potency, and amount of p-chloroaniline present (a substance that is produced when CHX is degraded). Both formulations passed the stability test, and there was no significant difference in potency, pH, or purity. The potency of the gel formulation tended to decrease (although it remained within the acceptable range) probably because sufficient homogeneity was not achieved during laboratory testing without a proper homogenizer. In commercial production, this is unlikely to be an issue. Based on these results on the stability of the product in this 6-month accelerated study, PATH estimates a 24-month shelf life at room temperature across all climatic zones listed above. 8. Cultivating demand from caregivers Most of the recent work on CHX for umbilical cord care (Nepal, Pakistan, Bangladesh, Zambia, and Tanzania) has focused on community-level use of the product. In these contexts, some caregivers may have full medical training, but most are community health workers or TBAs. In each case, CHX for C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     16   umbilical cord care has been well received when presented by program staff, with specific highlights in Table 11. Table 11. Caregiver demand. Location Caregiver Synthesis of comment or direct quotes Pemba (Tanzania) Unspecified “We are willing to use it. Mothers can apply if they are trained.” “Most mothers will be willing to use this medicine. They pray for such thing to be introduced in the community as they are very useful.” Bangladesh TBA TBAs were the single largest source of CHX, even when the product was both given away through government community outreach workers and sold in pharmacies. The TBAs appeared to appreciate the product as a special service they could offer (and potentially resell) to their clientele. India ASHA* As part of government training, ASHAs are instructed to advocate for dry cord care in Uttar Pradesh. However, they are often frustrated by mothers who insist on dressing the cord in one way or another despite their advice. As dry cord care is unable to displace traditional practices, ASHAs are excited to recommend CHX as a way to finally have something to offer mothers in their communities. Nepal FCHV FCHWs have enthusiastically embraced the product in the four districts where it is currently used today and have been able to ensure correct usage of CHX in close to 70% of all births in their catchment areas. Training is incorporated into existing FCHV training programs on other maternal and neonatal health topics. *ASHA: Accredited Social Health Activist. A critical component of cultivating caregiver demand has been training caregivers to understand the CHX product and administer it correctly. In Nepal, FCHVs were trained using dolls modified to have umbilical cords made from balloons as well as the instructional aide pictured below (Figure 4). In a follow-up study, FCHVs trained using these tools were able to ensure correct administration of CHX by household caregivers to roughly 70% of the newborns in their catchment areas. Figure 4. Instructional aide and correct chlorhexidine application. 9. Cultivating demand from consumers Discouraging mothers from putting anything on the cord has been a persistent challenge in communities around the world. Qualitative studies in India, Nepal, Uganda, Ghana, and Malawi show that mothers are often hesitant to leave the cord dry due to concerns that the cord might take longer to separate, cause the C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     17   baby discomfort, or leave the baby vulnerable to various maladies. In fact, in Uttar Pradesh, India, despite government programs to promote dry cord care, 83% of mothers apply some substance to the cord.19 Formative work in Zambia and Pemba (Tanzania) also show that mothers have a strong desire to put something on the umbilical cord stump. Specific motivations to dress the stump vary by region and by individual, but the most common reasons include a desire to make the cord stump separate faster and to prevent infection. The actual substances applied to the stump vary widely, sometimes even between individuals within the same community, but often fall into a few main categories: • Edible oils and butters including ghee and shea butter, and mustard, palm, peanut, and coconut oils (India, Nepal, Bangladesh, Ethiopia, Mozambique, Tanzania, Nigeria, Zambia, and others areas). • Medicinal products including powders, alcohols, iodine, and antibiotics (India, Ghana, Guinea Bissau, Malawi, Mozambique, Nigeria, Tanzania, Uganda, Zambia, and other areas). • Waste products including animal feces, ash, dust, sand, dirt (India, Nepal, Nigeria, Tanzania, Zambia, Malawi, Uganda, and other areas). Where studied, there appears to be a significant latent demand for purpose-built umbilical cord care products like CHX and often a willingness to displace existing practice with a product specifically packaged for this purpose. Mothers in many communities around the world are eager for a product to use in cord care and appear likely to adopt CHX once they are made aware of its existence. 10. Monitoring and Evaluation There are several different ways to monitor and evaluate the transformation of CHX for umbilical cord care from being an overlooked commodity to status as a widely used intervention. A number of metrics (Table 12) may be useful in monitoring that progression and identifying where additional attention may be required. Table 12. Monitoring and evaluation metrics. Supply Metrics • Global monthly production volume of a 4% CHX product for neonatal use. • Geographic and demographic reach of manufacturers. • Quality of manufactured product. Demand Metrics • Number of countries recommending CHX for newborn care. • Volume of public tenders for CHX products. • % of public and private facilities with CHX in stock. • % of wholesale and retail pharmacies stocking CHX. • % of caregivers recommending the use of CHX. • % of consumers accepting CHX.                                                                                                                                         19  Varma  DS,  Khan  ME,  Hazra  A.  Increasing  postnatal  care  of  mothers  and  newborns  including  follow-­‐up  cord  care  and   thermal  care  in  rural  Uttar  Pradesh.  Journal  of  Family  Welfare.  2010;56(special  issue):31–41.   C A S E   S T U D Y   Ch lo rhex id ine   f o r  Umb i l i c a l   Co rd  Ca re     18   Correct-Use Metrics • % of babies receiving CHX. • % of above within 2 hours of birth. • % of above where 3 g or more of product were used. • % of above where product was applied to the stump and surrounding areas. • % of mothers who report applying CHX and no other substance to the cord. Impact Metrics • Neonatal mortality rate. • Neonatal mortality from infection. 11. Recommendations Several simple activities could increase the uptake and impact of chlorhexidine for umbilical cord care around the world: • Add 4% chlorhexidine (7.1% chlorhexidine digluconate) for umbilical cord care to the WHO model list of essential medicines for children. • Correct the common misconception that WHO advocates dry cord care only. The WHO umbilical cord care guidelines recommend that antimicrobials be used “…as a temporary measure, according to a local situation (e.g., in neonatal tetanus-endemic areas or to replace a harmful traditional substance).” These exceptions are rarely cited in discussions of WHO’s dry cord care recommendation but may apply to a more than half of all births around the world. • Fast track registration of 4% chlorhexidine (7.1% chlorhexidine digluconate) for umbilical cord care with national regulatory authorities and encourage additional manufacturers to produce the drug with guaranteed minimum volumes. • Train birth attendants to correctly apply chlorhexidine to the umbilical cord, as part of newborn care training programs. • Allocate resources to integrate chlorhexidine for umbilical cord care into essential newborn care programs in order to generate sustainable demand and attractive manufacturing volumes for the product. Through these actions, we are much more likely to see increased use of this overlooked intervention, thereby contributing to hundreds of thousands of newborn lives saved annually.

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