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Dental tissues of sickle cell anemia and its impact on the quality of life related to oral health

ABSTRACT

Objective:

The aim of this study was to determine the association between dental tissues and sickle cell anemia (SCA) and how it impacts the quality of life related to oral health.

Materials and Methods:

It was a cohort study of 154 Congolese participants with and without SCA conducted in the dental service of SCA at the Yolo Center, Kinshasa, aged at least 6 years and without a history of clinically severe conditions (hospitalization and blood transfusion), who were regularly monitored. The inclusion criteria were the diagnosis confirmation of SCA at the health service in a period of at least 6 months before enrollment in this study. Dental tissues were assessed by a clinical examination using a dental mirror and probe. The index of Decayed-Missing-Filled Teeth (DMFT) was used to assess the dental state of the participants. For Oral Health-related Quality of Life (OHrQoL), the Congolese versions of the perception questionnaires, modified from the Oral Health Impacts Profile (OHIP-23), were used for participants. Each question had to be answered by yes or no, depending on whether the participant was satisfied (outcome = 1) or dissatisfied (outcome = 0) about an oral health-related quality of life.

Results:

Of the 154 participants, aged from 6 to 64 years, with a mean age of 19.5 ± 7 (SD) years, 96 presented with SCA and only 68 were correctly followed; 102 did not present SCA and only 86 were correctly followed. The DMFT and dmft indexes were higher in the SCA group, being 2.9 and 2.5, respectively. The difference between the SCA group and the control group was significant for decayed teeth, missing teeth, filled teeth and no caries. Of the different dimensions of quality of life that were compared between the SCA group and control group, 15 of 23 items were statistically significant.

Conclusion:

The present study strongly confirmed an association between dental caries and missing teeth with sickle cell anemia. Secondly, the quality of life for SCA participants seems to be poor, compared to the control group.

Keywords:
Dental caries; Tooth loss; Oral health; Quality of life; Sickle cell anemia

Introduction

Sickle Cell Anemia (SCA) is a qualitative hemoglobinopathy characterized by the substitution of glutamic acid for valine at the sixth codon of beta chain s globin.11 Mikobi TM, Lukusa PT, Aloni MN, et al. Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the a3.7triplication in Congolese patients than in worldwide series. J Clin Lab Anal. 2018;32:e22186. Global estimates suggest that more than 312,000 infants are born with SCA each year.22 De Franceschi L, Corrocher R. Established and experimental treatment for sickle cell disease. Haematologica. 2004;89: 348-56. The United States and Europe represent 2 % of annual SCA births worldwide.33 Fonseca MA, Oueis HS, Casamassimo PS. Sickle cell anemia: a review for the pediatric dentistry. Pediatr Dent. 2007;29(2): 159-69. The vast majority of sickle cell births occur in developing countries, with an estimated number of 230,000 annual SCA births in sub-Saharan Africa. The reported mortality reaches up to 92 %.44 Kanyana M, Mutombo M, Leta L, Nyembue T, Mantshumba M. Motifs de consultation des drépanocytaires au service de stomatologie du centre de médecine mixte et d’anémie SS/Yolo en République Démocratique du Congo. J de l’IRSS. 2016;2:83-8.,55 Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN. Global burden of sickle cell anemia in children under FIVE, 20102050: modeling based on DEMOGRAPHICS, excess mortality, and interventions. PLoS Med. 2013;vol.10(no.7). The Democratic Republic of the Congo (DRC) has the highest incidence of SCA patients in Africa after Nigeria.66 Agasa B, Bosunga K, Opara A, Tshilumba K, Dupont E, Vertongen F, Cotton F, Gulbis B. Prevalence of sickle cell disease in a northeastern region of the Democratic Republic of Congo: what impact on transfusion policy? Transfus Med Oxf Engl. 2010;20:62-5.,77 Mayank K, Kristen H, Megha S, Szilva A, Leslie S, Adela. Orofacial manifestation and dental management of sickle cell disease: a scooping review. Anemia. 2021. https://doi.org/10.1155/5556708. ID 5556708.
https://doi.org/10.1155/5556708....
,88 Tshilolo L, Aissi LM, Lukusa D, Kinsiama C, Wembonyama S, Gulbis B, Vertongen F. Neonatal screening for sickle cell anemia in the Democratic Republic of the Congo: experience from a pioneer project on 31204 newborns. J Clin Pathol. 2009;62: 35-8. The number of children born with SCA is expected to grow by nearly 30 % from 2010 to 2050.77 Mayank K, Kristen H, Megha S, Szilva A, Leslie S, Adela. Orofacial manifestation and dental management of sickle cell disease: a scooping review. Anemia. 2021. https://doi.org/10.1155/5556708. ID 5556708.
https://doi.org/10.1155/5556708....

In SCA, the life span of red blood cells is severely diminished from the usual 90 to 120 days to about 10 days.99 U.S. Department of Health and Human Services, (n.d.). Sickle Cell Disease. Bethesda, MD, USA: National Heart Lung and Blood Institute; 2021. Due to atypical hemoglobin and their sickle shape, red blood cells break down prematurely in the spleen, causing fever and hyperbilirubinemia. This leads to a structural modification responsible for changes in the stability, solubility and structure of erythrocytes, which take on a sickle shape when exposed to low oxygen tension, acidosis or dehydration.1010 Switzer JA, Hess DC, Nichols FT, Adams RJ. Pathophysiology and treatment of stroke in sickle cell disease: present and future. Lancet Neural. 2006;5(6):501-12. Hemoglobin in the red blood cell is the main molecule that delivers oxygen to all the cells throughout the body. SCA results in multiple symptoms of oxygen deficit, including fatigue, irritability, dizziness, lightheadedness, tachycardia and shortness of breath.

In the literature, SCA has been linked to dental caries, tooth erosion, hypomineralization, hypercementosis, pulp stones, and asymptomatic pulp necrosis.1111 Fernandes ML, Kawachi I, Correa-Faria P, Pattusi MP, Paiva SM, Pordeus IA. Caries prevalence and impact on oral health related quality of life in children with sickle cell disease: cross-section study. BMC Oral Health. 2015;15:68. https://doi.org/10.1186/s12903-015-0052-4.
https://doi.org/10.1186/s12903-015-0052-...
Mutombo et al.; found that the most common oral manifestations of SCA are mucosal pallor, yellow tissue coloration, disorders of enamel and dentin mineralization, changes to the superficial cells of the tongue; multiple caries and periodontal disease that can lead to an odontogenic abscess.1212 Mutombo MA, Nyimi BF, Kanyana M, Ngueyi K, Mantshumba MA. Management of odontogenic abscessing patients with sickle cell anemia: 5 cases reports. Br J Med Med Res. 2017; 20:1-5. Additionally, frequent admission drug treatments and diminished oral hygiene are high-risk factors for caries in SCA patients.1313 yue Hui, xu Xinxin, Liu Qin, Li Xiaozhi, jiang Wei, Hu Bo. Association between sickle cell disease and dental caries: a systemic review and meta- analysis. Hematology. 2020;25(1): 309-19.

Oral health is part of general health and recognized as an essential component of quality of life (QoL) that may affect the general health.1414 Petersen PE. The World Oral Health Report 2003; continuous improvement health in the 21st century approach of the WHO Global oral health Program. Community Dent Oral Epidemiol. 2003;321:3-24. The quality of life and the familial conditions are critical in determining the process of health and disease.1515 Fernandes ML, Kawachi I, Correa-Faria P, Pattusi MP, Paiva SM, Pordeus IA. The impact of the oral condition of children with sickle cell disease on family quality of life. Braz Oral Res. 2016;30:1-21. Several conditions affect the quality of life1616 Slade GD, Spencer AJ. Development and evaluation of the oral health impact profile. Community Dent Health. 1994;11:3-11. related to oral health in the daily lives of many patients. Many of them throughout the world, especially the poorest or those with inadequate oral hygiene are still affected by oral problems, such as caries and periodontal diseases.1717 Spanemberg JC, Cardoso JA, Slob EMGB, López-López J. Quality of life related to oral health and its impact in adults. J Stomatol, Oral Maxillofac Surg. 2019;120(3):234-9.

The aim of this study was to determine the effect of SCA on dental tissues and oral health-related quality of life of the patients treated at the dental service of the SCA Center at the Yolo Center, in relation to the control group.

Materials and methods

Study design and sampling

A cohort random study with a non-probabilistic sampling design of Congolese participants with and without Sickle Cell Anemia (SCA) was conducted at the dental service of SCA at the Yolo Center Kinshasa. The SCA dental service at the Yolo Center is the only institution accredited by the Congolese health ministry of the government of the Democratic Republic of the Congo. The participants’ medical records were obtained from the interview, dental examination and biological examination or blood examination report performed before or after treatment.

A total of 214 participants from January 2020 to December 2020 were invited to participate in the study. Of these, 154 agreed to participate (adhesion rate = 72 %). Only those participants who had completed all items on the clinical questionnaire and measuring instruments (OHIP-C, DMFT), aged at least six years, were included in the final sample. They were randomly assigned to 2 groups, an SCA group and a control group of healthy participants.

The inclusion criteria for the SCA patients were as follows: the diagnosis confirmation of sickle cell anemia for a period of at least six months prior to enrollment, hemoglobin electrophoresis revealing a genotype HbSS, the determination of the hemoglobin concentration analysis1818 Brandao CF, Oliveira VMB, Santos A, da Silva TMM, Vilella VQC, Simas G, et al. Association between sickle cell disease and the oral health condition of children and adolescents. BMC Oral Health. 2018;18:169. and the absence of painful crisis at the time of the survey, of medical conditions other than SCA, of emergency dental appointments in the past six months, or of a history of clinically health severe conditions (hospitalization and blood transfusion), being regularly monitored by the dental service of SCA at the Yolo Center.

The eligibility criteria for the healthy participant (control group) included the absence of organic, physiologic, or psychiatric disturbances, of intellectual disability, or of emergency dental appointments in the past six months. The exclusion criteria were the inability to meet the above requirements and refusal to participate in the study. The patients enrolled in the groups (SCA group and control group) and those lost to follow-up and their reason is detailed in the flowchart of patients enrolled and randomly followed in the study (Figure 1).

Figure 1
Flow chart of patients enrolled and randomly followed in the Study.

Study variables

The study variables were gender, age, visiting dental service to predict economic situation, dental status (decayed teeth, missing teeth and filled teeth), functional limitations, psychological discomfort, physical inability and physical pain were evaluated.

Data collection and measurements

Interviews and dental exams were performed in the dental service room during the day. Data on the demographics and socioeconomic characteristics were collected through direct questioning of the participants themselves or their parents or guardians. An intra-oral examination on each patient using a disposable mirror, CPI probes and gauzes was performed by 2 experienced and qualified periodontologists.

The assessment of the dental status was made by a clinical examination using a dental mirror and probe. The index of DMFT (Decayed-Missing-Filled Teeth), described by Klein et al.,1919 Klein H, Palmer CE, Knutson JW. Studies on dental caries: a procedure for recording and statistical proceeding of dental examinations findings. J Dent Restorat. 1940;19:243-52. was used to assess the dental state of the participants.2020 World Health Organization. Oral Health Surveys: Basic Methodic. 4th ed. Geneva: World Health Organization; 1997. Score 0: lack of caries, Score 1: Presence of caries, Score 2: Caries filled, Score 3: Filling without caries, Score 4: Loss of teeth before prosthodontics restauration, Score 5: Loss of teeth after prosthodontic restauration and Score 6: Loss of tooth due to the periodontal diseases after prosthodontic restoration. During the clinical examination, the dentist wore personal protective equipment (PPE) that met biosecurity standards.

As for the Oral Health-related Quality of Life (OHrQoL), the Congolese versions of the perception questionnaires,2121 Mantshumba MA, Joke D, Bourleyi SI, Shenda LP, Fidele NB. The effect of partial removable denture use on oral health related quality of life and masticatory function, after 5 years use. Open J Stomatol. 2016;6:201-10. modified from the OHIP-232222 Slade GD, Spencer AJ, Roberts-Thomson K. Tooth loss and chewing capacity among older adults in Adelaide. Aust N Z J Public Health. 1996;20:76-82. were used for participants. The questionnaires were prepared in the French language and helped to conduct a face-to-face pilot interview with 15 patients with Sickle Cell Anemia. After a normality pretest, data were analyzed with the Kolmogorov-Smirnov test and Cronbach’s a correlation coefficient, with p ≥ 0.05, indicating the survey had normal data distribution. The results of the pilot study were not included in the present study. Each question had to be answered by yes or no, depending on whether the participant was satisfied (outcome = 1) or dissatisfied (outcome = 0) about a specific aspect of his or her oral health-related quality of life. The overall oral health-related quality of life per participant was represented by the sum of the outcomes of the individual questions. The questions are similar for both groups.

Statistical analysis

Statistical analysis was performed using the Statistical Package for the Social Sciences (SPSS version 23.0). Descriptive and univariate analyses were performed separately for the SCA group and control group (healthy participants). The responses to categorical questions by the group were compared using either a chi-square test. The ANOVA test was used to compare medians of continuous variables between the SCA and control groups. The p < 0.05 was considered a level of statistically significant difference.

Ethical aspects

This study was authorized by the Research Ethics Committee of the National Center of Research for Dental Sciences in DR Congo-CNRSBD, which approved this study under the protocol number CNRSBD1504.215 and conducted according to the tenets outlined in the Declaration of Helsinki and to the STROBE guidelines. The study included only individuals at least 6 years of age who agreed and signed the Free and Informed Consent Form. Authorizations for the use of the instruments were acquired together with the authors (OHIP23) and the competent guardian.

Results

Of the 214 participants who were included, only 154 remained after correct follow-up until January 2021 (Figure 1) and constituted the final sample, from which the data were collected and statistically analyzed.

There was a male predominance in the SCA group and a female predominance in the control group. The most represented age group was ≤ 10 years in the SCA group and the age group of 11 to 20 years in the control group. The most frequent education level was primary school in the SCA group and middle school in the control group. A higher income was found in the control group. The difference between the SCA group and the control group was significant, as described in Table 1. The DMTF and dmft indexes were higher in the SCA group. The difference between the SCA group and the control group was significant for all the dental status, as described in Table 2. Among the different dimensions of quality of life that were compared between the SCA group the and control group, 15 out of 23 items were significant, as described in Table 3.

Table 1
Socio-demographic characteristics of the sample.
Table 2
Dental status of the sample.
Table 3
Oral health impact profile of sample.

Discussion

Sickle Cell Anemia (SCA) has several common oral manifestations. In the Democratic Republic of the Congo, out of the studies investigated by,1,4,8,12 not one evaluated the SCA for dental tissues and oral health-related quality of life.

The result showed a significant association between dental caries and missing teeth and a more negative impact on the QoL in patients with SCA, as was similar to other authors,1818 Brandao CF, Oliveira VMB, Santos A, da Silva TMM, Vilella VQC, Simas G, et al. Association between sickle cell disease and the oral health condition of children and adolescents. BMC Oral Health. 2018;18:169. meaning that, although most oral problems do not represent an immediate risk of death, they are responsible for decreasing the QoL of individuals, as they prolong states of pain and suffering and cause functional, esthetic, nutritional and psychological problems. Additionally, the morbidity for pain crises is a risk factor for caries and missing teeth.4,23 The minor occurrence of dental caries and missing teeth in the control group may be justified by their high frequency of attending dental visits, while those of the SCA group do not attend dental visits. These participants received major healthcare surveillance provided via access to dental treatment at the SCA Center. This shows the great resilience capacity of patients with chronic diseases, including SCA, to maintain good oral health and to attend periodic annual dental visits.2424 Casey RL, Brown RT. Psychological aspects of hematologic diseases. Child Adolesc Psychiatr Clin N Am. 2003;12:567–84.,2525 Gil KM, Willams DA, Thompson Jr RJ, Kinney TR. Sickle cell disease in children and adolescents: the relation of child and parent pain coping strategies to adjustment. J Pediatr Psychol. 1991;16:643–63.

Certain authors reported that the greater incidence of dental caries in patients with SCA is associated with a poorly structured family context, as well as worse health conditions in socially marginalized areas.1515 Fernandes ML, Kawachi I, Correa-Faria P, Pattusi MP, Paiva SM, Pordeus IA. The impact of the oral condition of children with sickle cell disease on family quality of life. Braz Oral Res. 2016;30:1-21. A higher income was found in the control group (US$ 253 ± 86). The difference between both groups was significant for family income and dental visits. The age of the patients with dental caries and missing teeth in SCA maybe play an important role. The behavior of older patients may differ from that of the younger ones. Teenagers can see the supervision of their parents as a threat to their growing desire for independence, resulting in resistance to the appropriate behaviors for health.2626 Midence K, Fuggle Davies SC. Psychosocial aspects of sickle cell disease (SCD) in childhood and adolescence: a review. Br J Clin Psychol. 1993;32:271–80. The knowledge of the association between dental caries and tooth loss in the SCA group allows dentists to gain a greater understanding of the problem and the role of dentists in overall health. Regardless of the effect of SCA on dental tissues, the oral health of this population needs a preventive measure against infections that could precipitate a vaso-occlusive crisis with other complications.1212 Mutombo MA, Nyimi BF, Kanyana M, Ngueyi K, Mantshumba MA. Management of odontogenic abscessing patients with sickle cell anemia: 5 cases reports. Br J Med Med Res. 2017; 20:1-5.,2727 Almeida TF, Vianna MI, Cabral MB, Cangussu MC, Floriano FR. Family context and incidence of dental caries in preschool children living in areas covered by the Family Health Strategy in Salvador, Bahia State, Brazil. Cad Saúde Publica. 2012;28 (6):1183–93. However,2828 Possos CP, santos PR, Aguiar MC, Cangussu MC, Toralles MB, da Silva MC. Sickle cell disease does not predispose to caries or periodontal disease. Spec Care Dentistry. 2012;32 (2):55–60. found that SCA does not predispose an individual to dental caries. Prevention of disease, disability and suffering should be a primary goal of each society that hopes to provide a decent quality of life for its people. Prevention on the community- or population-based level is the most cost-effective approach and has the greatest impact on a community or population, whether it is a school, neighborhood, or nation. Many different approaches to preventing dental diseases exist and the most cost-effective method is health education.

The quality of life for patients with SCA is critical in determining the process of health and disease. There was a difference in the OHrQoL among the SCA and control groups, similar to that of Ralstrom et al.2929 Ralstrom E, da Fonseca MA, Rhodes M, et al. The impact of sickle cell disease on oral health-related quality of life. Pediatr Dent. 2014;36(1):24–8. This study only included participants who were not suffering from a painful crisis at the time of the survey, medical conditions other than SCA and emergency dental appointments in the past six months. These facts may have led to evaluating only participants in good health, masking the OHrQoL during the acute pain that is a characteristic of SCA. The concept of quality of life related to oral health requires consideration not only of factors, such as malaise, pain, or functional changes, but should also include emotional aspects and social functions associated with oral health. Oral health is a significant component in the general quality of life of people, with important implications for their health status. The SCA severity is associated with the vasculature vaso-occlusion and may account for the pain experienced.3030 Kawar N, et al. Sickle cell disease: an overview of orofacial and dental manifestations. Br Dent J. 2018;185(2):90–2.,3131 Laurence B, Haywood Jr C, Lanzkron S. Dental infections increase the likelihood of hospital admissions among adult patients with sickle cell disease. Community Dent Health. 2013;30:168–72.

Our findings related to the OHIP-23 showed that the participants enrolled in the control group were most satisfied with the oral health-related quality of life than the participants of the SCA group. The difference between both groups was significant for 15 out of 23 items: mastication, bad pronunciation, affected appearance, breathing, bad taste, affected food intake, difficult adaptation, pain in the jaw, dental sensitivity, dental pain, disquiet/miserable or unhappy, esthetic, unclear speech, lack of appetite and upset stomach. Lower income may be associated with lower oral health, as well as lower access to preventive health care information.3232 Meneghim Mde C, Kozlowski FC, Pereira AC, Ambrosano GM, Meneghim ZM. A socioeconomic classification and dental fluorosis. Cien Saúde Colet. 2007;12:523–9.,3333 Laurence B, George D, Woods D, et al. The association between sickle cell disease and dental caries in African Americans. Spec Care Dent: Off Public Am Assoc Hosp Dent, Acad Dent Handicapped, Am Soc Geriatr Dent. 2006;26:95–100.

The main limitation of this study was the fact we examined a specific population from Kinshasa, the capital of the Democratic Republic of the Congo. In addition, it is important to mention that the present results are of insufficient conclusiveness because only one oral index for clinical evaluation (DMFT) was used, as well as the fact that the analyses of some different domains related to quality of life were not included, but will be necessary for future studies. Prospective studies with larger samples may provide a better understanding of the relationship between SCA and dental tissues and the oral health-related quality of life.

Conclusion

Considering the findings of our study, dental caries are associated with sickle cell anemia and they negatively impact the quality of life. To prevent the occurrence of dental caries and tooth loss and to avoid complications in the general health of patients with SCA, the inclusion of dental visits and dental care in the management strategy of patients with SCA should be considered. The negative impacts that poor oral health of the population have on their QoL make this issue a relevant problem for public health. Consequently, dentists have an important role in preventing health complications in patients with SCA.

Acknowledgments

This study received support from the National Center of Research in Dental Sciences, Kinshasa, Democratic Republic of the Congo. The authors would like to thank Professor Frans Vinckier, Professor Joke Duyck and Doctor Philippe Vuylsteke from KU Leuven University for their support and collaboration.

REFERENCES

  • 1
    Mikobi TM, Lukusa PT, Aloni MN, et al. Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the a3.7triplication in Congolese patients than in worldwide series. J Clin Lab Anal. 2018;32:e22186.
  • 2
    De Franceschi L, Corrocher R. Established and experimental treatment for sickle cell disease. Haematologica. 2004;89: 348-56.
  • 3
    Fonseca MA, Oueis HS, Casamassimo PS. Sickle cell anemia: a review for the pediatric dentistry. Pediatr Dent. 2007;29(2): 159-69.
  • 4
    Kanyana M, Mutombo M, Leta L, Nyembue T, Mantshumba M. Motifs de consultation des drépanocytaires au service de stomatologie du centre de médecine mixte et d’anémie SS/Yolo en République Démocratique du Congo. J de l’IRSS. 2016;2:83-8.
  • 5
    Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN. Global burden of sickle cell anemia in children under FIVE, 20102050: modeling based on DEMOGRAPHICS, excess mortality, and interventions. PLoS Med. 2013;vol.10(no.7).
  • 6
    Agasa B, Bosunga K, Opara A, Tshilumba K, Dupont E, Vertongen F, Cotton F, Gulbis B. Prevalence of sickle cell disease in a northeastern region of the Democratic Republic of Congo: what impact on transfusion policy? Transfus Med Oxf Engl. 2010;20:62-5.
  • 7
    Mayank K, Kristen H, Megha S, Szilva A, Leslie S, Adela. Orofacial manifestation and dental management of sickle cell disease: a scooping review. Anemia. 2021. https://doi.org/10.1155/5556708. ID 5556708.
    » https://doi.org/10.1155/5556708. ID 5556708.
  • 8
    Tshilolo L, Aissi LM, Lukusa D, Kinsiama C, Wembonyama S, Gulbis B, Vertongen F. Neonatal screening for sickle cell anemia in the Democratic Republic of the Congo: experience from a pioneer project on 31204 newborns. J Clin Pathol. 2009;62: 35-8.
  • 9
    U.S. Department of Health and Human Services, (n.d.). Sickle Cell Disease. Bethesda, MD, USA: National Heart Lung and Blood Institute; 2021.
  • 10
    Switzer JA, Hess DC, Nichols FT, Adams RJ. Pathophysiology and treatment of stroke in sickle cell disease: present and future. Lancet Neural. 2006;5(6):501-12.
  • 11
    Fernandes ML, Kawachi I, Correa-Faria P, Pattusi MP, Paiva SM, Pordeus IA. Caries prevalence and impact on oral health related quality of life in children with sickle cell disease: cross-section study. BMC Oral Health. 2015;15:68. https://doi.org/10.1186/s12903-015-0052-4
    » https://doi.org/10.1186/s12903-015-0052-4.
  • 12
    Mutombo MA, Nyimi BF, Kanyana M, Ngueyi K, Mantshumba MA. Management of odontogenic abscessing patients with sickle cell anemia: 5 cases reports. Br J Med Med Res. 2017; 20:1-5.
  • 13
    yue Hui, xu Xinxin, Liu Qin, Li Xiaozhi, jiang Wei, Hu Bo. Association between sickle cell disease and dental caries: a systemic review and meta- analysis. Hematology. 2020;25(1): 309-19.
  • 14
    Petersen PE. The World Oral Health Report 2003; continuous improvement health in the 21st century approach of the WHO Global oral health Program. Community Dent Oral Epidemiol. 2003;321:3-24.
  • 15
    Fernandes ML, Kawachi I, Correa-Faria P, Pattusi MP, Paiva SM, Pordeus IA. The impact of the oral condition of children with sickle cell disease on family quality of life. Braz Oral Res. 2016;30:1-21.
  • 16
    Slade GD, Spencer AJ. Development and evaluation of the oral health impact profile. Community Dent Health. 1994;11:3-11.
  • 17
    Spanemberg JC, Cardoso JA, Slob EMGB, López-López J. Quality of life related to oral health and its impact in adults. J Stomatol, Oral Maxillofac Surg. 2019;120(3):234-9.
  • 18
    Brandao CF, Oliveira VMB, Santos A, da Silva TMM, Vilella VQC, Simas G, et al. Association between sickle cell disease and the oral health condition of children and adolescents. BMC Oral Health. 2018;18:169.
  • 19
    Klein H, Palmer CE, Knutson JW. Studies on dental caries: a procedure for recording and statistical proceeding of dental examinations findings. J Dent Restorat. 1940;19:243-52.
  • 20
    World Health Organization. Oral Health Surveys: Basic Methodic. 4th ed. Geneva: World Health Organization; 1997.
  • 21
    Mantshumba MA, Joke D, Bourleyi SI, Shenda LP, Fidele NB. The effect of partial removable denture use on oral health related quality of life and masticatory function, after 5 years use. Open J Stomatol. 2016;6:201-10.
  • 22
    Slade GD, Spencer AJ, Roberts-Thomson K. Tooth loss and chewing capacity among older adults in Adelaide. Aust N Z J Public Health. 1996;20:76-82.
  • 23
    Patel J, Serjeant GR. Newborn screening for sickle cell disease in India: the need for defining optimal clinical care. Indian J Pediatr. 2014;81:229-30.
  • 24
    Casey RL, Brown RT. Psychological aspects of hematologic diseases. Child Adolesc Psychiatr Clin N Am. 2003;12:567–84.
  • 25
    Gil KM, Willams DA, Thompson Jr RJ, Kinney TR. Sickle cell disease in children and adolescents: the relation of child and parent pain coping strategies to adjustment. J Pediatr Psychol. 1991;16:643–63.
  • 26
    Midence K, Fuggle Davies SC. Psychosocial aspects of sickle cell disease (SCD) in childhood and adolescence: a review. Br J Clin Psychol. 1993;32:271–80.
  • 27
    Almeida TF, Vianna MI, Cabral MB, Cangussu MC, Floriano FR. Family context and incidence of dental caries in preschool children living in areas covered by the Family Health Strategy in Salvador, Bahia State, Brazil. Cad Saúde Publica. 2012;28 (6):1183–93.
  • 28
    Possos CP, santos PR, Aguiar MC, Cangussu MC, Toralles MB, da Silva MC. Sickle cell disease does not predispose to caries or periodontal disease. Spec Care Dentistry. 2012;32 (2):55–60.
  • 29
    Ralstrom E, da Fonseca MA, Rhodes M, et al. The impact of sickle cell disease on oral health-related quality of life. Pediatr Dent. 2014;36(1):24–8.
  • 30
    Kawar N, et al. Sickle cell disease: an overview of orofacial and dental manifestations. Br Dent J. 2018;185(2):90–2.
  • 31
    Laurence B, Haywood Jr C, Lanzkron S. Dental infections increase the likelihood of hospital admissions among adult patients with sickle cell disease. Community Dent Health. 2013;30:168–72.
  • 32
    Meneghim Mde C, Kozlowski FC, Pereira AC, Ambrosano GM, Meneghim ZM. A socioeconomic classification and dental fluorosis. Cien Saúde Colet. 2007;12:523–9.
  • 33
    Laurence B, George D, Woods D, et al. The association between sickle cell disease and dental caries in African Americans. Spec Care Dent: Off Public Am Assoc Hosp Dent, Acad Dent Handicapped, Am Soc Geriatr Dent. 2006;26:95–100.

Publication Dates

  • Publication in this collection
    11 Nov 2024
  • Date of issue
    2024

History

  • Received
    20 Oct 2022
  • Accepted
    08 Aug 2023
  • Published
    19 Oct 2023
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular (ABHH) R. Dr. Diogo de Faria, 775 cj 133, 04037-002, São Paulo / SP - Brasil - São Paulo - SP - Brazil
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